Clinical and pathological staging, AJCC 2009
In this chapter, cutaneous metastases from malignant melanoma will be analyzed from a clinical and a prognostic point of view.
This non rare condition is often distressing for the patient, as cutaneous lesions increase progressively in number and size and are frequently worsened by ulceration, bleeding and pain.
After a general introduction about the incidence of cutaneous involvement in melanoma natural history, clinical classification of skin metastases will be provided. Then, the impact of cutaneous localizations on prognosis will be evaluated. In the last paragraph, the different therapeutic options for the management of patients with loco-regional or diffused cutaneous metastases will be reviewed.
Skin metastases from solid tumor are not rare. They affect an estimated percentage of patients ranging from 0.7 to 9% in several literature series (Spencer & Helm 1987, Lookingbill, Spangler & Helm 1993, Schwartz 1995, Hu et al. 2008), in the late phases of disease progression or, in more than 7% of patients, as first sign of disseminated disease (Lookingbill, Spangler & Helm 1993, Rosen 1980). Breast cancer is the most commonly involved tumor, accounting for more than 60% of cases of cutaneous spread, followed by colon carcinoma (Krathen, Orengo & Rosen 2003). Moreover, cutaneous metastatic disease is commonly seen with cancer of the lung, kidney and ovary and with sarcoma, lymphoma or leukemia.
As expected, tumor types are differently distributed among the two genders: lung, colon and head and neck tumours together with melanoma account for the majority of skin metastases in males; whereas, breast cancer is the most common neoplasm related to the development of cutaneous secondary lesions in females (Hu et al 2008).
Focusing on melanoma, skin metastases represent a relatively frequent event in the natural history of the disease and can develop in early as well as in late stage of disease. Cutaneous or subcutaneous lesions arise in 10-17% of patients affected by melanoma and almost the 50% of patients with metastatic disease develops skin involvement (Lookingbill, Spangler & Helm 1993, Schwartz 1995, Krathen, Orengo & Rosen 2003).
No specific clinical or histological characteristics were found in patients with cutaneous metastases from melanoma if compared to those with visceral localizations (Savoia et al 2009). However, known risk factors related to prognosis impact on the metastatic melanoma potential.
On the basis of the distance from the primary melanoma, skin metastases are described as local recurrences, in transit disease or distant metastases.
True local recurrences are defined as the reappearance of melanoma in -or contiguous with- an excision scar or a graft and bearing an in situ component (Olsen et al 1970; Brown & Zitelli 1995). The prognosis of local recurrence defined strictly in this way is much better than that associated with in transit disease and 5-year survival rate is related only to the thickness of the primary melanoma. These recurrences are in fact considered as a result of a uncompleted resection of primary melanoma, and are for this reason becoming rare.
In-transit disease (satellitosis) indicates cutaneous or subcutaneous disease between the primary site and the regional lymph nodes. Satellite nodules and in-transit disease are associated with worse prognosis (super imposable to a melanoma with nodal metastases; stage III disease), and the distance of cutaneous deposits from the primary site has no prognostic significance (Balch et al 2009).
Distant cutaneous metastases are defined as tumour lesions that grow in any skin site over the regional lymph nodes. The presence of any distant metastases delineates a stage IV disease, even if patients with sole distant skin metastases (and normal serum LDH levels) have a relatively better prognosis if compared with those of other metastatic patients (Balch et al 2009). Obviously, distant skin melanoma localization can appear together with or in absence of other visceral metastases. Stage and prognosis vary according to AJCC classification as shown in table 1 (Balch et al 2009).
|Clinical Staging||Pathological Staging|
|III||any T||N 1-3||M0||IIIA||T1-T4a||N1a/2a||M0|
|IV||any T||any N||M 1||IV||any T||any N||M 1|
4. Clinical features
Skin metastases from melanoma can arise as single or multiple nodules. The most common presentations of cutaneous metastatic disease are brown to black or skin colored papules and nodules, sometimes ulcerated. In the majority of these cases cutaneous metastases were correctly identified by the clinician before the pathologic diagnosis was given; dermoscopy could help in diagnosis, even if skin melanoma metastases have often aspects that are indistinguishable from the characteristic pattern of blue nevi (Carlos-Ortega, de Oca-Monroy & Isyta-Morales 2008). Epidermotropic melanoma metastases are histopatologically characterized by aggregates of atypical melanocytes within the dermis with thinning of the epidermis. Usually there is no lateral extension of atypical melanocytes within the epidermis beyond the concentration of the metastases on the dermis. Metastases differs from primary melanoma by the absence of inflammatory infiltrate and junctional activity, even if a prominent lymphocytic infiltrated can be sometimes observed. In few cases metastatic cells are small and nevoid, with few or any mitoses and differentiation from compound nevi is difficult (Elder E et al, 2005. Tumours and Cysts in dermis and Subcutis, in
Less frequently, a wide morphological spectrum of lesions has been described, including erythematous patches or plaques, inflammatory erysipela-like lesions, diffuse sclerodermiform lesions with indurations of the skin (‘‘en cuirasse’’ metastatic carcinoma), telangiectatic papulovesicles, purpuric plaques mimicking vasculitis, and alopecia aerate-like scalp lesions (Saeed, Keehn & Morgan 2004, Sariya et al 2007). In these cases, clinical diagnosis could be more challenging and metastases can be suspicious for benign entities (Figure 1).
Moreover, there are also rare cases of so-called zosteriform metastases, with vesicobullous herpetiform lesions or papules and nodules distributed along one or more dermatomes. A previous Varicella Zoster Virus (VZV) infection or widespread lymphatic obstruction by tumor cells can justify the zosteriform pattern (Figure 2).
From a clinical point of view, if bleeding and super-infection are not present, superficial skin metastases are usually asymptomatic, even if patients frequently report localized pain and paresthesiae anticipating the onset of clinically evident cutaneous lesions; these symptoms are related to oedema and mechanical stress on the near tissues and usually disappear in a few days. On the other hand, when subcutaneous lesions grow deep infiltrating muscles or nerves become very painful. The management of pain in these cases could be difficult and requires a multidisciplinary approach.
As mentioned earlier, bleeding and super-infections are the most frequent complications of skin metastases and can significantly impact on the patient's quality of life (Kaheler, Egeberts & Hauschild 2010). These complications can also compromise general conditions. Massive bleeding from cutaneous metastases could become life threatening; sepsis related to the bacterial dissemination of infected metastases represents an uncommon but not rare event, that lead to septic shock and death (Figure 3).
5. Pattern of cutaneous localizations
Cutaneous secondary lesions can occur on all anatomic sites, with skin metastases from other solid tumours more frequently found on the head, neck, anterior chest and abdomen, whereas lower extremities are rarely involved (Schwartz, 1995). Conversely
6. Clinical course and prognosis
In more than half of the cases, skin represents the first site of metastatic involvement after the primary melanoma diagnosis. In about one third of cases, patients develop skin involvement after evidences of regional lymph nodal metastatic disease.
The finding of concomitant distant cutaneous, visceral and nodal metastases account for more than 10% of cases, whereas skin involvement after visceral dissemination is rare, and occurs only in about the 3% of patients (Savoia et al 2009).
Cutaneous metastases are loco regional in nearly 80% of cases, whereas distant metastases were documented in the remaining 20% of patients. A different pattern of cutaneous metastases was related to the time of onset: when cutaneous metastases arise as the first site of relapse, there is a significant higher percentage of locoregional localizations, whereas distant skin involvement was more frequently observed after visceral involvement. No significant differences were found between patients with regional and those with distant metastases regarding to the known risk factors, such as Breslow thickness, Clark level, histotype of the primary melanoma and ulceration (Savoia et al 2009).
It is noteworthy that in patients with distant metastases, primary melanomas arose predominantly at trunk and back, whereas patients with cutaneous loco-regional spreading were affected mainly by primary located at leg and foot. As we know, loco-regional metastases develop as a result of tumour cell embolization in the dermal lymphatic vessels between the primary tumour site and the draining regional lymph node basin; lymphatic stasis to lower limbs consequent to nodal dissection represents an additional risk factor for cutaneous locoregional dissemination.
In contrast, the correlation between disseminated skin lesions and primary melanoma located to the trunk could be explained by the fact that the lymph drainage of this region is not strictly dependent on a single station, but it could be resulted from more than one lymphatic basin, together with a possible role of haematogenous spreading.
Disease free survival evaluated from the first melanoma diagnosis varies in relation to the first site of metastatization. In our experience, loco regional cutaneous relapses develop early, but show a very late progression to visceral disease. On the contrary, patients with disseminated skin lesions as first site of relapse had a longer disease free interval from the first diagnosis but a shorter time to progression to visceral metastases (Savoia et al 2009).
7. Treatment and clinical management
The choice of the modality of treatment for cutaneous melanoma metastases depends on several factors, including location and number of lesions, presence of systemic involvement, age and general health conditions of patients. Moreover, the prognostic differences between patients with loco-regional and distant skin metastases justify different approaches in their clinical management.
Important therapeutic options including surgery, isolated limb perfusion, local or systemic chemo- and immuno-therapy and radiotherapy are discussed in detail below.
Surgery is the gold standard and represents the most effective treatment for limited in-transit disease, when technically feasible. It is an adequate treatment when the lesions are relatively small and clustered in a reasonable circumscribed area. Primary melanoma should be excised widely with a 1-2 cm margin depending on Breslow thickness, whereas wide surgical margins are unnecessary for the treatment of cutaneous metastases. Usually, metastases are clearly demarcated from the surrounding normal dermis and overlying epidermis and the better approach is the complete macroscopical excision of the lesion. When microscopical involvement of margins is documented, reintervention is not mandatory (Hoekstra, 2008).
If technically possible, direct wound closure is to prefer; the second choice is represented by skin graft, because plastic surgical reconstruction can affect the lymphatic drainage pattern.
Palliative treatment should be considered when results in the control of local complications (e.g. bleeding) and/or in a consistent quality of life improvement.
Amputation should be only considered as palliation for imminent exsanguinating haemorrhage or fungation unacceptable for the patient.
7.2. Isolated limb perfusion
Isolated limb perfusion (ILP) -firstly described by Creech and Krementz in 1958- can deliver high doses of cytotoxic agents to a limb, minimizing systemic toxicity. The dose received regionally can be up to tenfold higher than the systemic mean tolerated dose. Isolated limb perfusion is widely indicated for patients with advanced or recurrent in-transit disease, showing a complete response rate around the 50% in the majority of the published series, with an overall response rate up to 80% (Lens & Dawes 2003, Rossi et al 2010). On the contrary, the role of isolated limb perfusion as adjuvant therapy is still debated (Hoeckstra 2008). The tumour response after perfusion is the only demonstrated prognostic factor affecting local control of the disease and overall survival (Rossi et al 2010).
The usual agent employed is melphalan, with or without tumour necrosis factor (TNF); TNF increases response rate thanks to its selective disruption of the tumour microvasculate, with a consequent ischemic damage of melanoma cells, even if seems not to influence the long term local control (Di Filippo et al 2006). Dacarbazine is less effective when administered regionally; other combinations of cytostatics (dactinomycin, nitrogen mustard, vindesine, thio-TEPA) have also been proposed but the published series are too small to give absolute conclusions (Daryanani et al 2000, de Wilt et al 2000, Hoeckstra 2008). Hyperthermia, with temperature between 39 to 41 act sinergically with high dose chemotherapy, even if can exacerbate loco regional toxicity (Hoeckstra 2008).
General anesthesia is required. However, age does not represent a contraindication to ILP. Systemic side effects, due to drug releasing into the systemic circulation are rare and mainly represented by nausea, vomiting and mild bone marrow suppression. Local toxic reactions are more frequently described and ranges from mild erythema to deep tissue inflammation; nearly 25% of patients develop neuropathy or pain, whereas chronic edema is usually related to lymphoadenenctomy (Bonifati et al 2000, Rossi et al 2002).
Recently, electrochemotherapy (ECT) has been proposed as a new treatment modality for skin metastases of different malignancy, including melanoma. ECT enhances membrane permeability by electric pulses thus permitting a major drug delivery in neoplastic cells and a better cytotoxic effect.
Bleomycin and cisplatin are the drugs more frequently used in ECT with an increased efficacy up to 8.000-fold for bleomicyn, and up to 80-fold for cisplatin (Gaudy et al 2006).
The ECT technique requires only a regional anesthesia or mild general sedation with a lower duration if compared to isolated limb perfusion. With respect to ILP, ECT shows a minimal systemic toxicity; treatment is generally well tolerated; side effects were mainly represented by erythema and edema at the site of treated lesions, superficial erosions, scars and permanent marks from the electrodes (Quaglino et al 2008). Thus ECT can be performed also in patients with major co morbidities.
The first large study about effectiveness of ECT in melanoma treatment, was the multi center European Standard Operating Procedure of Eettrochemoterapy (ESOPE), based on the new CliniporatorTM Elettric Pulse Generator; this study enrolled twenty melanoma patients, with an overall response rate of more than 20% (Marty et al 2008). Several papers recently published confirm these encouraging results of ECT in the control of skin metastases (Campana et al 2009, Moller et al 2009). In our experience, the global response rate was of 79.4, with a percentage of complete remissions of 23.2%(Quaglino et al 2008); complete response was defined in accordance World Health Organiziation (WHO) guidelines as the total clinical disappearance of the tumor (WHO. From
The lesion size was the most predictive parameter for response; response rate for larger lesions was significantly lower. Moreover, a second limit is represented by the possible relapse of new lesions on untreated areas: ECT represent in fact a local treatment. However, it is possible to repeat ECT, both on new metastases in untreated areas and on already treated lesions with a previous partial remission or no changes. In our experience, new responses were obtained in about 60% of retreated lesions.
Appropriate dressing should be performed with the aim to control ulceration of cutaneous tumours, local infectious complications and to ensure an acceptable quality of life.
The effectiveness of radiotherapy in the treatment of melanoma metastases is still debated. A poor response was historically observed on in vitro cultures from melanoma cells treated with external-beam radiation (Barranco, Romsdahl & Humphrey 1971). So, radiotherapy was mainly used as palliation when disease was too extensive for surgery and other modalities of treatment were inadvisable or ineffective in stage III and IV melanoma patients. However, a retrospective review (Fenig et al 2009) showed a 52% response rate in stage IV patients who received radiotherapy with palliative intent and others studies (Sause et al 1991; Seegenschmeid et al 1999) demonstrated an overall response rate ranging from 60 to 79% for stage III disease. Moreover, disease-free and overall survival seems to be significant longer in patients who received radiotherapy (Olivier et al, 2007).
Usually, chemotherapy plays a role in the treatment of stage IV melanoma patients with visceral metastases. Regarding cutaneous metastases, chemotherapy can be used in patients with wide spread skin lesions not eligible for local treatments, with or without a concomitant visceral involvement.
Chemotherapy could be used also in stage III, when other loco-regional treatments have failed or are technically not feasable (e.g. cutaneous lesions diffused at trunk or back).
The global response rate is less than 25% for single agent treatment. The gold standard is still represented by Dacarbazine; new molecules as Temozolomide and Fotemustine showed a super imposable disease-free and overall survival, with major toxicity (Middelton et al, 2000). Combination regimens or chemo-immunotherapy give higher response rate but also more severe side effects. However, response to chemo-immunoterapy is not related to statistically significant benefit in term of overall survival when compared with a single-agent treatment.
Recently, Ipilimumab, a human anti-CTLA4 monoclonal antibody showed objective responses or disease stabilization in patients with advanced melanoma (O'Day et al, 2010). No data about the effectiveness of Ipilimumab in the treatment of cutaneous metastases are available, even if several studies are ongoing.
The response rate for in transit metastases treated with dacarbazine is 15-20%; the majority of the responses are partial with a median response duration less than 6 months. Chemoimunotherapy showed also no survival benefit (Hoekstra 2008).
Finally, the clinical efficacy of RAF inhibitors in BRAF mutated melanoma patients are under evaluation after some encouraging preliminary report; a phase I study on patients with both disseminated cutaneous and visceral metastases reported an 81% of clinical responses in patients treated with selective BRAF inhibitor, with a median time to progression of 6-9 months (Flaherty, 2010).
7.6.1. Laser ablation
Patients with small (<2 cm) and superficial lesions who are not suitable for isolated limb perfusion, ECT or other conventional modalities of treatment can be considered for carbon dioxide (CO2) laser ablation. This therapy is minimally invasive: only local anesthesia is required and the resultant defect does not require surgical closure but can be covered with a dressing until secondary healing (Lingam & McKay, 1996; Gibson, Byrne & Mc Kay, 2004). So, can be considered a minimally invasive and effective method of palliation; the role as first line treatment is still debated, in fact the technique can be used to treat only visible and superficial lesions, while deep subcutaneous metastases, large volume lesions and microscopic disease can not be treated with laser ablation (Gimbel, Delman & Zager, 2008).
This technique uses temperatures from -50 C to -60 C (with nitrogen spray) to obtain direct tissue destruction. The heat transfer results in vascular stasis, ice crystal and disruption of cell membranes, Ph changes, hypertonic damage and thermal shock that lead to tissue damage and necrosis. Low temperature causes the development of a bulla and a secondary healing with a scar. After the introduction of laser ablation and ECT, cryosurgery is less frequently used in the treatment of cutaneous metastases from melanoma (Hoekstra, 2008).
7.6.3. Intralesional therapy
The intralesional injection of bacillus Calmette-Guérin (BCG) was the first immunotherapy used in the local treatment of cutaneous metastases from melanoma. This procedure was accompanied by sever complications such as ulceration, skin necrosis, and superinfection without significative improvement of lesions treated (Tan & Ho, 1993). Other drugs such as IL-2, INF alpha and dinitrochlorobenzene, with or without sistemic dacarbazine, were more recently used as intralesional therapy (Radny et al, 2003; Strobbe et al, 1997); results are still debating and further investigations are necessary. Encouraging results regarding high-dose intratumoral IL-2 administration in melanoma patients with cutaneous secondarities has been reported (Weide et al, 2010): a complete local response was described in more than 60% of melanoma patients and seemed to be associated with an increased responses to subsequent chemotherapies. Recently, phase I studies confirmed the safety and an enhanced immune response for intralesional injection of Allovectin in metastatic melanoma patients. Unfortunately, phase II studies showed a complete response in only the 3.1% of treated patients, with an overall response rate of 11.8% and a median time-to-progression of 1.6 months (Beidikan et al, 2010).
Rose bengal has been proposed as a possible intralesional treatment, with an objective response rate ranging from 27 to 69%, related to the dose of injection (Thompson, Hersey & Wachter, 2008). Sistemic toxicity is low, even if phototoxic reactions have been described.
An interesting therapeutic option is represented by topical imiquimod. It enhances the immune system activity leading to an induction of melanoma-specific cytotoxic T-cells by cross presentation of melanoma antigen by dendritic cells. Partial remission of locoregional cutaneous metastases treated with imiquimod was demonstrated (Wolf, Richtig, Kopera & Kerl H, 2004).
Skin metastases from melanoma are a frequent finding in the natural history of the disease with various clinical, morphological and histopathologic backgrounds. The presence of progressively increasing metastases is often distressing for the patient, and ulceration, bleeding and super-infections can negatively impact on the life-quality. To date, many treatments are available for the clinical management of these lesions. Thus, clinicians should be informed about the prognostic implications and the therapeutic options in order to choose the best cost-effectiveness treatment modality.