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Revisiting bleomycin from pathophysiology to safe clinical use

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Auteur
Froudarakis, M.; Hatzimichael, E.; Kyriazopoulou, L.; Lagos, K.; Pappas, P.; Tzakos, A. G.; Karavasilis, V.; Daliani, D.; Papandreou, C.; Briasoulis, E.
Date
2013
DOI
10.1016/j.critrevonc.2012.12.003
Sujet
Bleomycin
Hodgkin's Lymphoma
Testicular germ-cell tumour
Lung injury
Therapeutics
Safe clinical use
Toxicity
GERM-CELL TUMORS
INDUCED PULMONARY TOXICITY
CANCER COOPERATIVE GROUP
INDUCED LUNG DAMAGE
INDUCED PNEUMONITIS
HODGKINS-LYMPHOMA
COMBINATION
CHEMOTHERAPY
RANDOMIZED-TRIAL
CISPLATIN CHEMOTHERAPY
EUROPEAN
ORGANIZATION
Oncology
Hematology
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Résumé
Bleomycin is a key component of curative chemotherapy regimens employed in the treatment of curable cancers, such as Hodgkin lymphoma (HL) and testicular germ-cell tumours (GCT), yet its use may cause bleomycin-induced lung injury (BILI), which is associated with significant morbidity and a mortality rate of 1-3%. Diagnosis of BILI is one of exclusion and physicians involved in the care of HL and GCT patients should be alerted. Pharmacogenomic studies could contribute towards the identification of molecular predictors of bleomycin toxicity on the aim to optimize individual use of bleomycin. We review all existing data on bleomycin's most recent integrated chemical biology, molecular pharmacology and mature clinical data and provide guidelines for its safe clinical use. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
URI
http://hdl.handle.net/11615/27578
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