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Systemic treatment of metastatic uveal melanoma: review of literature and future perspectives

机译:转移性葡萄膜黑色素瘤的系统治疗:文献综述和未来展望

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摘要

Up to 50% of patients with uveal melanoma develop metastatic disease with poor prognosis. Regional, mainly liver-directed, therapies may induce limited tumor responses but do not improve overall survival. Response rates of metastatic uveal melanoma (MUM) to systemic chemotherapy are poor. Insights into the molecular biology of MUM recently led to investigation of new drugs. In this study, to compare response rates of systemic treatment for MUM we searched Pubmed/Web of Knowledge databases and ASCO website (1980–2013) for “metastatic/uveal/melanoma” and “melanoma/eye.” Forty studies (one case series, three phase I, five pilot, 22 nonrandomized, and two randomized phase II, one randomized phase III study, data of three expanded access programs, three retrospective studies) with 841 evaluable patients were included in the numeric outcome analysis. Complete or partial remissions were observed in 39/841 patients (overall response rate [ORR] 4.6%; 95% confidence intervals [CI] 3.3–6.3%), no responses were observed in 22/40 studies. Progression-free survival ranged from 1.8 to 7.2, median overall survival from 5.2 to 19.0 months as reported in 21/40 and 26/40 studies, respectively. Best responses were seen for chemoimmunotherapy (ORR 10.3%; 95% CI 4.8–18.7%) though mainly in first-line patients. Immunotherapy with ipilimumab, antiangiogenetic approaches, and kinase inhibitors have not yet proven to be superior to chemotherapy. MEK inhibitors are currently investigated in a phase II trial with promising preliminary data. Despite new insights into genetic and molecular background of MUM, satisfying systemic treatment approaches are currently lacking. Study results of innovative treatment strategies are urgently awaited.Forty clinical studies on metastatic uveal melanoma were reviewed regarding responses to systemic treatments. New insights into genetic and molecular background led to investigation of new substances but promising in vitro data have not yet been translated into satisfying treatment responses; however, preliminary results of ongoing studies are highly encouraging.
机译:葡萄膜黑色素瘤患者中多达50%会发展为转移性疾病,预后不良。区域性治疗(主要是针对肝脏的治疗)可能会诱导有限的肿瘤反应,但不会改善总体生存率。转移性葡萄膜黑色素瘤(MUM)对全身化疗的反应率很低。最近对MUM分子生物学的洞察力导致了对新药的研究。在本研究中,为了比较MUM全身治疗的反应率,我们在Pubmed / Web of Knowledge数据库和ASCO网站(1980-2013年)中搜索了“转移性/葡萄膜/黑色素瘤”和“黑色素瘤/眼”。数值结果包括40项研究(一项病例系列,三个I期,五个先导,22个非随机和两个II期,一项随机III期研究,三个扩展访问计划的数据,三个回顾性研究),包括841名可评估患者分析。在39/841例患者中观察到全部或部分缓解(总缓解率[ORR] 4.6%; 95%可信区间[CI] 3.3-6.3%),在22/40研究中未观察到缓解。 21/40和26/40研究分别报告无进展生存期为1.8至7.2,中位总生存期为5.2至19.0个月。化学免疫治疗反应最好(ORR 10.3%; 95%CI 4.8-18.7%),尽管主要是在一线患者中。依匹莫单抗,抗血管生成方法和激酶抑制剂的免疫疗法尚未被证明优于化学疗法。目前,MEK抑制剂已在II期试验中进行了研究,初步数据令人鼓舞。尽管对MUM的遗传和分子背景有了新的见解,但目前仍缺乏令人满意的全身治疗方法。迫切需要创新治疗策略的研究结果。综述了40例关于转移性葡萄膜黑色素瘤的临床研究对全身治疗的反应。对遗传和分子背景的新见解导致对新物质的研究,但有希望的体外数据尚未转化为令人满意的治疗反应。但是,正在进行的研究的初步结果令人鼓舞。

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