Department of Dermatology, Chiba University, Chiba, Japan.
Department of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.
J Dermatol Sci. 2023 Apr;110(1):19-26. doi: 10.1016/j.jdermsci.2023.03.008. Epub 2023 Mar 31.
Efficacy of anti-PD-1 antibody monotherapy (PD1) or anti-PD-1 plus anti-CTLA-4 combination therapy (PD1 +CTLA4) for melanoma is affected by its clinical subtype. The amount of tumor mutation burden (TMB) caused by cumulative sun damage (CSD) is occasionally used to explain this; however, their relationship in Japanese nonacral cutaneous melanoma (NACM) is still unclear.
To analyze the ICI efficacy and its relationship with CSD of the primary lesion in Japanese patients with NACM.
Japanese patients with advanced BRAF wild-type NACM who received first-line ICIs were recruited. Objective response rate (ORR), progression-free survival (PFS), and overall survival (OS), and the degree of solar elastosis (SE) were evaluated.
A total of 146 patients (PD1 group 113 and PD1 +CTLA4 group 33) were included. No significant differences in ORR were observed between the PD1 and PD1 +CTLA4 groups (35 % vs. 36 %; P = 0.67) or PFS and OS (median PFS 6.1 months vs. 8.5 months; P = 0.46, median OS 28.1 months vs. not reached; P = 0.59). Multivariate survival analysis revealed that PD1 +CTLA4 did not prolong the PFS and OS. The SE score had no effect on either PFS or OS.
ICI efficacy was not as high as those reported in Western countries, and PD1 +CTLA4 did not present better clinical efficacy compared to PD1. Indicators of CSD did not serve as a predictor for clinical advantage. These findings may partially support the theory that ICI efficacy is affected by CSD; however, other unrecognized factors may also exist.
抗 PD-1 抗体单药治疗(PD1)或抗 PD-1 联合抗 CTLA-4 联合治疗(PD1+CTLA4)对黑色素瘤的疗效受其临床亚型的影响。由累积太阳损伤(CSD)引起的肿瘤突变负担(TMB)量偶尔用于解释这一点;然而,它们在日本非肢端皮肤黑色素瘤(NACM)中的关系仍不清楚。
分析日本 NACM 患者中ICI 的疗效及其与原发性病变 CSD 的关系。
招募接受一线 ICI 治疗的晚期 BRAF 野生型 NACM 日本患者。评估客观缓解率(ORR)、无进展生存期(PFS)和总生存期(OS)以及太阳弹性蛋白(SE)程度。
共纳入 146 例患者(PD1 组 113 例,PD1+CTLA4 组 33 例)。PD1 和 PD1+CTLA4 组之间的 ORR 无显著差异(35%比 36%;P=0.67),PFS 和 OS 也无显著差异(中位 PFS 6.1 个月比 8.5 个月;P=0.46,中位 OS 28.1 个月比未达到;P=0.59)。多变量生存分析显示,PD1+CTLA4 并未延长 PFS 和 OS。SE 评分对 PFS 或 OS 均无影响。
ICI 的疗效不如西方国家报道的那么高,PD1+CTLA4 与 PD1 相比并未表现出更好的临床疗效。CSD 的指标不能作为临床优势的预测指标。这些发现可能部分支持 ICI 疗效受 CSD 影响的理论,但也可能存在其他未被认识到的因素。