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吉西他滨治疗后纳米脂质体伊立替康联合氟尿嘧啶和亚叶酸钙治疗晚期胰腺癌患者的疗效和安全性:一项多中心前瞻性观察研究

Treatment Effect and Safety of Nanoliposomal Irinotecan with Fluorouracil and Folinic Acid after Gemcitabine-Based Therapy in Patients with Advanced Pancreatic Cancer: A Multicenter, Prospective Observational Study.

作者信息

Miki Masami, Fujimori Nao, Ueda Keijiro, Lee Lingaku, Murakami Masatoshi, Takamatsu Yu, Shimokawa Yuzo, Niina Yusuke, Oono Takamasa, Hisano Terumasa, Furukawa Masayuki, Ogawa Yoshihiro

机构信息

Department of Hepato-Biliary-Pancreatology, National Hospital Organization, Kyushu Cancer Center, Fukuoka 811-1347, Japan.

Department of Medicine and Bioregulatory Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.

出版信息

J Clin Med. 2022 Aug 30;11(17):5084. doi: 10.3390/jcm11175084.

DOI:10.3390/jcm11175084
PMID:36079012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9457338/
Abstract

Although the combination of nanoliposomal irinotecan plus fluorouracil/folinic acid (nal-IRI/FF) exhibited survival benefits in gemcitabine-refractory patients with advanced pancreatic cancer (APC) in the phase III NAPOLI-1 trial, there is limited data on the efficacy and safety of this regimen in real-world settings in Japan. This multicenter, prospective observational study enrolled patients with APC who received nal-IRI/FF after a gemcitabine-based regimen from July 2020 to June 2021. We collected and analyzed clinical data and conducted survival and multivariate analyses. Thirty-one (78%) of the 40 patients had metastases. Nal-IRI/FF was the second-line therapy in 36 patients (90%). The median duration was 3.2 months. The disease control rate was 57%. The median progression-free survival and overall survival (OS) were 4.5 months (95% confidence interval [CI]: 2.8−5.5) and 7.4 months (95% CI: 5.1−10.6), respectively. Common ≥grade 3 toxicities included neutropenia (28%) and fatigue (23%). Fatigue led to treatment discontinuation in 6 out of 10 patients. Multivariate analysis showed that a neutrophil-to-lymphocyte ratio > 4 was a significant risk factor for a short OS (hazard ratio (HR) = 3.08, 95% CI: 1.21−7.85, p = 0.02). In conclusion, nal-IRI/FF is an appropriate treatment option for APC following gemcitabine-containing regimens.

摘要

尽管在III期NAPOLI-1试验中,纳米脂质体伊立替康联合氟尿嘧啶/亚叶酸(nal-IRI/FF)对吉西他滨难治的晚期胰腺癌(APC)患者显示出生存获益,但在日本真实世界环境中,关于该方案疗效和安全性的数据有限。这项多中心前瞻性观察性研究纳入了2020年7月至2021年6月期间接受基于吉西他滨方案治疗后再接受nal-IRI/FF治疗的APC患者。我们收集并分析了临床数据,并进行了生存和多因素分析。40例患者中有31例(78%)发生转移。nal-IRI/FF是36例患者(90%)的二线治疗方案。中位治疗持续时间为3.2个月。疾病控制率为57%。中位无进展生存期和总生存期(OS)分别为4.5个月(95%置信区间[CI]:2.8−5.5)和7.4个月(95%CI:5.1−10.6)。常见的≥3级毒性包括中性粒细胞减少(28%)和疲劳(23%)。10例患者中有6例因疲劳导致治疗中断。多因素分析显示,中性粒细胞与淋巴细胞比值>4是OS短的显著危险因素(风险比[HR]=3.08,95%CI:1.21−7.85,p=0.02)。总之,nal-IRI/FF是含吉西他滨方案治疗后APC的合适治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b72d/9457338/a36678223dfb/jcm-11-05084-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b72d/9457338/d859fc2f5a49/jcm-11-05084-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b72d/9457338/a36678223dfb/jcm-11-05084-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b72d/9457338/d859fc2f5a49/jcm-11-05084-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b72d/9457338/a36678223dfb/jcm-11-05084-g002.jpg

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