Infante Jeffrey R, Yardley Denise A, Burris Howard A, Greco F Anthony, Farley Cindy P, Webb Charles, Spigel David R, Hainsworth John D
Tennessee Oncology, PLLC, Nashville, TN, USA.
Clin Breast Cancer. 2009 Feb;9(1):23-8. doi: 10.3816/CBC.2009.n.004.
The combinations of trastuzumab/docetaxel and trastuzumab/vinorelbine are highly active in the treatment of patients with HER2-positive metastatic breast cancer (MBC). We investigated the feasibility and safety of a 3-drug combination of trastuzumab, docetaxel, and vinorelbine as first-line therapy in this patient group.
Sixty patients with previously untreated, measurable HER2-positive MBC (immunohistochemistry 3+ and/or fluorescence in situ hybridization positive) were treated with docetaxel 30 mg/m2 intravenously (I.V.) and vinorelbine 25 mg/m2 I.V. on days 1 and 8 of each 3-week cycle. Trastuzumab was given weekly (4-mg/kg loading dose followed by 2 mg/kg/week). Patients were evaluated after 6 weeks; responders/stable patients continued treatment until progression.
Patients received a median of 11 treatment cycles (range, 1-22 cycles). Forty-one of 60 patients (68%) had major responses (16 complete responses [27%], 25 partial responses [42%]). An additional 13 patients (22%) had stable disease for > or = 6 months. After a median follow-up of 58 months, median progression-free survival was 12 months (95% CI, 9.1-16.3 months), and the median overall survival was 40.8 months (95% CI, 25-not reached). Neutropenia (72% grade 4) was the most common hematologic toxicity; 8 patients were hospitalized for febrile neutropenia. A total of 67% of patients required dose modifications for neutropenia during cycles 1 or 2. Other grade 3/4 toxicities included fatigue (12%), hyperglycemia (7%), and myalgias (7%). There were no treatment-related deaths.
The combination of trastuzumab, docetaxel, and vinorelbine is highly active as first-line treatment for patients with HER2-positive MBC. However, this regimen offers no obvious advantages over other less myelosuppressive trastuzumab-containing regimens, and its routine use is not supported by the study.
曲妥珠单抗/多西他赛和曲妥珠单抗/长春瑞滨联合方案在HER2阳性转移性乳腺癌(MBC)患者的治疗中具有高度活性。我们研究了曲妥珠单抗、多西他赛和长春瑞滨三药联合作为该患者群体一线治疗的可行性和安全性。
60例既往未接受过治疗、可测量的HER2阳性MBC患者(免疫组化3+和/或荧光原位杂交阳性),在每3周周期的第1天和第8天接受静脉注射多西他赛30mg/m²和静脉注射长春瑞滨25mg/m²治疗。曲妥珠单抗每周给药(4mg/kg负荷剂量,随后2mg/kg/周)。6周后对患者进行评估;缓解者/病情稳定患者继续治疗直至病情进展。
患者接受治疗的中位周期数为11个周期(范围1 - 22个周期)。60例患者中有41例(68%)有主要缓解(16例完全缓解[27%],25例部分缓解[42%])。另外13例患者(22%)病情稳定≥6个月。中位随访58个月后,中位无进展生存期为12个月(95%CI,9.1 - 16.3个月),中位总生存期为40.8个月(95%CI,25 - 未达到)。中性粒细胞减少(72%为4级)是最常见的血液学毒性;8例患者因发热性中性粒细胞减少住院。共有67%的患者在第1或第2周期因中性粒细胞减少需要调整剂量。其他3/4级毒性包括疲劳(12%)、高血糖(7%)和肌痛(7%)。无治疗相关死亡。
曲妥珠单抗、多西他赛和长春瑞滨联合作为HER2阳性MBC患者的一线治疗具有高度活性。然而,该方案与其他骨髓抑制性较小的含曲妥珠单抗方案相比并无明显优势,本研究不支持其常规使用。