Alcohol and HER2 polymorphisms as risk factor for cardiotoxicity in breast cancer treated with trastuzumab

Anticancer Res. 2013 Jun;33(6):2569-76.

Abstract

Background: Trastuzumab has no major side-effects except the potential for cardiac toxicity. The main objective of this study was to evaluate the association between trastuzumab-associated cardiac toxicity and two potential risk factors: alcohol intake and HER2 polymorphisms.

Patients and methods: In a retrospective cohort study of 237 women with non-metastatic HER2-positive breast cancer treated with trastuzumab, traditional risk factors were assessed by review of medical records, alcohol use by an administered questionnaire to women (n=132), and HER2 polymorphisms (Ile655Val and Ala1170Pro) using TaqMan assays (n=73).

Results: Association was observed between alcohol intake (10 drinks and more per week) during the trastuzumab treatment and cardiac toxicity (p=0.04). For polymorphisms, compared to Ile/Ile carriers, HER2 Ile/Val was associated with a higher risk of cardiac toxicity (p=0.02).

Conclusion: Heavy alcohol use during the course of trastuzumab treatment and the HER2 Ile/Val genotype may constitute risk factors for cardiac toxicity.

Keywords: Alcohol; HER2 polymorphism; cardiac risk factors; trastuzumab.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Alcohol Drinking*
  • Antibodies, Monoclonal, Humanized / adverse effects*
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Antineoplastic Agents / adverse effects*
  • Antineoplastic Agents / therapeutic use
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics
  • Cardiotoxins*
  • Cohort Studies
  • Female
  • Genes, erbB-2*
  • Genotype
  • Heart / drug effects
  • Heart Diseases / chemically induced*
  • Heart Failure / chemically induced
  • Humans
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism
  • Retrospective Studies
  • Risk Factors
  • Surveys and Questionnaires
  • Trastuzumab
  • Ventricular Function, Left / drug effects

Substances

  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Cardiotoxins
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • Trastuzumab