Wong Chun-Ka, Ho Isaac, Choo Ali, Lau Rachel, Ma Ting-Fung, Chiu Alston Conrad Ho-On, Lam Tsun-Ho, Lin Minqing, Leung Ricky Wang-Hei, Chor-Cheung Tam Frankie, Foo Dominic Chi Chung, Tse Hung-Fat
Department of Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Department of Clinical Oncology, Queen Mary Hospital, Hong Kong SAR, China.
Cardiooncology. 2025 Jan 15;11(1):3. doi: 10.1186/s40959-024-00294-2.
Fluoropyrimidines, including 5-fluorouracil and capecitabine, are the most common chemotherapeutic agents for colorectal carcinoma. Although previous studies have suggested varying degrees of cardiotoxicity with these drugs, there is a notable lack of large-scale investigations with appropriate control groups. This study aimed to evaluate cardiovascular outcome among colorectal carcinoma patients treated with fluoropyrimidines.
A retrospective propensity score- matched cohort study was conducted in patients diagnosed with colorectal carcinoma between January 1, 1993 and December 31, 2021 at public hospitals in Hong Kong. Cardiovascular outcomes in patients prescribed fluoropyrimidines were compared with controls. Further analyses to compare 5-fluroracil and capecitabine were performed.
A total of 51,888 colorectal carcinoma patients were identified. After 1:1 propensity score matching, 21,216 patients were included in the final analysis, with 10,608 patients in each group. 1.06% patients experienced a major adverse cardiovascular event (MACE) at 1 year. There was no significant difference in MACE risk between the two groups (HR 0.91, 95% confidence interval (95%CI): 0.70-1.18, p = 0.46). Risk of cardiovascular death was similar between the two groups (HR 1.05, 95%CI: 0.69-1.60, p = 0.82). Subgroup analysis did not demonstrate a statistically significant elevated risk of MACE during fluoropyrimidine use in high-risk patient groups. Further comparison of 5-fluorouracil and capecitabine did not reveal a difference in MACE (0.80% vs. 0.98%; HR 1.09, 95%CI: 0.64-1.85, p < 0.75).
Fluoropyrimidine use in patients with colorectal carcinoma did not increase the risk of MACE, cardiovascular death, or other specific cardiovascular conditions. There was no significant difference in cardiovascular risk between 5-fluorouracil and capecitabine.
氟嘧啶,包括5-氟尿嘧啶和卡培他滨,是结直肠癌最常用的化疗药物。尽管先前的研究表明这些药物存在不同程度的心脏毒性,但缺乏有适当对照组的大规模调查。本研究旨在评估接受氟嘧啶治疗的结直肠癌患者的心血管结局。
对1993年1月1日至2021年12月31日在香港公立医院诊断为结直肠癌的患者进行一项回顾性倾向评分匹配队列研究。将使用氟嘧啶的患者的心血管结局与对照组进行比较。进一步分析比较了5-氟尿嘧啶和卡培他滨。
共识别出51,888例结直肠癌患者。经过1:1倾向评分匹配后,21,216例患者纳入最终分析,每组10,608例。1.06%的患者在1年时发生了主要不良心血管事件(MACE)。两组之间的MACE风险无显著差异(HR 0.91,95%置信区间(95%CI):0.70-1.18,p = 0.46)。两组之间的心血管死亡风险相似(HR 1.05,95%CI:0.69-1.60,p = 0.82)。亚组分析未显示高危患者组在使用氟嘧啶期间MACE风险有统计学意义的升高。5-氟尿嘧啶和卡培他滨的进一步比较未发现MACE有差异(0.80%对0.98%;HR 1.09,95%CI:0.64-1.85,p < 0.75)。
结直肠癌患者使用氟嘧啶不会增加MACE、心血管死亡或其他特定心血管疾病的风险。5-氟尿嘧啶和卡培他滨之间的心血管风险无显著差异。