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既往 S-1 治疗对转移性胰腺癌患者接受伊立替康脂质体联合氟尿嘧啶和亚叶酸治疗疗效的影响。

Impact of previous S-1 treatment on efficacy of liposomal irinotecan plus 5-fluorouracil and leucovorin in patients with metastatic pancreatic cancer.

机构信息

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.

出版信息

Pancreatology. 2024 Jun;24(4):600-607. doi: 10.1016/j.pan.2024.03.014. Epub 2024 Mar 25.

DOI:10.1016/j.pan.2024.03.014
PMID:38565467
Abstract

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.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

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。

方法

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。

结果

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)。

结论

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。

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