4.5 Article

Subcutaneous trastuzumab with pertuzumab and docetaxel in HER2-positive metastatic breast cancer: Final analysis of MetaPHER, a phase IIIb single-arm safety study

Journal

BREAST CANCER RESEARCH AND TREATMENT
Volume 187, Issue 2, Pages 467-476

Publisher

SPRINGER
DOI: 10.1007/s10549-021-06145-3

Keywords

HER2-positive breast cancer; Metastatic breast cancer; Pertuzumab; Route of administration; Safety; Subcutaneous trastuzumab

Categories

Funding

  1. F. Hoffmann-La Roche Ltd.

Ask authors/readers for more resources

The study assessed the safety and tolerability of subcutaneous trastuzumab with intravenous pertuzumab and chemotherapy in HER2-positive mBC patients globally. Results showed that the safety and efficacy of this treatment were consistent with historical evidence of intravenous trastuzumab, without affecting its safety/efficacy profiles in HER2-positive BC and providing increased flexibility in patient care.
Purpose Intravenous trastuzumab, pertuzumab, and docetaxel are first-line standard of care for patients with HER2-positive metastatic breast cancer (mBC). MetaPHER is the first study assessing the safety and tolerability of subcutaneous trastuzumab plus intravenous pertuzumab and chemotherapy in a global patient population with HER2-positive mBC. Methods In this open-label, single-arm, multicenter, phase 3b study, eligible patients were >= 18 years old with histologically/cytologically confirmed previously untreated HER2-positive mBC. All received >= 1 subcutaneous trastuzumab 600 mg fixed dose plus intravenous pertuzumab (loading dose: 840 mg/kg; maintenance: 420 mg/kg) and docetaxel (>= 6 cycles; initial dose 75 mg/m(2)) every 3 weeks. The primary objective was safety and tolerability; secondary objectives included efficacy. Results At clinical cutoff, 276 patients had completed the study; median duration of follow-up was 27 months. The most common any-grade adverse events were diarrhea, alopecia, and asthenia; the most common grade >= 3 events were neutropenia, febrile neutropenia, and hypertension. There were no cardiac deaths and mean left ventricular ejection fraction was stable over time. Median investigator-assessed progression-free survival was 18.7 months; objective response rate was 75.6%. Conclusions Safety and efficacy with subcutaneous trastuzumab plus intravenous pertuzumab and docetaxel in mBC are consistent with historical evidence of intravenous trastuzumab with this combination. Findings further support subcutaneous administration not affecting safety/efficacy profiles of trastuzumab in HER2-positive BC with increased flexibility in patient care. A fixed-dose combination of pertuzumab and trastuzumab for subcutaneous injection has recently been approved for the treatment of HER2-positive early/mBC, further addressing the increasing relevance of and need for patient-centric treatment strategies.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available