Impact of complex NOTCH1 mutations on survival in paediatric T-cell leukaemia


Autoria(s): Mansur, Marcela Braga; Hassan, Rocio; Barbosa, Thayana C.; Splendore, Alessandra; Jotta, Patricia Y.; Yunes, Jose Andres; Wiemels, Joseph L.; Pombo-de-Oliveira, Maria S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

06/11/2013

06/11/2013

2012

Resumo

Background: Molecular alterations occur frequently in T-ALL and the potential impact of those abnormalities on outcome is still controversial. The current study aimed to test whether NOTCH1 mutations and additional molecular abnormalities would impact T-ALL outcome in a series of 138 T-ALL paediatric cases. Methods: T-ALL subtypes, status of SIL-TAL1 fusion, ectopic expression of TLX3, and mutations in FBXW7, KRAS, PTEN and NOTCH1 were assessed as overall survival (OS) and event-free survival (EFS) prognostic factors. OS and EFS were determined using the Kaplan-Meier method and compared using the log-rank test. Results: The frequencies of mutations were 43.5% for NOTCH1, while FBXW7, KRAS and PTEN exhibited frequencies of 19.1%, 9.5% and 9.4%, respectively. In 78.3% of cases, the coexistence of NOTCH1 mutations and other molecular alterations was observed. In multivariate analysis no statistical association was revealed between NOTCH1 mutations and any other variable analyzed. The mean length of the follow-up was 68.4 months and the OS was 50.7%. SIL-TAL1 was identified as an adverse prognostic factor. NOTCH1 mutation status was not associated with outcome, while the presence of NOTCH1 complex mutations (indels) were associated with a longer overall survival (p = 0.031) than point mutations. Conclusion: NOTCH1 mutations alone or in combination with FBXW7 did not impact T-ALL prognosis. Nevertheless, complex NOTCH1 mutations appear to have a positive impact on OS and the SIL-TAL1 fusion was validated as a negative prognostic marker in our series of T-ALL.

CNPq [473124/2008-4, 302423/2010-9]

CNPq

INCT para Controle do Cancer, CNPq [573806/2008-0]

INCT para Controle do Cancer, CNPq

FAPERJ [E26/170.026/2008]

FAPERJ

CAPES Foundation

CAPES Foundation

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2008/10034-1]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

INCT para Controle do Cancer INCA

INCT para Controle do Cancer INCA

Leukemia and Lymphoma Society

Leukemia and Lymphoma Society [6026-10]

Identificador

BMC CANCER, LONDON, v. 12, n. 3, supl., Part 3, pp. 282-288, 38718, 2012

1471-2407

http://www.producao.usp.br/handle/BDPI/42510

10.1186/1471-2407-12-9

http://dx.doi.org/10.1186/1471-2407-12-9

Idioma(s)

eng

Publicador

BIOMED CENTRAL LTD

LONDON

Relação

BMC CANCER

Direitos

openAccess

Copyright BIOMED CENTRAL LTD

Palavras-Chave #ACUTE LYMPHOBLASTIC-LEUKEMIA #GAMMA-SECRETASE INHIBITORS #PROGNOSTIC-SIGNIFICANCE #MOLECULAR PATHOGENESIS #FBXW7 MUTATIONS #GENE #PTEN #EXPRESSION #LEUKEMOGENESIS #ABNORMALITIES #ONCOLOGY
Tipo

article

original article

publishedVersion