Department of Dermatology and Allergy, School of Medicine, Technical University of Munich, Bavarian Cancer Research Center (BZKF), Munich, Germany.
Department of Dermatology and Venereology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
J Immunother. 2024;47(9):384-387. doi: 10.1097/CJI.0000000000000537. Epub 2024 Aug 29.
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.
大多数晚期黑色素瘤患者有已知的原发部位[已知原发性黑色素瘤 (MKP)]。然而,有 2%-9%的患者被诊断为黑色素瘤不明原发灶转移 (MUP)。由于 MUP 和 MKP 具有相似的紫外线诱导突变和分子特征,因此推测 MUP 患者的原发肿瘤已完全消退。由于原发肿瘤的消退可能表明黑色素瘤抗原的识别增强,我们假设与 MKP 相比,晚期 MUP 患者的预后更好。
对来自 10 家德国大学医院的晚期 MUP 患者进行回顾性分析,并根据系统治疗类型(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 进行匹配。共确定 337 例 MUP 患者,其中 152 例接受 PD-1 和 CTLA-4 抑制剂治疗,142 例接受 PD-1 抑制剂治疗,101 例接受 BRAF 和 MEK 抑制剂治疗。
与 MKP 相比,接受 PD-1 单药治疗的 MUP 患者(17 个月,95%CI:9-25,P = 0.002)和接受 PD-1 和 CTLA-4 联合治疗的 MUP 患者(11 个月,95%CI:4.5-17.5,P < 0.0001)的治疗失败时间明显延长,而接受 PD-1 单药治疗的 MUP 患者(5 个月,95%CI:3.4-6.6)的治疗失败时间明显延长。与 MKP 相比,接受 PD-1 和 CTLA-4 联合治疗的 MUP 患者(4 个月,95%CI:2.9-5.1)的治疗失败时间明显延长。
MKP 和 MUP 患者接受 BRAF 和 MEK 抑制剂治疗的免疫相关不良事件发生情况和治疗失败时间相似。在我们的多中心研究中,与 MKP 相比,MUP 患者接受免疫治疗的效果更好。