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Impact of pre-transplant induction and consolidation cycles on AML allogeneic transplant outcomes: a CIBMTR analysis in 3113 AML patients

Authors :
Boyiadzis, Michael
Zhang, Mei-Jie
Chen, Karen
Abdel-Azim, Hisham
Abid, Muhammad Bilal
Aljurf, Mahmoud
Bacher, Ulrike
Badar, Talha
Badawy, Sherif M.
Battiwalla, Minoo
Bejanyan, Nelli
Bhatt, Vijaya Raj
Brown, Valerie I.
Castillo, Paul
Cerny, Jan
Copelan, Edward A.
Craddock, Charles
Dholaria, Bhagirathbhai
Perez, Miguel Angel Diaz
Ebens, Christen L.
Gale, Robert Peter
Ganguly, Siddhartha
Gowda, Lohith
Grunwald, Michael R.
Hashmi, Shahrukh
Hildebrandt, Gerhard C.
Iqbal, Madiha
Jamy, Omer
Kharfan-Dabaja, Mohamed A.
Khera, Nandita
Lazarus, Hillard M.
Lin, Richard
Modi, Dipenkumar
Nathan, Sunita
Nishihori, Taiga
Patel, Sagar S.
Pawarode, Attaphol
Sharma, Akshay
Solh, Melhem
Wagner, John L.
Wang, Trent
Williams, Kirsten M.
Winestone, Lena E.
Wirk, Baldeep
Hourigan, Christopher S.
Litzow, Mark
Kebriaei, Partow
de Lima, Marcos
Page, Kristin
Weisdorf, Daniel J.
Source :
Leukemia; 20220101, Issue: Preprints p1-12, 12p
Publication Year :
2022

Abstract

We investigated the impact of the number of induction/consolidation cycles on outcomes of 3113 adult AML patients who received allogeneic hematopoietic cell transplantation (allo-HCT) between 2008 and 2019. Patients received allo-HCT using myeloablative (MAC) or reduced-intensity (RIC) conditioning in first complete remission (CR) or with primary induction failure (PIF). Patients who received MAC allo-HCT in CR after 1 induction cycle had 1.3-fold better overall survival (OS) than 2 cycles to CR and 1.47-fold better than ≥3 cycles. OS after CR in 2 or ≥3 cycles was similar. Relapse risk was 1.65-fold greater in patients receiving ≥3 cycles to achieve CR. After RIC allo-HCT, the number of induction cycles to CR did not affect OS. Compared to CR in 1 cycle, relapse risk was 1.24-1.41-fold greater in patients receiving 2 or ≥3 cycles. For patients receiving only 1 cycle to CR, consolidation therapy prior to MAC allo-HCT was associated with improved OS vs. no consolidation therapy. Detectable MRD at the time of MAC allo-HCT did not impact outcomes while detectable MRD preceding RIC allo-HCT was associated with an increased risk of relapse. For allo-HCT in PIF, OS was significantly worse than allo-HCT in CR after 1–3 cycles.

Details

Language :
English
ISSN :
08876924 and 14765551
Issue :
Preprints
Database :
Supplemental Index
Journal :
Leukemia
Publication Type :
Periodical
Accession number :
ejs61070834
Full Text :
https://doi.org/10.1038/s41375-022-01738-3