Incidence and management of diarrhea with adjuvant pertuzumab and trastuzumab in patients with human epidermal growth factor receptor 2-positive breast cancer Journal Article


Authors: Bines, J.; Procter, M.; Restuccia, E.; Viale, G.; Zardavas, D.; Suter, T.; Arahmani, A.; Van Dooren, V.; Baselga, J.; Clark, E.; Eng-Wong, J.; Gelber, R. D.; Piccart, M.; Mobus, V.; de Azambuja, E.; on behalf of the APHINITY Steering Committee and Investigators
Article Title: Incidence and management of diarrhea with adjuvant pertuzumab and trastuzumab in patients with human epidermal growth factor receptor 2-positive breast cancer
Abstract: In the APHINITY study, a randomized adjuvant trial that included 4805 patients, diarrhea was a common adverse event. The incidence was higher with the combination of a taxane and human epidermal growth factor receptor 2-targeted treatment and decreased after chemotherapy was stopped. Most episodes were low grade and manageable with common antidiarrheal agents. © 2019 Elsevier Inc. Background: The APHINITY (BIG 4-11) study showed that pertuzumab significantly improved the rates of invasive disease-free survival among patients with human epidermal growth factor receptor 2 (HER2)-positive, operable breast cancer when added to adjuvant trastuzumab and chemotherapy. Because diarrhea was a common adverse event that could compromise treatment administration, we evaluated the incidence and management of diarrhea in the APHINITY study. Patients and Methods: The APHINITY trial is a prospective, randomized, multicenter, multinational, double-blind, placebo-controlled trial. The eligible patients were randomly assigned to receive standard adjuvant chemotherapy and 1 year of trastuzumab combined with pertuzumab or placebo. The diarrhea incidence, severity (National Cancer Institute common terminology criteria for adverse events, version 4.0), onset, and management were analyzed. Results: A total of 4805 patients were randomized. Diarrhea of any grade was the most common adverse event and occurred in 71% of patients in the pertuzumab arm versus 45% in the placebo arm. Diarrhea grade 3 to 4 was observed in 10% and 4% in the pertuzumab and placebo arms, respectively. The greatest incidence of diarrhea was reported during the concomitant administration of HER2-targeted therapy and taxane (61% vs. 34% of patients experienced an event with pertuzumab vs. placebo, respectively). A marked decrease was observed on chemotherapy cessation. Antidiarrheal agents were commonly used, and diarrhea rarely caused treatment dose modifications or discontinuation. Conclusion: Diarrhea was a common adverse event in the APHINITY study. Most episodes were low grade and were generally manageable with common antidiarrheal agents. The incidence of diarrhea was greater with the combination of a taxane and HER2-targeted treatment and decreased once chemotherapy was stopped. © 2019 Elsevier Inc.
Keywords: adult; controlled study; aged; major clinical study; placebo; cancer combination chemotherapy; diarrhea; drug safety; drug withdrawal; cancer patient; breast cancer; incidence; cohort analysis; docetaxel; cancer hormone therapy; disease severity; adjuvant chemotherapy; taxane derivative; trastuzumab; anthracycline; treatment withdrawal; clinical observation; her2; pertuzumab; antidiarrheal agent; adjuvant; randomized controlled trial (topic); molecularly targeted therapy; phase 3 clinical trial (topic); multicenter study (topic); human epidermal growth factor receptor 2 positive breast cancer; human; article; national cancer institute common terminology criteria for adverse events version 4.0; side effect assessment
Journal Title: Clinical Breast Cancer
Volume: 20
Issue: 2
ISSN: 1526-8209
Publisher: Elsevier Inc.  
Date Published: 2020-04-01
Start Page: 174
End Page: 181.e3
Language: English
DOI: 10.1016/j.clbc.2019.06.016
PUBMED: 31924513
PROVIDER: scopus
DOI/URL:
Notes: Article -- Source: Scopus
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  1. Jose T Baselga
    484 Baselga