Department of Medical Oncology, Mayo Clinic, Rochester, MN.
Department of Medical Oncology, Mayo Clinic, Rochester, MN.
Clin Colorectal Cancer. 2019 Mar;18(1):52-57. doi: 10.1016/j.clcc.2018.09.006. Epub 2018 Oct 10.
Coronary vasospasm associated with fluoropyrimidine (FP)-based chemotherapy is a potentially serious complication and reported to occur more often with infusional 5-fluorouracil (5-FU) or capecitabine than with bolus 5-FU. Given the additional benefit of oxaliplatin over FP alone in the management of colorectal cancer, retaining oxaliplatin in the treatment regimen is desirable, but the safety of combining bolus 5-FU with oxaliplatin in patients with FP-induced vasospasm is not well established. We performed a retrospective review to explore the safety of substituting FLOX (bolus 5-FU, oxaliplatin, leucovorin) for FOLFOX (infusional 5-FU, oxaliplatin, leucovorin) and CAPOX (capecitabine, oxaliplatin) in patients who had FP-induced coronary vasospasm.
The pharmacy database of Mayo Clinic was queried to identify patients who developed coronary vasospasm associated with FOLFOX or CAPOX between January 2011 and January 2018 and were subsequently treated with FLOX. Detailed information was obtained on these patients by retrospective electronic chart review.
A total of 10 patients (median age, 56.5 years; range, 36-77 years) were identified, 9 with FOLFOX and 1 with CAPOX. Among the patients treated with FOLFOX, 8 patients had chest pain as the presenting complaint that had started within 48 hours of beginning of the 5-FU infusion. In 9 of 10 patients, coronary vasospasm occurred with the first cycle of therapy. All patients made full recovery after discontinuation of infusional 5-FU or capecitabine. All patients subsequently received FLOX with 7 median bolus 5-FU doses (range, 2-22 doses) and 7 median oxaliplatin doses (range, 2-12 doses) at 7 days to 18 months after the event, with 7 patients treated within 4 weeks of the event. FLOX did not cause any cardiovascular adverse events in any of the 10 patients.
Bolus 5-FU in combination with oxaliplatin is safe in patients who have experienced coronary vasospasm with infusional 5-FU or capecitabine.
与氟嘧啶(FP)为基础的化疗相关的冠状动脉痉挛是一种潜在的严重并发症,据报道,与推注 5-氟尿嘧啶(5-FU)或卡培他滨相比,输注 5-FU 或卡培他滨更常发生。鉴于奥沙利铂在结直肠癌治疗中优于 FP,保留奥沙利铂在治疗方案中是可取的,但 FP 诱导的血管痉挛患者中推注 5-FU 与奥沙利铂联合使用的安全性尚未得到充分证实。我们进行了一项回顾性研究,以探讨在发生 FP 诱导的冠状动脉痉挛的患者中,用 FLOX(推注 5-FU、奥沙利铂、亚叶酸)替代 FOLFOX(输注 5-FU、奥沙利铂、亚叶酸)和 CAPOX(卡培他滨、奥沙利铂)的安全性。
通过检索梅奥诊所的药房数据库,确定了 2011 年 1 月至 2018 年 1 月期间因 FOLFOX 或 CAPOX 引起的冠状动脉痉挛并随后接受 FLOX 治疗的患者。通过回顾性电子病历回顾获得这些患者的详细信息。
共确定了 10 例患者(中位年龄 56.5 岁;范围 36-77 岁),其中 9 例为 FOLFOX,1 例为 CAPOX。在接受 FOLFOX 治疗的患者中,8 例以胸痛为首发症状,胸痛发生在 5-FU 输注开始后 48 小时内。在 10 例患者中,9 例患者在第一周期治疗中发生冠状动脉痉挛。所有患者在停止输注 5-FU 或卡培他滨后完全康复。所有患者随后在事件发生后 7 天至 18 个月内接受 FLOX,其中 7 例在事件发生后 4 周内接受治疗。在这 10 例患者中,FLOX 均未引起任何心血管不良事件。
在接受输注 5-FU 或卡培他滨治疗后发生冠状动脉痉挛的患者中,5-FU 推注联合奥沙利铂是安全的。