TY - JOUR
T1 - Allogeneic hematopoietic stem cell transplantation for adults with therapy-related acute myeloid leukaemia
T2 - a retrospective multicentre study on behalf of the SFGM-TC
AU - Rey, Gaëlle
AU - Daguenet, Elisabeth
AU - Bonjean, Paul
AU - Devillier, Raynier
AU - Fegueux, Nathalie
AU - Forcade, Edouard
AU - Srour, Micha
AU - Chevallier, Patrice
AU - Robin, Marie
AU - Suarez, Felipe
AU - Micol, Jean Baptiste
AU - Labussière-Wallet, Hélène
AU - Bilger, Karin
AU - Daguindau, Etienne
AU - Bay, Jacques Olivier
AU - Fayard, Amandine
AU - Bulabois, Claude Eric
AU - Nguyen-Quoc, Stéphanie
AU - Genthon, Alexis
AU - Orvain, Corentin
AU - Turlure, Pascal
AU - Loschi, Michael
AU - Poiré, Xavier
AU - Guillerm, Gaëlle
AU - Beguin, Yves
AU - Maillard, Natacha
AU - Mear, Jean Baptiste
AU - Chalayer, Emilie
AU - Cornillon, Jérôme
AU - Tavernier, Emmanuelle
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2023/12/1
Y1 - 2023/12/1
N2 - We report the results from a multicentre retrospective study of 220 adult patients who underwent allogeneic hematopoietic stem cell transplantation (alloHSCT) for therapy-related acute myeloid leukaemia (t-AML). Median age at t-AML diagnosis was 56 years, with a prior history of haematological (45%) or breast (34%). Median time from cytotoxic exposure to t-AML diagnosis was 54.7 months. At transplant, around 20% of patients had measurable residual disease and 3% of patients were not in complete remission. The median follow-up was 21.4 months (Q1–Q3, 5.9–52.8). At 12 months, overall survival (OS), event-free survival (EFS), and graft-versus-host-disease (GVHD)-free-relapse-free survival (GRFS) were 60.7% (95% CI 54.6–67.5), 52.8% (95% CI 46.5–68.4), and 44.1% (95% CI 37.6–51.8), respectively. At 5 years, OS, EFS, and GRFS were 44.1% (95% CI 37.4–52.1), 40.4% (95% CI 33.9–48.1), and 35.3% (95% CI 28.8–43.3), respectively. At last follow-up, 44% of patients were in complete remission (n = 96) and transplant-related mortality accounted for 21% of all deaths (n = 119). Multivariable analysis revealed that uncontrolled t-AML at transplant was associated with lower EFS (HR 1.94, 95% CI 1.0–3.7, p = 0.041). In conclusion, alloHSCT for t-AML shows encouraging results and offers additional opportunity with the emergence of novel pre-graft therapies.
AB - We report the results from a multicentre retrospective study of 220 adult patients who underwent allogeneic hematopoietic stem cell transplantation (alloHSCT) for therapy-related acute myeloid leukaemia (t-AML). Median age at t-AML diagnosis was 56 years, with a prior history of haematological (45%) or breast (34%). Median time from cytotoxic exposure to t-AML diagnosis was 54.7 months. At transplant, around 20% of patients had measurable residual disease and 3% of patients were not in complete remission. The median follow-up was 21.4 months (Q1–Q3, 5.9–52.8). At 12 months, overall survival (OS), event-free survival (EFS), and graft-versus-host-disease (GVHD)-free-relapse-free survival (GRFS) were 60.7% (95% CI 54.6–67.5), 52.8% (95% CI 46.5–68.4), and 44.1% (95% CI 37.6–51.8), respectively. At 5 years, OS, EFS, and GRFS were 44.1% (95% CI 37.4–52.1), 40.4% (95% CI 33.9–48.1), and 35.3% (95% CI 28.8–43.3), respectively. At last follow-up, 44% of patients were in complete remission (n = 96) and transplant-related mortality accounted for 21% of all deaths (n = 119). Multivariable analysis revealed that uncontrolled t-AML at transplant was associated with lower EFS (HR 1.94, 95% CI 1.0–3.7, p = 0.041). In conclusion, alloHSCT for t-AML shows encouraging results and offers additional opportunity with the emergence of novel pre-graft therapies.
UR - http://www.scopus.com/inward/record.url?scp=85169166296&partnerID=8YFLogxK
U2 - 10.1038/s41409-023-02082-5
DO - 10.1038/s41409-023-02082-5
M3 - Article
AN - SCOPUS:85169166296
SN - 0268-3369
VL - 58
SP - 1331
EP - 1338
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 12
ER -