Zhou Shi-Qiong, Wan Peng, Zhang Seng, Ren Yuan, Li Hong-Tao, Ke Qing-Hua
Department of Chemoradiotherapy, The First Affiliated Hospital of Yangtze University, Jingzhou 434000, Hubei Province, China.
World J Clin Oncol. 2025 Feb 24;16(2):98079. doi: 10.5306/wjco.v16.i2.98079.
Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive cancer with poor prognosis. When it metastasizes to the liver, treatment options become particularly limited and challenging. Current treatment options for liver metastatic PDAC are limited, and chemotherapy alone often proves insufficient. Immunotherapy, particularly programmed cell death 1 (PD-1) inhibitors like sintilimab, shows potential efficacy for various cancers but has limited reports on PDAC. This study compares the efficacy and safety of sintilimab plus S-1 and gemcitabine S-1 and gemcitabine alone in liver metastatic PDAC.
To explore the feasibility and effectiveness of combined PD-1 inhibitor sintilimab and S-1 and gemcitabine (combination group) S-1 and gemcitabine used alone (chemotherapy group) for treating liver metastatic pancreatic adenocarcinoma.
Eligible patients were those with only liver metastatic PDAC, an Eastern Cooperative Oncology Group performance status of 0-1, adequate organ and marrow functions, and no prior anticancer therapy. Participants in the combination group received intravenous sintilimab 200 mg every 3 weeks, oral S-1 40 mg/m² twice daily on days 1-14 of a 21-day cycle, and intravenous gemcitabine 1000 mg/m² on days 1 and 8 of the same cycle for up to eight cycles or until disease progression, death, or unacceptable toxicity. Participants in the chemotherapy group received oral S-1 40 mg/m² twice daily on days 1-14 of a 21-day cycle and intravenous gemcitabine 1000 mg/m² on days 1 and 8 of the same cycle for up to eight cycles. Between June 2020 and December 2021, 66 participants were enrolled, with 32 receiving the combination treatment and 34 receiving chemotherapy alone.
The group receiving the combined therapy exhibited a markedly prolonged median overall survival (18.8 months compared to 10.3 months, < 0.05) and progression-free survival (9.6 months 5.4 months, < 0.05). compared to the chemotherapy group. The incidence of severe adverse events did not differ significantly between the two groups ( > 0.05).
The combination of PD-1 inhibitor sintilimab with S-1 and gemcitabine demonstrated effectiveness and safety for treating liver metastatic PDAC, meriting further investigation.
胰腺导管腺癌(PDAC)是一种侵袭性很强的癌症,预后较差。当它转移到肝脏时,治疗选择变得特别有限且具有挑战性。目前肝转移PDAC的治疗选择有限,单纯化疗往往证明是不够的。免疫疗法,特别是程序性细胞死亡1(PD-1)抑制剂如信迪利单抗,对各种癌症显示出潜在疗效,但关于PDAC的报道有限。本研究比较了信迪利单抗联合S-1和吉西他滨与单独使用S-1和吉西他滨治疗肝转移PDAC的疗效和安全性。
探讨联合使用PD-1抑制剂信迪利单抗与S-1和吉西他滨(联合治疗组)以及单独使用S-1和吉西他滨(化疗组)治疗肝转移胰腺腺癌的可行性和有效性。
符合条件的患者为仅患有肝转移PDAC、东部肿瘤协作组体能状态为0-1、器官和骨髓功能良好且未接受过先前抗癌治疗的患者。联合治疗组的参与者每3周静脉注射200mg信迪利单抗,在21天周期的第1-14天每天口服两次S-1,剂量为40mg/m²,在同一周期的第1天和第8天静脉注射吉西他滨,剂量为1000mg/m²,共进行8个周期或直至疾病进展、死亡或出现不可接受的毒性。化疗组的参与者在21天周期的第1-14天每天口服两次S-1,剂量为40mg/m²,在同一周期的第1天和第8天静脉注射吉西他滨,剂量为1000mg/m²,共进行8个周期。在2020年6月至2021年12月期间,招募了66名参与者,其中32名接受联合治疗,34名仅接受化疗。
与化疗组相比,接受联合治疗的组中位总生存期显著延长(18.8个月对10.3个月,P<0.05),无进展生存期也显著延长(9.6个月对5.4个月,P<0.05)。两组严重不良事件的发生率无显著差异(P>0.05)。
PD-1抑制剂信迪利单抗与S-1和吉西他滨联合使用对治疗肝转移PDAC显示出有效性和安全性,值得进一步研究。