Menaa Farid
Department of Oncology, Stem Cells and Nanomedicine, Fluorotronics, Inc., 2453 Cades Way, Building C, San Diego, CA 92081, USA.
J Skin Cancer. 2013;2013:735282. doi: 10.1155/2013/735282. Epub 2013 Feb 24.
Nowadays, oncogene-directed therapy and immunotherapy represent the two most promising avenues for patients with metastatic melanoma. The recent oncogene-directed therapeutic, vemurafenib, usually produces high level of tumor shrinkage and survival benefits in many patients with B-RAF (V600E) mutant melanomas, although the fast and high degrees of responses are likely short-lived. Conversely, the newly-approved immunotherapeutic, ipilimumab, produces durable responses in patients presenting CTLA-4 T-cell surface protein. Nevertheless, the possible synergy in combining these two therapeutic strategies primarily rely on the rational design of medical protocols (e.g., sequence and timing of agent administration; drug selectivity; compatibility of combined therapies i.e., adoptive T cell or agents, i.e., MEK inhibitor trametinib, PD-1 and PDL-1 blockers). Improved therapeutic protocols shall overcome therapeutic limitations such as the (i) tolerability and safety (i.e., minimal toxic side-effects); (ii) progression free survival (e.g., reduced relapse disease frequency); (iii) duration response (i.e., decreased drug resistance). Eventually, multidisciplinary approaches are still requested (e.g., genomics for personalized medicine, nanomedicine to overcome low free-drug bioavailability and targeting, systematic search of "melanoma stem cells" to enhance the prognosis and develop more valuable theranostics). In this paper, I will mainly present and discuss the latest and promising treatments for advanced cutaneous melanomas.
如今,针对癌基因的疗法和免疫疗法是转移性黑色素瘤患者最有希望的两条治疗途径。最近的针对癌基因的治疗药物维莫非尼,通常能使许多携带B-RAF(V600E)突变的黑色素瘤患者产生高水平的肿瘤缩小并带来生存益处,尽管快速且高度的反应可能是短暂的。相反,新批准的免疫治疗药物伊匹单抗,能使表达CTLA-4 T细胞表面蛋白的患者产生持久反应。然而,将这两种治疗策略相结合可能产生的协同作用主要依赖于医疗方案的合理设计(例如,药物给药的顺序和时间;药物选择性;联合疗法的兼容性,即过继性T细胞或药物,如MEK抑制剂曲美替尼、PD-1和PDL-1阻断剂)。改进的治疗方案应克服诸如(i)耐受性和安全性(即最小的毒副作用);(ii)无进展生存期(例如,降低疾病复发频率);(iii)反应持续时间(即降低耐药性)等治疗局限性。最终,仍需要多学科方法(例如,用于个性化医疗的基因组学、用于克服低游离药物生物利用度和靶向性的纳米医学、系统搜索“黑色素瘤干细胞”以改善预后并开发更有价值的诊疗方法)。在本文中,我将主要介绍和讨论晚期皮肤黑色素瘤的最新且有前景的治疗方法。