Zhang Xuchen, Zhang Chuantao, Hou Helei, Zhang Yuming, Jiang Peng, Zhou Hai, Wang Lele, Zhou Na, Zhang Xiaochun
Department of Oncology, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao 266000, China; Qingdao Medical College, Qingdao University, Qingdao 266000, China.
Qingdao Medical College, Qingdao University, Qingdao 266000, China.
Transl Oncol. 2023 May;31:101657. doi: 10.1016/j.tranon.2023.101657. Epub 2023 Mar 17.
PD-1 blockade has been shown to have promising efficacy and acceptable safety profiles in advanced and metastatic gastric cancer; however, the efficacy and safety of neoadjuvant PD-1 blockade-based immunotherapy plus chemotherapy in locally advanced gastric cancer (LAGC) remain uncertain.
We performed a retrospective review of patients with LAGC who received neoadjuvant treatment followed by D2 radical resection at the Affiliated Hospital of Qingdao University from 2019 to 2021. The primary aim was to investigate the difference in pathological response rates between neoadjuvant PD-1 immunotherapy plus chemotherapy and neoadjuvant chemotherapy alone. Multivariable models for pathological complete response (pCR) were constructed to investigate the factors that facilitate pCR.
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A total of 77 patients were included in the analysis, among whom 34 (44.2%) received neoadjuvant PD-1 blockade immunotherapy plus chemotherapy. A higher pCR rate was observed in the neoadjuvant PD-1 blockade immunotherapy plus chemotherapy group (8 of 34, 23.5% vs. 2 of 43, 4.7%, P=0.019). Multivariate logistic regression analysis of pCR revealed neoadjuvant PD-1 blockade plus chemotherapy regimen promoted pCR (OR 12.95, P=0.016). Regarding safety, 76.5% (26 of 34) of patients in the PD-1 blockade plus chemotherapy group and 76.7% (33 of 43) of patients in the chemotherapy group experienced treatment-related adverse events (TRAEs), and grade 3 or worse adverse events were 29.4% (10 of 34) and 34.9% (15 of 43), respectively.
Neoadjuvant PD-1 blockade plus chemotherapy induced a higher pCR rate than neoadjuvant chemotherapy, and the combined therapy was tolerable in LAGC patients.
PD - 1阻断疗法已被证明在晚期和转移性胃癌中具有可观的疗效和可接受的安全性;然而,基于新辅助PD - 1阻断的免疫疗法联合化疗在局部晚期胃癌(LAGC)中的疗效和安全性仍不确定。
我们对2019年至2021年在青岛大学附属医院接受新辅助治疗后行D2根治性切除术的LAGC患者进行了回顾性研究。主要目的是探讨新辅助PD - 1免疫疗法联合化疗与单纯新辅助化疗在病理缓解率上的差异。构建了病理完全缓解(pCR)的多变量模型,以研究促进pCR的因素。
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共有77例患者纳入分析,其中34例(44.2%)接受了新辅助PD - 1阻断免疫疗法联合化疗。新辅助PD - 1阻断免疫疗法联合化疗组的pCR率更高(34例中的8例,23.5% vs. 43例中的2例,4.7%,P = 0.019)。对pCR进行多因素逻辑回归分析显示,新辅助PD - 1阻断联合化疗方案可促进pCR(OR 12.95,P = 0.016)。在安全性方面,PD - 1阻断联合化疗组76.5%(34例中的26例)的患者和化疗组76.7%(43例中的33例)的患者发生了治疗相关不良事件(TRAEs),3级或更严重不良事件分别为29.4%(34例中的10例)和34.9%(43例中的15例)。
新辅助PD - 1阻断联合化疗诱导的pCR率高于新辅助化疗,且该联合疗法在LAGC患者中耐受性良好。