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Outcomes following second allogeneic haematopoietic cell transplantation in patients with myelofibrosis: a retrospective study of the Chronic Malignancies Working Party of EBMT
M. Nabergoj, K. Mauff, M. Robin, N. Kröger, E. Angelucci, X. Poiré, J. Passweg, A. Radujkovic, U. Platzbecker, S. Robinson, A. Rambaldi, SL. Petersen, F. Stölzel, M. Stelljes, F. Ciceri, J. Mayer, M. Ladetto, LC. de Wreede, L. Koster, PJ. Hayden,...
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články
NLK
Free Medical Journals
od 1997 do Před 1 rokem
Freely Accessible Science Journals
od 1997 do Před 1 rokem
ProQuest Central
od 1997-01-01 do Před 1 rokem
Open Access Digital Library
od 1997-01-01
Health & Medicine (ProQuest)
od 1997-01-01 do Před 1 rokem
- MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory * MeSH
- nemoc štěpu proti hostiteli * MeSH
- primární myelofibróza * terapie MeSH
- příprava pacienta k transplantaci MeSH
- retrospektivní studie MeSH
- transplantace hematopoetických kmenových buněk * MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Therapeutic management of patients with primary or secondary myelofibrosis (MF) who experience relapse or graft failure following allogeneic haematopoietic cell transplantation (allo-HCT) remains heterogeneous. We retrospectively analyzed 216 patients undergoing a second allo-HCT for either relapse (56%) or graft failure (31%) between 2010 and 2017. Median age was 57.3 years (range 51-63). The same donor as for the first allo-HCT was chosen in 66 patients (31%) of whom 19 received an HLA-identical sibling donor, whereas a different donor was chosen for 116 patients (54%). Median follow-up was 40 months. Three-year overall survival (OS) and relapse-free survival (RFS) were 42% and 39%, respectively. Three-year non-relapse mortality (NRM) and relapse rates were 36% and 25%, respectively. Grade II-IV and III-IV acute GVHD occurred in 25% and 11% of patients, respectively, and the 3-year incidence of chronic GVHD was 33% including 14% for extensive grade. Graft-failure incidence at 1 year was 14%. In conclusion, our data suggest that a second allo-HCT is a potential option for patients failing first allo-HCT for MF albeit careful patient assessment is fundamental to identify individual patients who could benefit from this approach.
Bone Marrow Transplant Unit Copenhagen Denmark
Bristol Royal Hospital for Children Bristol UK
CHU de Lille univ Lille INSERM U1286 INFINITE 59000 Lille France
Cliniques Universitaires St Luc Brussels Belgium
Department of Biomedical Data Sciences Leiden University Medical Center Leiden the Netherlands
Department of Haematology Guy's and St Thomas' NHS Foundation Trust London UK
Department of Haematology Trinity College Dublin St James's Hospital Dublin Ireland
Department of Hematology and Cellular Therapy University Hospital of Leipzig Leipzig Germany
Department of Hematology Hospital Clínico Universitario Valencia Spain
EBMT Data Office Leiden the Netherlands
EBMT Statistical Unit Date Office Leiden the Netherlands
Ematologia e Centro Trapianti IRCCS Ospedale Policlinico San Martino Genova Italy
H SS Antonio e Biagio Alessandria Italy
Hôpital Saint Louis APHP Université Paris 7 Paris France
Maria Skłodowska Curie Institute Cancer Center Gliwice Branch Gliwice Poland
Ospedale San Raffaele Milano Italy
Universitaetsklinikum Dresden Dresden Germany
University Hospital Basel Switzerland
University Hospital Brno Brno Czech Republic
University Hospital Eppendorf Hamburg Germany
University of Heidelberg Heidelberg Germany
University of Milan and Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII Bergamo Italy
Citace poskytuje Crossref.org
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- $a Therapeutic management of patients with primary or secondary myelofibrosis (MF) who experience relapse or graft failure following allogeneic haematopoietic cell transplantation (allo-HCT) remains heterogeneous. We retrospectively analyzed 216 patients undergoing a second allo-HCT for either relapse (56%) or graft failure (31%) between 2010 and 2017. Median age was 57.3 years (range 51-63). The same donor as for the first allo-HCT was chosen in 66 patients (31%) of whom 19 received an HLA-identical sibling donor, whereas a different donor was chosen for 116 patients (54%). Median follow-up was 40 months. Three-year overall survival (OS) and relapse-free survival (RFS) were 42% and 39%, respectively. Three-year non-relapse mortality (NRM) and relapse rates were 36% and 25%, respectively. Grade II-IV and III-IV acute GVHD occurred in 25% and 11% of patients, respectively, and the 3-year incidence of chronic GVHD was 33% including 14% for extensive grade. Graft-failure incidence at 1 year was 14%. In conclusion, our data suggest that a second allo-HCT is a potential option for patients failing first allo-HCT for MF albeit careful patient assessment is fundamental to identify individual patients who could benefit from this approach.
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