This review summarizes evidence on the smoking/lung cancer relationship, based on the author's 50 years’ experience. It starts by illustrating variations in national rates by time and sex. It then demonstrates that the relationship of smoking to overall lung cancer risk is strong, consistently seen and dose‐related with amount smoked, duration, age of start and time of quitting. Relative risks vary markedly by country, but little by sex, age, race, occupation, genetics and other factors. Though precisely estimating the smoking risk is difficult, the relationship is clearly causal, not explained by bias or confounding. The risk from smoking is reduced in lower tar filter cigarettes, and essentially independent of mentholation and type of curing. Lung cancer risk is not increased by smokeless tobacco use. The relative risk is much greater for squamous/small‐cell carcinoma than for adeno/large‐cell carcinoma. The argument that the increasing ratio of squamous to adenocarcinoma results from changes in cigarettes is shown to be weak, the increase also being seen in never smokers, starting before filters were introduced, and associated with diagnostic changes. Most of the weak association of lung cancer with passive smoking is explicable by confounding and by misclassification of some ever smokers as never smokers.
- lung cancer
- dose response
- quitting smoking
- tar reduction
- histological type
- passive smoking
While, at the beginning of the twentieth century, lung cancer was a rare disease, it was diagnosed progressively more often over the next 50 years, and various suggestions were made during this period that cigarette smoking might be the cause, deriving mainly from the simple fact that the incidence and cigarette consumption were increasing concomitantly . Although earlier case‐control studies had been conducted in Germany [2, 3], it was not until studies in the UK  and in the USA  published in the 1950s that serious attention was given to the possibility that smoking might cause lung cancer. Following additional evidence from a number of large prospective studies, the US Surgeon General concluded  that ‘cigarette smoking is a cause of lung cancer in men, and a suspected cause of lung cancer in women’, and later reports [7–9] have confirmed and extended the conclusions.
Following a section which concerns trends in lung cancer rates, this review summarizes the evidence on a number of aspects of the relationship of smoking with lung cancer, and also considers the evidence on environmental tobacco smoke (ETS) or ‘passive smoking’. In general, less attention is given to those aspects that are well‐known and non‐contentious, while dealing more fully with areas where the evidence is more open to interpretation. Concentration also tends to be in areas where the author and his colleagues have been involved in detailed reviews of the evidence. As the author has some 50 years of experience, this covers quite a wide range of topics, though not all.
2. Trends in lung cancer rates
Figure 1 shows trends in lung cancer rates in eight countries over the period 1946–2010. They are presented separately for males and females and for age 15+, weighted according to the age distribution of the European standard population. As can be seen, rates in males always substantially exceed rates in females. While in each country rates in males have risen to a peak and then declined, rates of females have tended to rise over the whole period, though there is evidence of flattening out in some countries. The differing trends in the two sexes are consistent with differing trends in the take up of smoking, which can be clearly seen in the detailed data presented in International Smoking Statistics .
For both sexes, there is striking variation by country in the trends seen. Points to note are the relatively low rates in Sweden and in Japan, and the rapidly accelerating rates in Hungary, so that in males, rates are now almost double those elsewhere. It is interesting that the lung cancer rates in Canada and the USA are so similar, given the type of tobacco predominantly used in Canada is made only from flue‐cured tobacco, while American cigarettes are blended, a topic discussed further in Section 3.5.
Trends in the UK are markedly different from those in other countries, particularly in males. In the 1950s, rates in males were much higher than in other countries, but following a much earlier and steeper decline than elsewhere, are now below those in all countries except Japan and Sweden. In 1998, Lee and Forey  attempted to determine whether the trends could be fully explained by trends in cigarette consumption, concluding that they could not, with factors other than cigarette smoking contributing importantly to risk. A contributor to the declining trend may have been the introduction of the Clean Air Act in the UK in 1956.
The trends in the UK are very different from those in the USA. Thus, UK rates, once much higher than in the USA, are now lower in both sexes. To some extent, this may have coloured differing national opinions on the benefits (or otherwise) of changes from high tar plain cigarettes to low‐tar filtered cigarettes. In 2003, Lee and Forey  looked in detail at the question as to why the trends in the US and UK are so different. Their analyses took into account detailed data on trends in the age of starting and stopping smoking, amount smoked per smoker and tar levels, and demonstrated clearly that the differing trends in lung cancer rates could not be explained by these factors. They concluded that the explanation must lie in changes over time in aspects of smoking not considered in the analyses and/or exposure to risk factors other than smoking. Evidence relating to a number of possible such smoking variables or other risk factors was considered, but no clear explanation of the differing trends could be found. Lee and Forey  also criticised views expressed in NCI Monograph 13 , in particular that tar reduction has been ineffective in lowering lung cancer risk, and that trends in US lung cancer rates fit in well with trends in smoking habits.
3. Relationship of smoking to overall lung cancer risk
In order to describe the main characteristics of the relationship, this section leans heavily on a recently published systematic review with meta‐analysis by Lee et al. . This involved all epidemiological studies published before 2000 which included at least 100 lung cancer cases, and which provided relevant information on risks associated with smoking. The meta‐analyses involved almost 300 studies, far more than in any other published meta‐analysis.
3.1. Dose‐related increase in risk in current and former smokers
Although the relative risk (RR) estimates vary considerably between studies, the evidence of an association is extremely clear from the meta‐analyses , with overall random‐effects relative risk estimates of 5.50 (95% confidence interval [CI] 5.07–5.96) for ever smokers, 8.43 (7.63–9.31) for current smokers and 4.30 (3.93–4.71) for ex‐smokers, these
That there is a tendency for the RR to increase with number of cigarettes smoked per day is abundantly clear. Because studies vary in the groupings used to categorize amount smoked, analyses were included in the systematic review  comparing ever smoking
Later Fry et al. , based on model‐fitting techniques, successfully fitted the linear with baseline model log e RR = 0.833 log e (1 + 0.81c ) to 97 independent data blocks, where
For years smoked, the shape of the dose response was best fitted by a power model log e RR = 0.792 (y / 10 ) 0.74, where
Although there is uncertainty as to the actual shape of the true dose‐relationship, and misclassification of smoking status and dose may bias the fitted relationships to some extent, it is abundantly clear that risk of lung cancer increases markedly with increasing dose, whether quantified by increased daily amount smoked, increased duration of smoking, or earlier age of starting to smoke.
It is also clear that risk declines, relative to continuing smokers, in those who quit smoking. This is evident, not only from the lower
A later paper , investigated whether the decline in RR of lung cancer following quitting (expressed relative to never smokers) could be adequately fitted by a simple, negative exponential, model. In this model, the excess relative risk ER (=
As shown subsequently , the negative exponential model can quite simply be adapted to predict risk following changes in exposure more generally. The adaptation was shown to satisfactorily predict results from those (relatively few) studies that have investigated the effect of reducing cigarette consumption, and suggests it may be useful for predicting changes in risk following switching to a reduced exposure product.
3.2. Factors affecting risk
The age‐specific absolute risk of lung cancer is known to be related to many factors other than smoking. These include alcohol, occupation, air pollution, diet, viruses and genetic factors .
However, the evidence considered in this section relates not to which factors modify the risk of lung cancer, but to which affect the RR associated with smoking.
There has been considerable discussion about whether smoking increases the risk of lung cancer more in women than in men, e.g. . Based on the systematic review of Lee et al. , there was little evidence of any difference, though RR estimates generally tended to be higher for men than for women. This conclusion was supported by additional analyses comparing
Though the absolute risk of lung cancer rises steeply with age, both in never and ever smokers, it is far less clear whether the RR also does, particularly when the great majority of published studies do not give results by age. However, a number of studies considered in the systematic review  did provide RR estimates for ever or current smoking separately by age, and it was possible to carry out meta‐analyses based on the ratio within study of the estimate for the oldest age group for which data were available, compared to that for the youngest. While the meta‐analysis did show a significantly higher risk in the oldest age group, the estimated average ratio (1.17, 95% CI 1.10–1.25) was quite modest. Clearly, any variation in RR by age is much smaller than the RR itself.
There is a striking variation between study locations in the estimated RR associated with smoking. For current smoking, where the overall RR estimate for the sexes combined from meta‐analyses , based on 195 estimates, was 8.43 (95% CI 7.63–9.31), the estimate was higher than this for studies based in North America (11.68, 10.61–12.85), and markedly lower than this for studies in China (2.94, 2.23–3.88), Japan (3.55, 3.05–4.14), and other parts of Asia (2.90, 2.04–4.13), with estimates intermediate in the United Kingdom (7.53, 5.40–10.50), Scandinavia (8.68, 7.14–10.54) and other parts of Europe (8.65, 5.98–12.51). The pattern of variation by location is similar if comparisons are based on ever rather than current smoking. The extent to which these quite clear differences are due to the product smoked, amount smoked, genetics or other factors, is a question which deserves further attention.
The systematic review  generally showed a tendency for
Few studies considered in the systematic review  provided comparable
Other risk factors were not considered in detail in the systematic review . However, reference is briefly made below to some of these.
3.2.6. Asbestos and other occupational exposures
It is well‐known that asbestos exposure increases risk of lung cancer, though the increase depends materially on the type of asbestos. In an early large study of US insulation workers 
There are, of course, numerous occupational factors which affect risk of lung cancer. Nearly all, such as arsenic, chromium, nickel, chloromethyl ethers and polycyclic aromatic hydrocarbons increase risk, though a reduced risk has been reported for exposure to endotoxins . The author is not aware of any occupation known to materially affect the RR associated with smoking. As smokers are more likely to work (or have worked) in ‘dirty’ occupations, there is a possible confounding effect of occupation. However, numerous epidemiological studies have adjusted for occupation (or indicators of it such as social grade) and the systematic review  found that the RR for smoking was hardly affected at all by the extent of adjustment for other risk factors.
3.2.7. Genetics and family history
A review by Lee in 1993  considered the limited evidence then available on family history, concluding that risk was approximately doubled in those who have a relative with lung cancer. The association has been confirmed in a recent pooled analysis  of data from 24 studies, with the RR of lung cancer associated with having a first degree relative with lung cancer estimated as 1.51 (1.39–1.63). The
The demonstration of an association of family history with lung cancer does not necessarily prove there is a genetic determinant of lung cancer, as family members may share aspects of smoking such as amount smoked, depth of inhalation and type of product smoked, or be exposed to common environmental factors other than smoking (e.g. heating and cooking practices). In recent years, there have been a very large number of studies aiming at looking more directly at how a whole range of genotypes are associated with lung cancer risk or with propensity to smoke. The author's impression of the literature is that associations reported are often non‐significant and never strong. Even for well‐studied relationships, such as chromosome 15q25, the evidence [28–31] only suggests that the variants are associated with an increased cigarette consumption of about one cigarette per day, and an increased lung cancer risk of about 30–50%. Furthermore, evidence obtained on whether the variants differentially affect lung cancer risk in never smokers is very limited. There seems to be no evidence that
3.3. Difficulties in the precise estimation of risk from smoking
3.3.1. Inaccuracy of diagnosis of lung cancer
A review in 1994 by Lee  demonstrated substantial evidence of disagreement between autopsy, clinical and death certificate diagnosis of lung cancer. Even though autopsy does not ensure 100% accuracy even if clinical history is taken into account, it offers the possibility of substantially improving the level of accuracy of death certificate data, which is affected by fashion and the particular interests and perceptions of certifying doctors. For example, knowledge that a person is a smoker affects diagnostic procedures so that lung cancer in a non‐smoker is less likely to be detected clinically than in a non‐smoker. The review also bemoaned the decline in autopsy rates, noting that advances in clinical diagnostic techniques seem not to be compensating for this in reducing inaccuracy.
While in many Western countries, autopsy rates are very low, this is not so in Hungary, or other countries in the old Austro‐Hungarian empire. Autopsies were for many years routinely carried out there on all patients dying in hospital. A study there  showed a substantial discrepancy between pre‐ and post‐autopsy diagnosis. In that study, 59% (36/61) of lung cancer seen at autopsy were not detected pre‐autopsy, while 50% (25.50) of those diagnosed pre‐autopsy were not confirmed at autopsy. Accuracy of diagnosis increased with the number of diagnostic techniques applied, but was still far from perfect in the absence of necropsy. Under‐diagnosis was commoner in non‐smokers and over‐diagnosis commoner in smokers. Although improved diagnostic procedures could have increased accuracy of diagnosis, the results certainly imply the possibility of considerable bias to the estimated RR for lung cancer and smoking.
3.3.2. Inaccuracy in determining smoking habits
In comparing the risk of ever smokers and never smokers, random misclassification of smoking habits tends to dilute any true association with lung cancer risk. Thus, if the true
3.3.3. Confounding factors
In the systematic review of Lee et al.  adjustment for age and other factors was found to have very little effect on the overall estimate of the RR associated with smoking. The conclusion of a minimal effect of confounding is consistent with that from an analysis of data from the very large US Cancer Prevention Study II . It is in any case clear that the smoking RR is too large to be explained by confounding. For an RR which comfortably exceeds 10 for heavy smokers to be an artefact of confounding would require there to be another risk factor which is both extremely strongly related to lung cancer and to which smokers are very much more commonly exposed than non‐smokers. While some rare risk factors (e.g. bis(chloromethyl)ethyl exposure) increase lung cancer risk very markedly, and smokers and non‐smokers do differ in a range of characteristics, no factor (or group of factors) has emerged which can come close to explaining the observed RR for smoking in terms of confounding. Certainly there is no good evidence to support early theories by Fisher  and Burch  that the association of smoking with lung cancer might be totally explained by genetic factors. This theory seems, in any case, to be refuted by the observation that in smoking‐discordant identical twins, risk of lung cancer was much higher in the twin who smoked [37–38].
Confounding is a more relevant issue when considering the dose‐related aspects of smoking. As shown in the systematic review , adjustment for other aspects of smoking (typically including amount smoked) consistently reduces associations of lung cancer risk with age of starting to smoke, duration of smoking, years quit and tar level. This is because earlier starters and high tar smokers tend to smoke more heavily than do later starters and low‐tar smokers, and lighter smokers tend to be more ready to quit smoking.
3.3.4. Publication bias
The tendency for researchers to be more likely to want to publish, and editors more likely to accept for publication, studies finding a statistically significant association may cause important bias for some relatively weak associations of exposure to disease [39, 40]. However, the association of smoking with lung cancer is too strong and consistently reported for publication bias to be a material explanation of the strong relationship.
3.3.5. Recall bias
In case‐control studies, the smoking habits reported by a case may be affected by knowledge of the disease, particularly where the disease is widely reported to be caused by smoking. However, the fact that smoking
3.3.6. Assessment of conclusions
While there are a number of factors that affect precise estimation of the risk of lung cancer from smoking, it is very clear that smoking is an important determinant of risk. Looking back at the Bradford Hill criteria for determining whether an association is due to causation  the available evidence discussed above clearly demonstrates strength, consistency, temporality (with the exposure preceding the disease) and biological gradient (or dose response). The relationship also satisfies plausibility, given the numerous known carcinogens in tobacco smoke, and coherence, the evidence not conflicting with known facts concerning the natural history and biology of lung cancer. There is also experimental evidence, partly in humans in relation to the decline of risk following quitting, and partly in animals, with exposure to tobacco for having been shown to increase risk of skin cancer in mice and exposure to tobacco smoke having been shown to elicit lung tumours in rodents . One could also argue analogy with regular inhalation of other pollutants increasing risk of lung cancer. Of the nine Bradford Hill criteria, the only one it fails is specificity. Smoking is clearly not a necessary condition for lung cancer to arise, inasmuch as there are other causes of lung cancer. Nor is it sufficient, as many smokers do not contract the disease. Though some old dictionary definitions appear to equate ‘cause’ to ‘necessary and sufficient cause’, this is not what is meant by saying that smoking causes lung cancer.
3.4. Types of product
While in most countries the majority of cigarette smokers smoke manufactured cigarettes, with relatively few smokers using hand‐rolled cigarettes, in some countries, e.g. the Netherlands and Norway, hand‐rolled smoking is relatively common . The systematic review of studies in the 1900s  included 20 independent within‐study estimates of the ratio of risk in hand‐rolled versus manufactured cigarette smokers, which produced a combined
That systematic review  also included results indicating that the RR of lung cancer was substantially lower for smokers of pipes and cigars than for cigarette smokers. Thus, for current smoking, while the
There has been considerable research into the health risks of smokeless tobacco in Western populations, mainly based on data for Sweden, where a type of moist snuff known as snus is the dominant product, and for the USA, where chewing tobacco is common, and moist and dry snuff are also used [43–45]. The results provide no indication of any increased risk of lung cancer associated with smokeless tobacco use. They may help to explain the relatively low risk of lung cancer in Sweden (see Figure 1), where snus use is a common alternative to cigarette smoking.
3.5. Type of manufactured cigarette
Over the second half of the last century, the characteristics of manufactured cigarettes have changed substantially . In the mid‐1950s, cigarettes were typically of the non‐filter plain variety with average tar levels exceeding 30 mg/cigarette. By now, nearly all cigarettes smoked have filters and average tar levels are around 10 mg/cigarette in many countries. Nicotine yields per cigarette have reduced by a similar factor.
An important question is whether these changes, introduced in order to reduce risk, have actually done so. Two points are worth making at the outset. The first is that, though the observed rise in RR for current smokers over the second half of the last century which was noted above would appear to suggest that the risk of cigarettes might have increased, this is not necessarily so, as changes in average duration of smoking by smokers have clearly had a major effect, and may mask any effects of the switch to lower tar filter cigarettes.
The second is that there is clear evidence of what is commonly termed ‘compensation’. Thus, whereas one might expect smokers switching from cigarettes with a nicotine yield (machine‐measured under standard smoking conditions) of, say, 2 mg/cigarette, to cigarettes with a nicotine yield of 1 mg/cigarette to halve their nicotine uptake, the reduction in measured dose is typically much less than this. This may, in theory, be because smokers increase their daily consumption or because they change how they smoke the cigarettes, the second possibility being more plausible given that consumption per smoker has changed little over the years in most countries .
Scherer and Lee  recently reviewed the available evidence on the extent of compensation, based partly on brand‐switching and partly on cross‐sectional studies. Using estimates based on nicotine biomarkers, commonly cotinine, they estimated a weighted mean compensation index of 0.781 (95% CI 0.720–0.842), where a value of 1 indicates complete and 0 no compensation. The index is estimated from a formula in which the biomarker,
Various reviews have assessed the evidence on risk associated with the switch to lower tar filter cigarettes. In one of the earliest reviews , it was calculated, based on 43 sex‐specific estimates, that the risk of lung cancer was 36% lower (95% CI 27–44%) in filter than in plain cigarettes, and 23% lower (95% CI 27–44%) for lower than higher tar cigarettes. The estimated reduction, seen in both sexes, equated to 2–3% risk reduction per mg tar per cigarette. Following publication of a report by the National Cancer Institute  claiming that the apparent benefits of lower delivery cigarettes may be illusory if
It should be noted that the evidence considered is limited by the range of tar levels tested in any one study being often quite small (as all long‐term smokers have experienced reducing tar levels), and also by there being essentially no evidence on risk of ultra‐low (≤3 mg) tar cigarettes. Also, there are various other limitations, including difficulties in obtaining individual results in a comparable format, inadequate reporting of results, possible unreliability of the data recorded on cigarette type, and lack of adjustment in some studies for potential confounding variables. However, the results clearly suggest that the switch to lower tar filter cigarettes has been beneficial, though the benefit has been substantially reduced by compensation.
That cigarette mentholation might increase risk of lung cancer has some plausibility. First, the acute respiratory effects of menthol might affect inhalation of cigarette smoke, and secondly, in the USA, Black men (who have a very strong preference for mentholated cigarettes) have lung cancer rates that are substantially higher than those for White men. However, a systematic review by Lee  concluded that the epidemiological evidence is actually consistent with mentholation having no effect on the lung carcinogenicity of cigarettes. That review identified eight generally good quality studies, all but one conducted in the USA, which gave a combined RR estimate for ever versus never use of mentholated cigarettes of 0.93 (95% CI 0.84–1.02), with no significant evidence of any effect in males or females, or in Blacks or Whites. Noting also that, in the USA, Black women (who also have a very strong menthol preference) have lung cancer rates which are no higher than in Whites, the high rates in Black men cannot be explained by their greater preference for mentholated cigarettes.
Based on the tobacco they include, most cigarettes sold can be divided into two categories; flue‐cured (or 100% Virginia) cigarettes, and blended (or American blended) cigarettes. The tobacco in flue‐cured cigarettes is cured over a short period (about a week) at high temperatures, while blended cigarettes are based on three types of tobacco (flue‐cured, Burley or Oriental) blended together . Burley and Oriental tobaccos are air‐cured over a period of about 6 weeks, the three tobacco types being genetically different. Different countries tend to predominantly use the different types of cigarettes. For example Austria, Denmark, Germany and the US use mainly blended cigarettes, while Australia, Canada and UK use mainly flue‐cured cigarettes . Comparing lung cancer risk for smokers of flue‐cured and blended cigarettes is not straightforward since epidemiological studies are typically conducted in a single country where the smokers are likely to all (or virtually all) use one cigarette type or the other. An alternative approach tried by Lee et al.  was to compare lung cancer risk (for 1971–2000) by sex, age and period for those four countries listed above which traditionally use blended cigarettes, and those three listed countries which use flue‐cured cigarettes. The comparisons were made both unadjusted and adjusted for prevalence of current and former smoking and for consumption per smoker. This approach was not particularly sensitive, due to the limited number of countries which (a) could both be clearly categorized by type, (b) had relevant data available and (c) did not have a large proportion of smokers of products other than cigarettes. However, it did not suggest any material effect of cigarette type on risk. Particularly noteworthy are the quite similar lung cancer rates and trends in the USA and in Canada shown in Figure 1, with one country using blended and the other flue‐cured cigarettes.
4. Differential effect of smoking on histological type of lung cancer
4.1. Classification and diagnosis of histological type
The classification of lung cancer based on its microscopic characteristics, formulated nearly 100 years ago , has changed little in general structure, with the great majority of lung cancers classified into one of four basic types—squamous cell carcinoma, adenocarcinoma, small‐cell carcinoma and large‐cell carcinoma. However, successive WHO classifications [51–53] have differed in how tumours should be ascribed to these types, and there are considerable difficulties in ensuring an accurate and consistent diagnosis, with evidence of intra‐ and inter‐observer variability of classification [54–56]. Part of the problem lies in the morphological heterogeneity of lung cancers with some tumours, and occasionally even in a single tissue block, presenting evidence of more than one type of lung cancer . It is also clear that the morphological type of tumour is influenced by its site within the lung and by how the specimen was obtained.
4.2. Variation in relative risk of lung cancer by histological type
In their systematic review of studies published in the twentieth century , Lee et al. presented a range of RR estimates, not only for all lung cancer but also for squamous cell carcinoma. More limited results are also shown for small‐cell and large‐cell carcinoma. For current smoking overall
For all lung cancer types
4.3. Possible explanations for the time shift in the relative frequency of adenocarcinoma and squamous cell carcinoma
A shift in the relative frequency of adenocarcinoma to squamous cell carcinoma over time has been clearly evident in many countries , and in 2014, the US Surgeon General  argued that the increasing incidence and relative frequency of adenocarcinoma has resulted ‘from changes in the design and consumption of cigarettes since the 1950s’. The argument that the switch from higher tar, plain cigarettes to lower tar, filtered cigarettes is responsible for the rise in adenocarcinoma had been made previously [60–62] and supported by various researchers [63, 64]. However, there are a number of reasons which indicate that this conclusion is, to say the least, over‐simplistic.
One reason for doubting the claim is that the observed shift in the relative frequency of adenocarcinoma to squamous cell carcinoma began well before the increase in consumption of low‐tar filtered cigarettes started .
Had there been an adverse effect of low‐tar filter cigarettes on risk of adenocarcinoma, one might have expected to see that for adenocarcinoma, the filter versus plain RR would be significantly increased. However, this is not the case [14, 42, 47], the systematic review  giving
Although the US Surgeon General  dismissed changes in diagnostic procedures as unimportant, there is quite clear evidence they are relevant, as indicated by three facts. First, schemes for classifying histological type of lung cancer have changed over time, notable being the reallocation of one of the four classes of large‐cell carcinoma in the WHO classification  to adenocarcinoma in the 1981 classification . Secondly, large studies where diagnoses of histological type made some years earlier were reviewed later by pathologists using later classification schemes generally report an increase in numbers of adenocarcinoma . Finally, studies using standard criteria to review cases collected over a period of at least 10 years found no increase in the proportion of lung cancers classified as adenocarcinoma [68, 69]. Interestingly one of those studies  reported a substantial rise in the rate of bronchioloalveolar carcinoma, which affected smokers and non‐smokers alike, and which the authors suggested may have a viral origin.
A huge weakness in the Surgeon General's argument  is that it would predict that the shift from squamous cell carcinoma to adenocarcinoma would be confined to smokers. Two pieces of work clearly indicate that there has been a clear change in never smokers. An analysis in 2013  indirectly estimated absolute lung cancer mortality rates by smoking habit, time period‐ and histological‐type‐based studies published in the twentieth century, coupled with WHO mortality data for the same country and period. Thus, while in never smoker rates of squamous cell carcinoma per 100,000 per year were estimated to vary little by time period (7.6, 12.6, 12.7, 10.2 and 11.6 for, respectively, 1930–1960, 1961–1970, 1971–1980, 1981–1990 and 1991–1999) the corresponding rates for adenocarcinoma increased sharply for the same time period, (6.9, 17.0, 18.1, 29.0 and 33.9).
The change in never smokers is illustrated more clearly in a recent publication  which examined how the proportion of adenocarcinoma in never smokers varied by time, sex and region, based on 219 sex‐ and period‐specific blocks of data drawn from 157 publications. Compared to the period 1950–1960, the ratio of adenocarcinoma to squamous cell carcinoma was higher by factors of 1.67, 1.97, 2.35 and 3.93 for, respectively, 1970–1979, 1980–1989, 1990–1999 and 2000 onwards. This publication presents arguments that the time trends could not be explained by changes in ETS exposure, or misclassification of ever smokers as never smokers.
While the switch to lower tar filtered cigarettes may have affected the relative frequency of adenocarcinoma to squamous cell carcinoma, the epidemiological evidence suggests that this is because changes in cigarettes have reduced risk of squamous cell carcinoma, not because they have increased risk of adenocarcinoma. The evidence also suggests that the differing trends by histological type are due partly to changes in diagnosis and classification and partly to other factors that have affected both non‐smokers and smokers. What these factors are requires further research.
5. Relationship of ETS exposure to lung cancer risk
As active smoking causes lung cancer, and as ETS contains many of the carcinogens in tobacco smoke, one might expect there to be some increased risk from ETS exposure. However, exposure to smoke constituents from ETS is very much less than exposure from active smoking, with studies based on cotinine (the major metabolite of nicotine) suggesting relative exposure factors of order 0.06% –0.4% . For particulate matter, a series of studies conducted in different countries by Phillips et al., e.g. [73, 74], suggests a lower factor still, of about 0.005–0.02%. Given that the chemical compositions of ETS and of tobacco smoke are not identical, and given doubts about the shape of the dose response at low doses, it is not clear what increase in risk one might expect to be associated with ETS exposure. However, two things are evident. First, any increase in risk is likely to be quite low, if it exists at all, making it extremely difficult to detect reliably using epidemiological methods. Second, any increase in risk is only likely to be demonstrable in never smokers or in those with a smoking history that is very limited or ceased a long time ago .
Since the first publications in the early 1980s [76–79], reports of studies of ETS and lung cancer in never smokers have proliferated, and a recent meta‐analysis  presented a systematic review of 102 studies. Except where noted, the conclusions reached are based on this review.
5.1. Relative risk by source of exposure
The early studies were mainly conducted in women, comparing risk in never smokers married to smokers and in never smokers married to non‐smokers. There were good reasons for this: a much larger proportion of women than men had, at that time, never smoked; whether a spouse smoked or not could be determined quite reliably; and studies showed that cotinine levels in never smokers married to smokers were clearly (about three times) higher than in never smokers married to non‐smokers . However, over the years, evidence has been collected on a wide range of markers of ETS exposure, with some studies collecting extremely detailed histories of exposure.
Based on the meta‐analyses  using random‐effects estimates to account for the substantial between‐study heterogeneity, significant (
5.2. Factors affecting relative risk estimates
In order to study heterogeneity further the review  looked at the 119 relative risk estimates for smoking by the husband or wife (or nearest equivalent), where the overall estimate was 1.21 (95% CI 1.14–1.29), and found evidence that the largest relative risks were seen in small studies of fewer than 50 cases (1.47, 1.15–1.88), in the earliest studies, published before 1990 (1.38, 1.24–1.54), and in studies that did not adjust for age (1.42, 1.18–1.71). However, with one minor exception, some increase was seen in all the subgroups studied (which included location and study design).
There was also evidence of an increase, for spousal smoking, both for squamous cell carcinoma and adenocarcinoma.
5.3. Difficulties in interpreting the association
Whereas the RR for active smoking is large and cannot plausibly be attributed to bias or confounding, that for ETS exposure is substantially smaller, making a causal conclusion difficult to establish with any certainty. In the recent review , various potential sources of bias were discussed. Some sources were dismissed as being unlikely to be very relevant. These include publication bias, because large studies, which contribute most to the overall estimates, seem likely to publish their findings regardless of the results; recall bias, because the overall estimates varied little according to whether the study design was prospective (where recall bias is not an issue) or case‐control (where it is), or according to diagnostic inaccuracy, because estimates were quite similar for studies that did or did not require full histological confirmation. Bias due to the reference group (never smokers married to never smokers) actually having some ETS exposure was considered, with comments made in the review  on the ‘background correction’ of Hackshaw et al.  aimed at converting an RR for marriage to a smoker to an RR expressed relative to never smokers with no ETS exposure at all. It was noted that this background correction only makes sense when the original association, with marriage to a smoker, derives from a causal relationship, and only applies to the
However, the review  did demonstrate clearly that confounding and misclassification of active smoking were extremely important issues which had a profound effect on the interpretation of the observed association of ETS exposure with lung cancer risk. The evidence that confounding may be a material issue derived from observations made some years ago [82, 83] strongly suggesting that, for a wide range of risk factors, exposure to the risk factor is higher in non‐smokers exposed to ETS than in those not exposed to ETS. For some of these risk factors, available data are inadequate to provide any sort of reliable quantitative estimate of their relationship to lung cancer risk in non‐smokers, but for four, increased dietary fat consumption, reduced fruit consumption, reduced vegetable consumption and fewer years of education, it was established that they were associated both with increased lung cancer risk and with increased ETS exposure in non‐smokers. The review  found that adjustment for confounding reduced the
Bias from misclassification of active smoking arises partly because some current or former smokers are known to deny having smoked, so being wrongly described as never smokers [84, 85], and partly as smokers tend to marry smokers [75, 81]. Taken together, these two tendencies, if ignored, will bias the observed association of smoking by the husband to lung cancer risk in never smokers [81, 86, 87]. Based on what were regarded as reasonable estimates of the extent to which misclassification occurs and of the magnitude of the concordance between spouse's smoking habits it was found that correction for misclassification of smoking habits further reduced the confounder‐adjusted estimates to 1.077 (0.999–1.162) for husband smoking and to 1.032 (0.994–1.071) for 10 cigs/day.
Given that adjustment for confounding and misclassification correction substantially weakens the association of lung cancer with the index of ETS exposure that is most usually considered (smoking by the husband) and renders it non‐significant, and given that these adjustments and corrections may be incomplete, it seems that one cannot reliably conclude that any true causal effect of ETS exposure on lung cancer risk has been demonstrated. If there were any true relationship, it would certainly be much weaker than suggested by meta‐analyses that do not adjust for confounding and misclassification.
6. Final comments
Some of the conclusions expressed here may disagree with those of other researchers. These include the risks of smoking being similar in men and women; the modest benefits of the switch to lower tar filter cigarettes; the inaccuracy of many diagnoses of lung cancer; the lack of evidence that cigarettes made from blended tobaccos (as used in the USA) are more harmful than cigarettes made from flue‐cured tobacco (as used in the UK); the rise in the relative frequency of adenocarcinoma to squamous cell carcinoma (seen in never smokers, and affected by changes in diagnosis and classification) not being explained by changes in cigarettes; and the observed association of ETS exposure to lung cancer risk being to a large extent due to bias and confounding. However, it should be emphasised that all the conclusions arrived at from a detailed and careful study of the evidence, including as far as possible all relevant papers that have been published on these subjects, with in some cases reference back to the raw data.
I thank Japan Tobacco International who supported my time in preparing their paper. I also thank them and the numerous other tobacco companies and organizations who have supported my work over the last 50 years. The late Dr. Francis Roe provided inspiration for much of my work. Particular thanks are also due to the staff of my company P.N. Lee Statistics and Computing Ltd. who have, over many years, made an invaluable contribution to my research. These include Barbara Forey, John Fry, Jan Hamling, Alison Thornton and Katharine Coombs who have all featured as co‐authors in many of my papers, and Diana Morris, Pauline Wassell and Yvonne Cooper who typed my manuscripts and obtained relevant references.
Doll, R. Uncovering the effects of smoking: historical perspective. Statistical Methods in Medical Research. 1998; 7:87–117.
Müller, F.H. Tabakmißbrauch und Lungencarcinom (Tobacco abuse and lung carcinoma). Z. Krebsforsch. 1939; 49:57–85.
Schairer, E., Schöniger, E. Lung cancer and tobacco consumption. Zeitschrift für Krebsforschung. 1943; 54:261–71.
Doll, R., Hill, A.B. Smoking and carcinoma of the lung. Preliminary report. British Medical Journal. 1950; 2:739–48.
Wynder, E.L., Graham, E.A. Tobacco smoking as a possible etiologic factor in bronchiogenic carcinoma. A study of 684 proved cases. JAMA. 1950; 143:329–36.
Advisory Committee to the Surgeon General of the Public Health Service. Smoking and health. Report of the Advisory Committee to the Surgeon General of the Public Health Service. Washington DC: US Department of Health, Education, and Welfare; Public Health Service; 1964. 387 p.
US Surgeon General. The health consequences of smoking—50 years of progress: a report of the Surgeon General. Atlanta, Georgia: US Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Chronic Disease Prevention and Health Promotion, Office on Smoking and Health; 2014. 944 p.
US Surgeon General. Reducing the health consequences of smoking. 25 years of progress. A report of the Surgeon General. Rockville, Maryland: US Department of Health and Human Services; Public Health Services; 1989. 703 p.
International Agency for Research on Cancer. Tobacco smoke and involuntary smoking—IARC Monographs on the evaluation of carcinogenic risks to humans. Lyon, France: IARC; 2004. 1452 p. IARC2004
Forey, B., Hamling, J., Hamling, J., Thornton, A., Lee, P., editors. International Smoking Statistics. A collection of worldwide historical data. Web edition ed. Sutton, Surrey: P N Lee Statistics and Computing Ltd; 2006–2016.
Lee, P.N., Forey, B.A. Trends in cigarette consumption cannot fully explain trends in British lung cancer rates. Journal of Epidemiology and Community Health. 1998; 52(2):82–92.
Lee, P.N., Forey, B.A. Why are lung cancer rate trends so different in the United States and United Kingdom? Inhalation Toxicology. 2003; 15:909–49.
National Cancer Institute. Risks associated with smoking cigarettes with low machine‐measured yields of tar and nicotine. Smoking and Tobacco Control. Monograph No. 13 ed. Bethesda, MD: US Department of Health and Human Services, National Institutes of Health, National Cancer Institute; 2001. 235 p.
Lee, P.N., Forey, B.A., Coombs, K.J. Systematic review with meta‐analysis of the epidemiological evidence in the 1900s relating smoking to lung cancer. BMC Cancer. 2012; 12:385. DOI: 10.1186/1471‐2407‐12‐385
Fry, J.S., Lee, P.N., Forey, B.A., Coombs, K.J. Dose–response relationship of lung cancer to amount smoked, duration and age starting. World Journal of Meta‐Analysis. 2013; 1(2):57–77.
Fry, J.S., Lee, P.N., Forey, B.A., Coombs, K.J. How rapidly does the excess risk of lung cancer decline following quitting smoking? A quantitative review using the negative exponential model. Regulatory Toxicolology Pharmacology. 2013; 67:13–26. DOI: 10.1016/j.yrtph.2013.06.001
Lee, P.N., Hamling, J., Fry, J., Forey, B. Using the negative exponential model to describe changes in risk of smoking‐related diseases following changes in exposure to tobacco. Advances in Epidemiology. 2015;Article ID 487876: 13 pages. DOI: 10.1155/2015/487876
Schottenfeld, D., Fraumeni, J.F., Jr., editors. Cancer epidemiology and prevention. 3rd editionrd ed. New York: Oxford University Press; 2006. 1392 p.
De Matteis, S., Consonni, D., Pesatori, A.C., Bergen, A.W., Bertazzi, P.A., Caporaso, N.E., Lubin, J.H., Wacholder, S., Landi, M.T. Are women who smoke at higher risk for lung cancer than men who smoke? American Journal of Epidemiology. 2013; 177(7):601–12.
Bain, C., Feskanich, D., Speizer, F.E., Thun, M., Hertzmark, E., Rosner, B.A., Colditz, G.A. Lung cancer rates in men and women with comparable histories of smoking. JNCI. 2004; 98(11):826–34.
Lee, P.N. Systematic review of the epidemiological evidence comparing lung cancer risk in smokers of mentholated and unmentholated cigarettes. BMC Pulmonary Medicine. 2011; 11:18. DOI: 10.1186/1471‐2466‐11‐18.
Hammond, E.C., Selikoff, I.J., Seidman, H. Asbestos exposure, cigarette smoking and death rates. Annals of the New York Academy of Sciences. 1979; 330:473–90.
Lee, P.N. Relation between exposure to asbestos and smoking jointly and the risk of lung cancer. Occupational and Environmental Medicine. 2001; 58(3):145–53.
Enterline, P.E., Keleti, G., Sykora, J.L., Lange, J.H. Endotoxins, cotton dust, and cancer. Lancet. 1985; 2(October 26):934–35.
Lee, P.N. Epidemiological studies relating to family history of lung cancer to risk of the disease. Indoor Environment. 1993; 2:129–42.
Coté, M.L., Liu, M., Bonassi, S., Neri, M., Schwartz, A.G., Christiani, D.C., et. al. Increased risk of lung cancer in individuals with a family history of the disease: a pooled analysis from the International Lung Cancer Consortium. European Journal of Cancer. 2012; 48(13):1957–68.
Lissowska, J., Foretova, L., Dąbek, J., Zaridze, D., Szeszenia‐Dabrowska, N., Rudnai, P. Family history and lung cancer risk: international multicentre case–control study in Eastern and Central Europe and meta‐analyses. Cancer Causes Control. 2010; 21(7):1091–104.
Wang, Y., Broderick, P., Matakidou, A, Eisen, T., Houlston, R.S. Chromosome 15q25 (CHRNA3‐CHRNA5) variation impacts indirectly on lung cancer risk. PLoS ONE. 2011; 6(4):e19085.
Timofeeva, M.N., McKay, J.D., Davey Smith, G., Johansson, M., Byrnes, G.B., Chabrier, A., et al. Genetic polymorphisms in 15q25 and 19q13 loci, cotinine levels, and risk of lung cancer in EPIC. Cancer Epidemiology Biomarkers & Prevention. 2011; 20(10):2250–61.
Munafò, M.R., Timofeeva, M.N., Morris, R.W., Prieto‐Merino, D., Sattar, N., Brennan, P., et al. Association between genetic variants on chromosome 15q25 locus and objective measures of tobacco exposure. Journal of National Cancer Institute. 2012; 104(10):740–8.
Gabrielsen, M.E., Romundstad, P., Langhammer, A., Krokan, H.E., Skorpen, F. Association between a 15q25 gene variant, nicotine‐related habits, lung cancer and COPD among 56307 individuals from the HUNT study in Norway. European Journal of Human Genetics. 2013; 21(11):1293–99.
Lee, P.N. Comparison of autopsy, clinical and death certificate diagnosis with particular reference to lung cancer. A review of the published data. APMIS. 1994; 102 (Suppl 45):42.
Kendrey, G., Szende, B., Lapis, K., Marton, T., Hargitai, B., Roe, F.J.C., et al. Misdiagnosis of lung cancer in a 2000 consecutive autopsy study in Budapest. General and Diagnostic Pathology. 1995; 141:169–78.
Thun, M.J., Apicella, L.F., Henley, S.J. Smoking vs other risk factors as the cause of smoking‐attributable deaths. Confounding in the courtroom. JAMA. 2000; 284(6):706–12.
Fisher, R.A. Dangers of cigarette‐smoking. British Medical Journal. 1957; 2:297–8.
Burch, P.R.J. Does smoking cause lung cancer? New Scientist. 1974; 61:458–67.
Floderus, B., Cederlöf, R., Friberg, L. Smoking and mortality: a 21‐year follow‐up based on the Swedish Twin Registry. International Journal of Epidemiology. 1988; 17(2):332–40.
Kaprio, J., Koskenvuo, M.. Cigarette smoking as a cause of lung cancer and coronary heart disease. A study of smoking‐discordant twin pairs. Acta Geneticae Medicae et Gemellologiae. 1990; 39:25–34.
Easterbrook, P.J., Berlin, J.A., Gopalan, R., Matthews, D.R. Publication bias in clinical research. Lancet. 1991; 337(8746):867–72. DOI: 10.1016/0140‐6736(91)90201‐Y
Thornton, A., Lee, P. Publication bias in meta‐analysis: its causes and consequences. Journal of Clinical Epidemiology. 2000; 53:207–16.
Hill, A.B. The environment and disease: association or causation? Proceedings of the Royal Society of Medicine. 1965; 58(5):295–300.
Lee, P.N. Lung cancer and type of cigarette smoked. Inhalation Toxicology. 2001; 13:951–76.
Lee, P.N., Hamling, J.S. Systematic review of the relation between smokeless tobacco and cancer in Europe and North America. BMC Medicine. 2009; 7:36. DOI: 10.1186/1741‐7015‐7‐36
Lee, P.N. Summary of the epidemiological evidence relating snus to health. Regulatory Toxicology and Pharmacology. 2011; 59:197–214.
Lee, P.N. Epidemiological evidence relating snus to health—an updated review based on recent publications. Harm Reduction Journal. 2013; 10(1):36. DOI: 10.1186/1477‐7517‐10‐36
Scherer, G., Lee, P.N. Smoking behaviour and compensation: a review of the literature with meta‐analysis. Regulatory Toxicology and Pharmacology. 2014; 70(3):615–28. DOI: 10.1016/j.yrtph.2014.09.008
Lee, P.N., Sanders, E. Does increased cigarette consumption nullify any reduction in lung cancer risk associated with low‐tar filter cigarettes? Inhalation Toxicology. 2004; 16:817–33.
Tso, T.C. Maturity, harvesting, and curing. In: Production, physiology, and biochemistry of tobacco plant. Beltsville, Maryland: IDEALS, Inc; 1992. pp. 105–24.
Lee, P.N., Forey, B.A., Fry, J.S., Hamling, J.S., Hamling, J.F., Sanders, E.B., Carchman, R.A. Does use of flue‐cured rather than blended cigarettes affect international variation in mortality from lung cancer and COPD? Inhalation Toxicology. 2009; 21(5):404–30.
Marchesani, W. Über den primären bronchialkrebs. Frankfurt Z. Path. 1924; 30:158–90.
Kreyberg, L. Histological typing of lung tumors—International histological classification of tumours. Geneva: World Health Organization; 1967. 28 p.
World Health Organization. The World Health Organization histological typing of lung tumours. Second edition. American Journal of Clinical & Patholology. 1982; 77(2):123–36.
Travis, W.D., Colby, T.V., Corrin, B., Shimosato, Y., Brambilla, E. Histological typing of lung and pleural tumours. Third Edition ed. Berlin Heidelberg: Springer; 1999. 156 p.
Feinstein, A.R., Gelfman, N.A., Yesner, R., Auerbach, O., Hackel, D.B., Pratt, P.C. Observer variability in the histopathologic diagnosis of lung cancer. American Review of Respiratory Disease. 1970; 101:671–84.
Auerbach, O., Garfinkel, L., Parks, V.R. Histologic type of lung cancer in relation to smoking habits, year of diagnosis and sites of metastases. Chest. 1975; 67:382–7.
Cane, P., Linklater, K.M., Nicholson, A.G., Peake, M.D., Gosney, J. Morphological and genetic classification of lung cancer: variation in practice and implications for tailored treatment. Histopathology. 2015; 67(2):216–24. DOI: 10.1111/his.12638
Roggli, V.L., Vollmer, R.T., Greenberg, S.D., McGavran, M.H., Spjut, H.J., Yesner, R. Lung cancer heterogeneity: a blinded and randomized study of 100 consecutive cases. Human Patholology. 1985; 16(6):569–79.
Fry, J.S., Lee, P.N., Forey, B.A., Coombs, K.J. Is the shape of the decline in risk following quitting smoking similar for squamous cell carcinoma and adenocarcinoma of the lung? A quantitative review using the negative exponential model. Regulatory Toxicology and Pharmacology. 2015; 72:49–57. DOI: 10.1016/j.yrtph.2015.02.010
Devesa, S.S., Bray, F., Vizcaino, A.P., Parkin, D.M. International lung cancer trends by histologic type: male: female differences diminishing and adenocarcinoma rates rising. International Journal of Cancer. 2005; 117(2):294–9.
Burns, D.M., Anderson, C.M., Gray, N. Do changes in cigarette design influence the rise in adenocarcinoma of the lung?. Cancer Causes & Control. 2011; 22:13–22.
Thun, M.J., Burns, D.M. Health impact of “reduced yield” cigarettes: a critical assessment of the epidemiological evidence. Tobacco Control. 2001; 10(Suppl I):i4–i11.
Thun, M.J., Lally, C.A., Flannery, J.T., Calle, E.E., Flanders, W.D., Heath, C.W., Jr. Cigarette smoking and changes in the histopathology of lung cancer. Journal of the National Cancer Institute. 1997; 89(21):1580–6.
Brooks, D.R., Austin, J.H.M., Heelan, R.T., Ginsberg, M.S., Shin, V., Olson, S.H., Muscat, J.E., Stellman, S.D. Influence of type of cigarette on peripheral versus central lung cancer. Cancer Epidemiology Biomarkers & Prevention. 2005; 14:576–81.
Ito, H., Matsuo, K., Tanaka, H., Koestler, D.C., Ombao, H., Fulton, J., et al. Nonfilter and filter cigarette consumption and the incidence of lung cancer by histological type in Japan and the United States: analysis of 30‐year data from population‐based cancer registries. International Journal of Cancer. 2011; 128(8):1918–28.
Chen, F., Bina, W.F., Cole, P. Declining incidence rate of lung adenocarcinoma in the United States. Chest. 2007; 131:1000–5.
Marugame, T., Sobue, T., Nakayama, T., Suzuki, T., Kuniyoshi, H., Sunagawa, K., et al. Filter cigarette smoking and lung cancer risk; a hospital‐based case–control study in Japan. British Journal of Cancer. 2004; 90:646–51.
Papadopoulos, A., Guida, F., Cénée, S., Cyr, D., Schmaus, A., Radoï, L., et al. Cigarette smoking and lung cancer in women: results of the French ICARE case–control study. Lung Cancer. 2011; 74(3):369–77.
Lee, P.N., Forey, B.A., Coombs, K.J., Lipowicz, P.J., Appleton, S. Time trends in never smokers in the relative frequency of the different histological types of lung cancer, in particular adenocarcinoma. Regulatory Toxicology and Pharmacology. 2016; 74:12–22. DOI: 10.1016/j.yrtph.2015.11.016
Barsky, S.H., Cameron, R., Osann, K.E., Tomita, D., Holmes, E.C. Rising incidence of bronchioloalveolar lung carcinoma and its unique clinicopathologic features. Cancer. 1994; 73(4):1163–70.
Lee, P.N., Forey, B.A. Indirectly estimated absolute lung cancer mortality rates by smoking status and histological type based on a systematic review. BMC Cancer. 2013; 13(1):189–224. DOI: 10.1186/1471‐2407‐13‐189
Pirkle, J.L., Flegal, K.M., Bernert, J.T., Brody, D.J., Etzel, R.A., Maurer, K.R. Exposure of the US population to environmental tobacco smoke. The Third National Health and Nutrition Examination Survey, 1988 to 1991. JAMA. 1996; 275:1233–40. DOI: 10.1001/jama.275.16.1233
Office of Population Censuses and Surveys. Health survey for England 1994. Volume I: Findings. Volume II: Survey methodology & documentation. Series HS no. 4 ed. London: HMSO; 1996. 607 p.
Phillips, K., Bentley, M.C., Howard, D.A., Alván, G. Assessment of air quality in Stockholm by personal monitoring of nonsmokers for respirable suspended particles and environmental tobacco smoke. Scandinavian Journal of Work, Environment and Health. 1996; 22(Suppl 1):1–24.
Phillips, K., Howard, D.A., Bentley, M.C., Alván, G. Assessment of air quality in Turin by personal monitoring of nonsmokers for respirable suspended particles and environmental tobacco smoke. Environment International. 1997; 23:851–71. DOI: 10.1016/S0160‐4120(97)00097‐4
Lee, P.N. Environmental tobacco smoke and mortality. A detailed review of epidemiological evidence relating environmental tobacco smoke to the risk of cancer, heart disease and other causes of death in adults who have never smoked. Basel: Karger; 1992. 224 p.
Hirayama, T. Non‐smoking wives of heavy smokers have a higher risk of lung cancer: a study from Japan. British Medical Journal. 1981; 282:183–5. DOI: 10.1136/bmj.282.6259.183
Garfinkel, L. Time trends in lung cancer mortality among nonsmokers and a note on passive smoking. Journal of the National Cancer Institute. 1981; 66(6):1061–6. DOI: 10.1093/jnci/66.6.1061
Trichopoulos, D., Kalandidi, A., Tzonou, A. Incidence and distribution of lung cancer in Greece. Excerpta Medica International Congress Series. 1982; 558:10–7.
Chan, W.C., Fung, S.C. Lung cancer in non‐smokers in Hong Kong. In: Grundmann, E., editors. Cancer Epidemiology. Stuttgart, New York: Gustav Fischer Verlag; 1982. pp. 199–202.
Lee, P.N., Fry, J.S., Forey, B., Hamling, J.S., Thornton, A.J. Environmental tobacco smoke exposure and lung cancer: a systematic review. World Journal of Meta‐Analysis. 2016; 4(2):10–43. DOI: 10.13105/wjma.v4.i2.10
Hackshaw, A.K., Law, M.R., Wald, N.J. The accumulated evidence on lung cancer and environmental tobacco smoke. BMJ. 1997; 315:980–8. DOI: 10.1136/bmj.315.7114.980
Thornton, A., Lee, P., Fry, J. Differences between smokers, ex‐smokers, passive smokers and non‐smokers. Journal of Clinical Epidemiology. 1994; 47(10):1143–62. DOI: 10.1016/0895‐4356(94)90101‐5
Matanoski, G., Kanchanaraksa, S., Lantry, D., Chang, Y. Characteristics of nonsmoking women in NHANES I and NHANES I epidemiologic follow‐up study with exposure to spouses who smoke. American Journal of Epidemiology. 1995; 142(2):149–57.
Lee, P.N., Forey, B.A. Misclassification of smoking habits as determined by cotinine or by repeated self‐report—a summary of evidence from 42 studies. Jouranal Smoking‐Related Disease.. 1995; 6:109–29.
Connor‐Gorber, S., Schofield‐Hurwitz, S., Hardt, J., Levasseur, G., Tremblay, M. The accuracy of self‐reported smoking: a systematic review of the relationship between self‐reported and cotinine‐assessed smoking status. Nicotine & Tobacco Research. 2009; 11(1):12–24. DOI: 10.1093/ntr/ntn010
Lee, P.N., Forey, B.A. Misclassification of smoking habits as a source of bias in the study of environmental tobacco smoke and lung cancer. Statistics in Medicine. 1996; 15(6):581–605. DOI: 10.1002/(SICI)1097‐0258(19960330)15
Lehnert, G., Garfinkel, L., Hirayama, T., Schmähl, D., Uberla, K., Wynder, E.L., Lee, P. Roundtable discussion. Preventive Medicine. 1984; 13(6):730–46.