首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Clinical activity of ipilimumab for metastatic uveal melanoma: A retrospective review of the Dana-Farber Cancer Institute, Massachusetts General Hospital, Memorial Sloan-Kettering Cancer Center, and University Hospital of Lausanne experience
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Clinical activity of ipilimumab for metastatic uveal melanoma: A retrospective review of the Dana-Farber Cancer Institute, Massachusetts General Hospital, Memorial Sloan-Kettering Cancer Center, and University Hospital of Lausanne experience

机译:伊匹木单抗治疗转移性葡萄膜黑色素瘤的临床活动:对达纳-法伯癌症研究所,麻萨诸塞州总医院,斯隆-凯特琳纪念癌症中心和洛桑大学医院的回顾性回顾

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BACKGROUND Uveal melanoma exhibits a high incidence of metastases; and, to date, there is no systemic therapy that clearly improves outcomes. The anticytotoxic T-lymphocyte-associated protein 4 (anti-CTLA-4) antibody ipilimumab is a standard of care for metastatic melanoma; however, the clinical activity of CTLA-4 inhibition in patients with metastatic uveal melanoma is poorly defined. METHODS To assess ipilimumab in this setting, the authors performed a multicenter, retrospective analysis of 4 hospitals in the United States and Europe. Clinical characteristics, toxicities, and radiographic disease burden, as determined by central, blinded radiology review, were evaluated. RESULTS Thirty-nine patients with uveal melanoma were identified, including 34 patients who received 3 mg/kg ipilimumab and 5 who received 10 mg/kg ipilimumab. Immune-related response criteria and modified World Health Organization criteria were used to assess the response rate (RR) and the combined response plus stable disease (SD) rate after 12 weeks, after 23 weeks, and overall (median follow-up, 50.4 weeks [12.6 months]). At week 12, the RR was 2.6%, and the response plus SD rate was 46.%; at week 23, the RR was 2.6%, and the response plus SD rate was 28.2%. There was 1 complete response and 1 late partial response (at 100 weeks after initial SD) for an immune-related RR of 5.1%. Immune-related adverse events were observed in 28 patients (71.8%) and included 7 (17.9%) grade 3 and 4 events. Immune-related adverse events were more frequent in patients who received 10 mg/kg ipilimumab than in those who received 3 mg/kg ipilimumab. The median overall survival from the first dose of ipilimumab was 9.6 months (95% confidence interval, 6.3-13.4 months; range, 1.6-41.6 months). Performance status, lactate dehydrogenase level, and an absolute lymphocyte count ≥1000 cells/μL at week 7 were associated significantly with survival. CONCLUSIONS In this multicenter, retrospective analysis of 4 hospitals in the United States and Europe of patients with uveal melanoma, durable responses to ipilimumab and manageable toxicity were observed. Cancer 2013;119:3687-3695.
机译:背景葡萄膜黑色素瘤表现出高转移率。迄今为止,还没有可以明显改善预后的全身疗法。抗细胞毒性T淋巴细胞相关蛋白4(抗CTLA-4)抗体ipilimumab是转移性黑色素瘤的治疗标准;但是,对于转移性葡萄膜黑色素瘤患者,CTLA-4抑制的临床活性尚不清楚。方法为了评估在这种情况下的ipilimumab,作者对美国和欧洲的4家医院进行了多中心回顾性分析。根据中央,盲法放射学检查确定的临床特征,毒性和影像学疾病负担进行了评估。结果确定了39例葡萄膜黑色素瘤患者,其中34例接受3 mg / kg的ipilimumab的患者和5例接受10 mg / kg的ipilimumab的患者。在12周,23周后以及总体(中位随访时间为50.4周)后,使用免疫相关缓解标准和经修改的世界卫生组织标准评估缓解率(RR)以及综合缓解率加上稳定疾病(SD)率[12.6个月]。在第12周时,RR为2.6%,反应加SD率为46.%;在第23周时,RR为2.6%,反应加SD率为28.2%。免疫相关的RR为5.1%,有1个完全缓解和1个晚期部分缓解(在初始SD后100周)。在28例患者(71.8%)中观察到了与免疫相关的不良事件,其中7例(17.9%)发生了3级和4级事件。接受10 mg / kg ipilimumab的患者的免疫相关不良事件比接受3 mg / kg ipilimumab的患者更为频繁。首次服用ipilimumab的中位总生存期为9.6个月(95%置信区间为6.3-13.4个月;范围为1.6-41.6个月)。在第7周时的生产状况,乳酸脱氢酶水平和绝对淋巴细胞计数≥1000细胞/μL与生存率显着相关。结论在该多中心研究中,对美国和欧洲的4所葡萄膜黑色素瘤患者,对ipilimumab的持久反应和可控制的毒性进行了回顾性分析。癌症2013; 119:3687-3695。

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