The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD 21231-1000, USA.
Breast Cancer Res Treat. 2010 May;121(1):111-20. doi: 10.1007/s10549-010-0838-7. Epub 2010 Mar 24.
The purpose of this trial was to determine cardiac toxicity and overall efficacy of the pegylated liposome doxorubicin (PLD)-docetaxel couplet alone if HER2-negative metastatic breast cancer (internal control) or with trastuzumab if HER2-positive disease. Upon central HER2 confirmation, 84 eligible patients received induction with PLD (30 mg/m(2)) and docetaxel (60 mg/m(2)) every 3 weeks (maximum eight cycles), alone if HER2-negative (arm A; N = 38) or plus trastuzumab (4 mg/kg once, then 2 mg/kg weekly) if HER2-positive disease (arm B; N = 46) as first-line therapy. Maintenance therapy (without PLD) allowed. Primary objectives were to determine whether congestive heart failure (CHF) rate >3% and the efficacy/toxicity of each arm. CHF rate was <3% in each arm. Response rate, median progression-free-, and overall survival in arms A and B were 47.4 and 45.7%, 11 and 10.6 months, and 24.6 and 31.8 months, respectively. Trastuzumab arm was associated with higher rates of hand foot syndrome (grade 3: 22 vs. 38%; P = 0.16; overall 51 vs. 75%, P = 0.03) and treatment discontinuation due to toxicity/patient withdrawal (13 vs. 28%; P = 0.11). Febrile neutropenia occurred in approximately 10% of patients. In conclusion, concurrent administration of trastuzumab with PLD-docetaxel was not associated with higher risk of cardiac toxicity compared with PLD-docetaxel alone, but led to excessive hand-foot syndrome.
本试验旨在确定多柔比星脂质体(PLD)-多西紫杉醇联合方案(单独用于 HER2 阴性转移性乳腺癌[内部对照]或联合曲妥珠单抗用于 HER2 阳性疾病)的心脏毒性和总体疗效。在中心 HER2 确认后,84 名符合条件的患者接受了 PLD(30mg/m²)和多西紫杉醇(60mg/m²)的诱导治疗,每 3 周一次(最多 8 个周期),如果 HER2 阴性(A 组;N=38)则单独使用,如果 HER2 阳性疾病(B 组;N=46)则联合曲妥珠单抗(4mg/kg 一次,然后每周 2mg/kg)作为一线治疗。允许维持治疗(不使用 PLD)。主要目标是确定每个组的心力衰竭(CHF)发生率>3%和疗效/毒性情况。每个组的 CHF 发生率<3%。A 组和 B 组的反应率、中位无进展生存期和总生存期分别为 47.4%和 45.7%、11 个月和 10.6 个月、24.6 个月和 31.8 个月。曲妥珠单抗组的手足综合征(3 级:22%比 38%;P=0.16;总体:51%比 75%;P=0.03)和因毒性/患者退出而停止治疗的发生率(13%比 28%;P=0.11)较高。大约 10%的患者发生发热性中性粒细胞减少症。结论:与单独使用 PLD-多西紫杉醇相比,曲妥珠单抗与 PLD-多西紫杉醇联合使用并未增加心脏毒性的风险,但导致手足综合征过度发生。