Literature DB >> 28971504

Relatively favorable outcome after allogeneic stem cell transplantation for BCR-ABL1-positive AML: A survey from the acute leukemia working party of the European Society for blood and marrow transplantation (EBMT).

Vladimir Lj Lazarevic1, Myriam Labopin2, Wu Depei3, Ibrahim Yakoub-Agha4, Anne Huynh5, Per Ljungman6, Nicolaas Schaap7, Jan J Cornelissen8, Natacha Maillard9, Pietro Pioltelli10, Tobias Gedde-Dahl11, Stig Lenhoff1, Mohamed Houhou2, Jordi Esteve12, Mohamad Mohty2, Arnon Nagler2,13.   

Abstract

The aim of the study was to assess the role of allogeneic stem cell transplantation (SCT) in patients diagnosed with BCR-ABL1-positive acute myeloid leukemia (AML). Fifty-seven patients (median age, 48 years, range: 19-67) with BCR-ABL1 positive AML undergoing SCT were identified. The majority of the patients (70%) received a TKI before the transplant. At SCT 48 patients were in CR (45 in CR1), while 9 patients were transplanted in a more advanced stage of the disease. MRD was negative (BCR-ABL1/ABL < 104 ) at time of SCT in 36.1% (14/40). After SCT, 16 (61.5%) out of 26 patients with MRD positive at transplantation reached MRD negativity. After a median follow-up of 6.3 years (0.7-14.2), NRM, RI, LFS, OS, and GRFS at 5 years were 18.1%, 37%, 44.2%, 53.8%, and 32.1%, respectively. The cumulative incidence of acute GvHD grade II-IV was 16.4%, incidence of chronic GvHD 24.9%, and of extensive cGvHD 21.4%, respectively. In patients who received SCT in CR1, 5-yr NRM, RI, LFS, OS, and GRFS were 15.9%, 36.4%, 46.5%, 59.4%, and 34.9%, respectively. Univariate analysis showed that age (<50 vs. ≥50 years) was associated with RI (5-yr: 22.7 vs. 50%), LFS (5-yr: 61.9 vs. 31.8%), and GRFS (5-yr: 52.4 vs. 18.2%), whereas MRD-negative status before SCT was associated with an improved GRFS (38.9 vs. 16.7%). We conclude that the outcome of patients <50 years of age with BCR-ABL1-positive AML receiving allogeneic SCT in CR is relatively favorable, possibly reflecting the beneficial effect of the use of TKI.
© 2017 Wiley Periodicals, Inc.

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Year:  2017        PMID: 28971504     DOI: 10.1002/ajh.24928

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  3 in total

1.  BCR-ABL+ acute myeloid leukemia: are we always dealing with a high-risk disease?

Authors:  Nina Rosa Neuendorff; Philipp Hemmati; Renate Arnold; Jana Ihlow; Bernd Dörken; Carsten Müller-Tidow; Jörg Westermann
Journal:  Blood Adv       Date:  2018-06-26

2.  Allogeneic hematopoietic cell transplantation efficacy in patients with Philadelphia chromosome-positive acute myeloid leukemia in complete remission.

Authors:  Shohei Mizuno; Masamitsu Yanada; Koji Kawamura; Masayoshi Masuko; Naoyuki Uchida; Yukiyasu Ozawa; Koji Iwato; Kazuteru Ohashi; Kazuhiro Ikegame; Sung-Won Kim; Masatsugu Tanaka; Tetsuya Eto; Yoshinobu Kanda; Takahiro Fukuda; Yoshiko Atsuta; Shingo Yano; Akiyoshi Takami
Journal:  Bone Marrow Transplant       Date:  2020-07-31       Impact factor: 5.483

3.  Successful treatment with ABL tyrosine kinase inhibitor for patients with acute myeloid leukemia with BCR-ABL1.

Authors:  Asako Takeuchi; Toshinori Kondo; Taizo Tasaka; Seiko Yamada; Tadashi Hirose; Hirofumi Fukuda; Risa Shimizu; Yoshiko Matsuhashi; Eisei Kondo; Hideho Wada
Journal:  Leuk Res Rep       Date:  2020-12-14
  3 in total

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