Autologous and allogeneic stem cell transplantations for poor-risk chronic lymphocytic leukemia
We report here on the long-term follow-up on 162 patients with high-risk chronic lymphocytic leukemia (CLL) who have undergone hematopoietic stem cell transplantation (SCT) at a single center from 1989 to 1999. Twenty-five patients with human leukocyte antigen (HLA)-matched sibling donors underwent...
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Veröffentlicht in: | Blood 2005-12, Vol.106 (13), p.4389-4396 |
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creator | Gribben, John G. Zahrieh, David Stephans, Katherine Bartlett-Pandite, Lini Alyea, Edwin P. Fisher, David C. Freedman, Arnold S. Mauch, Peter Schlossman, Robert Sequist, Lecia V. Soiffer, Robert J. Marshall, Blossom Neuberg, Donna Ritz, Jerome Nadler, Lee M. |
description | We report here on the long-term follow-up on 162 patients with high-risk chronic lymphocytic leukemia (CLL) who have undergone hematopoietic stem cell transplantation (SCT) at a single center from 1989 to 1999. Twenty-five patients with human leukocyte antigen (HLA)-matched sibling donors underwent T-cell-depleted allogeneic SCT, and 137 patients without HLA-matched sibling donors underwent autologous SCT. The 100-day mortality was 4% for both groups, but later morbidity and mortality were negatively affected on outcome. Progression-free survival was significantly longer following autologous than allogeneic SCT, but there was no difference in overall survival and no difference in the cumulative incidence of disease recurrence or deaths without recurrence between the 2 groups. At a median follow-up of 6.5 years there is no evidence of a plateau of progression-free survival. The majority of patients treated with donor lymphocyte infusions after relapse responded, demonstrating a significant graft-versus-leukemia effect in CLL. From these findings we have altered our approach for patients with high-risk CLL and are currently exploring the role of related and unrelated allogeneic SCT following reduced-intensity conditioning regimens. |
doi_str_mv | 10.1182/blood-2005-05-1778 |
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Twenty-five patients with human leukocyte antigen (HLA)-matched sibling donors underwent T-cell-depleted allogeneic SCT, and 137 patients without HLA-matched sibling donors underwent autologous SCT. The 100-day mortality was 4% for both groups, but later morbidity and mortality were negatively affected on outcome. Progression-free survival was significantly longer following autologous than allogeneic SCT, but there was no difference in overall survival and no difference in the cumulative incidence of disease recurrence or deaths without recurrence between the 2 groups. At a median follow-up of 6.5 years there is no evidence of a plateau of progression-free survival. The majority of patients treated with donor lymphocyte infusions after relapse responded, demonstrating a significant graft-versus-leukemia effect in CLL. From these findings we have altered our approach for patients with high-risk CLL and are currently exploring the role of related and unrelated allogeneic SCT following reduced-intensity conditioning regimens.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2005-05-1778</identifier><identifier>PMID: 16131571</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Disease Progression ; Female ; Follow-Up Studies ; Hematologic and hematopoietic diseases ; Hematopoietic Stem Cell Transplantation ; Humans ; Immunoglobulin Heavy Chains - genetics ; Leukemia, Lymphocytic, Chronic, B-Cell - pathology ; Leukemia, Lymphocytic, Chronic, B-Cell - surgery ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Middle Aged ; Mutation - genetics ; Prognosis ; Recurrence ; Risk Factors ; Survival Rate ; Transplantation ; Transplantation, Homologous ; Treatment Outcome</subject><ispartof>Blood, 2005-12, Vol.106 (13), p.4389-4396</ispartof><rights>2005 American Society of Hematology</rights><rights>2006 INIST-CNRS</rights><rights>2005 by The American Society of Hematology 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c578t-f41eeb61bc4a40949caf8fbf1a308bef8c4a71ec4368303f507f5c9cd85e862b3</citedby><cites>FETCH-LOGICAL-c578t-f41eeb61bc4a40949caf8fbf1a308bef8c4a71ec4368303f507f5c9cd85e862b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17346364$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16131571$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gribben, John G.</creatorcontrib><creatorcontrib>Zahrieh, David</creatorcontrib><creatorcontrib>Stephans, Katherine</creatorcontrib><creatorcontrib>Bartlett-Pandite, Lini</creatorcontrib><creatorcontrib>Alyea, Edwin P.</creatorcontrib><creatorcontrib>Fisher, David C.</creatorcontrib><creatorcontrib>Freedman, Arnold S.</creatorcontrib><creatorcontrib>Mauch, Peter</creatorcontrib><creatorcontrib>Schlossman, Robert</creatorcontrib><creatorcontrib>Sequist, Lecia V.</creatorcontrib><creatorcontrib>Soiffer, Robert J.</creatorcontrib><creatorcontrib>Marshall, Blossom</creatorcontrib><creatorcontrib>Neuberg, Donna</creatorcontrib><creatorcontrib>Ritz, Jerome</creatorcontrib><creatorcontrib>Nadler, Lee M.</creatorcontrib><title>Autologous and allogeneic stem cell transplantations for poor-risk chronic lymphocytic leukemia</title><title>Blood</title><addtitle>Blood</addtitle><description>We report here on the long-term follow-up on 162 patients with high-risk chronic lymphocytic leukemia (CLL) who have undergone hematopoietic stem cell transplantation (SCT) at a single center from 1989 to 1999. Twenty-five patients with human leukocyte antigen (HLA)-matched sibling donors underwent T-cell-depleted allogeneic SCT, and 137 patients without HLA-matched sibling donors underwent autologous SCT. The 100-day mortality was 4% for both groups, but later morbidity and mortality were negatively affected on outcome. Progression-free survival was significantly longer following autologous than allogeneic SCT, but there was no difference in overall survival and no difference in the cumulative incidence of disease recurrence or deaths without recurrence between the 2 groups. At a median follow-up of 6.5 years there is no evidence of a plateau of progression-free survival. The majority of patients treated with donor lymphocyte infusions after relapse responded, demonstrating a significant graft-versus-leukemia effect in CLL. From these findings we have altered our approach for patients with high-risk CLL and are currently exploring the role of related and unrelated allogeneic SCT following reduced-intensity conditioning regimens.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Humans</subject><subject>Immunoglobulin Heavy Chains - genetics</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - pathology</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - surgery</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mutation - genetics</subject><subject>Prognosis</subject><subject>Recurrence</subject><subject>Risk Factors</subject><subject>Survival Rate</subject><subject>Transplantation</subject><subject>Transplantation, Homologous</subject><subject>Treatment Outcome</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFvFSEQx4nR2NfqF_Bg9qK3VVhgYRNj0jRaTZp40TNh2aEPy8IKbJP37cv6XqxeTCaBgd9_GOaP0CuC3xEiu_ejj3FqO4x5W4MIIZ-gHeGdbDHu8FO0wxj3LRsEOUPnOf_EmDDa8efojPSEEi7IDqnLtUQfb-OaGx2mRvuaQABnmlxgbgx435SkQ168DkUXF0NubEzNEmNqk8t3jdmnGKrAH-ZlH82hbHtY72B2-gV6ZrXP8PK0XqAfnz99v_rS3ny7_np1edMaLmRpLSMAY09GwzTDAxuMttKOlmiK5QhW1nNBwDDaS4qp5VhYbgYzSQ6y70Z6gT4e6y7rOMNkINSmvVqSm3U6qKid-vcmuL26jfeKyIF3lNcCb08FUvy1Qi5qdnn7vQ5Qh6N6KbkQfAO7I2hSzDmB_fMIwWrzRf32RW2-qBqbL1X0-u_2HiUnIyrw5gTobLS3deLG5UdOUNbTnlXuw5GDOsx7B0ll4yAYmFwCU9QU3f_6eAAa86-k</recordid><startdate>20051215</startdate><enddate>20051215</enddate><creator>Gribben, John G.</creator><creator>Zahrieh, David</creator><creator>Stephans, Katherine</creator><creator>Bartlett-Pandite, Lini</creator><creator>Alyea, Edwin P.</creator><creator>Fisher, David C.</creator><creator>Freedman, Arnold S.</creator><creator>Mauch, Peter</creator><creator>Schlossman, Robert</creator><creator>Sequist, Lecia V.</creator><creator>Soiffer, Robert J.</creator><creator>Marshall, Blossom</creator><creator>Neuberg, Donna</creator><creator>Ritz, Jerome</creator><creator>Nadler, Lee M.</creator><general>Elsevier Inc</general><general>The Americain Society of Hematology</general><general>2005 by The American 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><scope>5PM</scope></search><sort><creationdate>20051215</creationdate><title>Autologous and allogeneic stem cell transplantations for poor-risk chronic lymphocytic leukemia</title><author>Gribben, John G. ; Zahrieh, David ; Stephans, Katherine ; Bartlett-Pandite, Lini ; Alyea, Edwin P. ; Fisher, David C. ; Freedman, Arnold S. ; Mauch, Peter ; Schlossman, Robert ; Sequist, Lecia V. ; Soiffer, Robert J. ; Marshall, Blossom ; Neuberg, Donna ; Ritz, Jerome ; Nadler, Lee M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c578t-f41eeb61bc4a40949caf8fbf1a308bef8c4a71ec4368303f507f5c9cd85e862b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Humans</topic><topic>Immunoglobulin Heavy Chains - genetics</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - pathology</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - surgery</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. 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Twenty-five patients with human leukocyte antigen (HLA)-matched sibling donors underwent T-cell-depleted allogeneic SCT, and 137 patients without HLA-matched sibling donors underwent autologous SCT. The 100-day mortality was 4% for both groups, but later morbidity and mortality were negatively affected on outcome. Progression-free survival was significantly longer following autologous than allogeneic SCT, but there was no difference in overall survival and no difference in the cumulative incidence of disease recurrence or deaths without recurrence between the 2 groups. At a median follow-up of 6.5 years there is no evidence of a plateau of progression-free survival. The majority of patients treated with donor lymphocyte infusions after relapse responded, demonstrating a significant graft-versus-leukemia effect in CLL. From these findings we have altered our approach for patients with high-risk CLL and are currently exploring the role of related and unrelated allogeneic SCT following reduced-intensity conditioning regimens.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>16131571</pmid><doi>10.1182/blood-2005-05-1778</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Biological and medical sciences Disease Progression Female Follow-Up Studies Hematologic and hematopoietic diseases Hematopoietic Stem Cell Transplantation Humans Immunoglobulin Heavy Chains - genetics Leukemia, Lymphocytic, Chronic, B-Cell - pathology Leukemia, Lymphocytic, Chronic, B-Cell - surgery Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Middle Aged Mutation - genetics Prognosis Recurrence Risk Factors Survival Rate Transplantation Transplantation, Homologous Treatment Outcome |
title | Autologous and allogeneic stem cell transplantations for poor-risk chronic lymphocytic leukemia |
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