Morabito Alessandro, Longo Raffaele, Gattuso Domenico, Carillio Guido, Massaccesi Cristian, Mariani Luigi, Bonginelli Paola, Amici Scolastica, De Sio Livia, Fanelli Massimo, Torino Francesco, Bonsignori Maurizio, Gasparini Giampietro
Division of Medical Oncology, San Filippo Neri Hospital, Rome, Italy.
Oncol Rep. 2006 Aug;16(2):393-8.
The aim of this study was to evaluate the safety and efficacy of combined treatment with trastuzumab (T), gemcitabine (gem) and vinorelbine (vin) as second-line therapy for HER-2 overexpressing metastatic breast cancer, pretreated with anthracyclines and/or taxanes and/or trastuzumab. Eligible patients had HER-2/neu-positive disease (IHC 2+ or 3+), performance status (PS) <or=2 and normal L-VEF. Patients were treated with weekly T (4 mg/kg on day 0, then 2 mg/kg), in combination with gem (800 mg/m(2)) and vin (25 mg/m(2)) on days 1 and 8, every 21 days. Patients were restaged every 3 cycles. A total of 30 patients (median age, 58 years; range, 41-74) were enrolled in the study. Fifteen patients were HER-2 3+ and 26 (86.7%) presented >or=2 metastatic sites. Of the patients, 7 (23.3%) had received trastuzumab as first-line therapy. Treatment was well-tolerated with grade 4 neutropenia in 6 patients, grade 3 thrombocytopenia and grade 3 anemia in 1 patient, and grade 3 asthenia in 4 patients. Fifteen patients obtained an objective response (response rate, 50%; C.I. 95%, range, 31.3-68.7%). Among the patients with HER-2/neu 3+, the response rate was 73.3%. Noteworthy were 4 objective responses observed in patients with brain metastasis. Also, 7 patients had stable disease (23.3%). Median progression-free survival was 7 months (range 5-10), and median overall survival was 15 months (range 5-33). T-gem-vin is a safe and active regimen in this subgroup of patients with poor prognosis, and the efficacy of such a schedule was particularly satisfactory in patients with HercepTest 3+.
本研究的目的是评估曲妥珠单抗(T)、吉西他滨(gem)和长春瑞滨(vin)联合治疗作为蒽环类药物和/或紫杉烷类药物和/或曲妥珠单抗预处理后的HER-2过表达转移性乳腺癌二线治疗的安全性和有效性。符合条件的患者患有HER-2/neu阳性疾病(免疫组化2+或3+),体能状态(PS)≤2且左心室射血分数(L-VEF)正常。患者在第0天接受每周一次的T(4mg/kg,然后2mg/kg)治疗,并在第1天和第8天联合gem(800mg/m²)和vin(25mg/m²),每21天重复一次。每3个周期对患者进行重新分期。共有30例患者(中位年龄58岁;范围41-74岁)入组本研究。15例患者为HER-2 3+,26例(86.7%)出现≥2个转移部位。其中7例(23.3%)患者接受过曲妥珠单抗一线治疗。治疗耐受性良好,6例患者出现4级中性粒细胞减少,1例患者出现3级血小板减少和3级贫血,4例患者出现3级乏力。15例患者获得客观缓解(缓解率50%;95%置信区间,范围31.3-68.7%)。在HER-2/neu 3+的患者中,缓解率为73.3%。值得注意的是,在脑转移患者中观察到4例客观缓解。此外,7例患者疾病稳定(23.3%)。中位无进展生存期为7个月(范围5-10个月),中位总生存期为15个月(范围5-33个月)。T-gem-vin方案对于该预后较差的患者亚组是一种安全且有效的方案,并且该方案在HercepTest 3+的患者中疗效尤为令人满意。