Transplantation of ex vivo expanded cord blood
Umbilical cord blood (CB) from unrelated donors is increasingly used to restore hematopoiesis after myeloablative therapy. CB transplants are associated with higher rates of delayed and failed engraftment than are bone marrow transplants, particularly for adult patients. We studied the ex vivo expan...
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creator | Shpall, Elizabeth J Quinones, Ralph Giller, Roger Zeng, Chan Baron, Anna E Jones, Roy B Bearman, Scott I Nieto, Yago Freed, Brian Madinger, Nancy Hogan, Christopher J Slat-Vasquez, Vicki Russell, Peggy Blunk, Betsy Schissel, Deborah Hild, Elaine Malcolm, Janet Ward, William McNiece, Ian K |
description | Umbilical cord blood (CB) from unrelated donors is increasingly used to restore hematopoiesis after myeloablative therapy. CB transplants are associated with higher rates of delayed and failed engraftment than are bone marrow transplants, particularly for adult patients. We studied the ex vivo expansion of CB in an attempt to improve time to engraftment and reduce the graft failure rate in the recipients. In this feasibility study, 37 patients (25 adults, 12 children) with hematologic malignancies (n = 34) or breast cancer (n = 3) received high-dose therapy followed by unrelated allogeneic CB transplantation. A fraction of each patient's CB allograft was CD34-selected and cultured ex vivo for 10 days prior to transplantation in defined media with stem cell factor, granulocyte colony-stimulating factor, and megakaryocyte growth and differentiation factor. The remainder of the CB graft was infused without further manipulation. Two sequential cohorts of patients were accrued to the study. The first cohort had 40% and the second cohort had 60% of their CB graft expanded. Patients received a median of 0.99 x 10(7) total nucleated cells (expanded plus unexpanded) per kilogram. The median time to engraftment of neutrophils was 28 days (range, 15-49 days) and of platelets was 106 days (range, 38-345 days). All evaluable patients who were followed for 28 days or longer achieved engraftment of neutrophils. Grade III/IV acute GVHD was documented in 40% and extensive chronic GVHD in 63% of patients. At a median follow-up of 30 months, 13 (35%) of 37 of patients survived. This study demonstrates that the CD34 selection and ex vivo expansion of CB prior to transplantation of CB is feasible. Additional accrual will be required to assess the clinical efficacy of expanded CB progenitors.
Biol Blood Marrow Transplant 2002;8(7):368-76. |
doi_str_mv | 10.1053/bbmt.2002.v8.pm12171483 |
format | Article |
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Biol Blood Marrow Transplant 2002;8(7):368-76.</description><identifier>ISSN: 1083-8791</identifier><identifier>EISSN: 1523-6536</identifier><identifier>DOI: 10.1053/bbmt.2002.v8.pm12171483</identifier><identifier>PMID: 12171483</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Antigens, CD34 ; Breast Neoplasms - mortality ; Breast Neoplasms - therapy ; Cell Culture Techniques - methods ; Child ; Child, Preschool ; Cord Blood Stem Cell Transplantation - methods ; Cord Blood Stem Cell Transplantation - mortality ; Feasibility Studies ; Female ; Fetal Blood - cytology ; Graft Survival ; Hematologic Neoplasms - mortality ; Hematologic Neoplasms - therapy ; Humans ; Infant ; Leukocyte Count ; Male ; Middle Aged ; Neutrophils - cytology</subject><ispartof>Biology of blood and marrow transplantation, 2002-01, Vol.8 (7), p.368-376</ispartof><rights>2002 American Society for Blood and Marrow Transplantation</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c482t-b56c47bfd1e1414bdede6834f891e9452a8476af6153a5fab258c08a366f40513</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1053/bbmt.2002.v8.pm12171483$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>315,782,786,3554,27933,27934,46004</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12171483$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shpall, Elizabeth J</creatorcontrib><creatorcontrib>Quinones, Ralph</creatorcontrib><creatorcontrib>Giller, Roger</creatorcontrib><creatorcontrib>Zeng, Chan</creatorcontrib><creatorcontrib>Baron, Anna E</creatorcontrib><creatorcontrib>Jones, Roy B</creatorcontrib><creatorcontrib>Bearman, Scott I</creatorcontrib><creatorcontrib>Nieto, Yago</creatorcontrib><creatorcontrib>Freed, Brian</creatorcontrib><creatorcontrib>Madinger, Nancy</creatorcontrib><creatorcontrib>Hogan, Christopher J</creatorcontrib><creatorcontrib>Slat-Vasquez, Vicki</creatorcontrib><creatorcontrib>Russell, Peggy</creatorcontrib><creatorcontrib>Blunk, Betsy</creatorcontrib><creatorcontrib>Schissel, Deborah</creatorcontrib><creatorcontrib>Hild, Elaine</creatorcontrib><creatorcontrib>Malcolm, Janet</creatorcontrib><creatorcontrib>Ward, William</creatorcontrib><creatorcontrib>McNiece, Ian K</creatorcontrib><title>Transplantation of ex vivo expanded cord blood</title><title>Biology of blood and marrow transplantation</title><addtitle>Biol Blood Marrow Transplant</addtitle><description>Umbilical cord blood (CB) from unrelated donors is increasingly used to restore hematopoiesis after myeloablative therapy. CB transplants are associated with higher rates of delayed and failed engraftment than are bone marrow transplants, particularly for adult patients. We studied the ex vivo expansion of CB in an attempt to improve time to engraftment and reduce the graft failure rate in the recipients. In this feasibility study, 37 patients (25 adults, 12 children) with hematologic malignancies (n = 34) or breast cancer (n = 3) received high-dose therapy followed by unrelated allogeneic CB transplantation. A fraction of each patient's CB allograft was CD34-selected and cultured ex vivo for 10 days prior to transplantation in defined media with stem cell factor, granulocyte colony-stimulating factor, and megakaryocyte growth and differentiation factor. The remainder of the CB graft was infused without further manipulation. Two sequential cohorts of patients were accrued to the study. The first cohort had 40% and the second cohort had 60% of their CB graft expanded. Patients received a median of 0.99 x 10(7) total nucleated cells (expanded plus unexpanded) per kilogram. The median time to engraftment of neutrophils was 28 days (range, 15-49 days) and of platelets was 106 days (range, 38-345 days). All evaluable patients who were followed for 28 days or longer achieved engraftment of neutrophils. Grade III/IV acute GVHD was documented in 40% and extensive chronic GVHD in 63% of patients. At a median follow-up of 30 months, 13 (35%) of 37 of patients survived. This study demonstrates that the CD34 selection and ex vivo expansion of CB prior to transplantation of CB is feasible. Additional accrual will be required to assess the clinical efficacy of expanded CB progenitors.
Biol Blood Marrow Transplant 2002;8(7):368-76.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antigens, CD34</subject><subject>Breast Neoplasms - mortality</subject><subject>Breast Neoplasms - therapy</subject><subject>Cell Culture Techniques - methods</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cord Blood Stem Cell Transplantation - methods</subject><subject>Cord Blood Stem Cell Transplantation - mortality</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Fetal Blood - cytology</subject><subject>Graft Survival</subject><subject>Hematologic Neoplasms - mortality</subject><subject>Hematologic Neoplasms - therapy</subject><subject>Humans</subject><subject>Infant</subject><subject>Leukocyte Count</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neutrophils - cytology</subject><issn>1083-8791</issn><issn>1523-6536</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtPwzAQhC0EolD4C5ATtwQ7thPnWFW8pEpcytnyYy0ZJXGw0wj-Pala1COn3cM3M7uD0D3BBcGcPmrdjUWJcVlMohg6UpKaMEHP0BXhJc0rTqvzeceC5qJuyAJdp_SJMa6ZaC7R4o-_QsU2qj4NrepHNfrQZ8Fl8J1NfgrzHFRvwWYmRJvpNgR7gy6cahPcHucSfTw_bdev-eb95W292uSGiXLMNa8Mq7WzBAgjTM8mUAnKnGgINIyXSrC6Uq4inCrulC65MFgoWlWOYU7oEj0cfIcYvnaQRtn5ZKCd74SwS7ImTUMJFTNYH0ATQ0oRnByi71T8kQTLfVVyX5XcVyUnIU9Vzcq7Y8ROd2BPuhOwOgAwPzp5iDIZD70B6yOYUdrg_w35BUH8e8s</recordid><startdate>20020101</startdate><enddate>20020101</enddate><creator>Shpall, Elizabeth J</creator><creator>Quinones, Ralph</creator><creator>Giller, Roger</creator><creator>Zeng, Chan</creator><creator>Baron, Anna E</creator><creator>Jones, Roy B</creator><creator>Bearman, Scott I</creator><creator>Nieto, Yago</creator><creator>Freed, Brian</creator><creator>Madinger, Nancy</creator><creator>Hogan, Christopher J</creator><creator>Slat-Vasquez, Vicki</creator><creator>Russell, Peggy</creator><creator>Blunk, Betsy</creator><creator>Schissel, Deborah</creator><creator>Hild, Elaine</creator><creator>Malcolm, Janet</creator><creator>Ward, William</creator><creator>McNiece, Ian K</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>20020101</creationdate><title>Transplantation of ex vivo expanded cord blood</title><author>Shpall, Elizabeth J ; Quinones, Ralph ; Giller, Roger ; Zeng, Chan ; Baron, Anna E ; Jones, Roy B ; Bearman, Scott I ; Nieto, Yago ; Freed, Brian ; Madinger, Nancy ; Hogan, Christopher J ; Slat-Vasquez, Vicki ; Russell, Peggy ; Blunk, Betsy ; Schissel, Deborah ; Hild, Elaine ; Malcolm, Janet ; Ward, William ; McNiece, Ian K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-b56c47bfd1e1414bdede6834f891e9452a8476af6153a5fab258c08a366f40513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antigens, CD34</topic><topic>Breast Neoplasms - mortality</topic><topic>Breast Neoplasms - therapy</topic><topic>Cell Culture Techniques - methods</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cord Blood Stem Cell Transplantation - methods</topic><topic>Cord Blood Stem Cell Transplantation - mortality</topic><topic>Feasibility Studies</topic><topic>Female</topic><topic>Fetal Blood - cytology</topic><topic>Graft Survival</topic><topic>Hematologic Neoplasms - mortality</topic><topic>Hematologic Neoplasms - therapy</topic><topic>Humans</topic><topic>Infant</topic><topic>Leukocyte Count</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neutrophils - cytology</topic><toplevel>online_resources</toplevel><creatorcontrib>Shpall, Elizabeth J</creatorcontrib><creatorcontrib>Quinones, Ralph</creatorcontrib><creatorcontrib>Giller, Roger</creatorcontrib><creatorcontrib>Zeng, Chan</creatorcontrib><creatorcontrib>Baron, Anna E</creatorcontrib><creatorcontrib>Jones, Roy B</creatorcontrib><creatorcontrib>Bearman, Scott I</creatorcontrib><creatorcontrib>Nieto, Yago</creatorcontrib><creatorcontrib>Freed, Brian</creatorcontrib><creatorcontrib>Madinger, Nancy</creatorcontrib><creatorcontrib>Hogan, Christopher J</creatorcontrib><creatorcontrib>Slat-Vasquez, Vicki</creatorcontrib><creatorcontrib>Russell, Peggy</creatorcontrib><creatorcontrib>Blunk, Betsy</creatorcontrib><creatorcontrib>Schissel, Deborah</creatorcontrib><creatorcontrib>Hild, Elaine</creatorcontrib><creatorcontrib>Malcolm, Janet</creatorcontrib><creatorcontrib>Ward, William</creatorcontrib><creatorcontrib>McNiece, Ian K</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Biology of blood and marrow transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shpall, Elizabeth J</au><au>Quinones, Ralph</au><au>Giller, Roger</au><au>Zeng, Chan</au><au>Baron, Anna E</au><au>Jones, Roy B</au><au>Bearman, Scott I</au><au>Nieto, Yago</au><au>Freed, Brian</au><au>Madinger, Nancy</au><au>Hogan, Christopher J</au><au>Slat-Vasquez, Vicki</au><au>Russell, Peggy</au><au>Blunk, Betsy</au><au>Schissel, Deborah</au><au>Hild, Elaine</au><au>Malcolm, Janet</au><au>Ward, William</au><au>McNiece, Ian K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transplantation of ex vivo expanded cord blood</atitle><jtitle>Biology of blood and marrow transplantation</jtitle><addtitle>Biol Blood Marrow Transplant</addtitle><date>2002-01-01</date><risdate>2002</risdate><volume>8</volume><issue>7</issue><spage>368</spage><epage>376</epage><pages>368-376</pages><issn>1083-8791</issn><eissn>1523-6536</eissn><abstract>Umbilical cord blood (CB) from unrelated donors is increasingly used to restore hematopoiesis after myeloablative therapy. CB transplants are associated with higher rates of delayed and failed engraftment than are bone marrow transplants, particularly for adult patients. We studied the ex vivo expansion of CB in an attempt to improve time to engraftment and reduce the graft failure rate in the recipients. In this feasibility study, 37 patients (25 adults, 12 children) with hematologic malignancies (n = 34) or breast cancer (n = 3) received high-dose therapy followed by unrelated allogeneic CB transplantation. A fraction of each patient's CB allograft was CD34-selected and cultured ex vivo for 10 days prior to transplantation in defined media with stem cell factor, granulocyte colony-stimulating factor, and megakaryocyte growth and differentiation factor. The remainder of the CB graft was infused without further manipulation. Two sequential cohorts of patients were accrued to the study. The first cohort had 40% and the second cohort had 60% of their CB graft expanded. Patients received a median of 0.99 x 10(7) total nucleated cells (expanded plus unexpanded) per kilogram. The median time to engraftment of neutrophils was 28 days (range, 15-49 days) and of platelets was 106 days (range, 38-345 days). All evaluable patients who were followed for 28 days or longer achieved engraftment of neutrophils. Grade III/IV acute GVHD was documented in 40% and extensive chronic GVHD in 63% of patients. At a median follow-up of 30 months, 13 (35%) of 37 of patients survived. This study demonstrates that the CD34 selection and ex vivo expansion of CB prior to transplantation of CB is feasible. Additional accrual will be required to assess the clinical efficacy of expanded CB progenitors.
Biol Blood Marrow Transplant 2002;8(7):368-76.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>12171483</pmid><doi>10.1053/bbmt.2002.v8.pm12171483</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Antigens, CD34 Breast Neoplasms - mortality Breast Neoplasms - therapy Cell Culture Techniques - methods Child Child, Preschool Cord Blood Stem Cell Transplantation - methods Cord Blood Stem Cell Transplantation - mortality Feasibility Studies Female Fetal Blood - cytology Graft Survival Hematologic Neoplasms - mortality Hematologic Neoplasms - therapy Humans Infant Leukocyte Count Male Middle Aged Neutrophils - cytology |
title | Transplantation of ex vivo expanded cord blood |
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