Grossmann Kenneth F, Margolin Kim
Division of Oncology, Department of Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Division of Oncology, Stanford University, Stanford, CA, USA.
Ther Adv Med Oncol. 2015 May;7(3):181-91. doi: 10.1177/1758834015572284.
Historically, stage III-IV melanoma patients have had few options to achieve long-term survival. For patients with stage III disease, surgery alone may be curative for approximately 50%. Adjuvant treatment with a slightly greater impact on relapse-free survival at the cost of substantial toxicity, and studies are ongoing to test the adjuvant benefit of other immunotherapies that appear more active and less toxic in advanced melanoma. Achieving long term survival for stage IV patients had been rare until recently and progress was painfully slow with traditional cytotoxic chemotherapy; review of multiple phase II studies showed universally poor results. Fortunately, since the approval by the US Food and Drug Administration of agents targeting the cytotoxic T lymphocyte antigen-4 (CTLA-4) receptor, as well as those targeting B-raf and mitogen-activated protein kinase kinase (MEK) in the mitogen-activated protein kinase (MAPK) pathway for patients whose melanoma is 'driven' by a BRAF mutation, long-term survival of stage IV melanoma is increasing substantially. Here we review the examples of studies documenting potentially curative approaches to melanoma and propose suggestions for the use of various treatments in achieving this important goal.
从历史上看,III-IV期黑色素瘤患者实现长期生存的选择很少。对于III期疾病患者,单纯手术可能治愈约50%的患者。辅助治疗对无复发生存期有稍大影响,但代价是有相当大的毒性,目前正在进行研究以测试其他免疫疗法在晚期黑色素瘤中的辅助益处,这些免疫疗法似乎更有效且毒性更低。直到最近,IV期患者实现长期生存还很罕见,传统细胞毒性化疗的进展极其缓慢;对多项II期研究的回顾显示结果普遍不佳。幸运的是,自从美国食品药品监督管理局批准了针对细胞毒性T淋巴细胞抗原-4(CTLA-4)受体的药物,以及针对黑色素瘤由BRAF突变“驱动”的患者的有丝分裂原激活蛋白激酶(MAPK)途径中的B-raf和有丝分裂原激活蛋白激酶激酶(MEK)的药物以来,IV期黑色素瘤的长期生存率正在大幅提高。在此,我们回顾记录黑色素瘤潜在治愈方法的研究实例,并就使用各种治疗方法实现这一重要目标提出建议。