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抗 PD-1 治疗后紫杉醇和雷莫芦单抗联合化疗治疗晚期胃癌的疗效改善。

Improved efficacy of taxanes and ramucirumab combination chemotherapy after exposure to anti-PD-1 therapy in advanced gastric cancer.

机构信息

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.

出版信息

ESMO Open. 2020 Jul;4(Suppl 2). doi: 10.1136/esmoopen-2020-000775.

Abstract

BACKGROUND

The efficacy and safety of chemotherapy (CTx) after anti-PD-1 therapy in patients with advanced gastric cancer (AGC) remains unclear.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ef/7381840/adddc30d55da/esmoopen-2020-000775f01.jpg

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