Biganzoli Laura, Cufer Tanja, Bruning Peter, Coleman Robert E, Duchateau Luc, Rapoport Bernardo, Nooij Marianne, Delhaye François, Miles D, Sulkes Aaron, Hamilton A, Piccart Martine
IDBBC Unit, EORTC-IDBBC, Jules Bordet Institute, Boulevard de Waterloo 121, 7th floor, 1000 Brussels, Belgium.
Cancer. 2003 Jan 1;97(1):40-5. doi: 10.1002/cncr.10914.
The potential cardiotoxicity of the doxorubicin-paclitaxel regimen, when paclitaxel is given shortly after the end of the anthracycline infusion, is an issue of concern, as suggested by small single institution Phase II studies.
In a large multicenter Phase III trial, 275 anthracycline naive metastatic breast carcinoma patients were randomized to receive either doxorubicin (60 mg/m(2)) followed 30 minutes later by paclitaxel (175 mg/m(2) 3-hour infusion; AT) or a standard doxorubicin-cyclophosphamide regimen (AC; 60/600 mg/m(2)). Both treatments were given once every 3 weeks for a maximum of six cycles. Close cardiac monitoring was implemented in the study design.
Congestive heart failure (CHF) occurred in three patients in the AT arm and in one patient in the AC arm (P = 0.62). Decreases in left ventricular ejection fraction to below the limit of normal were documented in 33% AT and 19% AC patients and were not predictive of CHF development.
AT is devoid of excessive cardiac risk among metastatic breast carcinoma patients, when the maximum planned cumulative dose of doxorubicin does not exceed 360 mg/m(2).
如小型单机构II期研究所表明的,当在蒽环类药物输注结束后不久给予紫杉醇时,多柔比星 - 紫杉醇方案的潜在心脏毒性是一个令人担忧的问题。
在一项大型多中心III期试验中,275例未接受过蒽环类药物治疗的转移性乳腺癌患者被随机分为两组,一组先接受多柔比星(60mg/m²),30分钟后再接受紫杉醇(175mg/m²,3小时输注;AT方案),另一组接受标准的多柔比星 - 环磷酰胺方案(AC方案;60/600mg/m²)。两种治疗均每3周进行一次,最多进行6个周期。在研究设计中实施了密切的心脏监测。
AT方案组有3例患者发生充血性心力衰竭(CHF),AC方案组有1例患者发生CHF(P = 0.62)。记录到AT方案组33%的患者和AC方案组19%的患者左心室射血分数降至正常下限以下,且这并非CHF发生的预测指标。
当多柔比星的最大计划累积剂量不超过360mg/m²时,AT方案在转移性乳腺癌患者中不存在过度的心脏风险。