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Annals of Oncology 11:355-358, 2000
© 2000 European Society for Medical Oncology


other

Endometrial mesodermal mixed tumor occurring after tamoxifen treatment: Report on a new case and review of the literature

J. Dumortier1, G. Freyer1, A. J. Sasco2, L. Frappart3, T. Zénone4, P. Romestaing1 and V. Trillet-Lenoir1,

1Department of Radiotherapy and Oncology, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon Lyon
2Unit of Epidemiology for Cancer Prevention, International Agency for Research on Cancer, and Institut National de la Santé el de la Recherche Médicale Lyon
3Department of Pathology, Hopital Edouard Herriot Lyon, France
4Department of Internal Medicine, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon Lyon, France

Correspondence to: V. Trillet-Lenoir, MD, Medical Oncology Unit, Department of Radiotherapy and Oncology, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, France

Background: Anti oestrogenic treatment is widely used for breast cancer treatment and prevention of recurrence. Because of concomitant estrogenic effects, tamoxifen exerts carcinogenic properties on the endometrium. Although secondary endometrial cancers usually present as pure adenocarcinomas, other types of rare tumors have also been reported.

Patients and methods: Herein we describe the clinical, pathological as well as therapeutic aspects of a new case of endometrial mesodermal mixed tumor occurring after long-term tamoxifen therapy. Results: The present case occured five years after cessation of a five years tamoxifen treatment. The patient failed to respond to doxorubicin and cyclophosphamide when combined to 5-fluorouracil (5-FU), but she reached complete response when the same two drugs were used with carboplatin, suggesting the potential usefullness of platinum derivatives.

Conclusions: A longer latency period might be observed for endometrial mesodermal mixed tumors as compared to adenocarcinomas and could justify a prolonged clinical and ultra-sonographic follow-up of patients during and after tamoxifen treatment. When indicated, chemotherapy might require the use of platinum derivatives in this particular type of secondary tumor.

carcinogenesis, endometrium, tamoxifen


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JNCI J Natl Cancer InstHome page
R. E. Curtis, D. M. Freedman, M. E. Sherman, and J. F. Fraumeni Jr.
Risk of Malignant Mixed Mullerian Tumors After Tamoxifen Therapy for Breast Cancer
J Natl Cancer Inst, January 7, 2004; 96(1): 70 - 74.
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