WHO classification and WPSS predict posttransplantation outcome in patients with myelodysplastic syndrome: a study from the Gruppo Italiano Trapianto di Midollo Osseo (GITMO)

Author:

Alessandrino Emilio Paolo1,Della Porta Matteo Giovanni1,Bacigalupo Andrea2,Van Lint Maria Teresa2,Falda Michele3,Onida Francesco4,Bernardi Massimo5,Iori Anna Paola6,Rambaldi Alessandro7,Cerretti Raffaella8,Marenco Paola9,Pioltelli Pietro10,Malcovati Luca1,Pascutto Cristiana1,Oneto Rosi2,Fanin Renato11,Bosi Alberto12

Affiliation:

1. Division of Hematology, University of Pavia, Fondazione Policlinico San Matteo, Istituti di Ricovero e Cura a Carattere Scientifico (IRCCS), Pavia;

2. Division of Hematology, Ospedale San Martino, Genova;

3. Division of Hematology, Ospedale San Giovanni Battista, Torino;

4. Department of Hematology, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Milano;

5. Hematology and Bone Marrow Transplantation Unit, San Raffaele Scientific Institute, Milano;

6. Division of Hematology, Department of Cellular Biotechnologies and Hematology, University La Sapienza, Roma;

7. Division of Hematology, Ospedali Riuniti, Bergamo;

8. Hemato-Oncology Transplant Unit, University Tor Vergata, Roma;

9. Department of Hematology, Ospedale Niguarda Ca' Granda, Milano;

10. Division of Hematology and Transplant Unit, Ospedale San Gerardo, University of Milano-Bicocca, Monza;

11. Division of Hematology and Bone Marrow Transplantation, University of Udine, Udine; and

12. Department of Hematology, University of Florence, Florence, Italy

Abstract

Abstract We evaluated the impact of World Health Organization (WHO) classification and WHO classification–based Prognostic Scoring System (WPSS) on the outcome of patients with myelodysplastic syndrome (MDS) who underwent allogeneic stem cell transplantation (allo-SCT) between 1990 and 2006. Five-year overall survival (OS) was 80% in refractory anemias, 57% in refractory cytopenias, 51% in refractory anemia with excess blasts 1 (RAEB-1), 28% in RAEB-2, and 25% in acute leukemia from MDS (P = .001). Five-year probability of relapse was 9%, 22%, 24%, 56%, and 53%, respectively (P < .001). Five-year transplant-related mortality (TRM) was 14%, 39%, 38%, 34%, and 44%, respectively (P = .24). In multivariate analysis, WHO classification showed a significant effect on OS (P = .017) and probability of relapse (P = .01); transfusion dependency was associated with a reduced OS (P = .01) and increased TRM (P = .037), whereas WPSS showed a prognostic significance on both OS (P = .001) and probability of relapse (P < .001). In patients without excess blasts, multilineage dysplasia and transfusion dependency affected OS (P = .001 and P = .009, respectively), and were associated with an increased TRM (P = .013 and P = .031, respectively). In these patients, WPSS identified 2 groups with different OS and TRM. These data suggest that WHO classification and WPSS have a relevant prognostic value in posttransplantation outcome of MDS patients.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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1. Allogeneic Hematopoietic Cell Transplantation in Myelodysplastic Syndrome Patients;Manual of Hematopoietic Cell Transplantation and Cellular Therapies;2024

2. Iron chelation therapy;European Journal of Haematology;2023-02-08

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