Xiao Annie, Li Xiaochen, Wang Chongkai, Fakih Marwan
Department of Medical Oncology and Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, CA.
Department of Computational and Quantitative Medicine, Division of Biostatistics, City of Hope Comprehensive Cancer Center, Duarte, CA.
Clin Colorectal Cancer. 2025 Mar;24(1):32-38.e1. doi: 10.1016/j.clcc.2024.08.001. Epub 2024 Aug 18.
Patients with microsatellite-high (MSI-H) metastatic colorectal cancers (CRC) may experience long-lasting benefit from immune checkpoint inhibitors (ICI) upon stopping therapy. However, optimal timing and patient selection criteria for early treatment withdrawal remain undefined. In this single-center retrospective study, we characterized the clinical response and associated survival outcomes of patients who received elective early versus late treatment discontinuation.
We retrospectively analyzed patients with MSI-H metastatic CRC treated with ICI therapy from May 2015 to April 2024. Early ICI discontinuation was defined as treatment withdrawal before 2 years, and late ICI discontinuation as after 2 years. Response was assessed using Response Evaluation Criteria in Solid Tumors. Progression-free survival (PFS) and overall survival (OS) were estimated using the Kaplan Meier method. Efficacy outcomes between early and late ICI discontinuation groups were compared using a log-rank test.
Of 36 patients with MSI-H metastatic CRC, 12 underwent elective early ICI discontinuation and 9 experienced late ICI discontinuation. After a median follow-up of 32 months post-treatment, 91.7% (11/12) in the early discontinuation group remain off therapy without progression. PFS and OS outcomes between the early and late discontinuation groups were similarly favorable (P = .88 and P = .85, respectively), despite a 12-month difference in median duration of ICI therapy (13.3 and 25.6 months, respectively). The most common reason for elective early treatment discontinuation was clinical remission (n = 10), defined as a complete response, or a partial response with negative PET and/or ctDNA testing.
Early ICI discontinuation guided by response criteria resulted in low rates of recurrence. Survival outcomes between early and late ICI discontinuation groups were comparable, suggesting that treatment duration can be individualized based on clinical response without compromising favorable long-term prognosis.
微卫星高度不稳定(MSI-H)的转移性结直肠癌(CRC)患者在停止免疫检查点抑制剂(ICI)治疗后可能会获得长期益处。然而,早期停药的最佳时机和患者选择标准仍不明确。在这项单中心回顾性研究中,我们对接受选择性早期与晚期治疗停药的患者的临床反应及相关生存结果进行了特征分析。
我们回顾性分析了2015年5月至2024年4月期间接受ICI治疗的MSI-H转移性CRC患者。早期ICI停药定义为在2年之前停止治疗,晚期ICI停药定义为在2年之后停止治疗。使用实体瘤疗效评价标准评估反应。采用Kaplan-Meier方法估计无进展生存期(PFS)和总生存期(OS)。使用对数秩检验比较早期和晚期ICI停药组之间的疗效结果。
在36例MSI-H转移性CRC患者中,12例接受了选择性早期ICI停药,9例经历了晚期ICI停药。治疗后中位随访32个月,早期停药组中91.7%(11/12)的患者停止治疗且无疾病进展。早期和晚期停药组之间的PFS和OS结果同样良好(分别为P = 0.88和P = 0.85),尽管ICI治疗的中位持续时间相差12个月(分别为13.3个月和25.6个月)。选择性早期治疗停药的最常见原因是临床缓解(n = 10),定义为完全缓解,或PET和/或ctDNA检测为阴性的部分缓解。
根据反应标准进行早期ICI停药导致复发率较低。早期和晚期ICI停药组之间的生存结果相当,这表明治疗持续时间可以根据临床反应个体化,而不会影响良好的长期预后。