Medical Oncology, Institut Curie, Saint Cloud, France.
Institut du Thorax Curie-Montsouris, Institut Curie, Paris, France.
Cancer Immunol Immunother. 2022 Jul;71(7):1719-1731. doi: 10.1007/s00262-021-03114-z. Epub 2021 Nov 25.
The optimal treatment duration of ICIs for patients with advanced NSCLC remains uncertain. In phase 3 clinical trials, treatment continued for 2 years or until disease progression with similar long-term survival rates. Real-life data are missing.
This academic multicentric retrospective study aims at analyzing the characteristics of patients who discontinued treatment after at least 18 months of ICI monotherapy, in the setting of controlled disease.
Of the 1127 patients treated with immunotherapy in the given period in six centers, 107 patients had their tumor controlled after at least 18 months of treatment and 54 (50%) of them had discontinued ICI. The median duration of treatment was 26 months. Treatment was stopped due to prescriber choice or toxicity in 46% and 22% of cases, respectively. After a median follow-up of 21 months from ICI discontinuation (95% CI 15.0-26.1 months), 18 (33%) patients experienced tumor progression after a median time of 10.0 months (range 2-33). From discontinuation, 12-month overall survival (OS) and progression-free survival (PFS) were 90% (95% CI 77.7-95.7) and 71% (95% CI 56.8-81.5), respectively; 24-month OS and PFS were 84% (95% CI 68.7-92.2) and 63% (95% CI 46.1-76.2), respectively. Duration of disease control after ICI discontinuation was correlated with tumor response at treatment discontinuation: PFS rate at 12 months was 76% after complete response (CR n = 11) or partial response (PR n = 37) and 22% after only stable disease (SD n = 6) as best response, p-value = 0.0002. PFS rate at 12 months was 80% for CR and/or complete metabolic response with 18F-FDG PET/CT (CMR) and 65% for others. Fourteen patients out of the 18 relapse patients received a subsequent treatment: seven with ICI rechallenge (best response 14% PR and 86% SD) and five with localized therapy with 60% CR.
This real-life study provides new insight into long-term outcomes of patients with advanced NSCLC treated with ICI for at least 18 months before treatment discontinuation in the absence of PD. Tumor response and CMR with FDG PET just before therapy discontinuation may be a predictive factor of prolonged disease control upon discontinuation. These results call for caution in discontinuing treatment in patients with stable disease as the best response.
晚期 NSCLC 患者接受 ICIs 治疗的最佳持续时间仍不确定。在 3 期临床试验中,治疗持续 2 年或直至疾病进展,生存率相似。目前缺乏真实世界的数据。
本学术多中心回顾性研究旨在分析至少接受 18 个月 ICIs 单药治疗且疾病得到控制的患者在停药后的特征。
在 6 个中心规定的时间段内,1127 名接受免疫治疗的患者中有 107 名患者的肿瘤在治疗至少 18 个月后得到控制,其中 54 名(50%)停止了 ICI 治疗。中位治疗时间为 26 个月。因医生选择或毒性导致治疗停止的分别占 46%和 22%。从 ICI 停药开始,中位随访 21 个月(95%CI 15.0-26.1 个月)后,18 名(33%)患者在中位时间 10.0 个月(范围 2-33)后出现肿瘤进展。停药后 12 个月总生存率(OS)和无进展生存率(PFS)分别为 90%(95%CI 77.7-95.7)和 71%(95%CI 56.8-81.5);24 个月 OS 和 PFS 分别为 84%(95%CI 68.7-92.2)和 63%(95%CI 46.1-76.2)。ICI 停药后疾病控制时间与停药时肿瘤反应相关:完全缓解(CR n=11)或部分缓解(PR n=37)患者的 12 个月 PFS 率为 76%,仅稳定疾病(SD n=6)为最佳反应的患者 PFS 率为 22%,p 值=0.0002。CR 和/或 18F-FDG PET/CT(CMR)完全代谢缓解的患者 12 个月 PFS 率为 80%,而其他患者为 65%。18 名复发患者中有 14 名接受了后续治疗:7 名接受了 ICI 再挑战(最佳反应为 14%PR 和 86%SD),5 名接受了局部治疗,60%的患者获得了完全缓解。
本真实世界研究提供了新的见解,即晚期 NSCLC 患者在没有疾病进展的情况下接受至少 18 个月的 ICIs 治疗后停药,其长期结果。在停药前的 18F-FDG PET 检查中,肿瘤反应和 CMR 可能是停药后延长疾病控制的预测因素。这些结果提醒我们在疾病得到控制的患者中谨慎停药,因为最佳反应是稳定疾病。