Trifluridine/tipiracil with or without bevacizumab in metastatic colorectal cancer: results of a systematic review and meta-analysis

被引:12
作者
Yoshino, Takayuki [1 ]
Taieb, Julien [2 ]
Kuboki, Yasutoshi [3 ]
Pfeiffer, Per [4 ]
Kumar, Amit [5 ]
Hochster, Howard S. S. [6 ]
机构
[1] Natl Canc Ctr Hosp East, Dept Gastroenterol & Gastrointestinal Oncol, 6-5-1 Kashiwanoha, Kashiwa, Chiba 2778577, Japan
[2] Univ Paris Cite, Hop Europeen Georges Pompidou, SIRIC CARPEM, Paris, France
[3] Natl Canc Ctr Hosp East, Kashiwa, Japan
[4] Odense Univ Hosp, Odense, Denmark
[5] SmartAnalyst India Pvt Ltd, Gurugram, Haryana, India
[6] Rutgers Canc Inst New Jersey, New Brunswick, NJ USA
关键词
bevacizumab; meta-analysis; metastatic colorectal cancer; overall survival; progression-free survival; safety; trifluridine; tipiracil; TAS-102; MONOTHERAPY; DOUBLE-BLIND; OPEN-LABEL; PLACEBO; TRIAL; CHEMOTHERAPY; QUALITY; AGENT; CARE;
D O I
10.1177/17588359221146137
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background:Trifluridine/tipiracil plus bevacizumab (FTD/TPI + BEV) has shown efficacy and tolerability in refractory metastatic colorectal cancer (mCRC). Because randomized controlled trial (RCT) data comparing FTD/TPI + BEV with FTD/TPI are lacking, this meta-analysis evaluated outcomes with both regimens. Data Sources and Methods:Electronic databases, congress proceedings (past 3 years), trial registries, systematic review bibliographies, gray literature, and guidelines through June 2021 were searched for RCTs, non-RCTs, and prospective observational studies involving >20 previously treated patients with mCRC receiving FTD/TPI + BEV or FTD/TPI. Absolute and relative disease control rate (DCR), progression-free survival (PFS), overall survival (OS), adverse event (AE) rates, and discontinuation rates due to AEs were evaluated using fixed-effects and random-effects models. Study quality, heterogeneity, and publication bias were assessed. Results:In all, 29 of 875 screened publications were selected (26 studies: 5 RCTs, 11 non-RCTs, and 10 prospective observational studies). One RCT compared FTD/TPI + BEV with FTD/TPI. FTD/TPI + BEV versus FTD/TPI had a higher absolute DCR [64% (6 studies; n = 289) versus 43% (10 studies; n = 2809)], median PFS [4.2 (5 studies; n = 244) versus 2.6 (6 studies; n = 1781) months], 12-month PFS [9% (5 studies; n = 244) versus 3% (6 studies; n = 1781)], median OS [9.8 (5 studies; n = 244) versus 8.1 (6 studies; n = 1814) months], and 12-month OS [38% (5 studies; n = 244) versus 32% (6 studies; n = 1814)]. Grade & GT;3 febrile neutropenia, asthenia/fatigue, diarrhea, nausea, and vomiting rates were similar (1%-7%). Grade & GT;3 neutropenia rate was higher with FTD/TPI + BEV than with FTD/TPI [43% (6 studies; n = 294) versus 29% (12 studies; n = 7139)]. Discontinuation rates due to AEs were similar [8% (5 studies; n = 244) and 7% (10 studies; n = 3724)]. Low study quality, heterogeneity, and/or publication bias were detected in certain instances. Conclusion:Despite fewer patients treated with the combination, this meta-analysis consistently suggested that FTD/TPI + BEV provides benefits over FTD/TPI in refractory mCRC and has similar safety, except for more frequent grade & GT;3 neutropenia.
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页数:14
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