Centre for Dermatooncology, Department of Dermatology, Eberhard Karls University, Tuebingen, Germany.
Institute of Dermatology, Catholic University, Rome, Italy.
Eur J Cancer. 2016 Aug;63:201-17. doi: 10.1016/j.ejca.2016.05.005. Epub 2016 Jun 29.
Cutaneous melanoma (CM) is potentially the most dangerous form of skin tumour and causes 90% of skin cancer mortality. A unique collaboration of multi-disciplinary experts from the European Dermatology Forum, the European Association of Dermato-Oncology and the European Organisation of Research and Treatment of Cancer was formed to make recommendations on CM diagnosis and treatment, based on systematic literature reviews and the experts' experience. Diagnosis is made clinically using dermoscopy and staging is based upon the AJCC system. CMs are excised with 1-2 cm safety margins. Sentinel lymph node dissection is routinely offered as a staging procedure in patients with tumours >1 mm in thickness, although there is as yet no clear survival benefit for this approach. Interferon-α treatment may be offered to patients with stage II and III melanoma as an adjuvant therapy, as this treatment increases at least the disease-free survival and less clear the overall survival (OS) time. The treatment is however associated with significant toxicity. In distant metastasis, all options of surgical therapy have to be considered thoroughly. In the absence of surgical options, systemic treatment is indicated. For first-line treatment particularly in BRAF wild-type patients, immunotherapy with PD-1 antibodies alone or in combination with CTLA-4 antibodies should be considered. BRAF inhibitors like dabrafenib and vemurafenib in combination with the MEK inhibitors trametinib and cobimetinib for BRAF mutated patients should be offered as first or second line treatment. Therapeutic decisions in stage IV patients should be primarily made by an interdisciplinary oncology team ('Tumour Board').
皮肤黑色素瘤(CM)是最危险的皮肤肿瘤形式,导致 90%的皮肤癌死亡。为了基于系统文献回顾和专家经验就 CM 的诊断和治疗提出建议,来自欧洲皮肤病学会、欧洲皮肤肿瘤学会和欧洲癌症研究与治疗组织的多学科专家进行了独特的合作。诊断采用临床皮肤科检查,分期依据 AJCC 系统。CM 采用 1-2cm 安全边界切除。对于厚度>1mm 的肿瘤,常规进行前哨淋巴结清扫作为分期手术,但目前这种方法尚无明确的生存获益。对于 II 期和 III 期黑色素瘤患者,可以作为辅助治疗提供干扰素-α治疗,因为这种治疗至少增加无病生存期,对总生存期(OS)的影响不太明确。但该治疗方法存在显著毒性。在远处转移中,需要彻底考虑所有手术治疗方案。在没有手术选择的情况下,应进行全身治疗。对于一线治疗,特别是在 BRAF 野生型患者中,应考虑单独使用 PD-1 抗体或与 CTLA-4 抗体联合进行免疫治疗。对于 BRAF 突变患者,应提供达拉非尼和维莫非尼联合 MEK 抑制剂曲美替尼和 cobimetinib 作为一线或二线治疗。IV 期患者的治疗决策应由多学科肿瘤团队(“肿瘤委员会”)主导。