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Evaluation of a disease risk index for adult patients undergoing umbilical cord blood transplantation for haematological malignancies.

Authors :
Paviglianiti A
Ruggeri A
Volt F
Sanz G
Milpied N
Furst S
Esquirol A
Arcese W
Picardi A
Ferra C
Ifrah N
Bourhis JH
Raj K
von dem Borne PA
Sica S
Menard AL
Bloor A
Kenzey C
Gluckman E
Rocha V
Source :
British journal of haematology [Br J Haematol] 2017 Dec; Vol. 179 (5), pp. 790-801. Date of Electronic Publication: 2017 Oct 19.
Publication Year :
2017

Abstract

A disease risk index (DRI) has been defined for stratifying heterogeneous cohorts of patients undergoing allogeneic haematopoietic stem cell transplantation (HSCT). This index defines 4 distinct groups with different outcomes, dividing patients by disease type and status and considering cytogenetics for acute myeloid leukaemia and myelodysplastic syndromes (MDS). Recently, the DRI has been refined to include rare diseases and improve MDS stratification by blast percentage and response to prior therapy. Previous reports on DRI include only a small number of UCBT recipients. The current study aims to determine the applicability of the DRI for patients undergoing unrelated cord blood transplantation (UCBT). We retrospectively analysed 2530 adults receiving UCBT between 2004 and 2014. Diagnosis was acute leukaemia (AL) in 66% of the cases. Overall survival (OS) at 2 years was 56 ± 3% for patients with low DRI (n = 352), 46 ± 1% for intermediate DRI (n = 1403), 28 ± 2% for high (n = 489) and 20 ± 4% for very high DRI (n = 109) (P < 0·001). In the multivariate model, DRI remained an independent risk factor for OS. Similar findings were observed for PFS and DRI. Our results show the applicability of DRI for stratifying UCBT recipients and confirm the prognostic value of this simple and robust tool in this setting.<br /> (© 2017 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2141
Volume :
179
Issue :
5
Database :
MEDLINE
Journal :
British journal of haematology
Publication Type :
Academic Journal
Accession number :
29048109
Full Text :
https://doi.org/10.1111/bjh.14962