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A Retrospective Analysis of 450 TP53Mutations in a Real Life Cohort of CLL from the French Innovative Leukemia Organization (FILO) Group

Authors :
Baran-Marszak, Fanny
Vidal, Valerie
Hormi, Myriam
Eclache, Virginie
Veronese, Lauren
Tournilhac, Olivier
Davi, Frederic
Nguyen-Khac, Florence
Leblond, Veronique
Delabesse, Eric
Ysebaert, Loic
Bidet, Audrey
Dilhuydy, Marie-Sarah
Poulain, Stephanie
Herbaux, Charles
Estienne, Marie-Helene
Dartigeas, Caroline
Pastoret, Cedric
de Guibert, Sophie
Giraudier, Stephane
Dupuis, Jehan
Cornillet-Lefebvre, Pascale
Quinquenel, Anne
Laibe, Sophy
Aurran, Thérèse
Naguib, Dina
Troussard, Xavier
Sujobert, Pierre
Michallet, Anne-Sophie
Thieblemont, Catherine
Letestu, Remi
Lazarian, Gregory
Levy, Vincent
Soussi, Thierry
Raynaud, Sophie
Cymbalista, Florence
Source :
Blood; December 2017, Vol. 130 Issue: 1, Number 1 Supplement 1 p1722-1722, 1p
Publication Year :
2017

Abstract

In Chronic Lymphocytic Leukemia (CLL), it is well established that 17p deletions are associated with adverse prognosis and chemotherapy resistance. 17p deletions are most often associated with TP53mutations, but TP53mutations can occur in the absence of 17p deletion in about half of the cases with a similar unfavorable prognostic influence. Some patients harbor several subclones with different TP53mutations. Nonetheless, little is known on the functional effect of the various alterations and of their associations.

Details

Language :
English
ISSN :
00064971 and 15280020
Volume :
130
Issue :
1, Number 1 Supplement 1
Database :
Supplemental Index
Journal :
Blood
Publication Type :
Periodical
Accession number :
ejs56812064
Full Text :
https://doi.org/10.1182/blood.V130.Suppl_1.1722.1722