Patients with TP53 dysfunction, assessed by del(17p) or TP53 mutations, respond poorly to chemo-immunotherapy and fare better with the new therapies (BCR and BCL-2 inhibitors); however, it is unclear whether their response is similar to that of patients without anomalies or whether there is currently an adequate determination of TP53 dysfunction.

TP53 dysfunction in chronic lymphocytic leukemia : clinical relevance in the era of B-cell receptors and BCL-2 inhibitors / F. Morabito, M. Gentile, P. Monti, A.G. Recchia, P. Menichini, M. Skafi, M. Atrash, G. De Luca, S. Bossio, H. Al-Janazreh, S. Galimberti, Z. Salah, L. Morabito, A. Mujahed, M. Hindiyeh, M. Dono, F. Fais, G. Cutrona, A. Neri, G. Tripepi, G. Fronza, M. Ferrarini. - In: EXPERT OPINION ON INVESTIGATIONAL DRUGS. - ISSN 1354-3784. - (2020 Jun 27). [Epub ahead of print] [10.1080/13543784.2020.1783239]

TP53 dysfunction in chronic lymphocytic leukemia : clinical relevance in the era of B-cell receptors and BCL-2 inhibitors

A. Neri;
2020

Abstract

Patients with TP53 dysfunction, assessed by del(17p) or TP53 mutations, respond poorly to chemo-immunotherapy and fare better with the new therapies (BCR and BCL-2 inhibitors); however, it is unclear whether their response is similar to that of patients without anomalies or whether there is currently an adequate determination of TP53 dysfunction.
TP53 mutations; BCL2 inhibitor; BCR inhibitors; chronic Lymphocytic Leukemia; clinical outcome; del(17p); ibrutinib; idelalisib; venetoclax
Settore MED/15 - Malattie del Sangue
27-giu-2020
27-giu-2020
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/746786
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