Recently a new three-group clinical classification was reported by an International Consortium to stratify CMML patients with regard to prognosis. The groups were defined as follows: (1) Myelodysplastic (MD)-CMML: WBC <= 10 x 10(9)/l, circulating immature myeloid cells (IMC) = 0, no splenomegaly; (2) MD/MP (overlap)-CMML: WBC 10-20 x 10(9)/l or WBC <= 10 x 10(9)/l but IMC > 0 and/or splenomegaly; (3) Myeloproliferative (MP)-CMML: WBC > 20 x 10(9)/l. By analysing EBMT Registry patients who underwent allo-HCT for CMML between 1997 and 2016, we aimed to determine the impact of this classification on transplantation outcome and to make a comparison with the conventional WHO classification (CMML-0/CMML-1/CMML-2). Patient grouping was based on the data registered at time of transplantation, with IMC replaced by peripheral blasts. Among 151 patients included in the analysis, 38% were classified as MD-CMML, 42% as MD/MP-CMML and 20% as MP-CMML. With a median survival of 17 months in the whole series, MD-CMML patients were distinguished as a low-risk group with higher CR rate at transplant and a longer post-transplant 2-year progression-free survival in comparison to others (44.5% vs 33.5%, respectively), whereas the WHO classification was superior in identifying high-risk patients (CMML-2) with inferior survival outcomes.

Prognostic value of a new clinically-based classification system in patients with CMML undergoing allogeneic HCT. A retrospective analysis of the EBMT-CMWP / Onida, F; Sbianchi, G; Radujkovic, A; Sockel, K; Kroger, N; Sierra, J; Socie, G; Cornelissen, J; Poire, X; Raida, L; Bourhis, Jh; Finke, J; Passweg, J; Salmenniemi, U; Schouten, Hc; Beguin, Y; Martin, S; Deconinck, E; Ganser, A; Zver, S; Lioure, B; Rohini, R; Koster, L; Hayden, P; Iacobelli, S; Robin, M; Yakoub-Agha, I. - In: BONE MARROW TRANSPLANTATION. - ISSN 0268-3369. - 57:6(2022), pp. 896-902. [10.1038/s41409-021-01555-9]

Prognostic value of a new clinically-based classification system in patients with CMML undergoing allogeneic HCT. A retrospective analysis of the EBMT-CMWP

Iacobelli, S;
2022

Abstract

Recently a new three-group clinical classification was reported by an International Consortium to stratify CMML patients with regard to prognosis. The groups were defined as follows: (1) Myelodysplastic (MD)-CMML: WBC <= 10 x 10(9)/l, circulating immature myeloid cells (IMC) = 0, no splenomegaly; (2) MD/MP (overlap)-CMML: WBC 10-20 x 10(9)/l or WBC <= 10 x 10(9)/l but IMC > 0 and/or splenomegaly; (3) Myeloproliferative (MP)-CMML: WBC > 20 x 10(9)/l. By analysing EBMT Registry patients who underwent allo-HCT for CMML between 1997 and 2016, we aimed to determine the impact of this classification on transplantation outcome and to make a comparison with the conventional WHO classification (CMML-0/CMML-1/CMML-2). Patient grouping was based on the data registered at time of transplantation, with IMC replaced by peripheral blasts. Among 151 patients included in the analysis, 38% were classified as MD-CMML, 42% as MD/MP-CMML and 20% as MP-CMML. With a median survival of 17 months in the whole series, MD-CMML patients were distinguished as a low-risk group with higher CR rate at transplant and a longer post-transplant 2-year progression-free survival in comparison to others (44.5% vs 33.5%, respectively), whereas the WHO classification was superior in identifying high-risk patients (CMML-2) with inferior survival outcomes.
2022
humans; prognosis; retrospective studies; hematopoietic stem cell transplantation; leukemia; myelomonocytic; chronic
01 Pubblicazione su rivista::01a Articolo in rivista
Prognostic value of a new clinically-based classification system in patients with CMML undergoing allogeneic HCT. A retrospective analysis of the EBMT-CMWP / Onida, F; Sbianchi, G; Radujkovic, A; Sockel, K; Kroger, N; Sierra, J; Socie, G; Cornelissen, J; Poire, X; Raida, L; Bourhis, Jh; Finke, J; Passweg, J; Salmenniemi, U; Schouten, Hc; Beguin, Y; Martin, S; Deconinck, E; Ganser, A; Zver, S; Lioure, B; Rohini, R; Koster, L; Hayden, P; Iacobelli, S; Robin, M; Yakoub-Agha, I. - In: BONE MARROW TRANSPLANTATION. - ISSN 0268-3369. - 57:6(2022), pp. 896-902. [10.1038/s41409-021-01555-9]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1723052
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