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Reduced intensity conditioned allograft yields favorable survival for older adults with B-cell acute lymphoblastic leukemia.

Identifieur interne : 001372 ( PubMed/Corpus ); précédent : 001371; suivant : 001373

Reduced intensity conditioned allograft yields favorable survival for older adults with B-cell acute lymphoblastic leukemia.

Auteurs : Ashley Rosko ; Hai-Lin Wang ; Marcos De Lima ; Brenda Sandmaier ; H Jean Khoury ; Andrew Artz ; Johnathan Brammer ; Christopher Bredeson ; Sherif Farag ; Mohamed Kharfan-Dabaja ; Hillard M. Lazarus ; David I. Marks ; Rodrigo Martino Bufarull ; Joseph Mcguirk ; Mohamed Mohty ; Taiga Nishihori ; Ian Nivison-Smith ; Armin Rashidi ; Olle Ringden ; Matthew Seftel ; Daniel Weisdorf ; Veronika Bachanova ; Wael Saber

Source :

RBID : pubmed:27712033

English descriptors

Abstract

Older adults with B-cell acute lymphoblastic leukemia (B-ALL) have poor survival. We examined the effectiveness of reduced intensity conditioning (RIC) hematopoietic cell transplant (HCT) in adults with B-ALL age 55 years and older and explored prognostic factors associated with long-term outcomes. Using CIBMTR registry data, we evaluated 273 patients (median age 61, range 55-72) with B-ALL with disease status in CR1 (71%), >CR2 (17%) and Primary Induction Failure (PIF)/Relapse (11%), who underwent RIC HCT between 2001 and 2012 using mostly unrelated donor (59%) or HLA-matched sibling (32%). Among patients with available cytogenetic data, the Philadelphia chromosome (Ph+) was present in 50%. The 3-year cumulative incidences of nonrelapse mortality (NRM) and relapse were 25% (95% confidence intervals (CI): 20-31%) and 47% (95% CI: 41-53%), respectively. Three-year overall survival (OS) was 38% (95% CI: 33-44%). Relapse remained the leading cause of death accounting for 49% of all deaths. In univariate analysis, 3 year risk of NRM was significantly higher with reduced Karnofsky performance status (KPS <90: 34% (95% CI: 25-43%) versus KPS ≥90 (18%; 95% CI: 12-24%, P = 0.006). Mortality was increased in older adults (66+ vs. 55-60: Relative Risk [RR] 1.51 95% CI: 1.00-2.29, P = 0.05) and those with advanced disease (RR 2.13; 95% CI: 1.36-3.34, P = 0.001). Survival of patients in CR1 yields 45% (95% CI: 38-52%) at 3 years and no relapse occurred after 2 years. We report promising OS and acceptable NRM using RIC HCT in older patients with B-ALL. Disease status in CR1 and good performance status are associated with improved outcomes. Am. J. Hematol. 92:42-49, 2017. © 2016 Wiley Periodicals, Inc.

DOI: 10.1002/ajh.24575
PubMed: 27712033

Links to Exploration step

pubmed:27712033

Le document en format XML

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<name sortKey="Mohty, Mohamed" sort="Mohty, Mohamed" uniqKey="Mohty M" first="Mohamed" last="Mohty">Mohamed Mohty</name>
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<name sortKey="Seftel, Matthew" sort="Seftel, Matthew" uniqKey="Seftel M" first="Matthew" last="Seftel">Matthew Seftel</name>
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<name sortKey="Bachanova, Veronika" sort="Bachanova, Veronika" uniqKey="Bachanova V" first="Veronika" last="Bachanova">Veronika Bachanova</name>
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<name sortKey="Saber, Wael" sort="Saber, Wael" uniqKey="Saber W" first="Wael" last="Saber">Wael Saber</name>
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<name sortKey="Artz, Andrew" sort="Artz, Andrew" uniqKey="Artz A" first="Andrew" last="Artz">Andrew Artz</name>
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<nlm:affiliation>Section of Hematology/Oncology, University of Chicago School of Medicine, Chicago, IL.</nlm:affiliation>
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<nlm:affiliation>The Ottawa Hospital Blood and Marrow Transplant Program and the Ottawa Hospital Research Institute, Ottawa, ON, Canada.</nlm:affiliation>
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<name sortKey="Farag, Sherif" sort="Farag, Sherif" uniqKey="Farag S" first="Sherif" last="Farag">Sherif Farag</name>
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<name sortKey="Kharfan Dabaja, Mohamed" sort="Kharfan Dabaja, Mohamed" uniqKey="Kharfan Dabaja M" first="Mohamed" last="Kharfan-Dabaja">Mohamed Kharfan-Dabaja</name>
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<nlm:affiliation>Department of Blood and Marrow Transplantation, H. Lee Moffit Cancer Center and Research Institute, Tampa, FL.</nlm:affiliation>
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<name sortKey="Lazarus, Hillard M" sort="Lazarus, Hillard M" uniqKey="Lazarus H" first="Hillard M" last="Lazarus">Hillard M. Lazarus</name>
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<name sortKey="Marks, David I" sort="Marks, David I" uniqKey="Marks D" first="David I" last="Marks">David I. Marks</name>
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<nlm:affiliation>Adult Bone Marrow Transplant, University Hospitals Bristol NHS Trust, Bristol, United Kingdom.</nlm:affiliation>
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<name sortKey="Bufarull, Rodrigo Martino" sort="Bufarull, Rodrigo Martino" uniqKey="Bufarull R" first="Rodrigo Martino" last="Bufarull">Rodrigo Martino Bufarull</name>
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<nlm:affiliation>Division of Clinical Hematology, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.</nlm:affiliation>
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<name sortKey="Mcguirk, Joseph" sort="Mcguirk, Joseph" uniqKey="Mcguirk J" first="Joseph" last="Mcguirk">Joseph Mcguirk</name>
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<name sortKey="Mohty, Mohamed" sort="Mohty, Mohamed" uniqKey="Mohty M" first="Mohamed" last="Mohty">Mohamed Mohty</name>
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<name sortKey="Nishihori, Taiga" sort="Nishihori, Taiga" uniqKey="Nishihori T" first="Taiga" last="Nishihori">Taiga Nishihori</name>
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<nlm:affiliation>Department of Blood and Marrow Transplantation, H. Lee Moffit Cancer Center and Research Institute, Tampa, FL.</nlm:affiliation>
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<name sortKey="Nivison Smith, Ian" sort="Nivison Smith, Ian" uniqKey="Nivison Smith I" first="Ian" last="Nivison-Smith">Ian Nivison-Smith</name>
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<nlm:affiliation>St. Vincent's Hospital, Darlinghurst, NSW, Australia.</nlm:affiliation>
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<name sortKey="Rashidi, Armin" sort="Rashidi, Armin" uniqKey="Rashidi A" first="Armin" last="Rashidi">Armin Rashidi</name>
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<nlm:affiliation>Barnes Jewish Hospital, St. Louis, MO.</nlm:affiliation>
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<name sortKey="Ringden, Olle" sort="Ringden, Olle" uniqKey="Ringden O" first="Olle" last="Ringden">Olle Ringden</name>
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<nlm:affiliation>Division of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.</nlm:affiliation>
</affiliation>
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<name sortKey="Seftel, Matthew" sort="Seftel, Matthew" uniqKey="Seftel M" first="Matthew" last="Seftel">Matthew Seftel</name>
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<nlm:affiliation>Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.</nlm:affiliation>
</affiliation>
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<name sortKey="Weisdorf, Daniel" sort="Weisdorf, Daniel" uniqKey="Weisdorf D" first="Daniel" last="Weisdorf">Daniel Weisdorf</name>
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<nlm:affiliation>Divsion of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota Medical Center, Minneapolis, MN.</nlm:affiliation>
</affiliation>
</author>
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<name sortKey="Bachanova, Veronika" sort="Bachanova, Veronika" uniqKey="Bachanova V" first="Veronika" last="Bachanova">Veronika Bachanova</name>
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<nlm:affiliation>Bone and Marrow Transplant Program, University of Minnesota Medical Center, Minneapolis, MN.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Saber, Wael" sort="Saber, Wael" uniqKey="Saber W" first="Wael" last="Saber">Wael Saber</name>
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<nlm:affiliation>CIBMTR (Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.</nlm:affiliation>
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<term>Disease-Free Survival</term>
<term>Female</term>
<term>Hematopoietic Stem Cell Transplantation (methods)</term>
<term>Humans</term>
<term>Kaplan-Meier Estimate</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Precursor B-Cell Lymphoblastic Leukemia-Lymphoma (epidemiology)</term>
<term>Precursor B-Cell Lymphoblastic Leukemia-Lymphoma (therapy)</term>
<term>Proportional Hazards Models</term>
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<term>Disease-Free Survival</term>
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<term>Humans</term>
<term>Kaplan-Meier Estimate</term>
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<front>
<div type="abstract" xml:lang="en">Older adults with B-cell acute lymphoblastic leukemia (B-ALL) have poor survival. We examined the effectiveness of reduced intensity conditioning (RIC) hematopoietic cell transplant (HCT) in adults with B-ALL age 55 years and older and explored prognostic factors associated with long-term outcomes. Using CIBMTR registry data, we evaluated 273 patients (median age 61, range 55-72) with B-ALL with disease status in CR1 (71%), >CR2 (17%) and Primary Induction Failure (PIF)/Relapse (11%), who underwent RIC HCT between 2001 and 2012 using mostly unrelated donor (59%) or HLA-matched sibling (32%). Among patients with available cytogenetic data, the Philadelphia chromosome (Ph+) was present in 50%. The 3-year cumulative incidences of nonrelapse mortality (NRM) and relapse were 25% (95% confidence intervals (CI): 20-31%) and 47% (95% CI: 41-53%), respectively. Three-year overall survival (OS) was 38% (95% CI: 33-44%). Relapse remained the leading cause of death accounting for 49% of all deaths. In univariate analysis, 3 year risk of NRM was significantly higher with reduced Karnofsky performance status (KPS <90: 34% (95% CI: 25-43%) versus KPS ≥90 (18%; 95% CI: 12-24%, P = 0.006). Mortality was increased in older adults (66+ vs. 55-60: Relative Risk [RR] 1.51 95% CI: 1.00-2.29, P = 0.05) and those with advanced disease (RR 2.13; 95% CI: 1.36-3.34, P = 0.001). Survival of patients in CR1 yields 45% (95% CI: 38-52%) at 3 years and no relapse occurred after 2 years. We report promising OS and acceptable NRM using RIC HCT in older patients with B-ALL. Disease status in CR1 and good performance status are associated with improved outcomes. Am. J. Hematol. 92:42-49, 2017. © 2016 Wiley Periodicals, Inc.</div>
</front>
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<Year>2016</Year>
<Month>10</Month>
<Day>06</Day>
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<AbstractText>Older adults with B-cell acute lymphoblastic leukemia (B-ALL) have poor survival. We examined the effectiveness of reduced intensity conditioning (RIC) hematopoietic cell transplant (HCT) in adults with B-ALL age 55 years and older and explored prognostic factors associated with long-term outcomes. Using CIBMTR registry data, we evaluated 273 patients (median age 61, range 55-72) with B-ALL with disease status in CR1 (71%), >CR2 (17%) and Primary Induction Failure (PIF)/Relapse (11%), who underwent RIC HCT between 2001 and 2012 using mostly unrelated donor (59%) or HLA-matched sibling (32%). Among patients with available cytogenetic data, the Philadelphia chromosome (Ph+) was present in 50%. The 3-year cumulative incidences of nonrelapse mortality (NRM) and relapse were 25% (95% confidence intervals (CI): 20-31%) and 47% (95% CI: 41-53%), respectively. Three-year overall survival (OS) was 38% (95% CI: 33-44%). Relapse remained the leading cause of death accounting for 49% of all deaths. In univariate analysis, 3 year risk of NRM was significantly higher with reduced Karnofsky performance status (KPS <90: 34% (95% CI: 25-43%) versus KPS ≥90 (18%; 95% CI: 12-24%, P = 0.006). Mortality was increased in older adults (66+ vs. 55-60: Relative Risk [RR] 1.51 95% CI: 1.00-2.29, P = 0.05) and those with advanced disease (RR 2.13; 95% CI: 1.36-3.34, P = 0.001). Survival of patients in CR1 yields 45% (95% CI: 38-52%) at 3 years and no relapse occurred after 2 years. We report promising OS and acceptable NRM using RIC HCT in older patients with B-ALL. Disease status in CR1 and good performance status are associated with improved outcomes. Am. J. Hematol. 92:42-49, 2017. © 2016 Wiley Periodicals, Inc.</AbstractText>
<CopyrightInformation>© 2016 Wiley Periodicals, Inc.</CopyrightInformation>
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<LastName>Rosko</LastName>
<ForeName>Ashley</ForeName>
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<Affiliation>James Cancer Center, Ohio State University, Columbus, OH.</Affiliation>
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<LastName>Wang</LastName>
<ForeName>Hai-Lin</ForeName>
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