Impact of FLT3 Internal Tandem Duplication on the Outcome of Related and Unrelated Hematopoietic Transplantation for Adult Acute Myeloid Leukemia in First Remission: A Retrospective Analysis


Autoria(s): Brunet, Salut; Labopin, Myriam; Esteve, Jordi; Cornelissen, Jan; Socie, Gerard; Iori, Anna P.; Verdonck, Leo F.; Volin, Liisa; Gratwohl, Alois; Sierra, Jorge; Mohty, Mohamad; Rocha, Vanderson
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

23/09/2013

23/09/2013

2012

Resumo

Purpose Patients with acute myeloid leukemia (AML) and FLT3/internal tandem duplication (FLT3/ITD) have poor prognosis if treated with chemotherapy only. Whether this alteration also affects outcome after allogeneic hematopoietic stem-cell transplantation (HSCT) remains uncertain. Patients and Methods We analyzed 206 patients who underwent HLA-identical sibling and matched unrelated HSCTs reported to the European Group for Blood and Marrow Transplantation with a diagnosis of AML with normal cytogenetics and data on FLT3/ITD (present: n = 120, 58%; absent: n = 86, 42%). Transplantations were performed in first complete remission (CR) after myeloablative conditioning. Results Compared with FLT3/ITD-negative patients, FLT3/ITD-positive patients had higher median leukocyte count at diagnosis (59 v 21 x 10(9)/L; P < .001) and shorter interval from CR to transplantation (87 v 99 days; P = .04). Other characteristics were similar in the two groups. At 2 years, relapse incidence (RI; +/- standard deviation) was higher (30% +/- 5% v 16% +/- 5%; P = .006) and leukemia-free survival (LFS) lower (58% +/- 5% v 71% +/- 6%; P = .04) in FLT3/ITD-positive compared with FLT3/ITD-negative patients. In multivariate analyses, FLT3/ITD led to increased RI (hazard ratio [HR], 3.4; 95% CI, 1.46 to 7.94; P = .005), as did older age, female sex, shorter interval between CR and transplantation, and higher number of chemotherapy courses before achieving CR. FLT3/ITD positivity was associated with decreased LFS (HR, 0.37; 95% CI, 0.19 to 0.73; P = .002), along with older age and higher number of chemotherapy courses before achieving CR. Conclusion FLT3/ITD adversely affected the outcome of HSCT in the same direction it does after chemotherapy; despite this, more than half of the patients harboring this mutation who received transplants were alive and leukemia free at 2 years. To further improve the results, use of FLT3 inhibitors before or after HSCT deserves investigation.

Instituto de Salud Carlos III, Madrid [EC07/90065, PI080672, PI080413, RD06/0020/0101, RD06/0020/0004]

Instituto de Salud Carlos III, Madrid

Agency for Administration of University and Research Grants, Barcelona, Spain [2009-SGR-1246]

Agency for Administration of University and Research Grants, Barcelona, Spain

Novartis

Novartis

Amgen

Amgen

Jorge Sierra

Jorge Sierra

Celgene

Celgene

Identificador

JOURNAL OF CLINICAL ONCOLOGY, ALEXANDRIA, v. 30, n. 7, pp. 735-741, 2012

0732-183X

http://www.producao.usp.br/handle/BDPI/33598

10.1200/JCO.2011.36.9868

http://dx.doi.org/10.1200/JCO.2011.36.9868

Idioma(s)

eng

Publicador

AMER SOC CLINICAL ONCOLOGY

ALEXANDRIA

Relação

JOURNAL OF CLINICAL ONCOLOGY

Direitos

closedAccess

Copyright AMER SOC CLINICAL ONCOLOGY

Palavras-Chave #STEM-CELL TRANSPLANTATION #ACUTE MYELOGENOUS LEUKEMIA #NORMAL CYTOGENETICS #MARROW-TRANSPLANTATION #PROMYELOCYTIC LEUKEMIA #PERIPHERAL-BLOOD #POOR-PROGNOSIS #12 TRIALS #GROUP-B #MUTATIONS #ONCOLOGY
Tipo

article

original article

publishedVersion