Yan Chang, Wang Runzhi, Zhang Chaojun, Lin Guoxiang, Du Youqing, Chen Meiwen, Liu Fushuang, Li Ling, Qu Song, Zhu XiaoDong
Department of Radiation Oncology, Guangxi Medical University Cancer Hospital, Nanning, Guangxi 530021, China.
Department of Oncology, Wuming Hospital of Guangxi Medical University, Nanning, Guangxi 530199, China; Research Center of Carcinogenesis and Targeted Therapy, Xiangya Hospital, Central South University, Changsha, China.
Oral Oncol. 2025 Jan;160:107119. doi: 10.1016/j.oraloncology.2024.107119. Epub 2024 Nov 25.
Gemcitabine plus cisplatin (GP) and docetaxel plus cisplatin plus fluorouracil (TPF) are induction chemotherapy (IC) regimens for locally advanced nasopharyngeal carcinoma (LA-NPC). The oral convenience of capecitabine presents its potential as a fluorouracil substitute in the TPF regimen, which has yet to be thoroughly investigated. This study aims to compare the efficacy and safety of the docetaxel, cisplatin, and capecitabine (TPC) with GP and TPF in LA-NPC.
A retrospective analysis was conducted on newly diagnosed stage III-IVa nasopharyngeal carcinoma patients who received GP, TPC, or TPF induction chemotherapy followed by concurrent chemoradiotherapy (CCRT) between February 2019 and December 2021. A comparison of the prognostic outcomes and associated adverse reactions among patients receiving different IC regimens. Multivariate Cox regression was applied to analyze independent prognostic factors, and subgroup survival analyses were conducted based on these factors.
A total of 291 LA-NPC patients were included, with 70 receiving TPC, 119 receiving GP, and 102 receiving TPF. Kaplan-Meier survival analysis indicated no significant differences in OS, PFS, LRFS, and DMFS among the 3 groups. Multivariate Cox regression identified T classification and clinical stage as independent prognostic factors. Subgroup analyses revealed no significant differences in OS and PFS between the 3 groups across T1-2 and T3-4 classifications or III and IVa stages.The TPC group exhibited lower incidence rates of treatment-related acute toxicity reactions, including grade 3-4 toxicities.
The TPC induction chemotherapy regimen demonstrates comparable efficacy to GP and TPF, while maintaining a favorable safety profile.
吉西他滨联合顺铂(GP)以及多西他赛联合顺铂加氟尿嘧啶(TPF)是局部晚期鼻咽癌(LA-NPC)的诱导化疗方案。卡培他滨的口服便利性使其有潜力作为TPF方案中氟尿嘧啶的替代药物,但这一点尚未得到充分研究。本研究旨在比较多西他赛、顺铂和卡培他滨(TPC)与GP及TPF在LA-NPC治疗中的疗效和安全性。
对2019年2月至2021年12月期间新诊断的III-IVa期鼻咽癌患者进行回顾性分析,这些患者接受了GP、TPC或TPF诱导化疗,随后接受同步放化疗(CCRT)。比较接受不同诱导化疗方案患者的预后结果及相关不良反应。应用多因素Cox回归分析独立预后因素,并基于这些因素进行亚组生存分析。
共纳入291例LA-NPC患者,其中70例接受TPC,119例接受GP,102例接受TPF。Kaplan-Meier生存分析表明,三组患者的总生存期(OS)、无进展生存期(PFS)、局部区域无复发生存期(LRFS)和远处转移无复发生存期(DMFS)无显著差异。多因素Cox回归分析确定T分期和临床分期为独立预后因素。亚组分析显示,在T1-2和T3-4分期或III期和IVa期的三组患者中,OS和PFS无显著差异。TPC组与治疗相关的急性毒性反应发生率较低,包括3-4级毒性反应。
TPC诱导化疗方案显示出与GP和TPF相当的疗效,同时保持了良好的安全性。