Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center-Hospital East, Kashiwa, Chiba, Japan.
Courses of Advanced Clinical Research of Cancer, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan.
ESMO Open. 2020 Jul;4(Suppl 2). doi: 10.1136/esmoopen-2020-000775.
The efficacy and safety of chemotherapy (CTx) after anti-PD-1 therapy in patients with advanced gastric cancer (AGC) remains unclear.
Medical records of consecutive patients with AGC treated with both CTx (taxanes plus ramucirumab, taxanes monotherapy or irinotecan) and anti-PD-1 therapy from June 2015 to April 2019 were retrospectively analysed. Patients were divided into two groups based on prior exposure to anti-PD-1 therapy: anti-PD-1-exposed and anti-PD-1-naïve groups. CTx-related outcomes were compared between two groups in the overall population and each CTx population.
In total, 233 patients (67 anti-PD-1-exposed, 166 anti-PD-1-naïve) were included. In the overall population, the objective response rate (ORR) to CTX was 44.6% in the anti-PD-1-exposed group and 19.6% in the anti-PD-1-naïve group (p=0.001); the median progression-free survivals (PFS) were 3.7 months and 3.3 months (HR=0.82, p=0.20), respectively. Among patients receiving taxanes plus ramucirumab (n=149), ORR (60.6% vs 20.0%, p<0.001) and median PFS (4.8 vs 3.4 months, p=0.004, HR=0.56) were significantly better in the anti-PD-1-exposed group (n=39) compared with the anti-PD-1-naïve group (n=110). These differences were not observed in patients receiving taxane monotherapy (n=34) or irinotecan (n=50). CTx after anti-PD-1 therapy showed no severe or unexpected adverse events.
Prior anti-PD-1 therapy might increase tumour response to taxanes plus ramucirumab without unexpected adverse events, which warrants further investigations in a large cohort.
抗 PD-1 治疗后晚期胃癌(AGC)患者化疗(CTx)的疗效和安全性仍不清楚。
回顾性分析了 2015 年 6 月至 2019 年 4 月连续接受 CTx(紫杉烷加雷莫芦单抗、紫杉烷单药或伊立替康)和抗 PD-1 治疗的 AGC 患者的病历。根据既往是否接受过抗 PD-1 治疗,将患者分为两组:抗 PD-1 暴露组和抗 PD-1 初治组。比较了两组在全人群和各 CTx 人群中的 CTx 相关结局。
共纳入 233 例患者(67 例抗 PD-1 暴露组,166 例抗 PD-1 初治组)。在全人群中,抗 PD-1 暴露组 CTx 的客观缓解率(ORR)为 44.6%,抗 PD-1 初治组为 19.6%(p=0.001);中位无进展生存期(PFS)分别为 3.7 个月和 3.3 个月(HR=0.82,p=0.20)。在接受紫杉烷加雷莫芦单抗治疗的患者中(n=149),抗 PD-1 暴露组(n=39)的 ORR(60.6%比 20.0%,p<0.001)和中位 PFS(4.8 比 3.4 个月,p=0.004,HR=0.56)均显著优于抗 PD-1 初治组(n=110)。在接受紫杉醇单药治疗的患者(n=34)或伊立替康治疗的患者(n=50)中未观察到这些差异。抗 PD-1 治疗后 CTx 未出现严重或意外的不良事件。
抗 PD-1 治疗前可能会增加肿瘤对紫杉烷加雷莫芦单抗的反应,且无意外的不良事件,这需要在更大的队列中进一步研究。