Tentoni Nicolás, Combs Ryan, Hwang Miriam, Ward Suzanne, McCracken Andrea, Lowe Jennifer, Howard Scott C
Resonance, Memphis, TN 38104, USA.
Laboratory of Applied Statistics in the Health Sciences, Faculty of Medicine, University of Buenos Aires, Buenos Aires C1121 ABG, Argentina.
Cancers (Basel). 2024 Dec 3;16(23):4050. doi: 10.3390/cancers16234050.
We aimed to determine whether the occurrence of early-onset toxicities due to 5-fluorouracil (5-FU) in treatment-naive patients undergoing their first cycle of FOLFOX/FOLFIRINOX was associated with decreased overall survival, increased risk of treatment cessation, and hospitalization.
This was a retrospective cohort study using patient information from community oncology practices. Patients who received their first dose of 5-FU from 1 January 2015 through 1 August 2023 were included. The occurrence of an early-onset 5-FU-related toxicity (during 5-FU infusion or up to 96 h after infusion completion) in the first cycle of FOLFOX/FOLFIRINOX was the explanatory variable. The primary endpoint was overall survival (OS); secondary endpoints included early treatment cessation and early hospital admission.
In total, 3988 patients were included; the median age was 62.9 years and 57.5% were male. Early-onset toxicities were observed in 19.1%, with vomiting, thrombocytopenia, and diarrhea being most common. Patients with early-onset toxicities had a median OS of 2.5 years [95% CI 2.2 to 2.9] compared with 5.3 years [95% CI 4.7 to 5.8] in patients without early-onset toxicities ( < 0.001). The occurrence of early-onset toxicities was associated with an adjusted hazard ratio of 1.61 [95% CI 1.44 to 1.80] and was also significantly associated with early treatment cessation (odds ratio [OR] 1.53, 95% CI 1.30 to 1.80) and early hospital admission (OR 8.69, 95% CI 3.45 to 24.18).
Early-onset toxicities related to 5-FU during the first cycle of FOLFOX/FOLFIRINOX treatment were associated with poor outcomes. Early recognition and prompt intervention are pertinent to improve outcomes in patients receiving fluoropyrimidine chemotherapy.
我们旨在确定初次接受FOLFOX/FOLFIRINOX方案首个周期治疗的患者中,5-氟尿嘧啶(5-FU)所致早发性毒性的发生是否与总生存期缩短、治疗中断风险增加及住院有关。
这是一项回顾性队列研究,使用来自社区肿瘤医疗实践的患者信息。纳入2015年1月1日至2023年8月1日期间接受首剂5-FU治疗的患者。FOLFOX/FOLFIRINOX首个周期中早发性5-FU相关毒性(在5-FU输注期间或输注完成后96小时内)的发生情况为解释变量。主要终点为总生存期(OS);次要终点包括早期治疗中断和早期住院。
共纳入3988例患者;中位年龄为62.9岁,57.5%为男性。观察到19.1%的患者出现早发性毒性,最常见的是呕吐、血小板减少和腹泻。出现早发性毒性的患者中位OS为2.5年[95%置信区间(CI)2.2至2.9],而未出现早发性毒性的患者为5.3年[95%CI 4.7至5.8](P<0.001)。早发性毒性的发生与调整后的风险比为1.61[95%CI 1.44至1.80]相关,也与早期治疗中断(比值比[OR]1.53,95%CI 1.30至1.80)和早期住院(OR 8.69,95%CI 3.45至24.18)显著相关。
FOLFOX/FOLFIRINOX治疗首个周期中与5-FU相关的早发性毒性与不良预后相关。早期识别和及时干预对于改善接受氟嘧啶化疗患者的预后至关重要。