Nodular Regenerative Hyperplasia Induced by Trastuzumab Emtansine: Role of Emtansine?
Autor: | Dorothée Boucherle, Yves Ranchoup, Marion Allouchery, Jérôme Long, Céline Villier, Nathalie Sturm, François Le Marc’Hadour, Marion Lepelley |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Receptor ErbB-2 medicine.medical_treatment Specialties of internal medicine Ado-Trastuzumab Emtansine Targeted therapy chemistry.chemical_compound 0302 clinical medicine Trastuzumab Molecular Targeted Therapy skin and connective tissue diseases Biopsy Needle Carcinoma Ductal Breast Liver Neoplasms General Medicine Middle Aged Immunohistochemistry Magnetic Resonance Imaging RC581-951 030220 oncology & carcinogenesis Female Nodular regenerative hyperplasia medicine.drug Antibody-drug conjugate medicine.drug_class Breast Neoplasms Monoclonal antibody Risk Assessment 03 medical and health sciences Breast cancer Drug-induced disease medicine Humans Maytansine Trastuzumab emtansine Hyperplasia Hepatology business.industry medicine.disease 030104 developmental biology chemistry Withholding Treatment Cancer cell Cancer research business Follow-Up Studies |
Zdroj: | Annals of Hepatology, Vol 17, Iss 6, Pp 1067-1071 (2018) |
ISSN: | 1665-2681 |
Popis: | Trastuzumab is a monoclonal antibody targeted against the Human Epidermal Growth Factor Receptor 2 (HER2) overexpressed in some breast cancer. This targeted therapy significantly improves the prognosis of these cancers. Recently an anti-HER2 antibodydrug conjugate was shaped in order to facilitate the targeted delivery of potent cytotoxic drug to cancer cells and to reduce resistance. This formulation, called trastuzumab emtansine (T-DM1), consists of the monoclonal antibody trastuzumab linked to a cytotoxic drug (a derivative of maytansine) via a chemical linker. Little is known about adverse reactions due to this new formulation. Herein we described the case of a woman suffering from a HER2-positive breast cancer, treated with trastuzumab for 30 months followed by T-DM1 monotherapy. After 12 months of T-DM1 treatment, a nodular regenerative hyperplasia confirmed by liver biopsy occurred. T-DM1 was stopped and medical imagery showed a resolution of the nodular regenerative hyperplasia. Unfortunately, hepatic metastasis progressed. Few cases of nodular regenerative hyperplasia induced by T-DM1 have been described so far. Further studies are needed to explore pathogenesis of nodular regenerative hyperplasia with this new antibody-drug conjugate treatment. |
Databáze: | OpenAIRE |
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