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Outcomes after allogeneic hematopoietic cell transplant in patients diagnosed with blast phase of myeloproliferative neoplasms: A retrospective study from the Chronic Malignancies Working Party of the European Society for Blood and Marrow Transplantation

Articolo
Data di Pubblicazione:
2023
Abstract:
Allogeneic hematopoietic cell transplant (allo-HCT) provides the only potential route to long-term remission in patients diagnosed with blast phase transformation of myeloproliferative neoplasm (BP-MPN). We report on a large, retrospective European Society for Blood and Marrow Transplantation registry-based study of BP-MPN patients undergoing allo-HCT. BP-MPN patients undergoing first allo-HCT between 2005 and 2019 were included. A total of 663 patients were included. With a median follow-up of 62 months, the estimated 3-year overall survival (OS) was 36% (95% confidence interval [CI], 32–36). Factors associated with lower OS were Karnofsky Performance Score (KPS) <90 (hazard ratio [HR] 1.65, p <.001) and active disease at allo-HCT (HR 1.45, p <.001), whereas patients undergoing allo-HCT more recently associated with a higher OS (HR 0.96, p =.008). In a selected patient's population, the 3-year OS of patients undergoing allo-HCT in complete response (CR) and with a KPS ≥90 was 60%. KPS < 90 (HR 1.4, p =.001) and active disease (HR 1.44, p =.0004) were associated with a lower progression-free survival (PFS). Conversely, most recent allo-HCT associated with a higher PFS (HR 0.96, p =.008). Active disease at allo-HCT (HR 1.34, p =.03) was associated with a higher cumulative incidence of relapse (RI) and allo-HCT in earlier calendar years (HR 0.96, p =.02) associated with a lower RI. Last, KPS < 90 (HR 1.91, p <.001), active disease (HR 1.74, p =.003) and allo-HCT from mismatched related donors were associated with a higher non-relapse mortality (HR 2.66, p =.003). In this large series of BP-MPN patients, about one third were alive at 3 years after transplantation. Patients undergoing allo-HCT in the more recent era, with a KPS ≥90 and in CR at transplant had a better prognosis.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Orti, G.; Gras, L.; Zinger, N.; Finazzi, M. C.; Sockel, K.; Robin, M.; Forcade, E.; Avenoso, D.; Kroger, N.; Finke, J.; Radujkovic, A.; Hunault-Berger, M.; Schroyens, W.; Zuckerman, T.; Bourhis, J. H.; Chalandon, Y.; Bloor, A.; Schots, R.; de Wreede, L. C.; Drozd-Sokolowska, J.; Raj, K.; Polverelli, N.; Czerw, T.; Hernandez-Boluda, J. C.; Mclornan, D.; Yakoub-Agha, I.
Autori di Ateneo:
AVENOSO DANIELE
Link alla scheda completa:
https://iris.unibs.it/handle/11379/569793
Pubblicato in:
AMERICAN JOURNAL OF HEMATOLOGY
Journal
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