Paris-Saclay University, Department of Cancer Medicine, Gustave Roussy, Villejuif.
Department of Cancer Medicine, Hôpital Européen Georges-Pompidou, Paris, France.
ESMO Open. 2024 May;9(5):103004. doi: 10.1016/j.esmoop.2024.103004. Epub 2024 Apr 22.
Patients with solid organ transplant (SOT) and solid tumors are usually excluded from clinical trials testing immune checkpoint blockers (ICB). As transplant rates are increasing, we aimed to evaluate ICB outcomes in this population, with a special focus on lung cancer.
We conducted a multicenter retrospective cohort study collecting real data of ICB use in patients with SOT and solid tumors. Clinical data and treatment outcomes were assessed by using retrospective medical chart reviews in every participating center. Study endpoints were: overall response rate (ORR), 6-month progression-free survival (PFS), and grade ≥3 immune-related adverse events.
From August 2016 to October 2022, 31 patients with SOT (98% kidney) and solid tumors were identified (36.0% lung cancer, 19.4% melanoma, 13.0% genitourinary cancer, 6.5% gastrointestinal cancer). Programmed death-ligand 1 expression was positive in 29% of tumors. Median age was 61 years, 69% were males, and 71% received ICB as first-line treatment. In the whole cohort the ORR was 45.2%, with a 6-month PFS of 56.8%. In the lung cancer cohort, the ORR was 45.5%, with a 6-month PFS of 32.7%, and median overall survival of 4.6 months. The grade 3 immune-related adverse events rate leading to ICB discontinuation was 12.9%. Allograft rejection rate was 25.8%, and risk of rejection was similar regardless of the type of ICB strategy (monotherapy or combination, 28% versus 33%, P = 1.0) or response to ICB treatment.
ICB could be considered a feasible option for SOT recipients with some advanced solid malignancies and no alternative therapeutic options. Due to the risk of allograft rejection, multidisciplinary teams should be involved before ICB therapy.
患有实体器官移植(SOT)和实体肿瘤的患者通常被排除在测试免疫检查点抑制剂(ICB)的临床试验之外。随着移植率的增加,我们旨在评估该人群中 ICB 的结果,特别关注肺癌。
我们进行了一项多中心回顾性队列研究,收集了 SOT 和实体肿瘤患者使用 ICB 的真实数据。每个参与中心都通过回顾性病历审查评估临床数据和治疗结果。研究终点为:总缓解率(ORR)、6 个月无进展生存期(PFS)和≥3 级免疫相关不良事件。
从 2016 年 8 月至 2022 年 10 月,共确定了 31 名 SOT(98%为肾脏)和实体肿瘤患者(36.0%为肺癌,19.4%为黑色素瘤,13.0%为泌尿生殖系统癌症,6.5%为胃肠道癌症)。29%的肿瘤表达程序性死亡配体 1。中位年龄为 61 岁,69%为男性,71%接受 ICB 作为一线治疗。在整个队列中,ORR 为 45.2%,6 个月 PFS 为 56.8%。在肺癌队列中,ORR 为 45.5%,6 个月 PFS 为 32.7%,中位总生存期为 4.6 个月。因 3 级免疫相关不良事件而导致 ICB 停药的发生率为 12.9%。同种异体移植物排斥率为 25.8%,且无论 ICB 策略(单药或联合治疗,28%与 33%,P=1.0)或对 ICB 治疗的反应如何,排斥风险均相似。
对于患有某些晚期实体恶性肿瘤且无其他治疗选择的 SOT 受者,ICB 可被视为一种可行的选择。由于同种异体移植物排斥的风险,在开始 ICB 治疗之前,应涉及多学科团队。