免疫检查点抑制剂治疗 MSI/dMMR 胃肠道癌症的年龄相关结果以及毒性对疗效的影响:免疫MSI 队列研究

L. Mailly-Giacchetti , R. Colle , T. Samaille , D. Lopez-Trabada Ataz , L. Faucheux , A. Duval , T. Andre , R. Cohen
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引用次数: 0

摘要

背景免疫检查点抑制剂(ICIs)是微卫星不稳定性(MSI)转移性胃肠癌(mGIC)患者一线和二线治疗的标准疗法。我们比较了老年(年龄≥75岁)与非老年MSI mGIC患者对ICIs的耐受性和疗效,并分析了免疫相关不良事件(irAEs)与疗效之间的相关性。这项单中心前瞻性队列研究纳入了接受ICIs治疗的MSI mGIC患者,不包括化疗患者。结果201名患者中,24名为老年人(平均年龄75-90岁),177名为非老年人(平均年龄22-74岁)。在所有患者中,抗程序性细胞死亡蛋白1+抗细胞毒性T淋巴细胞相关抗原4的≥3级irAEs和E-irAEs发生率为40%,抗程序性细胞死亡蛋白1单药治疗的发生率为23%(P = 0.011)。29%的老年患者和40%的非老年患者接受了联合治疗。在老年/非老年患者中,单药治疗的≥3级irAEs和E-irAEs发生率为37%/29%(P = 0.48),联合治疗为57%/39%(P = 0.43)。在无进展生存期[危险比(HR)=1.15,95% 置信区间(CI)0.57-2.32,P = 0.7]和OS(HR = 1.61,95% CI 0.75-3.43,P = 0.25)方面,老年患者和非老年患者之间未观察到明显差异。以时间为变量的Cox回归分析显示,有/无≥3级irAEs和E-irAEs患者的生存率没有差异(无进展生存率:HR = 1.19,95% CI 0.64-2.19,P = 0.59;总生存率:HR = 0.91,95% CI 0.44-1.92,P = 0.81)。然而,客观反应率与免疫治疗相关不良事件发生率之间存在正相关[77%/59%,免疫治疗相关不良事件患者/其他人(P = 0.0012)]。有和没有≥3级irAEs和E-irAEs的患者的生存结果没有明显差异。
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Age-related outcomes in MSI/dMMR gastrointestinal cancers treated by immune checkpoint inhibitors and toxicity’s impact on efficacy: an immunoMSI cohort study

Background

Immune-checkpoint inhibitors (ICIs) are the standard of care for microsatellite instability (MSI) metastatic gastrointestinal cancer (mGIC) patients in first- and later-treatment lines. We compared tolerability and efficacy of ICIs in elderly (aged ≥75 years) versus non-elderly MSI mGIC patients and analyzed the correlation between immune-related adverse events (irAEs) and efficacy.

Patients and methods

This single-center prospective cohort study included MSI mGIC patients treated with ICIs, excluding chemotherapy. Assessments covered grade ≥3 irAEs and ≥2 endocrine irAEs (E-irAEs).

Results

Among 201 patients, 24 were elderly (mean age 75–90 years) and 177 non-elderly (mean age 22-74 years). In the overall population, grade ≥3 irAEs and E-irAEs incidence was 40% with the anti-programmed cell death protein 1 + anti-cytotoxic T lymphocyte-associated antigen 4 and 23% with anti-programmed cell death protein 1 monotherapy (P = 0.011). Treatment combination was administered to 29% of elderly and 40% of non-elderly patients. The incidence of grade ≥3 irAEs and E-irAEs was 37%/29% with monotherapy (P = 0.48) and 57%/39% with combination (P = 0.43) in elderly/non-elderly patients. No significant difference was observed in progression-free survival [hazard ratio (HR) = 1.15, 95% confidence interval (CI) 0.57-2.32, P = 0.7] and OS (HR = 1.61, 95% CI 0.75-3.43, P = 0.25) between elderly and non-elderly. Cox regression analysis with a time-dependent variable showed no survival difference between patients with/without grade ≥3 irAEs and E-irAEs (progression-free survival: HR = 1.19, 95% CI 0.64-2.19, P = 0.59; overall survival: HR = 0.91, 95% CI 0.44-1.92, P = 0.81). A positive association was found, however, between objective response rate and immune treatment-related adverse event occurrence [77%/59%, immune treatment-related adverse event patients/others (P = 0.0012)].

Conclusion

This study reveals comparable tolerability and efficacy of ICIs in elderly and non-elderly patients with MSI mGIC. Survival outcomes did not differ significantly between patients with and without grade ≥3 irAEs and E-irAEs.

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