晚期胰腺癌患者三周改良FOLFIRINOX治疗的临床结果和安全性。

IF 1.6 Q4 ONCOLOGY
Kana Hosokawa, Kenji Ikezawa, Yugo Kai, Ryoji Takada, Takumi Kinomoto, Takanori Masumoto, Masaki Kawabata, Hiroki Kishimoto, Kazuhiro Kozumi, Makiko Urabe, Kaori Mukai, Tasuku Nakabori, Kazuyoshi Ohkawa
{"title":"晚期胰腺癌患者三周改良FOLFIRINOX治疗的临床结果和安全性。","authors":"Kana Hosokawa, Kenji Ikezawa, Yugo Kai, Ryoji Takada, Takumi Kinomoto, Takanori Masumoto, Masaki Kawabata, Hiroki Kishimoto, Kazuhiro Kozumi, Makiko Urabe, Kaori Mukai, Tasuku Nakabori, Kazuyoshi Ohkawa","doi":"10.1007/s12029-025-01309-6","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Modified FOLFIRINOX (mFFX) therapy is widely used as first- or second-line treatment for advanced pancreatic cancer. However, adverse effects (AEs), such as cytopenia, often prevent the intended biweekly administration of mFFX therapy. Extending the dosing interval may decrease AEs and allow safer and longer mFFX therapy continuation. Therefore, this study evaluated the efficacy and safety of triweekly mFFX therapy at our institution.</p><p><strong>Methods: </strong>We retrospectively reviewed 17 patients with unresectable pancreatic ductal adenocarcinoma who received mFFX therapy for more than 3 months and switched to a triweekly administration schedule within 2 months of initiating therapy at our institution between April 2017 and December 2023.</p><p><strong>Results: </strong>Patient median age was 58 years (range: 36-75, 52.9% male). Eleven patients received mFFX therapy as the first-line treatment, while the other four patients received it as the second-line treatment. The median number of mFFX cycles was nine (range: 5-56). The median overall survival (OS) and progression-free survival (PFS) for all patients were 14.2 (95% confidence interval [CI], 10.5-26.3) and 6.7 (95% CI, 3.9-9.5) months, respectively. Regarding AEs, because patients with severe hematologic toxicity in the early phase were switched to triweekly treatment, the proportions of grade ≥ 3 leukopenia and neutropenia were high. In contrast, for grade ≥ 3 non-hematologic toxicity, diarrhea and anorexia were observed in only 1 of 17 patients.</p><p><strong>Conclusion: </strong>Triweekly mFFX therapy for unresectable pancreatic cancer may be a feasible treatment option, with relatively low toxicity and valid efficacy.</p>","PeriodicalId":15895,"journal":{"name":"Journal of Gastrointestinal Cancer","volume":"56 1","pages":"187"},"PeriodicalIF":1.6000,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinical Outcome and Safety of Triweekly Modified FOLFIRINOX Therapy in Patients with Advanced Pancreatic Cancer.\",\"authors\":\"Kana Hosokawa, Kenji Ikezawa, Yugo Kai, Ryoji Takada, Takumi Kinomoto, Takanori Masumoto, Masaki Kawabata, Hiroki Kishimoto, Kazuhiro Kozumi, Makiko Urabe, Kaori Mukai, Tasuku Nakabori, Kazuyoshi Ohkawa\",\"doi\":\"10.1007/s12029-025-01309-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Modified FOLFIRINOX (mFFX) therapy is widely used as first- or second-line treatment for advanced pancreatic cancer. However, adverse effects (AEs), such as cytopenia, often prevent the intended biweekly administration of mFFX therapy. Extending the dosing interval may decrease AEs and allow safer and longer mFFX therapy continuation. Therefore, this study evaluated the efficacy and safety of triweekly mFFX therapy at our institution.</p><p><strong>Methods: </strong>We retrospectively reviewed 17 patients with unresectable pancreatic ductal adenocarcinoma who received mFFX therapy for more than 3 months and switched to a triweekly administration schedule within 2 months of initiating therapy at our institution between April 2017 and December 2023.</p><p><strong>Results: </strong>Patient median age was 58 years (range: 36-75, 52.9% male). Eleven patients received mFFX therapy as the first-line treatment, while the other four patients received it as the second-line treatment. The median number of mFFX cycles was nine (range: 5-56). The median overall survival (OS) and progression-free survival (PFS) for all patients were 14.2 (95% confidence interval [CI], 10.5-26.3) and 6.7 (95% CI, 3.9-9.5) months, respectively. Regarding AEs, because patients with severe hematologic toxicity in the early phase were switched to triweekly treatment, the proportions of grade ≥ 3 leukopenia and neutropenia were high. In contrast, for grade ≥ 3 non-hematologic toxicity, diarrhea and anorexia were observed in only 1 of 17 patients.</p><p><strong>Conclusion: </strong>Triweekly mFFX therapy for unresectable pancreatic cancer may be a feasible treatment option, with relatively low toxicity and valid efficacy.</p>\",\"PeriodicalId\":15895,\"journal\":{\"name\":\"Journal of Gastrointestinal Cancer\",\"volume\":\"56 1\",\"pages\":\"187\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-09-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Gastrointestinal Cancer\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s12029-025-01309-6\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Gastrointestinal Cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s12029-025-01309-6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

目的:改良的FOLFIRINOX (mFFX)疗法广泛用于晚期胰腺癌的一线或二线治疗。然而,不良反应(ae),如细胞减少症,通常阻止mFFX治疗的预期双周给药。延长给药间隔可以减少不良反应,并允许更安全和更长的mFFX治疗持续时间。因此,本研究评估了我们机构每三周mFFX治疗的有效性和安全性。方法:我们回顾性分析了17例不可切除的胰腺导管腺癌患者,这些患者在2017年4月至2023年12月期间接受mFFX治疗超过3个月,并在开始治疗后的2个月内切换为三周给药计划。结果:患者中位年龄58岁(36-75岁,男性占52.9%)。11例患者接受mFFX治疗作为一线治疗,另外4例患者接受mFFX治疗作为二线治疗。mFFX周期的中位数为9(范围:5-56)。所有患者的中位总生存期(OS)和无进展生存期(PFS)分别为14.2个月(95%可信区间[CI], 10.5-26.3)和6.7个月(95% CI, 3.9-9.5)。对于不良反应,由于早期有严重血液学毒性的患者改为每三周治疗一次,因此≥3级白细胞减少和中性粒细胞减少的比例很高。相比之下,对于≥3级的非血液学毒性,17例患者中只有1例出现腹泻和厌食。结论:三周mFFX治疗不可切除的胰腺癌可能是一种可行的治疗方案,毒性较低,疗效有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Outcome and Safety of Triweekly Modified FOLFIRINOX Therapy in Patients with Advanced Pancreatic Cancer.

Purpose: Modified FOLFIRINOX (mFFX) therapy is widely used as first- or second-line treatment for advanced pancreatic cancer. However, adverse effects (AEs), such as cytopenia, often prevent the intended biweekly administration of mFFX therapy. Extending the dosing interval may decrease AEs and allow safer and longer mFFX therapy continuation. Therefore, this study evaluated the efficacy and safety of triweekly mFFX therapy at our institution.

Methods: We retrospectively reviewed 17 patients with unresectable pancreatic ductal adenocarcinoma who received mFFX therapy for more than 3 months and switched to a triweekly administration schedule within 2 months of initiating therapy at our institution between April 2017 and December 2023.

Results: Patient median age was 58 years (range: 36-75, 52.9% male). Eleven patients received mFFX therapy as the first-line treatment, while the other four patients received it as the second-line treatment. The median number of mFFX cycles was nine (range: 5-56). The median overall survival (OS) and progression-free survival (PFS) for all patients were 14.2 (95% confidence interval [CI], 10.5-26.3) and 6.7 (95% CI, 3.9-9.5) months, respectively. Regarding AEs, because patients with severe hematologic toxicity in the early phase were switched to triweekly treatment, the proportions of grade ≥ 3 leukopenia and neutropenia were high. In contrast, for grade ≥ 3 non-hematologic toxicity, diarrhea and anorexia were observed in only 1 of 17 patients.

Conclusion: Triweekly mFFX therapy for unresectable pancreatic cancer may be a feasible treatment option, with relatively low toxicity and valid efficacy.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
3.80
自引率
0.00%
发文量
121
期刊介绍: The Journal of Gastrointestinal Cancer is a multidisciplinary medium for the publication of novel research pertaining to cancers arising from the gastrointestinal tract.The journal is dedicated to the most rapid publication possible.The journal publishes papers in all relevant fields, emphasizing those studies that are helpful in understanding and treating cancers affecting the esophagus, stomach, liver, gallbladder and biliary tree, pancreas, small bowel, large bowel, rectum, and anus. In addition, the Journal of Gastrointestinal Cancer publishes basic and translational scientific information from studies providing insight into the etiology and progression of cancers affecting these organs. New insights are provided from diverse areas of research such as studies exploring pre-neoplastic states, risk factors, epidemiology, genetics, preclinical therapeutics, surgery, radiation therapy, novel medical therapeutics, clinical trials, and outcome studies.In addition to reports of original clinical and experimental studies, the journal also publishes: case reports, state-of-the-art reviews on topics of immediate interest or importance; invited articles analyzing particular areas of pancreatic research and knowledge; perspectives in which critical evaluation and conflicting opinions about current topics may be expressed; meeting highlights that summarize important points presented at recent meetings; abstracts of symposia and conferences; book reviews; hypotheses; Letters to the Editors; and other items of special interest, including:Complex Cases in GI Oncology:  This is a new initiative to provide a forum to review and discuss the history and management of complex and involved gastrointestinal oncology cases. The format will be similar to a teaching case conference where a case vignette is presented and is followed by a series of questions and discussion points. A brief reference list supporting the points made in discussion would be expected.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信