Cobleigh M A, Vogel C L, Tripathy D, Robert N J, Scholl S, Fehrenbacher L, Wolter J M, Paton V, Shak S, Lieberman G, Slamon D J
Rush-Presbyterian-St Luke's Medical Center, Chicago, IL 60612, USA.
J Clin Oncol. 1999 Sep;17(9):2639-48. doi: 10.1200/JCO.1999.17.9.2639.
Overexpression of the HER2 protein occurs in 25% to 30% of human breast cancers and leads to a particularly aggressive form of the disease. Efficacy and safety of recombinant humanized anti-HER2 monoclonal antibody as a single agent was evaluated in women with HER2-overexpressing metastatic breast cancer that had progressed after chemotherapy for metastatic disease.
Two hundred twenty-two women, with HER2-overexpressing metastatic breast cancer that had progressed after one or two chemotherapy regimens, were enrolled. Patients received a loading dose of 4 mg/kg intravenously, followed by a 2-mg/kg maintenance dose at weekly intervals.
Study patients had advanced metastatic disease and had received extensive prior therapy. A blinded, independent response evaluation committee identified eight complete and 26 partial responses, for an objective response rate of 15% in the intent-to-treat population (95% confidence interval, 11% to 21%). The median duration of response was 9.1 months; the median duration of survival was 13 months. The most common adverse events, which occurred in approximately 40% of patients, were infusion-associated fever and/or chills that usually occurred only during the first infusion, and were of mild to moderate severity. These symptoms were treated successfully with acetaminophen and/or diphenhydramine. The most clinically significant adverse event was cardiac dysfunction, which occurred in 4.7% of patients. Only 1% of patients discontinued the study because of treatment-related adverse events.
Recombinant humanized anti-HER2 monoclonal antibody, administered as a single agent, produces durable objective responses and is well tolerated by women with HER2-overexpressing metastatic breast cancer that has progressed after chemotherapy for metastatic disease. Side effects that are commonly observed with chemotherapy, such as alopecia, mucositis, and neutropenia, are rarely seen.
HER2蛋白过表达出现在25%至30%的人类乳腺癌中,并导致该疾病呈现一种特别侵袭性的形式。在HER2过表达的转移性乳腺癌且转移性疾病化疗后病情进展的女性患者中,评估重组人源化抗HER2单克隆抗体作为单一药物的疗效和安全性。
招募了222名HER2过表达的转移性乳腺癌女性患者,这些患者在接受一或两种化疗方案后病情进展。患者静脉注射4mg/kg的负荷剂量,随后每周间隔注射2mg/kg的维持剂量。
研究患者患有晚期转移性疾病且接受过广泛的前期治疗。一个盲法、独立的疗效评估委员会确定了8例完全缓解和26例部分缓解,意向性治疗人群的客观缓解率为15%(95%置信区间,11%至21%)。缓解的中位持续时间为9.1个月;中位生存期为13个月。最常见的不良事件发生在约40%的患者中,是与输注相关的发热和/或寒战,通常仅在首次输注时出现,且严重程度为轻至中度。这些症状用对乙酰氨基酚和/或苯海拉明治疗成功。最具临床意义的不良事件是心脏功能障碍,发生在4.7%的患者中。只有1%的患者因治疗相关不良事件而停止研究。
重组人源化抗HER2单克隆抗体作为单一药物给药,可产生持久的客观缓解,且HER2过表达的转移性乳腺癌且转移性疾病化疗后病情进展的女性患者对其耐受性良好。化疗常见的副作用,如脱发、粘膜炎和中性粒细胞减少,很少见。