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纳武利尤单抗联合伊匹木单抗用于未经化疗的不可切除晚期黑色素瘤的II期研究的最终分析。

Final analysis of a phase II study of nivolumab in combination with ipilimumab for unresectable chemotherapy-naive advanced melanoma.

作者信息

Namikawa Kenjiro, Kiyohara Yoshio, Takenouchi Tatsuya, Uhara Hisashi, Uchi Hiroshi, Yoshikawa Shusuke, Takatsuka Sumiko, Koga Hiroshi, Wada Naoko, Minami Hironobu, Hatsumichi Masahiro, Namba Yoshinobu, Yamazaki Naoya

机构信息

Department of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.

Dermatology Division, Shizuoka Cancer Center Hospital, Shizuoka, Japan.

出版信息

J Dermatol. 2020 Nov;47(11):1257-1266. doi: 10.1111/1346-8138.15514. Epub 2020 Aug 18.

Abstract

Nivolumab plus ipilimumab combination is currently one of the preferred regimens for advanced melanoma in recently updated clinical practice guidelines. However, the evidence on the efficacy of the combination for acral or mucosal subtypes remains less robust. This is the final analysis of a multicenter, open-label, uncontrolled phase II study that investigated the long-term efficacy and safety in treatment-naive Japanese patients with advanced melanoma, including acral or mucosal subtypes, and subsequent therapy after discontinuation of the investigational agents. Patients received four doses of nivolumab (1 mg/kg i.v.) in combination with ipilimumab (3 mg/kg i.v.) at 3-week intervals, followed by doses of nivolumab (3 mg/kg i.v.) at 2-week intervals. The median follow-up period was 20.8 months (range, 5.2-35.0). The centrally and locally assessed objective response rates were both 43.3% (13/30; 95% confidence interval [CI], 25.5-62.6). Median progression-free survival was not reached (95% CI, 3.02-not reached), and median overall survival was also not reached (95% CI, 19.52-not reached). The 30-month progression-free survival and overall survival rates were 50.3% and 54.2%, respectively. No new safety concerns were detected. After discontinuation of the investigational agents, 83.3% of patients received some form of subsequent therapy including 43.3% of patients who received nivolumab monotherapy and 26.7% of patients who received radiotherapy. Of the four patients who discontinued the investigational agents because of immune-related adverse events, two received subsequent therapy (nivolumab and ipilimumab, respectively) and the other two showed long-term treatment-free survival (659 and 590 days, respectively). Long-term survival with nivolumab plus ipilimumab was observed in Japanese patients with melanoma including acral and mucosal subtypes, which is consistent with the CheckMate 067 study. Many patients continued to receive some form of treatment safely after stopping treatment with nivolumab plus ipilimumab.

摘要

在最近更新的临床实践指南中,纳武利尤单抗联合伊匹木单抗方案是目前晚期黑色素瘤的首选方案之一。然而,该联合方案对肢端或黏膜亚型黑色素瘤疗效的证据仍不充分。这是一项多中心、开放标签、非对照的II期研究的最终分析,该研究调查了初治的日本晚期黑色素瘤患者(包括肢端或黏膜亚型)接受研究药物治疗的长期疗效和安全性,以及停药后的后续治疗情况。患者接受4剂纳武利尤单抗(1mg/kg静脉注射)联合伊匹木单抗(3mg/kg静脉注射),每3周一次,随后接受纳武利尤单抗(3mg/kg静脉注射),每2周一次。中位随访期为20.8个月(范围5.2 - 35.0个月)。中心评估和局部评估的客观缓解率均为43.3%(13/30;95%置信区间[CI],25.5 - 62.6)。中位无进展生存期未达到(95%CI,3.02 - 未达到),中位总生存期也未达到(95%CI,19.52 - 未达到)。30个月的无进展生存率和总生存率分别为50.3%和54.2%。未发现新的安全问题。停药后,83.3%的患者接受了某种形式的后续治疗,其中43.3%的患者接受了纳武利尤单抗单药治疗,26.7%的患者接受了放疗。在因免疫相关不良事件停药的4例患者中,2例接受了后续治疗(分别为纳武利尤单抗和伊匹木单抗),另外2例显示长期无治疗生存(分别为659天和590天)。在包括肢端和黏膜亚型的日本黑色素瘤患者中观察到纳武利尤单抗联合伊匹木单抗的长期生存情况,这与CheckMate 067研究结果一致。许多患者在停止使用纳武利尤单抗联合伊匹木单抗治疗后继续安全地接受某种形式治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b089/7693067/05d5f470925c/JDE-47-1257-g001.jpg

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