Literature DB >> 25802300

Combination pertuzumab, trastuzumab, and taxane for metastatic breast cancer after first progression: a single institution's experience.

Bao D Dao1, Hansen Ho2, Laura N Quintal2.   

Abstract

BACKGROUND: 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.
OBJECTIVE: Describe the progression-free survival of pertuzumab, trastuzumab, and taxane therapy for previously treated HER2-positive metastatic breast cancer.
METHODS: 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.
RESULTS: 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.
CONCLUSIONS: 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.
© The Author(s) 2015.

Entities:  

Keywords:  Metastatic breast cancer; pertuzumab; trastuzumab

Mesh:

Substances:

Year:  2015        PMID: 25802300     DOI: 10.1177/1078155215578494

Source DB:  PubMed          Journal:  J Oncol Pharm Pract        ISSN: 1078-1552            Impact factor:   1.809


  1 in total

1.  Efficacy and safety of HER2 inhibitors in combination with or without pertuzumab for HER2-positive breast cancer: a systematic review and meta-analysis.

Authors:  Shanshan Chen; Yu Liang; Zhangying Feng; Mingxia Wang
Journal:  BMC Cancer       Date:  2019-10-21       Impact factor: 4.430

  1 in total

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