Kasper Bernd, D'Hondt Veronique, Vereecken Pierre, Awada Ahmad
Clinic of Medical Oncology, Institut Jules Bordet, Boulevard de Waterloo 125, Brussels 1000, Belgium.
Crit Rev Oncol Hematol. 2007 Apr;62(1):16-22. doi: 10.1016/j.critrevonc.2006.11.007. Epub 2007 Jan 5.
Malignant melanoma is one of the most common cancer types among the Caucasian population. While the prognosis is excellent for patients diagnosed at an early stage and treated by adequate surgery, unresectable or advanced metastatic diseases shrink the overall survival at 5 years dramatically to less than 10%. For disseminated malignant melanoma, the appropriate systemic medical treatment is still controversial. Fortunately, progress in the molecular biology and in the understanding of pathogenesis has been made recently and should in the near future translate into molecular-based therapeutic strategies. In this review, we briefly describe the status of current treatment strategies and existing standards for malignant melanoma. We will focus on the new and emerging compounds including recent developments of targeted therapy such as antiangiogenic and immunomodulatory drugs, Bcl-2 antisense therapy, raf kinase inhibitors, heat shock protein modulators, anti-cytotoxic T lymphocyte-associated antigen (CTLA)-4 monoclonal antibody and finally PARP and proteasome inhibitors.
恶性黑色素瘤是白种人群中最常见的癌症类型之一。虽然早期诊断并接受充分手术治疗的患者预后良好,但无法切除或晚期转移性疾病会使5年总生存率大幅降至不到10%。对于播散性恶性黑色素瘤,合适的全身药物治疗仍存在争议。幸运的是,最近在分子生物学和发病机制理解方面取得了进展,有望在不久的将来转化为基于分子的治疗策略。在本综述中,我们简要描述了恶性黑色素瘤当前治疗策略的现状和现有标准。我们将重点关注新出现的化合物,包括抗血管生成和免疫调节药物等靶向治疗的最新进展、Bcl-2反义治疗、raf激酶抑制剂、热休克蛋白调节剂、抗细胞毒性T淋巴细胞相关抗原(CTLA)-4单克隆抗体,以及最后介绍的PARP和蛋白酶体抑制剂。