TP53 variant allele frequency and therapy‐related setting independently predict survival in myelodysplastic syndromes with del(5q)

Author:

Tefferi Ayalew1ORCID,Fleti Farah1,Chan Onyee1,Al Ali Najla H.2,Al‐Kali Aref1ORCID,Begna Kebede H.1,Foran James M.1ORCID,Badar Talha1ORCID,Khera Nandita1,Shah Mithun1ORCID,Hiwase Devendra3ORCID,Padron Eric2,Sallman David A.2ORCID,Pardanani Animesh1ORCID,Arber Daniel A.4ORCID,Orazi Attilio5,Reichard Kaaren K.1,He Rong1ORCID,Ketterling Rhett P.1,Gangat Naseema1ORCID,Komrokji Rami2ORCID

Affiliation:

1. Mayo Clinic Rochester/Jacksonville/Scottsdale Minnesota/Florida/Arizona USA

2. Department of Malignant Hematology H. Lee Moffitt Cancer Center Tampa Florida USA

3. Division of Blood Cells and Blood Cancer Walter and Eliza Hall Institute of Medical Research Melbourne Victoria Australia

4. Department of Pathology University of Chicago Chicago Illinois USA

5. Department of Pathology Texas Tech University Health Sciences Center El Paso Texas USA

Abstract

SummaryAmong 210 patients with myelodysplastic syndromes (MDSs) with del(5q), molecular information was available at diagnosis or at least 3 months before leukaemic transformation in 146 cases. Multivariate analysis identified therapy‐related setting (p = 0.02; HR 2.3) and TP53 variant allele frequency (VAF) ≥22% (p < 0.01; HR 2.8), but not SF3B1 mutation (p = 0.65), as independent risk factors for survival. Median survival was 11.7 versus 4 years (5/10‐year survival 73%/52% vs. 42%/14%) in the absence (N = 112) versus presence (N = 34) of ≥1 risk factors; leukaemia‐free survival was affected by TP53 VAF ≥22% (p < 0.01). Such information might inform treatment decision‐making in MDS‐del(5q) regarding allogeneic stem cell transplant.

Publisher

Wiley

Subject

Hematology

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