Impact of prior imatinib mesylate on the outcome of hematopoietic cell transplantation for chronic myeloid leukemia
Imatinib mesylate (IM, Gleevec) has largely supplanted allogeneic hematopoietic cell transplantation (HCT) as first line therapy for chronic myeloid leukemia (CML). Nevertheless, many people with CML eventually undergo HCT, raising the question of whether prior IM therapy impacts HCT success. Data f...
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creator | Lee, Stephanie J. Kukreja, Manisha Wang, Tao Giralt, Sergio A. Szer, Jeffrey Arora, Mukta Woolfrey, Ann E. Cervantes, Francisco Champlin, Richard E. Gale, Robert Peter Halter, Joerg Keating, Armand Marks, David I. McCarthy, Philip L. Olavarria, Eduardo Stadtmauer, Edward A. Abecasis, Manuel Gupta, Vikas Khoury, H. Jean George, Biju Hale, Gregory A. Liesveld, Jane L. Rizzieri, David A. Antin, Joseph H. Bolwell, Brian J. Carabasi, Matthew H. Copelan, Edward Ilhan, Osman Litzow, Mark R. Schouten, Harold C. Zander, Axel R. Horowitz, Mary M. Maziarz, Richard T. |
description | Imatinib mesylate (IM, Gleevec) has largely supplanted allogeneic hematopoietic cell transplantation (HCT) as first line therapy for chronic myeloid leukemia (CML). Nevertheless, many people with CML eventually undergo HCT, raising the question of whether prior IM therapy impacts HCT success. Data from the Center for International Blood and Marrow Transplant Research on 409 subjects treated with IM before HCT (IM+) and 900 subjects who did not receive IM before HCT (IM−) were analyzed. Among patients in first chronic phase, IM therapy before HCT was associated with better survival but no statistically significant differences in treatment-related mortality, relapse, and leukemia-free survival. Better HLA-matched donors, use of bone marrow, and transplantation within one year of diagnosis were also associated with better survival. A matched-pairs analysis was performed and confirmed a higher survival rate among first chronic phase patients receiving IM. Among patients transplanted with advanced CML, use of IM before HCT was not associated with treatment-related mortality, relapse, leukemia-free survival, or survival. Acute graft-versus-host disease rates were similar between IM+ and IM− groups regardless of leukemia phase. These results should be reassuring to patients receiving IM before HCT. |
doi_str_mv | 10.1182/blood-2008-02-141689 |
format | Article |
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Jean ; George, Biju ; Hale, Gregory A. ; Liesveld, Jane L. ; Rizzieri, David A. ; Antin, Joseph H. ; Bolwell, Brian J. ; Carabasi, Matthew H. ; Copelan, Edward ; Ilhan, Osman ; Litzow, Mark R. ; Schouten, Harold C. ; Zander, Axel R. ; Horowitz, Mary M. ; Maziarz, Richard T.</creator><creatorcontrib>Lee, Stephanie J. ; Kukreja, Manisha ; Wang, Tao ; Giralt, Sergio A. ; Szer, Jeffrey ; Arora, Mukta ; Woolfrey, Ann E. ; Cervantes, Francisco ; Champlin, Richard E. ; Gale, Robert Peter ; Halter, Joerg ; Keating, Armand ; Marks, David I. ; McCarthy, Philip L. ; Olavarria, Eduardo ; Stadtmauer, Edward A. ; Abecasis, Manuel ; Gupta, Vikas ; Khoury, H. Jean ; George, Biju ; Hale, Gregory A. ; Liesveld, Jane L. ; Rizzieri, David A. ; Antin, Joseph H. ; Bolwell, Brian J. ; Carabasi, Matthew H. ; Copelan, Edward ; Ilhan, Osman ; Litzow, Mark R. ; Schouten, Harold C. ; Zander, Axel R. ; Horowitz, Mary M. ; Maziarz, Richard T.</creatorcontrib><description>Imatinib mesylate (IM, Gleevec) has largely supplanted allogeneic hematopoietic cell transplantation (HCT) as first line therapy for chronic myeloid leukemia (CML). Nevertheless, many people with CML eventually undergo HCT, raising the question of whether prior IM therapy impacts HCT success. Data from the Center for International Blood and Marrow Transplant Research on 409 subjects treated with IM before HCT (IM+) and 900 subjects who did not receive IM before HCT (IM−) were analyzed. Among patients in first chronic phase, IM therapy before HCT was associated with better survival but no statistically significant differences in treatment-related mortality, relapse, and leukemia-free survival. Better HLA-matched donors, use of bone marrow, and transplantation within one year of diagnosis were also associated with better survival. A matched-pairs analysis was performed and confirmed a higher survival rate among first chronic phase patients receiving IM. Among patients transplanted with advanced CML, use of IM before HCT was not associated with treatment-related mortality, relapse, leukemia-free survival, or survival. Acute graft-versus-host disease rates were similar between IM+ and IM− groups regardless of leukemia phase. These results should be reassuring to patients receiving IM before HCT.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2008-02-141689</identifier><identifier>PMID: 18664621</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Antineoplastic Agents - therapeutic use ; Benzamides ; Biological and medical sciences ; Child ; Child, Preschool ; Disease-Free Survival ; Female ; Hematologic and hematopoietic diseases ; Hematopoietic Stem Cell Transplantation - methods ; HLA Antigens - metabolism ; Humans ; Imatinib Mesylate ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - therapy ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Middle Aged ; Piperazines - therapeutic use ; Pyrimidines - therapeutic use ; Registries ; Transplantation ; Treatment Outcome</subject><ispartof>Blood, 2008-10, Vol.112 (8), p.3500-3507</ispartof><rights>2008 American Society of Hematology</rights><rights>2009 INIST-CNRS</rights><rights>2008 by The American Society of Hematology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c557t-4685f5c6224f657efac0c255747823916d484b4e97af5f419d62a7d7c26e68843</citedby><cites>FETCH-LOGICAL-c557t-4685f5c6224f657efac0c255747823916d484b4e97af5f419d62a7d7c26e68843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20791780$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18664621$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Stephanie J.</creatorcontrib><creatorcontrib>Kukreja, Manisha</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Giralt, Sergio A.</creatorcontrib><creatorcontrib>Szer, Jeffrey</creatorcontrib><creatorcontrib>Arora, Mukta</creatorcontrib><creatorcontrib>Woolfrey, Ann E.</creatorcontrib><creatorcontrib>Cervantes, Francisco</creatorcontrib><creatorcontrib>Champlin, Richard E.</creatorcontrib><creatorcontrib>Gale, Robert Peter</creatorcontrib><creatorcontrib>Halter, Joerg</creatorcontrib><creatorcontrib>Keating, Armand</creatorcontrib><creatorcontrib>Marks, David I.</creatorcontrib><creatorcontrib>McCarthy, Philip L.</creatorcontrib><creatorcontrib>Olavarria, Eduardo</creatorcontrib><creatorcontrib>Stadtmauer, Edward A.</creatorcontrib><creatorcontrib>Abecasis, Manuel</creatorcontrib><creatorcontrib>Gupta, Vikas</creatorcontrib><creatorcontrib>Khoury, H. Jean</creatorcontrib><creatorcontrib>George, Biju</creatorcontrib><creatorcontrib>Hale, Gregory A.</creatorcontrib><creatorcontrib>Liesveld, Jane L.</creatorcontrib><creatorcontrib>Rizzieri, David A.</creatorcontrib><creatorcontrib>Antin, Joseph H.</creatorcontrib><creatorcontrib>Bolwell, Brian J.</creatorcontrib><creatorcontrib>Carabasi, Matthew H.</creatorcontrib><creatorcontrib>Copelan, Edward</creatorcontrib><creatorcontrib>Ilhan, Osman</creatorcontrib><creatorcontrib>Litzow, Mark R.</creatorcontrib><creatorcontrib>Schouten, Harold C.</creatorcontrib><creatorcontrib>Zander, Axel R.</creatorcontrib><creatorcontrib>Horowitz, Mary M.</creatorcontrib><creatorcontrib>Maziarz, Richard T.</creatorcontrib><title>Impact of prior imatinib mesylate on the outcome of hematopoietic cell transplantation for chronic myeloid leukemia</title><title>Blood</title><addtitle>Blood</addtitle><description>Imatinib mesylate (IM, Gleevec) has largely supplanted allogeneic hematopoietic cell transplantation (HCT) as first line therapy for chronic myeloid leukemia (CML). Nevertheless, many people with CML eventually undergo HCT, raising the question of whether prior IM therapy impacts HCT success. Data from the Center for International Blood and Marrow Transplant Research on 409 subjects treated with IM before HCT (IM+) and 900 subjects who did not receive IM before HCT (IM−) were analyzed. Among patients in first chronic phase, IM therapy before HCT was associated with better survival but no statistically significant differences in treatment-related mortality, relapse, and leukemia-free survival. Better HLA-matched donors, use of bone marrow, and transplantation within one year of diagnosis were also associated with better survival. A matched-pairs analysis was performed and confirmed a higher survival rate among first chronic phase patients receiving IM. Among patients transplanted with advanced CML, use of IM before HCT was not associated with treatment-related mortality, relapse, leukemia-free survival, or survival. Acute graft-versus-host disease rates were similar between IM+ and IM− groups regardless of leukemia phase. These results should be reassuring to patients receiving IM before HCT.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Benzamides</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hematopoietic Stem Cell Transplantation - methods</subject><subject>HLA Antigens - metabolism</subject><subject>Humans</subject><subject>Imatinib Mesylate</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - therapy</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Piperazines - therapeutic use</subject><subject>Pyrimidines - therapeutic use</subject><subject>Registries</subject><subject>Transplantation</subject><subject>Treatment Outcome</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU-PFCEQxYnRuOPqNzCGi95ageFfX0zMZtVNNvGiZ8LQhYNC0wK9yXx7GWeyqxdPlVC_96iqh9BLSt5Sqtm7Xcx5GhgheiBsoJxKPT5CGypYfyCMPEYbQogc-KjoBXpW6w9CKN8y8RRdUC0ll4xuUL1Ji3UNZ4-XEnLBIdkW5rDDCeoh2gY4z7jte1mbywmO5B46lJccoAWHHcSIW7FzXaKdW5d3he9Wbl_y3IF0gJjDhCOsPyEF-xw98TZWeHGul-jbx-uvV5-H2y-fbq4-3A5OCNUGLrXwwknGuJdCgbeOONZbXGm2HamcuOY7DqOyXnhOx0kyqyblmASpNd9eovcn32XdJZgczH3KaPqeyZaDyTaYfztz2Jvv-c6wUXAlaDd4czYo-dcKtZkU6nFdO0Neq5Gj5Jwz0kF-Al3JtRbw959QYo5pmT9pmWNahjBzSqvLXv094IPoHE8HXp8BW52Nvh_ZhXrPMaJGqjR52BT6Oe8CFFNdgNnBFAq4ZqYc_j_Jb-xFtmI</recordid><startdate>20081015</startdate><enddate>20081015</enddate><creator>Lee, Stephanie J.</creator><creator>Kukreja, Manisha</creator><creator>Wang, Tao</creator><creator>Giralt, Sergio A.</creator><creator>Szer, Jeffrey</creator><creator>Arora, Mukta</creator><creator>Woolfrey, Ann E.</creator><creator>Cervantes, Francisco</creator><creator>Champlin, Richard E.</creator><creator>Gale, Robert Peter</creator><creator>Halter, Joerg</creator><creator>Keating, Armand</creator><creator>Marks, David I.</creator><creator>McCarthy, Philip L.</creator><creator>Olavarria, Eduardo</creator><creator>Stadtmauer, Edward A.</creator><creator>Abecasis, Manuel</creator><creator>Gupta, Vikas</creator><creator>Khoury, H. 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Jean ; George, Biju ; Hale, Gregory A. ; Liesveld, Jane L. ; Rizzieri, David A. ; Antin, Joseph H. ; Bolwell, Brian J. ; Carabasi, Matthew H. ; Copelan, Edward ; Ilhan, Osman ; Litzow, Mark R. ; Schouten, Harold C. ; Zander, Axel R. ; Horowitz, Mary M. ; Maziarz, Richard T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c557t-4685f5c6224f657efac0c255747823916d484b4e97af5f419d62a7d7c26e68843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Benzamides</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hematopoietic Stem Cell Transplantation - methods</topic><topic>HLA Antigens - metabolism</topic><topic>Humans</topic><topic>Imatinib Mesylate</topic><topic>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy</topic><topic>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - therapy</topic><topic>Leukemias. 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Myelofibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Piperazines - therapeutic use</topic><topic>Pyrimidines - therapeutic use</topic><topic>Registries</topic><topic>Transplantation</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Stephanie J.</creatorcontrib><creatorcontrib>Kukreja, Manisha</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Giralt, Sergio A.</creatorcontrib><creatorcontrib>Szer, Jeffrey</creatorcontrib><creatorcontrib>Arora, Mukta</creatorcontrib><creatorcontrib>Woolfrey, Ann E.</creatorcontrib><creatorcontrib>Cervantes, Francisco</creatorcontrib><creatorcontrib>Champlin, Richard E.</creatorcontrib><creatorcontrib>Gale, Robert Peter</creatorcontrib><creatorcontrib>Halter, Joerg</creatorcontrib><creatorcontrib>Keating, Armand</creatorcontrib><creatorcontrib>Marks, David I.</creatorcontrib><creatorcontrib>McCarthy, Philip L.</creatorcontrib><creatorcontrib>Olavarria, Eduardo</creatorcontrib><creatorcontrib>Stadtmauer, Edward A.</creatorcontrib><creatorcontrib>Abecasis, Manuel</creatorcontrib><creatorcontrib>Gupta, Vikas</creatorcontrib><creatorcontrib>Khoury, H. 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Jean</au><au>George, Biju</au><au>Hale, Gregory A.</au><au>Liesveld, Jane L.</au><au>Rizzieri, David A.</au><au>Antin, Joseph H.</au><au>Bolwell, Brian J.</au><au>Carabasi, Matthew H.</au><au>Copelan, Edward</au><au>Ilhan, Osman</au><au>Litzow, Mark R.</au><au>Schouten, Harold C.</au><au>Zander, Axel R.</au><au>Horowitz, Mary M.</au><au>Maziarz, Richard T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of prior imatinib mesylate on the outcome of hematopoietic cell transplantation for chronic myeloid leukemia</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2008-10-15</date><risdate>2008</risdate><volume>112</volume><issue>8</issue><spage>3500</spage><epage>3507</epage><pages>3500-3507</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Imatinib mesylate (IM, Gleevec) has largely supplanted allogeneic hematopoietic cell transplantation (HCT) as first line therapy for chronic myeloid leukemia (CML). Nevertheless, many people with CML eventually undergo HCT, raising the question of whether prior IM therapy impacts HCT success. Data from the Center for International Blood and Marrow Transplant Research on 409 subjects treated with IM before HCT (IM+) and 900 subjects who did not receive IM before HCT (IM−) were analyzed. Among patients in first chronic phase, IM therapy before HCT was associated with better survival but no statistically significant differences in treatment-related mortality, relapse, and leukemia-free survival. Better HLA-matched donors, use of bone marrow, and transplantation within one year of diagnosis were also associated with better survival. A matched-pairs analysis was performed and confirmed a higher survival rate among first chronic phase patients receiving IM. Among patients transplanted with advanced CML, use of IM before HCT was not associated with treatment-related mortality, relapse, leukemia-free survival, or survival. Acute graft-versus-host disease rates were similar between IM+ and IM− groups regardless of leukemia phase. These results should be reassuring to patients receiving IM before HCT.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>18664621</pmid><doi>10.1182/blood-2008-02-141689</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Antineoplastic Agents - therapeutic use Benzamides Biological and medical sciences Child Child, Preschool Disease-Free Survival Female Hematologic and hematopoietic diseases Hematopoietic Stem Cell Transplantation - methods HLA Antigens - metabolism Humans Imatinib Mesylate Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy Leukemia, Myelogenous, Chronic, BCR-ABL Positive - therapy Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Middle Aged Piperazines - therapeutic use Pyrimidines - therapeutic use Registries Transplantation Treatment Outcome |
title | Impact of prior imatinib mesylate on the outcome of hematopoietic cell transplantation for chronic myeloid leukemia |
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