Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Department of Oncology, Uppsala University Hospital, Uppsala, Sweden.
Pigment Cell Melanoma Res. 2024 May;37(3):352-362. doi: 10.1111/pcmr.13156. Epub 2023 Dec 29.
Dacarbazine (DTIC) and its oral counterpart temozolomide (TMZ) have been the most used agents in advanced malignant melanoma (MM) patients and they are still used routinely. The preferred first line treatment, immune checkpoint inhibitors (CPIs) might shape the tumor and the tumor microenvironment, possibly affecting the response to subsequent therapies. The aim of this study was to investigate the treatment effect of DTIC/TMZ in MM patients after CPI therapy in a consecutive patient cohort and through systematic literature review and meta-analysis. Thirty-five patients with advanced MM treated with DTIC/TMZ after previous CPI therapy in three Swedish regions between 2017 and 2021 were recognized and seven case series studies were identified through systematic database review. Pooled data from all 345 patients showed a median real-world progression-free survival (rwPFS) of 1.9 months and overall survival (OS) of 6.0 months. Three of these studies were included in a meta-analysis comparing DTIC/TMZ after CPI treatment, versus no previous immunotherapy, showing no statistically significant differences in rwPFS or OS but higher real-world response rate to chemotherapy for the prior-CPI treated group (Odds Ratio: 2.24; 95% Confidence Interval: 1.04-4.86). The current study supports consideration of DTIC/TMZ in later line of treatment in the immunotherapy era.
达卡巴嗪(DTIC)及其口服类似物替莫唑胺(TMZ)是晚期恶性黑色素瘤(MM)患者最常用的药物,目前仍常规使用。首选的一线治疗药物——免疫检查点抑制剂(CPIs)可能会影响肿瘤和肿瘤微环境,从而可能影响对后续治疗的反应。本研究旨在通过连续患者队列和系统文献回顾及荟萃分析,调查 CPIs 治疗后 MM 患者使用 DTIC/TMZ 的治疗效果。在 2017 年至 2021 年间,瑞典三个地区的 35 名接受 CPIs 治疗的晚期 MM 患者接受了 DTIC/TMZ 治疗,通过系统数据库检索,我们确定了 7 项病例系列研究。所有 345 名患者的汇总数据显示,真实世界无进展生存期(rwPFS)的中位数为 1.9 个月,总生存期(OS)的中位数为 6.0 个月。其中三项研究被纳入荟萃分析,比较了 CPIs 治疗后使用 DTIC/TMZ 与未接受过免疫治疗的患者,结果显示 rwPFS 或 OS 无统计学显著差异,但先前接受 CPI 治疗的患者对化疗的真实世界反应率更高(优势比:2.24;95%置信区间:1.04-4.86)。本研究支持在免疫治疗时代将 DTIC/TMZ 作为后线治疗药物的考虑。