Measurable residual disease status and outcome of transplant in acute myeloid leukemia in second complete remission: a study by the acute leukemia working party of the EBMT
Language English Country United States Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
33980810
PubMed Central
PMC8116335
DOI
10.1038/s41408-021-00479-3
PII: 10.1038/s41408-021-00479-3
Knihovny.cz E-resources
- MeSH
- Leukemia, Myeloid, Acute diagnosis therapy MeSH
- Adult MeSH
- Remission Induction MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Prognosis MeSH
- Proportional Hazards Models MeSH
- Neoplasm, Residual diagnosis MeSH
- Aged MeSH
- Hematopoietic Stem Cell Transplantation * MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Measurable residual disease (MRD) prior to hematopoietic cell transplant (HCT) for acute myeloid leukemia (AML) in first complete morphological remission (CR1) is an independent predictor of outcome, but few studies address CR2. This analysis by the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation registry assessed HCT outcomes by declared MRD status in a cohort of 1042 adult patients with AML CR2 at HCT. Patients were transplanted 2006-2016 from human leukocyte antigen (HLA) matched siblings (n = 719) or HLA 10/10 matched unrelated donors (n = 293). Conditioning was myeloablative (n = 610) or reduced-intensity (n = 432) and 566 patients (54%) had in-vivo T cell depletion. At HCT, 749 patients (72%) were MRD negative (MRD NEG) and 293 (28%) were MRD positive (MRD POS). Time from diagnosis to HCT was longer in MRD NEG than MRD POS patients (18 vs. 16 months (P < 0.001). Two-year relapse rates were 24% (95% CI, 21-28) and 40% (95% CI, 34-46) in MRD NEG and MRD POS groups (P < 0.001), respectively. Leukemia-free survival (LFS) was 57% (53-61) and 46% (40-52%), respectively (P = 0.001), but there was no difference in terms of overall survival. Prognostic factors for relapse and LFS were MRD NEG status, good risk cytogenetics, and longer time from diagnosis to HCT. In-vivo T cell depletion predicted relapse.
CHU de Lille LIRIC INSER U995 Université de Lille Lille France
Department of Haematology Rigshospitalet Copenhagen Denmark
EBMT Paris study office CEREST TC Paris France
Hematologie Transplantation Hôpital St Louis Paris CEDEX 10 France
Hematology Division Chaim Sheba Medical Center Tel Hashomer Israel
Hematology Service Institute of Hematology and Blood Transfusion Prague Czech Republic
Hôpital Saint Antoine INSERM UMR 938 Paris France; Université Pierre et Marie Curie Paris France
Kapadokya BMT Center Kayseri Turkey
Leeds Teaching Hospitals Trust St James's University Hospital Leeds LS9 7TF United Kingdom
Manchester Royal Infirmary Manchester United Kingdom
University Hospital Bristol NHS Foundation Trust London United Kingdom
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