Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan; School of Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Department of Oncology, National Taiwan University Hospital and National Taiwan University, Taipei, Taiwan; Graduate Institute of Oncology, National Taiwan University College of Medicine, Taipei, Taiwan.
Pancreatology. 2024 Jun;24(4):600-607. doi: 10.1016/j.pan.2024.03.014. Epub 2024 Mar 25.
BACKGROUND/OBJECTIVES: Liposomal irinotecan plus 5-fluorouracil and leucovorin (nal-IRI + 5-FU/LV) provides survival benefits for metastatic pancreatic adenocarcinoma (mPDAC) refractory to gemcitabine-based treatment, mainly gemcitabine plus nab-paclitaxel (GA), in current practice. Gemcitabine plus S-1 (GS) is another commonly administered first-line regimen before nab-paclitaxel reimbursement; however, the efficacy and safety of nal-IRI + 5-FU/LV for mPDAC after failed GS treatment has not been reported and was therefore explored in this study.
In total, 177 patients with mPDAC received first-line GS or GA treatment, followed by second-line nal-IRI + 5-FU/LV treatment (identified from a multicenter retrospective cohort in Taiwan from 2018 to 2020); 85 and 92 patients were allocated to the GS and GA groups, respectively. Overall survival (OS), time-to-treatment failure (TTF), and adverse events were compared between the two groups.
The baseline characteristics of the two groups were generally similar; however, a higher median age (67 versus 62 years, p < 0.001) and fewer liver metastases (52% versus 78%, p < 0.001) were observed in the GS versus GA group. The median OS was 15.0 and 15.9 months in the GS and GA groups, respectively (p = 0.58). The TTF (3.1 versus 2.8 months, p = 0.36) and OS (7.6 versus 6.7 months, p = 0.83) after nal-IRI treatment were similar between the two groups. More patients in the GS group developed mucositis during nal-IRI treatment (15% versus 4%, p = 0.02).
The efficacy of second-line nal-IRI +5-FU/LV treatment was unaffected by prior S-1 exposure. GS followed by nal-IRI treatment is an alternative treatment sequence for patients with mPDAC.
背景/目的:脂质体伊立替康联合氟尿嘧啶和亚叶酸(nal-IRI+5-FU/LV)为转移性胰腺腺癌(mPDAC)提供了生存获益,这些患者对吉西他滨为基础的治疗(主要是吉西他滨联合 nab-紫杉醇(GA))耐药,这在当前实践中是常见的。吉西他滨联合替吉奥(GS)是 nab-紫杉醇报销前另一种常用的一线治疗方案;然而,nal-IRI+5-FU/LV 治疗 GS 治疗失败后的 mPDAC 的疗效和安全性尚未报道,因此本研究对此进行了探讨。
总共 177 名 mPDAC 患者接受了一线 GS 或 GA 治疗,随后二线 nal-IRI+5-FU/LV 治疗(2018 年至 2020 年期间从台湾的一个多中心回顾性队列中确定);85 名和 92 名患者分别分配到 GS 和 GA 组。比较两组的总生存期(OS)、治疗失败时间(TTF)和不良事件。
两组的基线特征总体相似;然而,GS 组的中位年龄(67 岁比 62 岁,p<0.001)和肝转移较少(52%比 78%,p<0.001)。GS 组和 GA 组的中位 OS 分别为 15.0 和 15.9 个月(p=0.58)。nal-IRI 治疗后的 TTF(3.1 个月比 2.8 个月,p=0.36)和 OS(7.6 个月比 6.7 个月,p=0.83)相似。GS 组在 nal-IRI 治疗期间发生粘膜炎的患者更多(15%比 4%,p=0.02)。
二线 nal-IRI+5-FU/LV 治疗的疗效不受 S-1 暴露的影响。GS 序贯 nal-IRI 治疗是 mPDAC 患者的另一种治疗选择。