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Long-term survival of patients with CLL after allogeneic transplantation: a report from the European Society for Blood and Marrow Transplantation
by
Potter, M
, Vitek, A
, Cornelissen, J J
, Kröger, N
, van Biezen, A
, Caballero, D
, de Wreede, L C
, Gramatzki, M
, Urbano-Ispízua, Á
, Anderson, N S
, Schetelig, J
, Putter, H
, Michallet, M
, van Gelder, M
, Yakoub-Agha, I
, Schönland, S
, Karas, M
, Beelen, D
, Blaise, D
, Niederwieser, D
, Russell, N H
, Henseler, A
, Bornhäuser, M
, Dreger, P
, Petersen, E
, Bunjes, D
, Chevallier, P
, Finke, J
, Volin, L
, Schoemans, H
in
692/308/174
/ 692/699/1541/1990/283/1895
/ Adolescent
/ Adult
/ Age Factors
/ Aged
/ Allografts
/ Bone marrow
/ Cancer treatment
/ Care and treatment
/ Cell Biology
/ Child
/ Chronic lymphocytic leukemia
/ Clinical Medicine
/ Confidence intervals
/ Disease-Free Survival
/ Europe - epidemiology
/ Female
/ Follow-Up Studies
/ Hematologi
/ Hematology
/ Hematopoietic Stem Cell Transplantation
/ Humans
/ Immunosuppressive agents
/ Internal Medicine
/ Klinisk medicin
/ Leukemia, Lymphocytic, Chronic, B-Cell - mortality
/ Leukemia, Lymphocytic, Chronic, B-Cell - therapy
/ Male
/ Medical and Health Sciences
/ Medicin och hälsovetenskap
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mortality
/ original-article
/ Patient outcomes
/ Patients
/ Public Health
/ Societies, Medical
/ Statistical analysis
/ Stem cell transplantation
/ Stem Cells
/ Survival
/ Survival analysis
/ Survival Rate
/ Time Factors
/ Transplantation
2017
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Long-term survival of patients with CLL after allogeneic transplantation: a report from the European Society for Blood and Marrow Transplantation
by
Potter, M
, Vitek, A
, Cornelissen, J J
, Kröger, N
, van Biezen, A
, Caballero, D
, de Wreede, L C
, Gramatzki, M
, Urbano-Ispízua, Á
, Anderson, N S
, Schetelig, J
, Putter, H
, Michallet, M
, van Gelder, M
, Yakoub-Agha, I
, Schönland, S
, Karas, M
, Beelen, D
, Blaise, D
, Niederwieser, D
, Russell, N H
, Henseler, A
, Bornhäuser, M
, Dreger, P
, Petersen, E
, Bunjes, D
, Chevallier, P
, Finke, J
, Volin, L
, Schoemans, H
in
692/308/174
/ 692/699/1541/1990/283/1895
/ Adolescent
/ Adult
/ Age Factors
/ Aged
/ Allografts
/ Bone marrow
/ Cancer treatment
/ Care and treatment
/ Cell Biology
/ Child
/ Chronic lymphocytic leukemia
/ Clinical Medicine
/ Confidence intervals
/ Disease-Free Survival
/ Europe - epidemiology
/ Female
/ Follow-Up Studies
/ Hematologi
/ Hematology
/ Hematopoietic Stem Cell Transplantation
/ Humans
/ Immunosuppressive agents
/ Internal Medicine
/ Klinisk medicin
/ Leukemia, Lymphocytic, Chronic, B-Cell - mortality
/ Leukemia, Lymphocytic, Chronic, B-Cell - therapy
/ Male
/ Medical and Health Sciences
/ Medicin och hälsovetenskap
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mortality
/ original-article
/ Patient outcomes
/ Patients
/ Public Health
/ Societies, Medical
/ Statistical analysis
/ Stem cell transplantation
/ Stem Cells
/ Survival
/ Survival analysis
/ Survival Rate
/ Time Factors
/ Transplantation
2017
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Do you wish to request the book?
Long-term survival of patients with CLL after allogeneic transplantation: a report from the European Society for Blood and Marrow Transplantation
by
Potter, M
, Vitek, A
, Cornelissen, J J
, Kröger, N
, van Biezen, A
, Caballero, D
, de Wreede, L C
, Gramatzki, M
, Urbano-Ispízua, Á
, Anderson, N S
, Schetelig, J
, Putter, H
, Michallet, M
, van Gelder, M
, Yakoub-Agha, I
, Schönland, S
, Karas, M
, Beelen, D
, Blaise, D
, Niederwieser, D
, Russell, N H
, Henseler, A
, Bornhäuser, M
, Dreger, P
, Petersen, E
, Bunjes, D
, Chevallier, P
, Finke, J
, Volin, L
, Schoemans, H
in
692/308/174
/ 692/699/1541/1990/283/1895
/ Adolescent
/ Adult
/ Age Factors
/ Aged
/ Allografts
/ Bone marrow
/ Cancer treatment
/ Care and treatment
/ Cell Biology
/ Child
/ Chronic lymphocytic leukemia
/ Clinical Medicine
/ Confidence intervals
/ Disease-Free Survival
/ Europe - epidemiology
/ Female
/ Follow-Up Studies
/ Hematologi
/ Hematology
/ Hematopoietic Stem Cell Transplantation
/ Humans
/ Immunosuppressive agents
/ Internal Medicine
/ Klinisk medicin
/ Leukemia, Lymphocytic, Chronic, B-Cell - mortality
/ Leukemia, Lymphocytic, Chronic, B-Cell - therapy
/ Male
/ Medical and Health Sciences
/ Medicin och hälsovetenskap
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mortality
/ original-article
/ Patient outcomes
/ Patients
/ Public Health
/ Societies, Medical
/ Statistical analysis
/ Stem cell transplantation
/ Stem Cells
/ Survival
/ Survival analysis
/ Survival Rate
/ Time Factors
/ Transplantation
2017
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Long-term survival of patients with CLL after allogeneic transplantation: a report from the European Society for Blood and Marrow Transplantation
Journal Article
Long-term survival of patients with CLL after allogeneic transplantation: a report from the European Society for Blood and Marrow Transplantation
2017
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Overview
Even with the availability of targeted drugs, allogeneic hematopoietic cell transplantation (allo-HCT) is the only therapy with curative potential for patients with CLL. Cure can be assessed by comparing long-term survival of patients to the matched general population. Using data from 2589 patients who received allo-HCT between 2000 and 2010, we used landmark analyses and methods from relative survival analysis to calculate excess mortality compared with an age-, sex- and calendar year-matched general population. Estimated event-free survival, overall survival and non-relapse mortality (NRM) 10 years after allo-HCT were 28% (95% confidence interval (CI), 25–31), 35% (95% CI, 32–38) and 40% (95% CI, 37–42), respectively. Patients who passed the 5-year landmark event-free survival (
N
=394) had a 79% probability (95% CI, 73–85) of surviving the subsequent 5 years without an event. Relapse and NRM contributed equally to treatment failure. Five-year mortality for 45- and 65-year-old reference patients who were event-free at the 5-year landmark was 8% and 47% compared with 3% and 14% in the matched general population, respectively. The prospect of long-term disease-free survival remains an argument to consider allo-HCT for young patients with high-risk CLL, and programs to understand and prevent late causes of failure for long-term survivors are warranted, especially for older patients.
Publisher
Nature Publishing Group UK,Nature Publishing Group
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