Dao Bao D, Ho Hansen, Quintal Laura N
Department of Pharmacy, University of California San Francisco Medical Center, San Francisco, CA, USA
Department of Pharmacy, University of California San Francisco Medical Center, San Francisco, CA, USA.
J Oncol Pharm Pract. 2016 Apr;22(2):261-4. doi: 10.1177/1078155215578494. Epub 2015 Mar 22.
The addition of pertuzumab to trastuzumab and taxane therapy was shown to be an effective first-line treatment for patients with HER2-positive metastatic breast cancer.
Describe the progression-free survival of pertuzumab, trastuzumab, and taxane therapy for previously treated HER2-positive metastatic breast cancer.
This case-series reviews 19 patients with metastatic breast cancer receiving treatment with pertuzumab, trastuzumab, taxane after progression and exposure to previous lines of HER2-directed therapy. Progression-free survival and adverse effects such as changes in ejection fraction and episodes of neutropenic fever were assessed.
The median progression-free survival of pertuzumab, trastuzumab, taxane therapy for previously treated metastatic breast cancer was 4.1 months. The mean baseline left ventricular ejection fraction change experienced by patients was -1%. Neutropenic fever events were not encountered.
Pertuzumab, trastuzumab, and taxane therapy seems to confer progression-free survival benefit for previously treated metastatic breast cancer. The use of the dual anti-HER2 antibodies, pertuzumab and trastuzumab, in addition to cytotoxic chemotherapy agents for previously treated metastatic breast cancer should be further evaluated.
在曲妥珠单抗和紫杉烷治疗中加入帕妥珠单抗被证明是HER2阳性转移性乳腺癌患者的一种有效的一线治疗方法。
描述帕妥珠单抗、曲妥珠单抗和紫杉烷治疗既往接受过治疗的HER2阳性转移性乳腺癌的无进展生存期。
本病例系列回顾了19例转移性乳腺癌患者,这些患者在病情进展并接受过先前几线HER2靶向治疗后,接受了帕妥珠单抗、曲妥珠单抗和紫杉烷治疗。评估了无进展生存期和不良反应,如射血分数变化和中性粒细胞减少性发热发作。
帕妥珠单抗、曲妥珠单抗、紫杉烷治疗既往接受过治疗的转移性乳腺癌的中位无进展生存期为4.1个月。患者经历的平均基线左心室射血分数变化为-1%。未发生中性粒细胞减少性发热事件。
帕妥珠单抗、曲妥珠单抗和紫杉烷治疗似乎能为既往接受过治疗的转移性乳腺癌带来无进展生存期益处。对于既往接受过治疗的转移性乳腺癌,除细胞毒性化疗药物外,联合使用双重抗HER2抗体帕妥珠单抗和曲妥珠单抗应进一步评估。