Pala Laura, Pagan Eleonora, Sala Isabella, Oriecuia Chiara, Oliari Matteo, De Pas Tommaso, Specchia Claudia, Cocorocchio Emilia, Zattarin Emma, Rossi Giovanna, Catania Chiara, Ceresoli Giovanni Luca, Laszlo Daniele, Canzian Jacopo, Valenzi Elena, Viale Giuseppe, Gelber Richard D, Mantovani Alberto, Bagnardi Vincenzo, Conforti Fabio
Division of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy.
Department of Statistics and Quantitative Methods, University of Milan-Bicocca, Milan, Italy.
EClinicalMedicine. 2024 Jun 20;73:102681. doi: 10.1016/j.eclinm.2024.102681. eCollection 2024 Jul.
The outcome of patients with metastatic tumors who discontinued immune checkpoint inhibitors (ICIs) not for progressive disease (PD) has been poorly explored. We performed a meta-analysis of all studies reporting the clinical outcome of patients who discontinued ICIs for reasons other than PD.
We searched PubMed, Embase and Scopus databases, from the inception of each database to December 2023, for clinical trials (randomized or not) and observational studies assessing PD-(L)1 and CTLA-4 inhibitors in patients with metastatic solid tumors who discontinued treatment for reasons other than PD. Each study had to provide swimmer plots or Kaplan-Meier survival curves enabling the reconstruction of individual patient-level data on progression-free survival (PFS) following the discontinuation of immunotherapy. The primary endpoint was PFS from the date of treatment discontinuation overall and according to tumor histotype, type of treatment and reason of discontinuation. The Combersure's method was used to estimate meta-analytical non-parametric summary survival curves assuming random effects at study level.
Thirty-six studies (2180 patients) were included. The pooled median PFS (mPFS) was 24.7 months (95% CI, 18.8-30.6) and the PFS-rate at 12, 24, and 36 months was respectively 69.8% (95% CI, 63.1-77.3), 51.0% (95% CI, 43.4-59.8) and 34.0% (95% CI, 27.0-42.9). Univariable analysis showed that the mPFS was significantly longer for patients with melanoma (43.0 months), as compared with non-small cell lung cancer (NSCLC, 13.5 months) and renal cell carcinoma (RCC, 10.0 months; between-strata comparison test p-value < 0.001); for patients treated with anti-PD-(L)1 + anti-CTLA-4 as compared with anti-PD-(L)1 monotherapy (44.6 versus 19.9 months; p-value < 0.001), and in NSCLC when the reason of treatment discontinuation was elective as compared with toxicity onset (19.6 versus 4.8 months; p-value = 0.003). The multivariable analysis confirmed these differences.
The long-term outcome of patients who stopped ICIs for reasons other than PD was substantially affected by clinicopathological features: PFS after treatment discontinuation was longer in patients with melanoma, and/or treated with anti-PD-(L)1 + anti-CTLA-4, and shorter in patients with RCC or in those patients with NSCLC who stopped treatment for toxicity onset.
The Italian Ministry of University and Research (PRIN 2022Y7HHNW).
转移性肿瘤患者因非疾病进展(PD)而停用免疫检查点抑制剂(ICI)的结局尚未得到充分研究。我们对所有报告因PD以外原因停用ICI的患者临床结局的研究进行了荟萃分析。
我们检索了PubMed、Embase和Scopus数据库,从每个数据库创建之初至2023年12月,查找评估转移性实体瘤患者中PD-(L)1和CTLA-4抑制剂的临床试验(无论是否随机)和观察性研究,这些患者因PD以外的原因停止治疗。每项研究都必须提供游泳者图或Kaplan-Meier生存曲线,以便重建免疫治疗停药后无进展生存期(PFS)的个体患者水平数据。主要终点是从治疗停药日期起的总体PFS,以及根据肿瘤组织学类型、治疗类型和停药原因的PFS。采用Combersure方法估计荟萃分析的非参数汇总生存曲线,假设研究水平存在随机效应。
纳入36项研究(2180例患者)。汇总的中位PFS(mPFS)为24.7个月(95%CI,18.8 - 30.6),12个月、24个月和36个月时的PFS率分别为69.8%(95%CI,63.1 - 77.3)、51.0%(95%CI,43.4 - 59.8)和34.0%(95%CI,27.0 - 42.9)。单变量分析显示,与非小细胞肺癌(NSCLC,13.5个月)和肾细胞癌(RCC,10.0个月;层间比较检验p值<0.001)相比,黑色素瘤患者的mPFS显著更长(43.0个月);与抗PD-(L)1单药治疗相比,接受抗PD-(L)1 +抗CTLA-4治疗的患者(44.6个月对19.9个月;p值<0.001),以及在NSCLC中,因择期原因停药的患者与因毒性发作停药的患者相比(19.6个月对4.8个月;p值 = 0.003),mPFS更长。多变量分析证实了这些差异。
因PD以外原因停用ICI的患者的长期结局受临床病理特征的显著影响:黑色素瘤患者、和/或接受抗PD-(L)1 +抗CTLA-4治疗的患者停药后的PFS更长,而RCC患者或因毒性发作而停药的NSCLC患者的PFS更短。
意大利大学与研究部(PRIN 2022Y7HHNW)