In 2012, rectal cancer affected 40,290 Americans. Colon and rectal cancer resulted in a mortality of 51,690 individuals during the same year . Patients affected with rectal cancer who have a clinical stage II (T3-T4, NO, MO) or III (Any T, N1-N3, M0) tumor are treated with pre-operative chemoradiation (CRT) followed by surgical intervention 5-10 weeks after the last CRT treatment. An adequate oncologic operation involves removal of the tumor and the entire mesorectum (total mesorectal excision). This has been demonstrated to decrease local recurrence substantially as the lymphatic drainage of the rectum is contained within the investing fascia (mesorectum). Distal rectal tumors involving the anorectal sphincter complex are classically treated with an abdominoperineal resection (APR); whereas, more proximal tumors might be treated with an anterior protosigmoidectomy with a primary colorectal anastomosis (LAR). There has been a substantial shift in the number of APR operations to LAR procedures over the past decade owing to the implementation of new circular stapling devices and the use of neoadjuvant CRT.
2. The rectum
In a Cochrane review of 19 clinical trials assessing preoperative radiotherapy
3. Indications for neoadjuvant chemoradiation
The addition of preoperative radiation therapy to TME decreases locoregional recurrence from approximately 8% to 2%. The combination of chemotherapy and radiation (CRT) further decreases local recurrence. Chemotherapy also increases the number of patients which achieve a pathologic complete response (pCR), i.e. no detectable tumor after resection. This modality also reduces tumor burden in some patients and might allow a sphincter preserving operation (i.e. LAR) as opposed to an APR, allowing a patient to avoid a permanent colostomy. The rate of pCR is approximately 25% [6;7]. Patients who achieve pCR have better long-term outcomes compared to patients who only have a partial response or no response at all . Current guide lines in the United States [4;5] dictate that patients with stage II (T3-T4) or stage III (any T with positive regional lymph nodes) should be treated with neoadjuvant CRT. Patients with stage I (T1-T2) disease or those with distant metastases (stage IV) generally do not receive neoadjuvant CRT. However, in instances of synchronous liver metastases for which liver resection is planned, neoadjuvant radiation may be considered. These recommendations emanate from the low rate of recurrence (4%) in patients with stage I tumors treated with surgery alone . Further, there is no difference in the rate of locoregional recurrence in patients with stage IV tumors treated with radiotherapy and surgery compared to palliative surgery alone . Similarly, there is no difference in outcomes in patients with distant metastases treated with neoadjuvant radiotherapy and surgery
4. Clinical staging of rectal cancer
Staging of rectal cancer begins with a thorough history and physical examination. The most common symptom of rectal cancer is bright red blood per rectum. Physical examination of the abdomen is important to identify any evidence of liver disease (ascites) or masses. A lymph node examination is important in any patient suspected of having cancer. Rectal examination will reveal distal tumors and is mandatory in the evaluation of patients with colorectal cancers. In such cases information regarding the size, degree of fixation, distance from the anal sphincters is important. In women, a rectovaginal examination may reveal extent of disease. A full colonoscopy is indicated to identify synchronous lesions (present in approximately 5% of cases). Rigid proctoscopy will define the distance of the lesion from the anus and can be critical in cases where the distance from the anus is not clear.
Because only stage II and III tumors are treated with pre-operative CRT, clinical staging is pivotal in guiding treatment options. There are currently two modalities to assess tumor stage (T stage) in the pre-operative setting: (1) endorectal ultrasound (EUS) and (2) Magnetic Resonance Imaging (MRI). The efficacy of these modalities has been assessed by two meta-analyses [10;11]. One study favors EUS  and the other MRI . In the first analysis, 90 studies were included and assessed the accuracy of EUS, MRI, and CT in pre-operatively staging rectal cancer. The results demonstrated that EUS and MRI were similar in terms of sensitivity (Sn) with regards to tumor depth into the muscularis propia (94%). EUS was superior in determining muscularis propia invasion [specificity (Sp) of 86%] compared to MRI (Sp = 69%) and was an overall sensitive strategy (Sn = 90%) for perirectal tumor invasion compared to MRI (Sn = 82%) . A second meta-analysis interrogated 84 studies. This study showed no difference in these modalities in evaluating the nodes (N-staging) . In seven studies, MRI was a superior strategy in evaluating involved circumferential margins . MRI seems to be emerging as a preferred modality for the assessment of rectal cancer staging in the pre-operative setting. However, the use of either of these modalities is largely based on institutional experience. The sensitivity of EUS following CRT is less compared to virgin tissue. Thus, MRI may be a preferred modality to determine response to neoadjuvant CRT.
5. Neoadjuvant chemoradiotherapy
The management of stage II and stage III rectal cancer is a tri-modality approach (Radiotherapy, Chemotherapy and Surgery) and patients are best managed following discussion at a multidisciplinary conference.
Initial studies evaluated the efficacy of radiotherapy without pre-operative chemotherapy. The data has been summarized in two meta-analyses addressing the benefit of preoperative radiation [12;13]. While the data on overall survival was not clear in these analyses, there was a clear decrease in the rate of local recurrence (46% in patients receiving preoperative radiation vs. 53% in the control group). These data established the benefits of preoperative radiotherapy followed by surgery.
5.1.1. Short course vs. long course radiotherapy
In Europe, small fractions of ionizing radiation 5.0 Grey (Gy) X 5.0 (over five days), for a total of 25.0 Gy without chemotherapy, are employed. With this strategy, the Swedish Rectal Cancer Trial found an improved rate of survival at five years with preoperative radiation . In the United States, the typical IR dose is 45.0 to 50.4 Gy given in small doses (1.8 Gy/day) for five to six weeks . In contrast to short course radiotherapy, in the United States, long course radiotherapy is given in combination with neoadjuvant chemotherapy. The interval between completion of radiation and subsequent operation is an area of some debate (see below) but is typically 5-10 weeks.
5.2. Neoadjuvant chemotherapy
Preoperative chemotherapy is generally used as a radiosensitizer. The EORTC group demonstrated that the addition of chemotherapy (5-FU) to the use of preoperative radiation reduced the risk of local recurrence by approximately 50%, from 17.1% to 8.7%. There was not a significant difference in overall survival in this study. Other trials have shown similar improvements in local control. Based on this data, the most established agent used in the pre-operative setting in combination with radiation has been 5-fluorouracil (5-FU). The oral form of 5-FU (Capecitabine) is also being widely used in place of 5-FU with similar results . Several chemotherapeutic agents used for the management of colon cancer in the adjuvant setting and for patients with metastases have been evaluated as possible radiosensitizers. These agents include: irinotecan , oxaliplatin , bevacizumab  and cetuximab . With such strategies, there is still a wide response to ionizing radiation and these agents are not in widespread use at this time.
5.3. Pathologic complete response
A pathologic complete response (pCR) occurs in patients who undergo resection of the rectum and no residual tumor is identified. Patients who have a pCR demonstrate superior survival than those without. The EORTC 22921 showed an increased rate of pCR in patients who underwent chemoradiotherapy (13.7%) compared to patients who received radiation therapy alone (5.3%). A European trial inclusive of 762 patients receiving preoperative chemoradiation compared to radiation alone, the pCR rate was 11.4%
In the United States current guidelines recommend pre-operative radiation [50.4 Gy] in 25-28 fractions combination with 5-FU infusional or bolus with leucovorin [425 mg/m2/d] or capecitibine [825 mg/m2]. Neoadjuvant treatment is followed by surgery five to ten weeks later. While some investigators have shown that longer periods between neoadjuvant CRT and surgery might be associated with an increase rate of pCR , this approach is still under investigation .
For stage II and III patients treated with CRT, surgical intervention must be planned within five to ten weeks after the last dose of chemoradiation. Although a longer window between neoadjuvant chemoradiation and operative intervention has been associated with higher rates of pCR, this must be assessed in case-to-case basis [21;22].
Transabdominal operations (LAR or APR) are the operations of choice for stage II and stage III rectal cancers. For small tumors with a good histology and for a patient with a prohibitive risk of surgical intervention, a transanal approach might be an alternative approach.
6.1. Transabdominal operations
Two operations are typically performed for rectal cancer. The abdominoperineal resection involves the removal of the distal rectum and perineum with clear tumor radial margins laterally to the pelvic sidewalls. Thus, part of this operation is the creation of a permanent colostomy. A low anterior resection involves the removal of the tumor and the creation of an anastomosis. This might require a temporary loop ileostomy especially in patients that have received neoadjuvant chemoradiation.
6.1.1. Abdominioperineal Resection (APR)
An abdominoperineal resection (Figure 1) necessitates a permanent colostomy, which frequently carries negative perception as a drastic change in quality of life for patients. Although a permanent stoma does necessitate some changes for patients, data is emerging that quality of life following an APR is not significantly less than that following an LAR . This is related to the relatively high rate of complications following LAR, including sexual dysfunction, pain and fecal incontinence. However, an APR is associated with a high rate of perineal wound infections . Furthermore, obtaining clear radial margins is more difficult with an APR compared to an LAR [23;25]. As a result, there is an oncologic advantage in peforming an LAR compared to an APR . Thus, in patients with preserved rectal tone, the operation of choice, is an LAR provided tumor associated factors make this possible.
6.1.2. Low Anterior Resection (LAR): Total Mesorectal Excision (TME)
An LAR (Figure 2) involves the creation of a primary anastomosis. The area confined within the investing fascia of the rectum and the presacral fascia involves the vascular and lymphatic structures of the mid-rectum. An en bloc resection of the rectum that circumscribes these structures is termed a TME (Figure 3). Superiorly, the mesorectum is defined at the level of the sacral promontory or the division of the right and left superior hemorrhoideal arteries. The mesorectum extends distally and reduces posteriorly at the level of the investing fasica of the levators (Waldeyer's Fascia). Prior to in the introduction of TME the rate of recurrence for rectal cancer was 25.0%. This rate has been reduced to 5.0% following the introduction of the TME .
6.1.3. Proximal margin of resection and level of arterial ligation
No studies have interrogated the length required for proximal resection. Because of the continuity with the colon this is not such a concern. NCI guidelines recommend a 5-cm segment of resection proximal to the tumor . While the inferior mesenteric artery (high ligation) was typically the level of arterial ligation recommended, this practice was associated with a decrease in innervation and perfusion to the anastomosis. The evidence demonstrating that this has a superior oncologic compared to ligation at the level of the superior rectal artery (low ligation) is lacking. Thus, low ligation has become the preferred strategy  (Figure 4).
6.2. Laparoscopic surgery for the management of adenocarcinoma of the rectum
Minimally invasive surgery has made laparoscopic resection of rectal cancer possible. However, at this juncture, this procedure remains investigational for the management of rectal cancer . It is currently, recommended to include patients in study protocol to continue to address the benefits of the laparoscopic approach in rectal cancer including: oncologic efficacy, complication rates, conversion rates, patient benefit, and cost-effectiveness.
Short term outcomes have not been different in patients treated with the laparoscopic approach compared to the open techniques . Multiple case series reporting laparoscopic TME have documented technical feasibility with satisfactory short term outcomes . While case reports have also reported the ability of a robotic proctectomy , these studies need to be replicated in large series compared to the “gold-standard” to determine the general applicability of innovative approaches.
In contrast to colon cancer, where laparoscopy has been compared to the open approach [31-33], for rectal cancer these studies are currently needed. The Conventional Versus Laparoscopic-Assisted Surgery in Colorectal Cancer (CLASICC) trial specifically addressed rectal cancer . In this study, the rate of complications was similar. However, the rate of positive CRM was twice in the laparoscopic approach compared to the open technique (12%
A randomized controlled trial  and institutional case series [35;36] indicate that the laparoscopic and the open TME have similar oncologic outcomes. More data on the long term outcomes of the laparoscopic approach will be shed with further analysis of the Colon Cancer Laparoscopic or Open Resection (COLOR) II  and the and the American College of Surgeons Oncology Group trial Z6051 is completed.
Thus, the current data suggest that the short-term outcomes of laparoscopic and open surgery are similar. It is crucial to analyze the current data of the available studies carefully as patient selection and the experience of the institution/surgeon are paramount in the current available literature. Long term data regarding oncologic outcome and functional status remain at large, as do data demonstrating patient benefit and cost effectiveness .
6.3. Transanal excision
An alternative treatment for early stage rectal cancers is a transanal excision. Candidates for this approach have small (≤ 3-cm) stage I (T1) tumors located within 8-cm from the anal verge that occupy less than 30% of the circumference of the bowel with good histological features is a transanal removal of the tumor with clear margins. There is a substantial risk for local recurrence with this approach. Local rates of recurrence with the transanal approach
7. Adjuvant chemotherapy
Patients with stage II/III rectal cancer should be treated with adjuvant chemotherapy as soon as they are able. Current regimens for this approach extrapolate the experience with colon cancer such that FOLFOX (5-FU/leucovorin, and oxaliplatin) for six months is recommended. 5-FU with or without leucovorin as well as capacitibine with or without oxaliplatin are also alternative options for treatment in the adjuvant setting .
8. Pathological analysis of rectal cancer
In rectal cancer staging, the prefix “p” refers to pathological staging and “yp” indicates pathological staging after neoadjuvant chemoradiation.
The number of recommended nodes to be retrieved to accurately stage tumors is 12 according to the NCCN guidelines . In patients treated with neoadjuvant therapy, the number of nodes resected during surgery is 3-6 less compared to patients treated with surgery alone [41-43]. Thus, care must be taken by the surgeon to remove all involved nodes and by pathology for a careful analysis of the specimen.
8.2. Pathological Inspection of the tumor
8.2.1. Circumferential Resection Margin (CRM)
The circumferential margin (CRM) is important during pathological assessment of tumors in rectal cancer . The CRM refers to assessment of the non-peritonealized area (bare area) of the rectum created by subperitoneal dissection during surgery. Tumors within 1 mm of the resection margin are defined as having a positive CRM. Additionally discontinuous spread or lymph node involvement within 1mm of the CRM is defined as positive. CRM is a predictor of local recurrence in patients receiving surgery as the only modality of treatment of rectal cancer [25;45]. Patients whose CRM is less that 2 mm have a recurrence rate of 16% compared to 5.8% for patients having a CMR over 2mm. The rate of metastases is also higher in patients with less than 2mm margins vs. greater that 2mm (37.6 vs. 12.7%; respectively) . This observation underscores the importance or radial margins in rectal surgery. Other studies have shown that the CRM is an important predictor of local recurrence, distant metastasis, and overall survival in patients receiving induction CRT compared to patients treated with surgery alone . Thus, pathological evaluation of the resected rectal tumor must include the distance to the tumor to the closest CRM.
8.2.2. Determining response to induction chemotherapy
Pathological tumor response following neoadjuvant therapy is graded from 0 to 3. A grade of 0 indicates complete response without any viable cells; while 3 denotes minimal or no response to treatment. It is important for the pathologist and the surgeon to note the response of CRT after surgery to determine if the current regimens are adequate for the patient population and also to determine the possible aggressiveness of the tumor and plan for adjuvant therapies.
9. Clinical Complete Response (cCR)
Studies continue to accumulate that document the possibility of observing patients who achieve a clinical complete response following neoadjuvant chemoradiation [46;47]. The first study was reported by Habr-Gama’s group in 2004 . In this study, 8% of patients considered to have recurrence had a complete pathological response following surgery. Patients with rectal tumors within 0-7 cm from the anal verge received pre-operative radiotherapy (50.4 Gy) and chemotherapy [5-FU (425 mg/m2/d) + folinic acid (20 mg/m2/d)]. Re-staging was performed 8 weeks after treatment and included proctoscopy with rectal biopsies. Complete clinical response was defined by the absence of any abnormalities during proctoscopy. A rectal scar or a positive biopsy was defined as an incomplete response. These patients did not receive postoperative chemotherapy unless they had recurrent disease. These findings were then reproduced by Maas et al .
Maas et al compared patients that achieved a cCR to patients who had a pathological complete response after surgery. Twenty-one subjects were included in the study arm and 20 in the control group. The major differences in these studies include the follow up in Maas vs. Habr-Gama’s studies (24.8
While there are some differences between the studies by Habr-Gama and Maas, they provide an excellent platform to build on further prospective cohort studies. Further, two other smaller studies have replicated these observations [48;49].
Complications from rectal surgery are typically associated with bladder and sexual dysfunction. A TME has been associated with bladder dysfunction (17.8%), loss of erection (27.7%), and lack of ejaculation (33.9%) . Up to 30% of patients with attempted curative surgical intervention will eventually develop regional (pelvic) recurrence . Treatment failure is largely dependent on the cohort of patients studied and combined to patients who develop metastasis, the rate is substantially high.
The management of rectal cancer is in dynamic evolution. Drastic improvements have occurred over the past 20 years. However, the 5-year survival for these patients remains unacceptably high. The tri-modality approach has demonstrated clear advantages. In a small segment of patients (~25%) the tri-modality approach might be reduced to a bimodality treatment avoiding surgery in patients that achieve a clinical complete response. However, this strategy should be undertaken only in the setting of an Institutional Board Review protocol. Efforts to improve local control and survival in rectal cancer are continuing in multiple clinical and preclinical studies. An understanding of specific molecular pathways leading to a response in neoadjuvant modalities will refine the segment of patients who might need an operation sooner compared to patients who might be observed. Ongoing trials on the laparoscopic approach for rectal cancer will shed light into the benefits of this practice.
Cancer statistics, Siegel R Naishadham D Jemal A 2012CA Cancer J Clin 2012; 62 1 10 29
De SS, Figueredo A. Pre-operative radiotherapy and curative surgery for the management of localized rectal carcinoma. Cochrane Database Syst Rev Wong R. K Tandan V 2007CD002102.
Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer. N Engl J Med Kapiteijn E Marijnen C. A Nagtegaal I. D Putter H Steup W. H Wiggers T et al 2001 345 9 638 646
Guidelines 2000 for colon and rectal cancer surgery. J Natl Cancer Inst Nelson H Petrelli N Carlin A Couture J Fleshman J Guillem J et al 2001 93 8 583 596
III, Chen YJ, Choti MA, Cooper HS et al. NCCN Clinical Practice Guidelines in Oncology: rectal cancer. J Natl Compr Canc Netw Engstrom P. F Arnoletti J. P Benson A. B 2009 7 8 838 881
Rectal cancer and importance of chemoradiation in the treatment. Adv Exp Med Biol Huerta S 2010 685 124 133
Tissue microarray constructs to predict a response to chemoradiation in rectal cancer. Dig Liver Dis Huerta S Hrom J Gao X Saha D Anthony T Reinhart H et al 2010 42 10 679 684
Long-term outcome in patients with a pathological complete response after chemoradiation for rectal cancer: a pooled analysis of individual patient data. Lancet Oncol Maas M Nelemans P. J Valentini V Das P Rodel C Kuo L. J et al 2010 11 9 835 844
Radiotherapy and concurrent radiochemotherapy for rectal cancer. Surg Oncol Rodel C Sauer R 2004
Rectal cancer: local staging and assessment of lymph node involvement with endoluminal US, CT, and MR imaging--a meta-analysis. Radiology Bipat S Glas A. S Slors F. J Zwinderman A. H Bossuyt P. M Stoker J 2004 232 3 773 783
van de Velde CJ, van Engelshoven JM et al. Imaging for predicting the risk factors--the circumferential resection margin and nodal disease--of local recurrence in rectal cancer: a meta-analysis. Semin Ultrasound CT MR Lahaye M. J Engelen S. M Nelemans P. J Beets G. L 2005 26 4 259 268
Adjuvant radiotherapy for rectal cancer: a systematic overview of 8patients from 22 randomised trials. Lancet 2001 358 9290 1291 1304
Preoperative radiotherapy for resectable rectal cancer: A meta-analysis. JAMA Camma C Giunta M Fiorica F Pagliaro L Craxi A Cottone M 2000 284 8 1008 1015
Improved survival with preoperative radiotherapy in resectable rectal cancerSwedish Rectal Cancer Trial. N Engl J Med 1997 336 14 980 987
Evolution of 5-fluorouracil-based chemoradiation in the management of rectal cancer. Anticancer Drugs Patel P. A 2011 22 4 311 316
Irinotecan and radiosensitization in rectal cancer. Anticancer Drugs Illum H 2011 22 4 324 329
Oxaliplatin as a radiosensitizing agent in rectal cancer. Anticancer Drugs Huerta S Hrom J 2011 22 4 317 323
Antiepidermal growth factor receptor radiosensitizers in rectal cancer. Anticancer Drugs Glynne-jones R Mawdsley S Harrison M 2011 22 4 330 340
Chemotherapy with preoperative radiotherapy in rectal cancer. N Engl J Med Bosset J. F Collette L Calais G Mineur L Maingon P Radosevic-jelic L et al 2006 355 11 1114 1123
Randomized phase II study of neoadjuvant combined-modality chemoradiation for distal rectal cancer: Radiation Therapy Oncology Group Trial 0012. J Clin Oncol Mohiuddin M Winter K Mitchell E Hanna N Yuen A Nichols C et al 2006 24 4 650 655
da Luz MA, Stocchi L, Dietz D, Kalady MF. Neoadjuvant therapy for rectal cancer: the impact of longer interval between chemoradiation and surgery. J Gastrointest Surg De Campos-lobato L. F Geisler D. P 2011 15 3 444 450
Interval between neoadjuvant chemoradiation and surgery for the management of rectal cancer. J Gastrointest Surg Huerta S 2011
Comparative quality of life in patients following abdominoperineal excision and low anterior resection for low rectal cancer. Dis Colon Rectum How P Stelzner S Branagan G Bundy K Chandrakumaran K Heald R. J et al 2012 55 4 400 406
MacFarlane JKRyall RD, Heald RJ. Mesorectal excision for rectal cancer. Lancet 1993 341 8843 457 460
What is the role for the circumferential margin in the modern treatment of rectal cancer? J Clin Oncol Nagtegaal I. D Quirke P 2008 26 2 303 312
Phase I/II study of preoperative cetuximab, capecitabine, and external beam radiotherapy in patients with rectal cancer. Ann Oncol Machiels J. P Sempoux C Scalliet P Coche J. C Van CE Humblet Y et al 2007 18 4 738 744
van de Velde CJ, Lange JF. Level of arterial ligation in rectal cancer surgery: low tie preferred over high tie. A review. Dis Colon Rectum Lange M. M Buunen M 2008 51 7 1139 1145
Laparoscopic- vs. hand-assisted ultralow anterior resection: a prospective study. Dis Colon Rectum Tjandra J. J Chan M. K Yeh C. H 2008 51 1 26 31
Laparoscopic resection for rectal cancers: lessons learned from 579 cases. Ann Surg Ng K. H Ng D. C Cheung H. Y Wong J. C Yau K. K Chung C. C et al 2009 249 1 82 86
Full robotic left colon and rectal cancer resection: technique and early outcome. Ann Surg Oncol Luca F Cenciarelli S Valvo M Pozzi S Faso F. L Ravizza D et al 2009 16 5 1274 1278
A comparison of laparoscopically assisted and open colectomy for colon cancer. N Engl J Med 2004; 350(20):2050-2059.
Short-term endpoints of conventional versus laparoscopic-assisted surgery in patients with colorectal cancer (MRC CLASICC trial): multicentre, randomised controlled trial. Lancet Guillou P. J Quirke P Thorpe H Walker J Jayne D. G Smith A. M et al 2005 365 9472 1718 1726
Laparoscopic surgery versus open surgery for colon cancer: short-term outcomes of a randomised trial. Lancet Oncol Veldkamp R Kuhry E Hop W. C Jeekel J Kazemier G Bonjer H. J et al 2005 6 7 477 484
Randomized clinical trial comparing laparoscopic and open surgery in patients with rectal cancer. Br J Surg Lujan J Valero G Hernandez Q Sanchez A Frutos M. D Parrilla P 2009 96 9 982 989
Laparoscopic versus open surgery for rectal cancer: long-term oncologic results. Ann Surg Laurent C Leblanc F Wutrich P Scheffler M Rullier E 2009 250 1 54 61
de OO, Jr., Trencheva KI, Pandey S, Lee SW, Sonoda T. Long-term outcomes of patients undergoing curative laparoscopic surgery for mid and low rectal cancer. Dis Colon Rectum Milsom J. W 2009 52 7 1215 1222
COLOR II. A randomized clinical trial comparing laparoscopic and open surgery for rectal cancer. Dan Med Bull Buunen M Bonjer H. J Hop W. C Haglind E Kurlberg G Rosenberg J et al 2009 56 2 89 91
Laparoscopic and open surgery for colorectal cancer: reaching equipoise? J Clin Oncol Wagman L. D 2007 25 21 2996 2998
Long-term survival after transanal excision of T1 rectal cancer. Dis Colon Rectum Nash G. M Weiser M. R Guillem J. G Temple L. K Shia J Gonen M et al 2009 52 4 577 582
Local excision of rectal cancer: what is the evidence? Dis Colon Rectum Sengupta S Tjandra J. J 2001 44 9 1345 1361
Impact of preoperative radiation for rectal cancer on subsequent lymph node evaluation: a population-based analysis. Int J Radiat Oncol Biol Phys Baxter N. N Morris A. M Rothenberger D. A Tepper J. E 2005 61 2 426 431
et al. Impact of number of nodes retrieved on outcome in patients with rectal cancer. J Clin Oncol Tepper J. E O Connell M. J Niedzwiecki D Hollis D Compton C Benson A. B Iii 2001 19 1 157 163
Effect of preoperative radiochemotherapy on lymph node retrieval after resection of rectal cancer. Arch Surg Wichmann M. W Muller C Meyer G Strauss T Hornung H. M Lau-werner U et al 2002 137 2 206 210
Key issues in reporting common cancer specimens: problems in pathologic staging of colon cancer. Arch Pathol Lab Med Compton C. C 2006 130 3 318 324
Circumferential margin involvement is still an important predictor of local recurrence in rectal carcinoma: not one millimeter but two millimeters is the limit. Am J Surg Pathol Nagtegaal I. D Marijnen C. A Kranenbarg E. K Van D V Van Krieken J. H 2002 26 3 350 357
Jr., Silva e Sousa AH Jr et al. Operative versus nonoperative treatment for stage 0 distal rectal cancer following chemoradiation therapy: long-term results. Ann Surg Habr-gama A Perez R. O Nadalin W Sabbaga J Ribeiro U 2004 240 4 711 717
Wait-and-see policy for clinical complete responders after chemoradiation for rectal cancer. J Clin Oncol Maas M Beets-tan R. G Lambregts D. M Lammering G Nelemans P. J Engelen S. M et al 2011 29 35 4633 4640
A single-centre experience of chemoradiotherapy for rectal cancer: is there potential for nonoperative management? Colorectal Dis Dalton R. S Velineni R Osborne M. E Thomas R Harries S Gee A. S et al 2012 14 5 567 571
Nonoperative management of rectal cancer with complete clinical response after neoadjuvant therapy. Ann Surg Smith J. D Ruby J. A Goodman K. A Saltz L. B Guillem J. G Weiser M. R et al 2012 256 6 965 972
Male sexual and urinary function after laparoscopic total mesorectal excision. Surg Endosc Morino M Parini U Allaix M. E Monasterolo G Brachet C. R Garrone C 2009 23 6 1233 1240