Shitara Kohei, Falcone Alfred, Fakih Marwan G, George Ben, Sundar Raghav, Ranjan Sandip, Van Cutsem Eric
National Cancer Center Hospital East, Chiba, Japan.
Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Oncologist. 2024 May 3;29(5):e601-e615. doi: 10.1093/oncolo/oyae007.
We performed a systematic literature review to identify and summarize data from studies reporting clinical efficacy and safety outcomes for trifluridine/tipiracil (FTD/TPI) combined with other antineoplastic agents in advanced cancers, including metastatic colorectal cancer (mCRC). We conducted a systematic search on May 29, 2021, for studies reporting one or more efficacy or safety outcome with FTD/TPI-containing combinations. Our search yielded 1378 publications, with 38 records meeting selection criteria: 35 studies of FTD/TPI-containing combinations in mCRC (31 studies second line or later) and 3 studies in other tumor types. FTD/TPI plus bevacizumab was extensively studied, including 19 studies in chemorefractory mCRC. Median overall survival ranged 8.6-14.4 months and median progression-free survival 3.7-6.8 months with FTD/TPI plus bevacizumab in refractory mCRC. Based on one randomized and several retrospective studies, FTD/TPI plus bevacizumab was associated with improved outcomes compared with FTD/TPI monotherapy. FTD/TPI combinations with chemotherapy or other targeted agents were reported in small early-phase studies; preliminary data indicated higher antitumor activity for certain combinations. Overall, no safety concerns existed with FTD/TPI combinations; most common grade ≥ 3 adverse event was neutropenia, ranging 5%-100% across all studies. In studies comparing FTD/TPI combinations with monotherapy, grade ≥ 3 neutropenia appeared more frequently with combinations (29%-67%) vs. monotherapy (5%-41%). Discontinuation rates due to adverse events ranged 0%-11% for FTD/TPI plus bevacizumab and 0%-17% with other combinations. This systematic review supports feasibility and safety of FTD/TPI plus bevacizumab in refractory mCRC. Data on non-bevacizumab FTD/TPI combinations remain preliminary and need further validation.
我们进行了一项系统的文献综述,以识别和总结报告曲氟尿苷/替匹嘧啶(FTD/TPI)与其他抗肿瘤药物联合用于晚期癌症(包括转移性结直肠癌[mCRC])的临床疗效和安全性结果的研究数据。我们于2021年5月29日进行了系统检索,以查找报告含FTD/TPI联合用药的一项或多项疗效或安全性结果的研究。我们的检索得到1378篇出版物,其中38条记录符合入选标准:35项关于含FTD/TPI联合用药治疗mCRC的研究(31项为二线或更晚期研究)以及3项关于其他肿瘤类型的研究。FTD/TPI联合贝伐单抗得到了广泛研究,其中包括19项关于化疗难治性mCRC的研究。在难治性mCRC中,FTD/TPI联合贝伐单抗治疗的总生存期中位数为8.6 - 14.4个月,无进展生存期中位数为3.7 - 6.8个月。基于一项随机研究和多项回顾性研究,与FTD/TPI单药治疗相比,FTD/TPI联合贝伐单抗与更好的结果相关。小型早期研究报告了FTD/TPI与化疗或其他靶向药物的联合用药情况;初步数据表明某些联合用药具有更高的抗肿瘤活性。总体而言,FTD/TPI联合用药不存在安全性问题;最常见的≥3级不良事件是中性粒细胞减少,在所有研究中的发生率为5% - 100%。在比较FTD/TPI联合用药与单药治疗的研究中,联合用药组≥3级中性粒细胞减少的出现频率(29% - 67%)高于单药治疗组(5% - 41%)。FTD/TPI联合贝伐单抗因不良事件导致的停药率为0% - 11%,其他联合用药组为0% - 17%。这项系统综述支持FTD/TPI联合贝伐单抗用于难治性mCRC的可行性和安全性。关于不含贝伐单抗的FTD/TPI联合用药的数据仍属初步,需要进一步验证。