Comparative Analysis of the Value of Allogeneic Hematopoietic Stem-Cell Transplantation in Acute Myeloid Leukemia With Monosomal Karyotype Versus Other Cytogenetic Risk Categories

Author:

Cornelissen Jan J.1,Breems Dimitri1,van Putten Wim L.J.1,Gratwohl Alois A.1,Passweg Jakob R.1,Pabst Thomas1,Maertens Johan1,Beverloo H. Berna1,van Marwijk Kooy Marinus1,Wijermans Pierre W.1,Biemond Bart J.1,Vellenga Edo1,Verdonck Leo F.1,Ossenkoppele Gert J.1,Löwenberg Bob1

Affiliation:

1. Jan J. Cornelissen, Wim L.J. van Putten, H. Berna Beverloo, and Bob L|f-wenberg, Erasmus University Medical Center, Rotterdam; Marinus van Marwijk Kooy and Leo F. Verdonck, Isala Clinics, Zwolle; Pierre W. Wijermans, Haga Hospital, the Hague; Bart J. Biemond, Academic Medical Center; Gert J. Ossenkoppele, Vrije Universiteit Medical Center, Amsterdam; Edo Vellenga, University Medical Center, Groningen, the Netherlands; Dimitri Breems, Hospital Campus Stuivenberg, Antwerp; Johan Maertens, University...

Abstract

Purpose To determine to what extent allogeneic hematopoietic stem-cell transplantation (alloHSCT) quantitatively reduces relapse in acute myeloid leukemia with monosomal karyotype (MK-AML) compared with alternative postremission therapy and how it compares with other cytogenetic subcategories. Patients and Methods Of 2,560 patients (younger than age 61 years) without core-binding factor abnormalities including 305 patients with MK-AML receiving first-line induction treatment, 1,975 patients (77%) achieved remission, and 1,588 received consolidation in the first complete remission (CR1) after two induction cycles. Consolidation treatment of 107 patients with MK-AML consisted of alloHSCT (n = 45), chemotherapy (n = 48), or autologous HSCT (n = 14). Results The 5-year overall survival after start of consolidation was 19% for patients with MK-AML who received alloHSCT and 9% for those who received chemotherapy or autoHSCT (P = .02). Relapse-free survival (RFS) at 5 years was 17% versus 7% (P = .003). Cox regression analysis was performed with alloHSCT as a time-dependent covariate. Hazard ratios (HRs) associated with alloHSCT for relapse and RFS were 0.30 (95% CI, 0.24 to 0.37; P < .001), and 0.52 (95% CI, 0.43 to 0.62; P < .001), respectively. HRs were similar in MK-AML and the other cytogenetic subgroups. Conclusion AlloHSCT, applied as consolidation in CR1, is associated with a significant reduction of relapse and improvement of survival in MK-AML, with the same relative reduction of relapse or death as in other cytogenetic risk categories.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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