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Leukemia relapse following unmanipulated haploidentical transplantation: a risk factor analysis on behalf of the ALWP of the EBMT

Authors :
Yener Koc
Zafar Gulbas
Didier Blaise
William Arcese
Dietrich W. Beelen
Simona Piemontese
Depei Wu
Arnon Nagler
Fabio Ciceri
Johanna Tischer
Benedetto Bruno
Annalisa Ruggeri
Ariane Boumendil
Giuseppe Irrera
Mohamad Mohty
Myriam Labopin
Mohamed Houhou
Christoph Schmid
Piemontese, Simona
Boumendil, Ariane
Labopin, Myriam
Schmid, Christoph
Ciceri, Fabio
Arcese, William
Koc, Yener
Gulbas, Zafar
Tischer, Johanna
Bruno, Benedetto
Wu, Depei
Blaise, Didier
Beelen, Dietrich
Irrera, Giuseppe
Ruggeri, Annalisa
Houhou, Mohamed
Mohty, Mohamad
Nagler, Arnon
Source :
Journal of Hematology & Oncology, Vol 12, Iss 1, Pp 1-11 (2019), Journal of Hematology & Oncology
Publication Year :
2019

Abstract

Background As information on incidence, risk factors, and outcome of acute leukemia (AL) relapse after unmanipulated haploidentical stem cell transplantation (haplo-SCT) is scarce, a retrospective registry study was performed by the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation. Methods Among 1652 transplants performed for lymphoblastic and myeloid AL between 2007 and 2014, 587 patients (acute lymphoblastic leukemia (ALL) 131, acute myeloid leukemia (AML) 456) with detailed information were analyzed aiming to identify risk factors for post-transplant relapse and for overall survival (OS) after relapse. Results The cumulative incidence of relapse at 3 years was 44% (35–53%) for ALL and 32% (27–36%) for AML (p = 0.023). In ALL, risk factors for relapse were disease status different from the first complete remission (CR1) at haplo-SCT (CR2 vs CR1: HR 2.85, p = 0.011; advanced vs CR1: HR 14.28, p < 0.0001) and male donor gender (HR 3.64, p = 0.0002), while in AML, risk factors were advanced disease at haplo-SCT (advanced vs CR1: HR 3.95, p < 0.0001) and comorbidities (HCT-CI) ≥ 3 (HR 1.75, p = 0.014). Transplants performed in more recent years were associated with lower relapse incidence (RI) in AML, but not in ALL (HR 0.91, p = 0.042). After relapse, median follow-up was 13 months (mos). OS at 1-year post relapse was 18%. Prognostic factors for superior OS after relapse were remission at time of haplo-SCT (CR vs advanced: HR 0.71, p = 0.028), time from transplant to relapse (≥ 5 mos vs < 5 mos: HR 0.530, p < 0.0001), and bone marrow as a stem cell source (peripheral blood (PB) vs bone marrow (BM): HR 1.473, p = 0.016). Conclusions Risk factors for relapse after haploidentical transplantation were disease specific. Longer OS after relapse was achieved in particular by patients both in CR at haplo-SCT and relapsing more than 5 months after transplant (1-year OS 33%). Electronic supplementary material The online version of this article (10.1186/s13045-019-0751-4) contains supplementary material, which is available to authorized users.

Details

Language :
English
Database :
OpenAIRE
Journal :
Journal of Hematology & Oncology, Vol 12, Iss 1, Pp 1-11 (2019), Journal of Hematology & Oncology
Accession number :
edsair.doi.dedup.....def6c12430a57e0360bb0709f9b7b6d8