{"title":"脂质体伊立替康作为晚期胰腺癌二线治疗的安全性和有效性:系统综述和荟萃分析。","authors":"","doi":"10.1016/j.critrevonc.2024.104386","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Nanoliposomal irinotecan (nal-IRI) is a novel regimen for pancreatic cancer, featuring a longer half-life and an increased area under the concentration-time curve. This study aims to assess the safety and efficacy of nal-IRI as a second-line treatment for advanced pancreatic cancer.</p></div><div><h3>Methods</h3><p>A systemic literature search was conducted based on articles published before September 26th, 2023 in databases, including PubMed, Cochrane Library, EMBASE and Web of Science. The fixed effects model was used to calculate the pooled mean difference for overall survival (OS) and progression-free survival (PFS), as well as the pooled odds ratio for the overall response rate (ORR) and the risk of adverse events.</p></div><div><h3>Results</h3><p>A total of 21 studies, including 3044 patients with locally advanced unresectable or metastatic pancreatic cancers, were considered eligible. The use of nal-IRI, combined with 5-fluorouracil and leucovorin, resulted in significantly improved PFS (pooled mean difference=1.01 months, 95 % confidence interval [CI]=0.97–1.05, <em>p<</em>0.01) and OS (pooled mean difference=0.29 months, 95 %CI=0.18–0.39, <em>p</em><0.01), as well as significantly better ORR (pooled odds ratio=2.06, 95 %CI=1.30–3.27, <em>p</em>=0.002) compared to other second-line regimens. Nonetheless, an increased risk of grade 3 or greater neutropenia, anemia, hypokalemia, diarrhea, and vomiting was also noted.</p></div><div><h3>Conclusion</h3><p>Second-line treatments based on nal-IRI exhibited significantly improved PFS, OS, and ORR compared to other available treatments in advanced pancreatic cancer. Further research is necessary to corroborate these findings and define the role of nal-IRI in both first and later lines of therapy.</p></div>","PeriodicalId":11358,"journal":{"name":"Critical reviews in oncology/hematology","volume":"201 ","pages":"Article 104386"},"PeriodicalIF":5.5000,"publicationDate":"2024-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Safety and efficacy of liposomal irinotecan as the second-line treatment for advanced pancreatic cancer: A systematic review and meta-analysis\",\"authors\":\"\",\"doi\":\"10.1016/j.critrevonc.2024.104386\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>Nanoliposomal irinotecan (nal-IRI) is a novel regimen for pancreatic cancer, featuring a longer half-life and an increased area under the concentration-time curve. This study aims to assess the safety and efficacy of nal-IRI as a second-line treatment for advanced pancreatic cancer.</p></div><div><h3>Methods</h3><p>A systemic literature search was conducted based on articles published before September 26th, 2023 in databases, including PubMed, Cochrane Library, EMBASE and Web of Science. The fixed effects model was used to calculate the pooled mean difference for overall survival (OS) and progression-free survival (PFS), as well as the pooled odds ratio for the overall response rate (ORR) and the risk of adverse events.</p></div><div><h3>Results</h3><p>A total of 21 studies, including 3044 patients with locally advanced unresectable or metastatic pancreatic cancers, were considered eligible. The use of nal-IRI, combined with 5-fluorouracil and leucovorin, resulted in significantly improved PFS (pooled mean difference=1.01 months, 95 % confidence interval [CI]=0.97–1.05, <em>p<</em>0.01) and OS (pooled mean difference=0.29 months, 95 %CI=0.18–0.39, <em>p</em><0.01), as well as significantly better ORR (pooled odds ratio=2.06, 95 %CI=1.30–3.27, <em>p</em>=0.002) compared to other second-line regimens. Nonetheless, an increased risk of grade 3 or greater neutropenia, anemia, hypokalemia, diarrhea, and vomiting was also noted.</p></div><div><h3>Conclusion</h3><p>Second-line treatments based on nal-IRI exhibited significantly improved PFS, OS, and ORR compared to other available treatments in advanced pancreatic cancer. Further research is necessary to corroborate these findings and define the role of nal-IRI in both first and later lines of therapy.</p></div>\",\"PeriodicalId\":11358,\"journal\":{\"name\":\"Critical reviews in oncology/hematology\",\"volume\":\"201 \",\"pages\":\"Article 104386\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2024-05-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Critical reviews in oncology/hematology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S104084282400129X\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Critical reviews in oncology/hematology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S104084282400129X","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
简介使用纳米脂质体伊立替康(nal-IRI)治疗胰腺癌是一种新型疗法,其特点是半衰期更长、浓度-时间曲线下面积增大。然而,很少有全面的系统综述或荟萃分析对其作为二线治疗的疗效进行评估。因此,本研究旨在回顾目前有关纳尔-IRI的证据,评估其对该疾病的整体临床表现:方法:根据 2023 年 9 月 26 日之前在 PubMed、Cochrane Library、EMBASE 和 Web of Science 数据库中发表的文章进行系统文献检索。采用固定效应模型计算总生存期(OS)、无进展生存期(PFS)、总反应率(ORR)和不良事件等基本结果的集合平均差和几率:共有 21 项研究符合条件,其中包括 3017 例局部晚期不可切除或转移性胰腺癌患者。纳尔-IRI与5-氟尿嘧啶和亮菌甲素一起使用可显著改善PFS和OS,汇总平均差异为1.01个月(95%置信区间(95%CI)=0.97-1.05,p):与其他现有疗法相比,基于Nal-IRI的晚期胰腺癌二线疗法的PFS、OS和ORR均有明显改善。有必要开展进一步研究,以证实这些发现,并确定纳尔-IRI在一线和二线治疗中的作用。
Safety and efficacy of liposomal irinotecan as the second-line treatment for advanced pancreatic cancer: A systematic review and meta-analysis
Introduction
Nanoliposomal irinotecan (nal-IRI) is a novel regimen for pancreatic cancer, featuring a longer half-life and an increased area under the concentration-time curve. This study aims to assess the safety and efficacy of nal-IRI as a second-line treatment for advanced pancreatic cancer.
Methods
A systemic literature search was conducted based on articles published before September 26th, 2023 in databases, including PubMed, Cochrane Library, EMBASE and Web of Science. The fixed effects model was used to calculate the pooled mean difference for overall survival (OS) and progression-free survival (PFS), as well as the pooled odds ratio for the overall response rate (ORR) and the risk of adverse events.
Results
A total of 21 studies, including 3044 patients with locally advanced unresectable or metastatic pancreatic cancers, were considered eligible. The use of nal-IRI, combined with 5-fluorouracil and leucovorin, resulted in significantly improved PFS (pooled mean difference=1.01 months, 95 % confidence interval [CI]=0.97–1.05, p<0.01) and OS (pooled mean difference=0.29 months, 95 %CI=0.18–0.39, p<0.01), as well as significantly better ORR (pooled odds ratio=2.06, 95 %CI=1.30–3.27, p=0.002) compared to other second-line regimens. Nonetheless, an increased risk of grade 3 or greater neutropenia, anemia, hypokalemia, diarrhea, and vomiting was also noted.
Conclusion
Second-line treatments based on nal-IRI exhibited significantly improved PFS, OS, and ORR compared to other available treatments in advanced pancreatic cancer. Further research is necessary to corroborate these findings and define the role of nal-IRI in both first and later lines of therapy.
期刊介绍:
Critical Reviews in Oncology/Hematology publishes scholarly, critical reviews in all fields of oncology and hematology written by experts from around the world. Critical Reviews in Oncology/Hematology is the Official Journal of the European School of Oncology (ESO) and the International Society of Liquid Biopsy.