Treatment, risk factors, and outcome of adults with relapsed AML after reduced intensity conditioning for allogeneic stem cell transplantation
Because information on management and outcome of AML relapse after allogeneic hematopoietic stem cell transplantation (HSCT) with reduced intensity conditioning (RIC) is scarce, a retrospective registry study was performed by the Acute Leukemia Working Party of EBMT. Among 2815 RIC transplants perfo...
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Published in | Blood Vol. 119; no. 6; pp. 1599 - 1606 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
Elsevier Inc
09.02.2012
Americain Society of Hematology |
Subjects | |
Online Access | Get full text |
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Abstract | Because information on management and outcome of AML relapse after allogeneic hematopoietic stem cell transplantation (HSCT) with reduced intensity conditioning (RIC) is scarce, a retrospective registry study was performed by the Acute Leukemia Working Party of EBMT. Among 2815 RIC transplants performed for AML in complete remission (CR) between 1999 and 2008, cumulative incidence of relapse was 32% ± 1%. Relapsed patients (263) were included into a detailed analysis of risk factors for overall survival (OS) and building of a prognostic score. CR was reinduced in 32%; remission duration after transplantation was the only prognostic factor for response (P = .003). Estimated 2-year OS from relapse was 14%, thereby resembling results of AML relapse after standard conditioning. Among variables available at the time of relapse, remission after HSCT > 5 months (hazard ratio [HR] = 0.50, 95% confidence interval [CI], 0.37-0.67, P < .001), bone marrow blasts less than 27% (HR = 0.53, 95% CI, 0.40-0.72, P < .001), and absence of acute GVHD after HSCT (HR = 0.67, 95% CI, 0.49-0.93, P = .017) were associated with better OS. Based on these factors, 3 prognostic groups could be discriminated, showing OS of 32% ± 7%, 19% ± 4%, and 4% ± 2% at 2 years (P < .0001). Long-term survival was achieved almost exclusively after successful induction of CR by cytoreductive therapy, followed either by donor lymphocyte infusion or second HSCT for consolidation. |
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AbstractList | Because information on management and outcome of AML relapse after allogeneic hematopoietic stem cell transplantation (HSCT) with reduced intensity conditioning (RIC) is scarce, a retrospective registry study was performed by the Acute Leukemia Working Party of EBMT. Among 2815 RIC transplants performed for AML in complete remission (CR) between 1999 and 2008, cumulative incidence of relapse was 32% ± 1%. Relapsed patients (263) were included into a detailed analysis of risk factors for overall survival (OS) and building of a prognostic score. CR was reinduced in 32%; remission duration after transplantation was the only prognostic factor for response (P = .003). Estimated 2-year OS from relapse was 14%, thereby resembling results of AML relapse after standard conditioning. Among variables available at the time of relapse, remission after HSCT > 5 months (hazard ratio [HR] = 0.50, 95% confidence interval [CI], 0.37-0.67, P < .001), bone marrow blasts less than 27% (HR = 0.53, 95% CI, 0.40-0.72, P < .001), and absence of acute GVHD after HSCT (HR = 0.67, 95% CI, 0.49-0.93, P = .017) were associated with better OS. Based on these factors, 3 prognostic groups could be discriminated, showing OS of 32% ± 7%, 19% ± 4%, and 4% ± 2% at 2 years (P < .0001). Long-term survival was achieved almost exclusively after successful induction of CR by cytoreductive therapy, followed either by donor lymphocyte infusion or second HSCT for consolidation. Abstract Because information on management and outcome of AML relapse after allogeneic hematopoietic stem cell transplantation (HSCT) with reduced intensity conditioning (RIC) is scarce, a retrospective registry study was performed by the Acute Leukemia Working Party of EBMT. Among 2815 RIC transplants performed for AML in complete remission (CR) between 1999 and 2008, cumulative incidence of relapse was 32% ± 1%. Relapsed patients (263) were included into a detailed analysis of risk factors for overall survival (OS) and building of a prognostic score. CR was reinduced in 32%; remission duration after transplantation was the only prognostic factor for response (P = .003). Estimated 2-year OS from relapse was 14%, thereby resembling results of AML relapse after standard conditioning. Among variables available at the time of relapse, remission after HSCT > 5 months (hazard ratio [HR] = 0.50, 95% confidence interval [CI], 0.37-0.67, P < .001), bone marrow blasts less than 27% (HR = 0.53, 95% CI, 0.40-0.72, P < .001), and absence of acute GVHD after HSCT (HR = 0.67, 95% CI, 0.49-0.93, P = .017) were associated with better OS. Based on these factors, 3 prognostic groups could be discriminated, showing OS of 32% ± 7%, 19% ± 4%, and 4% ± 2% at 2 years (P < .0001). Long-term survival was achieved almost exclusively after successful induction of CR by cytoreductive therapy, followed either by donor lymphocyte infusion or second HSCT for consolidation. |
Author | Ljungman, Per Falda, Michele Castagna, Luca Labopin, Myriam Schmid, Christoph Niederwieser, Dietger Jackson, Graham Polge, Emmanuelle Nagler, Arnon Rank, Andreas Tabrizi, Reza Stadler, Michael Vorlicek, Jiri Mohty, Mohamad Kuball, Jürgen Socié, Gerard Vindeløv, Lars Cornelissen, Jan Kröger, Nicolaus Rocha, Vanderson |
Author_xml | – sequence: 1 givenname: Christoph surname: Schmid fullname: Schmid, Christoph email: christoph.schmid@klinikum-augsburg.de organization: Klinikum Augsburg, University of Munich, Munich, Germany – sequence: 2 givenname: Myriam surname: Labopin fullname: Labopin, Myriam organization: EBMT Study Office, Faculté de Medicines St Antoine, Paris, France – sequence: 3 givenname: Arnon surname: Nagler fullname: Nagler, Arnon organization: Chaim Sheba Medical Center, Tel-Hashomer, Israel – sequence: 4 givenname: Dietger surname: Niederwieser fullname: Niederwieser, Dietger organization: University Hospital, Leipzig, Germany – sequence: 5 givenname: Luca surname: Castagna fullname: Castagna, Luca organization: Institute Paoli Calmettes, Marseilles, France – sequence: 6 givenname: Reza surname: Tabrizi fullname: Tabrizi, Reza organization: Centre Hospitalier Universitaire, Bordeaux, France – sequence: 7 givenname: Michael surname: Stadler fullname: Stadler, Michael organization: Michael Stadler Medizinische Hochschule, Hannover, Germany – sequence: 8 givenname: Jürgen surname: Kuball fullname: Kuball, Jürgen organization: University Medical Center, Utrecht, The Netherlands – sequence: 9 givenname: Jan surname: Cornelissen fullname: Cornelissen, Jan organization: Erasmus MC–Daniel den Hoed Cancer Centre, Rotterdam, The Netherlands – sequence: 10 givenname: Jiri surname: Vorlicek fullname: Vorlicek, Jiri organization: University Hospital, Brno, Czech Republik – sequence: 11 givenname: Gerard surname: Socié fullname: Socié, Gerard organization: Hôpital St Louis, Paris, France – sequence: 12 givenname: Michele surname: Falda fullname: Falda, Michele organization: Azienda Ospedaliera S. Giovanni, Torino, Italy – sequence: 13 givenname: Lars surname: Vindeløv fullname: Vindeløv, Lars organization: Rigshospitalet, Copenhagen, Denmark – sequence: 14 givenname: Per surname: Ljungman fullname: Ljungman, Per organization: Huddinge University Hospital, Huddinge, Sweden – sequence: 15 givenname: Graham surname: Jackson fullname: Jackson, Graham organization: Royal Victoria Infirmary, New Castle, United Kingdom – sequence: 16 givenname: Nicolaus surname: Kröger fullname: Kröger, Nicolaus organization: University Hospital Eppendorf, Hamburg, Germany – sequence: 17 givenname: Andreas surname: Rank fullname: Rank, Andreas organization: Klinikum Augsburg, University of Munich, Munich, Germany – sequence: 18 givenname: Emmanuelle surname: Polge fullname: Polge, Emmanuelle organization: EBMT Study Office, Faculté de Medicines St Antoine, Paris, France – sequence: 19 givenname: Vanderson surname: Rocha fullname: Rocha, Vanderson organization: Hôpital St Louis, Paris, France – sequence: 20 givenname: Mohamad surname: Mohty fullname: Mohty, Mohamad organization: Hôtel Dieu, University of Nantes, Nantes, France |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25518837$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/22167752$$D View this record in MEDLINE/PubMed http://kipublications.ki.se/Default.aspx?queryparsed=id:124068979$$DView record from Swedish Publication Index |
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Keywords | Human Acute myelogenous leukemia Relapse Prognosis Hematology Stem cell Hematopoietic cell Homograft Malignant hemopathy Non myeloablative treatment Epidemiology Treatment Allogeneic hematopoietic stem cell transplantation Risk factor Graft Adult Cancer |
Language | English |
License | This article is made available under the Elsevier license. CC BY 4.0 |
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Snippet | Because information on management and outcome of AML relapse after allogeneic hematopoietic stem cell transplantation (HSCT) with reduced intensity... Abstract Because information on management and outcome of AML relapse after allogeneic hematopoietic stem cell transplantation (HSCT) with reduced intensity... |
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SubjectTerms | Acute Disease Adolescent Adult Aged Biological and medical sciences Europe Female Hematologic and hematopoietic diseases Hematopoietic Stem Cell Transplantation - methods Humans Kaplan-Meier Estimate Leukemia, Myeloid - pathology Leukemia, Myeloid - surgery Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Medicin och hälsovetenskap Middle Aged Prognosis Recurrence Registries - statistics & numerical data Remission Induction Retrospective Studies Risk Factors Transplantation Conditioning - methods Transplantation, Homologous Treatment Outcome Young Adult |
Title | Treatment, risk factors, and outcome of adults with relapsed AML after reduced intensity conditioning for allogeneic stem cell transplantation |
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