dc.contributor.author | Guièze, R. | |
dc.contributor.author | Eikema, D.-J. | |
dc.contributor.author | Koster, L. | |
dc.contributor.author | Schetelig, J. | |
dc.contributor.author | Sengeloev, H. | |
dc.contributor.author | Passweg, J. | |
dc.contributor.author | Finke, J. | |
dc.date.accessioned | 2025-01-12T18:55:07Z | |
dc.date.available | 2025-01-12T18:55:07Z | |
dc.date.issued | 2024 | |
dc.identifier.issn | 0268-3369 | |
dc.identifier.uri | https://doi.org/10.1038/s41409-024-02256-9 | |
dc.identifier.uri | http://hdl.handle.net/11446/5060 | |
dc.description.abstract | Management of Richter transformation (RT) is particularly challenging, with survival estimates <1 year. We report on outcomes of 66 RT patients undergoing allogeneic-HCT (allo-HCT) between 2008 and 2018 registered with the EBMT. Median age at allo-HCT was 56.2 years (interquartile range (IQR), 51.3–63.1). Median time from RT to allo-HCT was 6.9 months (IQR, 4.9–11) and 28 (42.4%) were in complete remission (CR). The majority underwent reduced intensity conditioning (66.2%) using peripheral blood derived stem cells. Eighteen (27.3%) patients had a matched sibling donor, 24 (36.4%) a matched unrelated donor and the remaining were mismatched. Median follow-up was 6.6 years; 1- and 3- year overall and progression free survival (PFS) (95% CI) was 65% (54–77) and 39% (27–51) and 53% (41–65) and 29% (18–40), respectively. Patients in CR at time of allo-HCT had significantly better 3-year PFS (39% vs. 21%, p = 0.032). Cumulative incidences of grade II–IV acute graft versus host disease (GVHD) at day +100 was 41% (95% CI 29–53) and chronic GVHD at 3 years was 53% (95% CI 41–65). High rates of non-relapse mortality (NRM) were observed; 38% (95% CI, 26–50) at 3 years. Although potentially curative, approaches to reduce considerable NRM and chronic GVHD rates are required. © The Author(s), under exclusive licence to Springer Nature Limited 2024. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Springer Nature | en_US |
dc.relation.ispartof | Bone Marrow Transplantation | en_US |
dc.identifier.doi | 10.1038/s41409-024-02256-9 | |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Adult | en_US |
dc.subject | Allografts | en_US |
dc.subject | Female | en_US |
dc.subject | Graft vs Host Disease | en_US |
dc.subject | Hematopoietic Stem Cell Transplantation | en_US |
dc.subject | Humans | en_US |
dc.subject | Male | en_US |
dc.subject | Middle Aged | en_US |
dc.subject | Retrospective Studies | en_US |
dc.subject | Transplantation Conditioning | en_US |
dc.subject | Transplantation, Homologous | en_US |
dc.subject | acalabrutinib | en_US |
dc.subject | alemtuzumab | en_US |
dc.subject | cyclophosphamide | en_US |
dc.subject | cyclophosphamide plus doxorubicin plus prednisolone plus rituximab plus vincristine | en_US |
dc.subject | cyclosporine | en_US |
dc.subject | fludarabine | en_US |
dc.subject | ibrutinib | en_US |
dc.subject | idelalisib | en_US |
dc.subject | melphalan | en_US |
dc.subject | mycophenolate mofetil | en_US |
dc.subject | venetoclax | en_US |
dc.subject | acute graft versus host disease | en_US |
dc.subject | adult | en_US |
dc.subject | allogeneic hematopoietic stem cell transplantation | en_US |
dc.subject | Article | en_US |
dc.subject | chronic graft versus host disease | en_US |
dc.subject | chronic lymphatic leukemia | en_US |
dc.subject | Chronic Malignancies Working Party of the EBMT | en_US |
dc.subject | diffuse large B cell lymphoma | en_US |
dc.subject | female | en_US |
dc.subject | follow up | en_US |
dc.subject | graft versus host reaction | en_US |
dc.subject | histology | en_US |
dc.subject | Hodgkin disease | en_US |
dc.subject | human | en_US |
dc.subject | Karnofsky Performance Status | en_US |
dc.subject | male | en_US |
dc.subject | matched sibling donor | en_US |
dc.subject | matched unrelated donor | en_US |
dc.subject | medical society | en_US |
dc.subject | mortality | en_US |
dc.subject | multicenter study | en_US |
dc.subject | neutrophil count | en_US |
dc.subject | overall survival | en_US |
dc.subject | posttransplant lymphoproliferative disease | en_US |
dc.subject | progression free survival | en_US |
dc.subject | questionnaire | en_US |
dc.subject | reduced intensity conditioning | en_US |
dc.subject | relapse | en_US |
dc.subject | retrospective study | en_US |
dc.subject | Richter syndrome | en_US |
dc.subject | treatment response | en_US |
dc.subject | allograft | en_US |
dc.subject | allotransplantation | en_US |
dc.subject | hematopoietic stem cell transplantation | en_US |
dc.subject | middle aged | en_US |
dc.subject | procedures | en_US |
dc.subject | transplantation conditioning | en_US |
dc.title | Allogeneic hematopoietic stem-cell transplantation for patients with Richter transformation: a retrospective study on behalf of the Chronic Malignancies Working Party of the EBMT | en_US |
dc.type | article | en_US |
dc.department | DBÜ | en_US |
dc.identifier.issue | 7 | en_US |
dc.identifier.volume | 59 | en_US |
dc.identifier.startpage | 950 | en_US |
dc.identifier.endpage | 956 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.department-temp | Guièze R., CHU Estaing, Clermont-Ferrand University Hospital, Clermont-Ferrand, France; Eikema D.-J., EBMT Statistical Unit, Leiden, Netherlands; Koster L., EBMT Leiden Study Unit, Leiden, Netherlands; Schetelig J., University Hospital Dresden, Dresden, Germany; Sengeloev H., Rigshospitalet, Copenhagen, Denmark; Passweg J., University Hospital Basel, Basel, Switzerland; Finke J., University of Freiburg, Freiburg, Germany; Arat M., Demiroglu Bilim University Istanbul Florence Nightingale Hospital, Istanbul, Turkey; Broers A.E.C., Erasmus MC Cancer Institute, Rotterdam, Netherlands; Stölzel F., Department of Medicine II, Division for Stem Cell Transplantation and Cellular Immunotherapy, University Hospital Schleswig-Holstein Kiel, Kiel University, Kiel, Germany; Byrne J., Nottingham University, Nottingham, United Kingdom; Castilla-Llorente C., Gustave Roussy Cancer Campus, Villejuif, France; Dreger P., University of Heidelberg, Heidelberg, Germany; Eder M., Hannover Medical School, Hannover, Germany; Gedde-Dahl T., Oslo University Hospital, Rikshospitalet, Oslo, Norway; Kröger N., University Hospital Eppendorf, Hamburg, Germany; Ribera Santasusana J.M., ICO-Hospital Universitari Germans Trias i Pujol, Badalona, Spain; Richardson D., | en_US |
dc.identifier.pmid | 38503942 | en_US |
dc.identifier.scopus | 2-s2.0-85188059146 | en_US |
dc.authorscopusid | 8691824900 | |
dc.authorscopusid | 57216508282 | |
dc.authorscopusid | 57194647248 | |
dc.authorscopusid | 6602851628 | |
dc.authorscopusid | 57205523598 | |
dc.authorscopusid | 35243190200 | |
dc.authorscopusid | 55636592100 | |