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Annals of Oncology 2007 18(8):1335-1341; doi:10.1093/annonc/mdm181
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© 2007 European Society for Medical Oncology

breast cancer

Role of the HER2 [Ile655Val] genetic polymorphism in tumorogenesis and in the risk of trastuzumab-related cardiotoxicity

S Beauclair1, P Formento1, JL Fischel1, W Lescaut2, R Largillier2, E Chamorey3, P Hofman4, JM Ferrero2, G Pagès5,{dagger} and G Milano1,6,{dagger},*

1 Oncopharmacology unit (EA 3836), Centre Antoine Lacassagne, Nice
2 Medical Oncology Department, Centre Antoine Lacassagne, Nice
3 Biostatistics Unit, Centre Antoine Lacassagne, Nice
4 Equipe INSERM ESPRI 2006 and Laboratory of Clinical and Experimental Pathology, Faculté de Médecine, University of Nice–Sophia Antipolis
5 Institute of Signalling, Developmental Biology and Cancer Research UMR CNRS 6543
6 University of Nice-Sophia Antipolis Equipe labellisée Ligue Nationale contre le Cancer

* Correspondence to: Dr G. Milano, Oncopharmacology unit (EA 3836), Centre Antoine Lacassagne, 33 avenue de Valombrose 06189 Nice, France. E-mail: Gerard.milano{at}nice.fnclcc.fr

Background: To examine the impact of a frequent her2 gene polymorphism (Ile655Val) on tumor growth and on the pharmacodynamics of treatment by trastuzumab.

Patients and methods: Experimental study: The growth characteristics of cells expressing the Ile or Val isoform were examined in vitro and after injection into nude mice. The effect of trastuzumab was determined in both experimental models. Clinical study: 61 patients with advanced breast cancers and treated by trastuzumab were genotyped for HER2 by PCR–RFLP. The influence of HER2 genotype on the trastuzumab treatment was examined.

Results: Experimental study: HER2-expressing cells acquired the characteristics of tumor cells. The Val isoform-expressing cells showed the highest growth capacity and developed aggressive tumors sensitive to trastuzumab. Clinical study: There was no link between tumor response or survival and HER2 genotype. All cases of treatment-related cardiotoxicity were found in the Ile/Val group and there was no cardiac toxicity in the Val/Val and Ile/Ile patients.

Conclusions: This study establishes a clear-cut difference between the two HER2 isoforms regarding their tumorogenic potential with an advantage for the Val/HER2 isoform. In breast cancer patients treated with trastuzumab, the presence of a Val allele may constitute a risk factor for cardiac toxicity.

Key words: cardiotoxicity, gene polymorphism, HER 2, trastuzumab


{dagger} These authors co-directed the present work.

Received for publication January 31, 2007. Revision received March 28, 2007. Accepted for publication April 5, 2007.


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