Unrelated marrow transplantation for children with acute lymphoblastic leukemia in second remission
Allogeneic bone marrow transplantation (BMT) may be curative for more patients than chemotherapy for the child with relapsed acute lymphoblastic leukemia. This study reviewed the outcomes of 363 children with acute lymphoblastic leukemia in second remission who received unrelated donor BMT from 1988...
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Veröffentlicht in: | Blood 2002-05, Vol.99 (9), p.3151-3157 |
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description | Allogeneic bone marrow transplantation (BMT) may be curative for more patients than chemotherapy for the child with relapsed acute lymphoblastic leukemia. This study reviewed the outcomes of 363 children with acute lymphoblastic leukemia in second remission who received unrelated donor BMT from 1988 to 2000 in order to define prognostic factors that affect leukemia-free survival (LFS). Median patient age was 9 years (range, 0-19 years), and median follow-up 29 was months (range, 0-125 months). The median duration of first remission was 24 months (range, 0-109 months). Prognostic factors, including age, duration of first remission, HLA matching, and graft-versus-host (GVH) disease, were analyzed using both univariate and multivariate analyses. Overall survival was 38%, and LFS was 36% at 5 years. LFS was significantly worse for patients 15 years or older (log-rank, P = .009). HLA matching was associated with improved LFS. Acute GVH disease developed in 71%, with 29% having grades III-IV. The incidence of chronic GVH disease was 39% for patients who survived more than 80 days and was significantly higher for female patients receiving marrow from female donors (P = .0009). Transplantation-related mortality was 42% and was associated with HLA mismatches, age 15 years and older, and first remission less than 12 months. The 5-year estimate for relapse was 22%, with first remission at least 6 months associated with a lower risk. Results of unrelated donor BMT appear similar to multi-institutional studies of matched related donor BMT, and this approach appears to be curative for many patients. However, innovative approaches are needed for patients with initial remissions of less than 6 months and for older teenagers. |
doi_str_mv | 10.1182/blood.V99.9.3151 |
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This study reviewed the outcomes of 363 children with acute lymphoblastic leukemia in second remission who received unrelated donor BMT from 1988 to 2000 in order to define prognostic factors that affect leukemia-free survival (LFS). Median patient age was 9 years (range, 0-19 years), and median follow-up 29 was months (range, 0-125 months). The median duration of first remission was 24 months (range, 0-109 months). Prognostic factors, including age, duration of first remission, HLA matching, and graft-versus-host (GVH) disease, were analyzed using both univariate and multivariate analyses. Overall survival was 38%, and LFS was 36% at 5 years. LFS was significantly worse for patients 15 years or older (log-rank, P = .009). HLA matching was associated with improved LFS. Acute GVH disease developed in 71%, with 29% having grades III-IV. The incidence of chronic GVH disease was 39% for patients who survived more than 80 days and was significantly higher for female patients receiving marrow from female donors (P = .0009). Transplantation-related mortality was 42% and was associated with HLA mismatches, age 15 years and older, and first remission less than 12 months. The 5-year estimate for relapse was 22%, with first remission at least 6 months associated with a lower risk. Results of unrelated donor BMT appear similar to multi-institutional studies of matched related donor BMT, and this approach appears to be curative for many patients. However, innovative approaches are needed for patients with initial remissions of less than 6 months and for older teenagers.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.V99.9.3151</identifier><identifier>PMID: 11964277</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Age Factors ; Analysis of Variance ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Bone Marrow Transplantation - immunology ; Bone Marrow Transplantation - mortality ; Bone marrow, stem cells transplantation. Graft versus host reaction ; Child ; Child, Preschool ; Disease-Free Survival ; Graft vs Host Disease - mortality ; Hematologic and hematopoietic diseases ; Histocompatibility ; Humans ; Infant ; Infant, Newborn ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Medical sciences ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy ; Prognosis ; Remission Induction ; Retrospective Studies ; Survival Rate ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy ; Transplantation, Homologous - immunology ; Transplantation, Homologous - mortality</subject><ispartof>Blood, 2002-05, Vol.99 (9), p.3151-3157</ispartof><rights>2002 American Society of Hematology</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-39a89f7d8f90c0cbb45dc920d23120a6cccffd03b8e68c388571ed3936d854b63</citedby><cites>FETCH-LOGICAL-c418t-39a89f7d8f90c0cbb45dc920d23120a6cccffd03b8e68c388571ed3936d854b63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13623482$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11964277$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bunin, Nancy</creatorcontrib><creatorcontrib>Carston, Michael</creatorcontrib><creatorcontrib>Wall, Donna</creatorcontrib><creatorcontrib>Adams, Roberta</creatorcontrib><creatorcontrib>Casper, James</creatorcontrib><creatorcontrib>Kamani, Naynesh</creatorcontrib><creatorcontrib>King, Roberta</creatorcontrib><creatorcontrib>National Marrow Donor Program Working Group</creatorcontrib><creatorcontrib>the National Marrow Donor Program Working Group</creatorcontrib><title>Unrelated marrow transplantation for children with acute lymphoblastic leukemia in second remission</title><title>Blood</title><addtitle>Blood</addtitle><description>Allogeneic bone marrow transplantation (BMT) may be curative for more patients than chemotherapy for the child with relapsed acute lymphoblastic leukemia. This study reviewed the outcomes of 363 children with acute lymphoblastic leukemia in second remission who received unrelated donor BMT from 1988 to 2000 in order to define prognostic factors that affect leukemia-free survival (LFS). Median patient age was 9 years (range, 0-19 years), and median follow-up 29 was months (range, 0-125 months). The median duration of first remission was 24 months (range, 0-109 months). Prognostic factors, including age, duration of first remission, HLA matching, and graft-versus-host (GVH) disease, were analyzed using both univariate and multivariate analyses. Overall survival was 38%, and LFS was 36% at 5 years. LFS was significantly worse for patients 15 years or older (log-rank, P = .009). HLA matching was associated with improved LFS. Acute GVH disease developed in 71%, with 29% having grades III-IV. The incidence of chronic GVH disease was 39% for patients who survived more than 80 days and was significantly higher for female patients receiving marrow from female donors (P = .0009). Transplantation-related mortality was 42% and was associated with HLA mismatches, age 15 years and older, and first remission less than 12 months. The 5-year estimate for relapse was 22%, with first remission at least 6 months associated with a lower risk. Results of unrelated donor BMT appear similar to multi-institutional studies of matched related donor BMT, and this approach appears to be curative for many patients. However, innovative approaches are needed for patients with initial remissions of less than 6 months and for older teenagers.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Analysis of Variance</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Transplantation - immunology</subject><subject>Bone Marrow Transplantation - mortality</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Disease-Free Survival</subject><subject>Graft vs Host Disease - mortality</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Histocompatibility</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Medical sciences</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy</subject><subject>Prognosis</subject><subject>Remission Induction</subject><subject>Retrospective Studies</subject><subject>Survival Rate</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><subject>Transplantation, Homologous - immunology</subject><subject>Transplantation, Homologous - mortality</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kD1PHDEQhq0oKFxI-lTITdLt4Y_9sOkQCgkSEg2ktbzjWZ0T3_qwvSD-PYY7iSrVaKTnfTXzEPKNszXnSpyNIUa3_qP1Wq8l7_gHsuKdUA1jgn0kK8ZY37R64Mfkc85_GeOtFN0ncsy57lsxDCsC93PCYAs6urUpxSdakp3zLti52OLjTKeYKGx8cAln-uTLhlpYCtLwvN1t4hhsLh5owOUfbr2lfqYZIc6OprrnXCu-kKPJhoxfD_OE3F_9vLv83dzc_rq-vLhpoOWqNFJbpafBqUkzYDCObedAC-aE5ILZHgCmyTE5KuwVSKW6gaOTWvZOde3YyxPyY9-7S_FhwVxMPQAw1F8wLtkMvBeDbrsKsj0IKeaccDK75Ov7z4Yz8yrWvIk1VazR5lVsjZweupdxi-49cDBZge8HwGawYaoWwed3TvZCtkpU7nzPYTXx6DGZDB5nQOcTQjEu-v9f8QK3TZi8</recordid><startdate>20020501</startdate><enddate>20020501</enddate><creator>Bunin, Nancy</creator><creator>Carston, Michael</creator><creator>Wall, Donna</creator><creator>Adams, Roberta</creator><creator>Casper, James</creator><creator>Kamani, Naynesh</creator><creator>King, Roberta</creator><general>Elsevier Inc</general><general>The Americain Society of Hematology</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20020501</creationdate><title>Unrelated marrow transplantation for children with acute lymphoblastic leukemia in second remission</title><author>Bunin, Nancy ; Carston, Michael ; Wall, Donna ; Adams, Roberta ; Casper, James ; Kamani, Naynesh ; King, Roberta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-39a89f7d8f90c0cbb45dc920d23120a6cccffd03b8e68c388571ed3936d854b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Analysis of Variance</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Transplantation - immunology</topic><topic>Bone Marrow Transplantation - mortality</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Disease-Free Survival</topic><topic>Graft vs Host Disease - mortality</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Histocompatibility</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Medical sciences</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy</topic><topic>Prognosis</topic><topic>Remission Induction</topic><topic>Retrospective Studies</topic><topic>Survival Rate</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><topic>Transplantation, Homologous - immunology</topic><topic>Transplantation, Homologous - mortality</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bunin, Nancy</creatorcontrib><creatorcontrib>Carston, Michael</creatorcontrib><creatorcontrib>Wall, Donna</creatorcontrib><creatorcontrib>Adams, Roberta</creatorcontrib><creatorcontrib>Casper, James</creatorcontrib><creatorcontrib>Kamani, Naynesh</creatorcontrib><creatorcontrib>King, Roberta</creatorcontrib><creatorcontrib>National Marrow Donor Program Working Group</creatorcontrib><creatorcontrib>the National Marrow Donor Program Working Group</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bunin, Nancy</au><au>Carston, Michael</au><au>Wall, Donna</au><au>Adams, Roberta</au><au>Casper, James</au><au>Kamani, Naynesh</au><au>King, Roberta</au><aucorp>National Marrow Donor Program Working Group</aucorp><aucorp>the National Marrow Donor Program Working Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unrelated marrow transplantation for children with acute lymphoblastic leukemia in second remission</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2002-05-01</date><risdate>2002</risdate><volume>99</volume><issue>9</issue><spage>3151</spage><epage>3157</epage><pages>3151-3157</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Allogeneic bone marrow transplantation (BMT) may be curative for more patients than chemotherapy for the child with relapsed acute lymphoblastic leukemia. This study reviewed the outcomes of 363 children with acute lymphoblastic leukemia in second remission who received unrelated donor BMT from 1988 to 2000 in order to define prognostic factors that affect leukemia-free survival (LFS). Median patient age was 9 years (range, 0-19 years), and median follow-up 29 was months (range, 0-125 months). The median duration of first remission was 24 months (range, 0-109 months). Prognostic factors, including age, duration of first remission, HLA matching, and graft-versus-host (GVH) disease, were analyzed using both univariate and multivariate analyses. Overall survival was 38%, and LFS was 36% at 5 years. LFS was significantly worse for patients 15 years or older (log-rank, P = .009). HLA matching was associated with improved LFS. Acute GVH disease developed in 71%, with 29% having grades III-IV. The incidence of chronic GVH disease was 39% for patients who survived more than 80 days and was significantly higher for female patients receiving marrow from female donors (P = .0009). Transplantation-related mortality was 42% and was associated with HLA mismatches, age 15 years and older, and first remission less than 12 months. The 5-year estimate for relapse was 22%, with first remission at least 6 months associated with a lower risk. Results of unrelated donor BMT appear similar to multi-institutional studies of matched related donor BMT, and this approach appears to be curative for many patients. However, innovative approaches are needed for patients with initial remissions of less than 6 months and for older teenagers.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>11964277</pmid><doi>10.1182/blood.V99.9.3151</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Age Factors Analysis of Variance Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Bone Marrow Transplantation - immunology Bone Marrow Transplantation - mortality Bone marrow, stem cells transplantation. Graft versus host reaction Child Child, Preschool Disease-Free Survival Graft vs Host Disease - mortality Hematologic and hematopoietic diseases Histocompatibility Humans Infant Infant, Newborn Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Medical sciences Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy Prognosis Remission Induction Retrospective Studies Survival Rate Transfusions. Complications. Transfusion reactions. Cell and gene therapy Transplantation, Homologous - immunology Transplantation, Homologous - mortality |
title | Unrelated marrow transplantation for children with acute lymphoblastic leukemia in second remission |
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