Brief Communication: Treatment Outcomes for Advanced Melanoma of Unknown Primary Compared With Melanoma With Known Primary.

IF 3.2 4区 医学 Q3 IMMUNOLOGY Journal of Immunotherapy Pub Date : 2024-11-01 Epub Date: 2024-08-29 DOI:10.1097/CJI.0000000000000537
Oana-Diana Persa, Jessical Cecile Hassel, Theresa Steeb, Michael Erdmann, Bita Karimi, Henner Stege, Kai Christian Klespe, Kerstin Schatton, Dirk Tomsitz, Albert Rübben, Alexander Thiem, Carola Berking, Tilo Biedermann
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Abstract

Summary: Most patients with advanced melanomas have a known primary site [melanoma of known primary (MKP)]. However, 2%-9% of patients are diagnosed with melanoma metastasis of unknown primary (MUP). As MUP and MKP have similar UV-induced mutations and molecular signatures, it is proposed that the primary tumor has regressed completely in patients with MUP. As regression of the primary tumor could be indicative of enhanced recognition of melanoma antigens, we hypothesize that patients with advanced MUP have a better outcome compared with MKP.Patients with advanced MUP from 10 German university hospitals were retrospectively analyzed and matched with MKP based on the type of systemic treatment (BRAF and MEK inhibitors, PD-1 inhibitor monotherapy, combined CTLA-4 and PD-1 inhibitor therapy) therapy line (first or second line) and AJCC stage (IIIC, IV M1a-M1d). Three hundred thirty-seven patients with MUP were identified, and 152 treatments with PD-1 and CTLA-4 inhibitors, 142 treatments with PD-1 inhibitors, and 101 treatments with BRAF and MEK inhibitors were evaluated. Median time to treatment failure was significantly prolonged in patients with MUP treated with PD-1 monotherapy (17 mo, 95% CI: 9-25, P = 0.002) compared with MKP (5 mo, 95% CI: 3.4-6.6), as well as in MUP treated with combined PD-1 and CTLA-4 therapy (11 mo, 95% CI: 4.5-17.5, P < 0.0001) compared with MKP (4 mo, 95% CI: 2.9-5.1) Occurrence of immune-related adverse events and time to treatment failure for patients with BRAF and MEK inhibitors was similar in MKP and MUP. In our multicentre collective, patients with MUP have better outcomes under immunotherapy compared with MKP.

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简讯:原发灶不明的晚期黑色素瘤与已知原发灶黑色素瘤的治疗效果比较。
摘要:大多数晚期黑色素瘤患者的原发部位是已知的[已知原发黑色素瘤(MKP)]。然而,2%-9%的患者被诊断为原发部位不明的黑色素瘤转移(MUP)。由于 MUP 和 MKP 具有相似的紫外线诱导突变和分子特征,因此有人认为 MUP 患者的原发肿瘤已完全消退。我们对来自德国 10 家大学医院的晚期 MUP 患者进行了回顾性分析,并根据系统治疗的类型(BRAF 和 MEK 抑制剂、PD-1 抑制剂单药治疗、CTLA-4 和 PD-1 抑制剂联合治疗)、治疗线(一线或二线)和 AJCC 分期(IIIC、IV M1a-M1d)与 MKP 进行了配对。共确定了 337 例 MUP 患者,评估了 152 种使用 PD-1 和 CTLA-4 抑制剂的治疗方法、142 种使用 PD-1 抑制剂的治疗方法以及 101 种使用 BRAF 和 MEK 抑制剂的治疗方法。与MKP(5个月,95% CI:3.4-6.6)相比,接受PD-1单药治疗的MUP患者治疗失败的中位时间明显延长(17个月,95% CI:9-25,P = 0.002),接受PD-1和CTLA-4联合治疗的MUP患者治疗失败的中位时间也明显延长(11个月,95% CI:4.MKP和MUP中,BRAF和MEK抑制剂患者的免疫相关不良事件发生率和治疗失败时间相似。在我们的多中心研究中,MUP患者接受免疫疗法的疗效优于MKP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Immunotherapy
Journal of Immunotherapy 医学-免疫学
CiteScore
6.90
自引率
0.00%
发文量
79
审稿时长
6-12 weeks
期刊介绍: Journal of Immunotherapy features rapid publication of articles on immunomodulators, lymphokines, antibodies, cells, and cell products in cancer biology and therapy. Laboratory and preclinical studies, as well as investigative clinical reports, are presented. The journal emphasizes basic mechanisms and methods for the rapid transfer of technology from the laboratory to the clinic. JIT contains full-length articles, review articles, and short communications.
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