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Inferior outcome of allogeneic stem cell transplantation for secondary acute myeloid leukemia in first complete remission as compared to de novo acute myeloid leukemia
- Source :
- Blood Cancer Journal, Blood Cancer Journal, 2020, 10 (3), pp.26. ⟨10.1038/s41408-020-0296-3⟩, Blood Cancer Journal, Nature Publishing Group, 2020, 10 (3), ⟨10.1038/s41408-020-0296-3⟩, Blood Cancer Journal, 2020, 10 (3), ⟨10.1038/s41408-020-0296-3⟩, Blood Cancer Journal, Vol 10, Iss 3, Pp 1-9 (2020), Blood Cancer Journal, Nature Publishing Group, 2020, 10 (3), pp.26. ⟨10.1038/s41408-020-0296-3⟩, Blood Cancer Journal, 10(3):26. Nature Publishing Group
- Publication Year :
- 2020
- Publisher :
- HAL CCSD, 2020.
-
Abstract
- Following chemotherapy, secondary acute myeloid leukemia (sAML), occurring after antecedent hematologic diseases, previous chemotherapy or radiation, has an inferior prognosis compared with de novo AML. To define the outcome of sAML in the context of allogeneic stem cell transplantation (alloSCT), a retrospective, registry-based comparison was performed, including 11,439 patients with de novo and 1325 with sAML. Among transplants in first complete remission (CR1) (n = 8,600), the 3-year cumulative incidence of relapse (RI) and non-relapse mortality (NRM) was 28.5% and 16.4% for de novo, and 35% and 23.4% for sAML. Three-year overall survival (OS), leukemia-free survival (LFS) and Graft-versus-Host Disease/relapse-free survival (GRFS) was 60.8%, 55.1%, and 38.6% for de novo, and 46.7%, 41.6%, and 28.4% for sAML, respectively. In multivariate analysis, sAML was associated with a lower OS (HR = 1.33 [95% CI = 1.21–1.48]; p −5), LFS (HR = 1.32 [95% CI = 1.19–1.45]; p −5) and GRFS (HR = 1.2 [95% CI = 1.1–1.31]; p −4) and higher NRM (HR = 1.37 [95% CI = 1.17–1.59]; p −4) and RI (HR = 1.27 [95% CI = 1.12–1.44]; p −3). Results of the Cox model were confirmed in a matched-pair analysis. In contrast, results did not differ between de novo and sAML after alloSCT in induction failure or relapse. Hence, this analysis identified sAML as an independent risk factor for outcome after alloSCT in CR1.
- Subjects :
- Male
Oncology
Transplantation Conditioning
medicine.medical_treatment
[SDV]Life Sciences [q-bio]
Medizin
RELAPSE
THERAPY
0302 clinical medicine
AML
Secondary Acute Myeloid Leukemia
Cumulative incidence
ComputingMilieux_MISCELLANEOUS
Cancer stem cells
Remission Induction
Hematopoietic Stem Cell Transplantation
Myeloid leukemia
Neoplasms, Second Primary
Hematology
Middle Aged
Prognosis
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
CYTOGENETICS
Stem-cell research
[SDV] Life Sciences [q-bio]
Leukemia, Myeloid, Acute
030220 oncology & carcinogenesis
SURVIVAL
[SDV.IMM]Life Sciences [q-bio]/Immunology
Female
Adult
medicine.medical_specialty
Adolescent
3122 Cancers
Context (language use)
lcsh:RC254-282
Article
Young Adult
03 medical and health sciences
Internal medicine
medicine
Humans
Transplantation, Homologous
ddc:610
Risk factor
Aged
Chemotherapy
business.industry
Proportional hazards model
Transplantation
business
030215 immunology
Subjects
Details
- Language :
- English
- ISSN :
- 20445385
- Database :
- OpenAIRE
- Journal :
- Blood Cancer Journal, Blood Cancer Journal, 2020, 10 (3), pp.26. ⟨10.1038/s41408-020-0296-3⟩, Blood Cancer Journal, Nature Publishing Group, 2020, 10 (3), ⟨10.1038/s41408-020-0296-3⟩, Blood Cancer Journal, 2020, 10 (3), ⟨10.1038/s41408-020-0296-3⟩, Blood Cancer Journal, Vol 10, Iss 3, Pp 1-9 (2020), Blood Cancer Journal, Nature Publishing Group, 2020, 10 (3), pp.26. ⟨10.1038/s41408-020-0296-3⟩, Blood Cancer Journal, 10(3):26. Nature Publishing Group
- Accession number :
- edsair.doi.dedup.....bdb85aa28d959ec4a110483eb84f37ce