Kim Hyunho, Shin Kabsoo, Park Hyung Soon, Hong Tae Ho, Kim Younghoon, Lee Sung Hak, Kim In-Ho, Lee MyungAh, Park Se Jun
Division of Medical Oncology, Department of Internal Medicine, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Division of Medical Oncology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Front Oncol. 2025 Aug 13;15:1638606. doi: 10.3389/fonc.2025.1638606. eCollection 2025.
The combination of liposomal irinotecan with fluorouracil and leucovorin (Nal-IRI/FL) has shown efficacy in phase II trials for advanced biliary tract cancer (BTC) following gemcitabine-cisplatin (GP) therapy. However, its effectiveness and safety in real-world clinical settings have not been well established. This study aimed to assess the real-world outcomes of Nal-IRI/FL in BTC patients who experienced disease progression after gemcitabine-based treatment.
This retrospective, multicenter study evaluated patients with advanced BTC who received Nal-IRI/FL following progression on GP-based therapy between January 2022 and December 2024. Survival outcomes, radiologic responses, toxicities, and molecular alterations were evaluated, with key findings compared against those reported in prior clinical trials.
A total of 93 patients were included. The median progression-free survival (PFS) and overall survival (OS) were 2.1 and 4.2 months, respectively. Among 76 radiologic response evaluable patients, median PFS and OS were 2.5 and 5.0 months. The disease control rate was 40.8%, and objective response rate was 7.5%. Higher disease burden and poor performance status were associated with inferior outcomes. Efficacy did not significantly differ between second- and third-line settings or based on or mutation status. Hematological toxicities were common, including grade ≥3 neutropenia (38.7%) and febrile neutropenia (7.5%). The median relative dose intensity was 0.69. Treatment-related death occurred in 4 patients (4.3%).
Nal-IRI/FL showed modest effectiveness in real-world settings, with outcomes generally less favorable than clinical trials, potentially reflecting patient characteristics. Its efficacy was consistent across treatment lines and mutation subgroups, including patients with or mutations. Careful patient selection and proactive supportive care are essential. Further studies are warranted to clarify its role across diverse populations.
脂质体伊立替康联合氟尿嘧啶和亚叶酸钙(Nal-IRI/FL)在吉西他滨-顺铂(GP)治疗后的晚期胆管癌(BTC)II期试验中显示出疗效。然而,其在实际临床环境中的有效性和安全性尚未得到充分证实。本研究旨在评估Nal-IRI/FL在基于吉西他滨的治疗后疾病进展的BTC患者中的实际疗效。
这项回顾性多中心研究评估了2022年1月至2024年12月期间在基于GP的治疗进展后接受Nal-IRI/FL治疗的晚期BTC患者。评估了生存结果、放射学反应、毒性和分子改变,并将主要发现与先前临床试验报告的结果进行比较。
共纳入93例患者。中位无进展生存期(PFS)和总生存期(OS)分别为2.1个月和4.2个月。在76例可评估放射学反应的患者中,中位PFS和OS分别为2.5个月和5.0个月。疾病控制率为40.8%,客观缓解率为7.5%。较高的疾病负担和较差的体能状态与较差的预后相关。二线和三线治疗环境之间或基于 或 突变状态的疗效无显著差异。血液学毒性常见,包括≥3级中性粒细胞减少(38.7%)和发热性中性粒细胞减少(7.5%)。中位相对剂量强度为0.69。4例患者(4.3%)发生治疗相关死亡。
Nal-IRI/FL在实际临床环境中显示出适度的疗效,其结果总体上不如临床试验,这可能反映了患者特征。其疗效在各治疗线和突变亚组中一致,包括有 或 突变的患者。仔细的患者选择和积极的支持性治疗至关重要。有必要进一步研究以阐明其在不同人群中的作用。