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Pertuzumab

In the First-Line Treatment of HER2-Positive Metastatic Breast Cancer

Abstract

The humanized monoclonal antibody pertuzumab is the first in a new class of drugs, the human epidermal growth factor receptor (HER) dimerization inhibitors. Given that pertuzumab binds to a different epitope of the HER2 extracellular domain than trastuzumab, combination therapy with pertuzumab plus trastuzumab may result in more comprehensive blockade of HER2 signalling than can be achieved with trastuzumab alone.

The efficacy of adding pertuzumab to trastuzumab plus docetaxel for the first-line treatment of HER2-positive metastatic breast cancer was demonstrated in the randomized, double-blind, multinational, phase III CLEOPATRA trial. Both independently assessed progression-free survival (primary endpoint) and investigator-assessed progression-free survival were significantly improved in patients receiving pertuzumab plus trastuzumab and docetaxel compared with those receiving placebo plus trastuzumab and docetaxel.

The prespecified interim analysis of survival revealed a strong trend towards a survival benefit associated with pertuzumab, although this was not considered statistically significant. The objective response rate was higher with pertuzumab than with placebo.

Intravenous pertuzumab had an acceptable tolerability profile when added to trastuzumab and docetaxel in the CLEOPATRA trial.

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Acknowledgements and Disclosures

The manuscript was reviewed by: A.M. Brufsky, University of Pittsburgh, Pittsburgh, PA, USA; D.W. Miles, Mount Vernon Cancer Centre, Mount Vernon Hospital, Northwood, Middlesex, UK.

The preparation of this review was not supported by any external funding. During the peer review process, the manufacturer of the agent under review was also offered an opportunity to comment on this article. Changes resulting from comments received were made by the author on the basis of scientific and editorial merit.

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Correspondence to Gillian M. Keating.

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Keating, G.M. Pertuzumab. Drugs 72, 353–360 (2012). https://doi.org/10.2165/11209000-000000000-00000

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Keywords

  • Docetaxel
  • Trastuzumab
  • Human Epidermal Growth Factor Receptor
  • Advanced Solid Tumour
  • Pertuzumab