Abiodun Aderonke Temilade, Ju Chengsheng, Welch Catherine A, Lai Jennifer, Tyrer Freya, Chambers Pinkie, Paley Lizz, Vernon Sally, Deanfield John, de Belder Mark, Rutherford Mark, Lambert Paul C, Slater Sarah, Shiu Kai Keen, Wei Li, Peake Michael D, Adlam David, Manisty Charlotte
University College London Institute of Cardiovascular Science, London, UK.
Barts Heart Centre, Barts Health NHS Trust, London, UK.
BMJ Oncol. 2024 Aug 8;3(1):e000323. doi: 10.1136/bmjonc-2024-000323. eCollection 2024.
Fluoropyrimidine chemotherapy is a first-line treatment for many gastrointestinal (GI) cancers, however, cardiotoxicity concerns may limit administration in patients with pre-existing cardiovascular disease (CVD). This study investigated the association of pre-existing CVD with use of fluoropyrimidine chemotherapy in tumour-eligible GI cancer patients.
National cancer registry data from the Virtual Cardio-Oncology Research Initiative from England between 2014 and 2018 was used to identify GI cancer patients eligible to receive fluoropyrimidine chemotherapy. Linkage to Hospital Episode Statistics and CVD registry data were used to ascertain prior CVD and outcomes. Primary outcome was first administration of fluoropyrimidine chemotherapy following cancer diagnosis. Cox proportional hazard models determined HR and 95% CIs for the association between initiation of fluoropyrimidine treatment and prior CVD.
112 726 eligible patients were identified (median age 71 years (IQR 62-80), 39.7% female). 33 026 (29.3%) had pre-existing CVD. 73 392 (65.1%) patients had a diagnosis of colorectal, 23 208 (20.6%) oesophageal, 14 788 (13.1%) gastric and 1338 (1.2%) small bowel cancer. Individuals with pre-existing CVD had a 27% reduced rate of receiving fluoropyrimidine chemotherapy (HR, 0.73; 95% CI 0.70 to 0.75) on multivariable analysis. Significantly reduced rates of fluoropyrimidine administration were found across all subtypes of pre-existing CVD.
GI cancer patients with all types of pre-existing CVD are less likely to receive fluoropyrimidine chemotherapy despite eligibility. This suggests widespread caution regarding administration of fluoropyrimidines across this population; further research is needed to assess whether such conservatism is justified.
氟嘧啶化疗是许多胃肠道(GI)癌症的一线治疗方法,然而,心脏毒性问题可能会限制其在已有心血管疾病(CVD)患者中的应用。本研究调查了已有CVD与符合条件的GI癌症患者使用氟嘧啶化疗之间的关联。
使用2014年至2018年英格兰虚拟心脏肿瘤研究倡议的国家癌症登记数据,以确定符合接受氟嘧啶化疗条件的GI癌症患者。通过与医院事件统计数据和CVD登记数据的关联,来确定既往CVD情况和治疗结果。主要结局是癌症诊断后首次给予氟嘧啶化疗。Cox比例风险模型确定了氟嘧啶治疗开始与既往CVD之间关联的HR和95%CI。
共确定了112726名符合条件的患者(中位年龄71岁(IQR 62 - 80),39.7%为女性)。33026名(29.3%)患者已有CVD。73392名(65.1%)患者被诊断为结直肠癌,23208名(20.6%)为食管癌,14788名(13.1%)为胃癌,1338名(1.2%)为小肠癌。多变量分析显示,已有CVD的个体接受氟嘧啶化疗的比例降低了27%(HR,0.73;95%CI 0.70至0.75)。在所有已有CVD的亚型中,氟嘧啶给药率均显著降低。
所有类型已有CVD的GI癌症患者尽管符合条件,但接受氟嘧啶化疗的可能性较小。这表明在这一人群中普遍对氟嘧啶的给药持谨慎态度;需要进一步研究以评估这种保守做法是否合理。