Hematopoietic Progenitor Cell Harvesting Is Feasible after Treatment with Brentuximab Vedotin in CD30+ Lymphoma Patients Who Received Multiple Prior Lines of Treatment

Abstract Brentuximab vedotin (BV), an antibody-drug conjugate that targets CD30, induces high response rates in CD30+ lymphoid malignancies. It is unknown if BV use affects procurement of autologous CD34+ stem cells and hematopoietic engraftment after autologous stem cell transplantation (ASCT). We...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biology of blood and marrow transplantation 2015-08, Vol.21 (8), p.1529-1531
Hauptverfasser: Afable, Manuel, Caimi, Paolo F, Hosing, Chitra, de Lima, Marcos, Khouri, Issa, William, Basem M, Nieto, Yago, Cooper, Brenda W, Anderlini, Paolo, Gerson, Stanton L, Lazarus, Hillard M, Champlin, Richard, Popat, Uday
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1531
container_issue 8
container_start_page 1529
container_title Biology of blood and marrow transplantation
container_volume 21
creator Afable, Manuel
Caimi, Paolo F
Hosing, Chitra
de Lima, Marcos
Khouri, Issa
William, Basem M
Nieto, Yago
Cooper, Brenda W
Anderlini, Paolo
Gerson, Stanton L
Lazarus, Hillard M
Champlin, Richard
Popat, Uday
description Abstract Brentuximab vedotin (BV), an antibody-drug conjugate that targets CD30, induces high response rates in CD30+ lymphoid malignancies. It is unknown if BV use affects procurement of autologous CD34+ stem cells and hematopoietic engraftment after autologous stem cell transplantation (ASCT). We examined 42 patients treated with BV before mobilization. Median times from diagnosis to transplantation, from initial BV treatment to transplantation, and from last BV treatment to stem cell collection were 21 months (range, 10 to 210), 5 months (range, 1.5 to 16.8), and 30 days (range, 2 to 280), respectively. Mobilization was successful on the first attempt in 38 patients (90.4%). The median number of infused CD34+ cells was 5.46 × 106 /kg (range, 1.65 to 54.78 × 106 /kg). The median times to neutrophil and platelet engraftment were 10 (range, 9 to 13), and 10.5 days (range, 7 to 35), respectively. BV before high-dose chemotherapy–ASCT did not adversely affect peripheral blood stem cell mobilization and subsequent engraftment in a cohort of heavily pretreated patients with CD30+ lymphomas.
doi_str_mv 10.1016/j.bbmt.2015.04.022
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4830276</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S1083879115002992</els_id><sourcerecordid>1697213737</sourcerecordid><originalsourceid>FETCH-LOGICAL-c580t-54581510bbc09edce252fe37002cd75b837bfb6ea3e800d315a39db3d21f26ff3</originalsourceid><addsrcrecordid>eNp9Ul2LEzEUHURx19U_4IPkUZDWm6SZD5CFtbp2oWLRVR9DkrnTps5MapKp9hf5N83Qdf14EAK5kHPOvTnnZtljClMKNH--nWrdxSkDKqYwmwJjd7JTKhif5ILnd1MNJZ-URUVPsgchbAGgmJXV_eyEiYoXvCpOsx8L7FR0O2cxWkNW3q2xt9F5Mse2JQvl9xii7dfkKpBLVMHqFolqInpy7VHFDvtIvtm4IS99KofvtlOafMLaJRZJZ_6KwzOyPHS7jesUWaloEy6QzxtH3qNBu8eavB3aaHdJeeVt6r20PQbimt8tHmb3GtUGfHRzn2UfL19fzxeT5bs3V_OL5cSIEuJEzERJBQWtDVRYG2SCNcgLAGbqQuiSF7rROSqOJUDNqVC8qjWvGW1Y3jT8LDs_6u4G3Y0CffSqlTufvuUP0ikr_37p7Uau3V7OSg6syJPA0xsB774OyTvZ2WCSl6pHNwRJ86pgNLlfJCg7Qo13IXhsbttQkGPCcivHhOWYsISZTAkn0pM_B7yl_Io0AV4cAZhs2lv0MpjkuMHaejRR1s7-X__8H7ppbW-Nar_gAcPWDb5PAUgqA5MgP4w7Nq4YFcnjqmL8J0yy0HY</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1697213737</pqid></control><display><type>article</type><title>Hematopoietic Progenitor Cell Harvesting Is Feasible after Treatment with Brentuximab Vedotin in CD30+ Lymphoma Patients Who Received Multiple Prior Lines of Treatment</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Afable, Manuel ; Caimi, Paolo F ; Hosing, Chitra ; de Lima, Marcos ; Khouri, Issa ; William, Basem M ; Nieto, Yago ; Cooper, Brenda W ; Anderlini, Paolo ; Gerson, Stanton L ; Lazarus, Hillard M ; Champlin, Richard ; Popat, Uday</creator><creatorcontrib>Afable, Manuel ; Caimi, Paolo F ; Hosing, Chitra ; de Lima, Marcos ; Khouri, Issa ; William, Basem M ; Nieto, Yago ; Cooper, Brenda W ; Anderlini, Paolo ; Gerson, Stanton L ; Lazarus, Hillard M ; Champlin, Richard ; Popat, Uday</creatorcontrib><description>Abstract Brentuximab vedotin (BV), an antibody-drug conjugate that targets CD30, induces high response rates in CD30+ lymphoid malignancies. It is unknown if BV use affects procurement of autologous CD34+ stem cells and hematopoietic engraftment after autologous stem cell transplantation (ASCT). We examined 42 patients treated with BV before mobilization. Median times from diagnosis to transplantation, from initial BV treatment to transplantation, and from last BV treatment to stem cell collection were 21 months (range, 10 to 210), 5 months (range, 1.5 to 16.8), and 30 days (range, 2 to 280), respectively. Mobilization was successful on the first attempt in 38 patients (90.4%). The median number of infused CD34+ cells was 5.46 × 106 /kg (range, 1.65 to 54.78 × 106 /kg). The median times to neutrophil and platelet engraftment were 10 (range, 9 to 13), and 10.5 days (range, 7 to 35), respectively. BV before high-dose chemotherapy–ASCT did not adversely affect peripheral blood stem cell mobilization and subsequent engraftment in a cohort of heavily pretreated patients with CD30+ lymphomas.</description><identifier>ISSN: 1083-8791</identifier><identifier>EISSN: 1523-6536</identifier><identifier>DOI: 10.1016/j.bbmt.2015.04.022</identifier><identifier>PMID: 25937397</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Autologous transplantation ; Brentuximab ; Female ; Hematology, Oncology and Palliative Medicine ; Hematopoietic Stem Cell Transplantation - methods ; Hodgkin Disease - therapy ; Humans ; Immunoconjugates - administration &amp; dosage ; Immunoconjugates - therapeutic use ; Ki-1 Antigen - metabolism ; Male ; Middle Aged ; Mobilization ; Retrospective Studies ; Stem Cells - metabolism ; Transplantation Conditioning - methods ; Young Adult</subject><ispartof>Biology of blood and marrow transplantation, 2015-08, Vol.21 (8), p.1529-1531</ispartof><rights>American Society for Blood and Marrow Transplantation</rights><rights>2015 American Society for Blood and Marrow Transplantation</rights><rights>Copyright © 2015 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c580t-54581510bbc09edce252fe37002cd75b837bfb6ea3e800d315a39db3d21f26ff3</citedby><cites>FETCH-LOGICAL-c580t-54581510bbc09edce252fe37002cd75b837bfb6ea3e800d315a39db3d21f26ff3</cites><orcidid>0000-0001-9376-9377</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1083879115002992$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25937397$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Afable, Manuel</creatorcontrib><creatorcontrib>Caimi, Paolo F</creatorcontrib><creatorcontrib>Hosing, Chitra</creatorcontrib><creatorcontrib>de Lima, Marcos</creatorcontrib><creatorcontrib>Khouri, Issa</creatorcontrib><creatorcontrib>William, Basem M</creatorcontrib><creatorcontrib>Nieto, Yago</creatorcontrib><creatorcontrib>Cooper, Brenda W</creatorcontrib><creatorcontrib>Anderlini, Paolo</creatorcontrib><creatorcontrib>Gerson, Stanton L</creatorcontrib><creatorcontrib>Lazarus, Hillard M</creatorcontrib><creatorcontrib>Champlin, Richard</creatorcontrib><creatorcontrib>Popat, Uday</creatorcontrib><title>Hematopoietic Progenitor Cell Harvesting Is Feasible after Treatment with Brentuximab Vedotin in CD30+ Lymphoma Patients Who Received Multiple Prior Lines of Treatment</title><title>Biology of blood and marrow transplantation</title><addtitle>Biol Blood Marrow Transplant</addtitle><description>Abstract Brentuximab vedotin (BV), an antibody-drug conjugate that targets CD30, induces high response rates in CD30+ lymphoid malignancies. It is unknown if BV use affects procurement of autologous CD34+ stem cells and hematopoietic engraftment after autologous stem cell transplantation (ASCT). We examined 42 patients treated with BV before mobilization. Median times from diagnosis to transplantation, from initial BV treatment to transplantation, and from last BV treatment to stem cell collection were 21 months (range, 10 to 210), 5 months (range, 1.5 to 16.8), and 30 days (range, 2 to 280), respectively. Mobilization was successful on the first attempt in 38 patients (90.4%). The median number of infused CD34+ cells was 5.46 × 106 /kg (range, 1.65 to 54.78 × 106 /kg). The median times to neutrophil and platelet engraftment were 10 (range, 9 to 13), and 10.5 days (range, 7 to 35), respectively. BV before high-dose chemotherapy–ASCT did not adversely affect peripheral blood stem cell mobilization and subsequent engraftment in a cohort of heavily pretreated patients with CD30+ lymphomas.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Autologous transplantation</subject><subject>Brentuximab</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Hematopoietic Stem Cell Transplantation - methods</subject><subject>Hodgkin Disease - therapy</subject><subject>Humans</subject><subject>Immunoconjugates - administration &amp; dosage</subject><subject>Immunoconjugates - therapeutic use</subject><subject>Ki-1 Antigen - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mobilization</subject><subject>Retrospective Studies</subject><subject>Stem Cells - metabolism</subject><subject>Transplantation Conditioning - methods</subject><subject>Young Adult</subject><issn>1083-8791</issn><issn>1523-6536</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Ul2LEzEUHURx19U_4IPkUZDWm6SZD5CFtbp2oWLRVR9DkrnTps5MapKp9hf5N83Qdf14EAK5kHPOvTnnZtljClMKNH--nWrdxSkDKqYwmwJjd7JTKhif5ILnd1MNJZ-URUVPsgchbAGgmJXV_eyEiYoXvCpOsx8L7FR0O2cxWkNW3q2xt9F5Mse2JQvl9xii7dfkKpBLVMHqFolqInpy7VHFDvtIvtm4IS99KofvtlOafMLaJRZJZ_6KwzOyPHS7jesUWaloEy6QzxtH3qNBu8eavB3aaHdJeeVt6r20PQbimt8tHmb3GtUGfHRzn2UfL19fzxeT5bs3V_OL5cSIEuJEzERJBQWtDVRYG2SCNcgLAGbqQuiSF7rROSqOJUDNqVC8qjWvGW1Y3jT8LDs_6u4G3Y0CffSqlTufvuUP0ikr_37p7Uau3V7OSg6syJPA0xsB774OyTvZ2WCSl6pHNwRJ86pgNLlfJCg7Qo13IXhsbttQkGPCcivHhOWYsISZTAkn0pM_B7yl_Io0AV4cAZhs2lv0MpjkuMHaejRR1s7-X__8H7ppbW-Nar_gAcPWDb5PAUgqA5MgP4w7Nq4YFcnjqmL8J0yy0HY</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Afable, Manuel</creator><creator>Caimi, Paolo F</creator><creator>Hosing, Chitra</creator><creator>de Lima, Marcos</creator><creator>Khouri, Issa</creator><creator>William, Basem M</creator><creator>Nieto, Yago</creator><creator>Cooper, Brenda W</creator><creator>Anderlini, Paolo</creator><creator>Gerson, Stanton L</creator><creator>Lazarus, Hillard M</creator><creator>Champlin, Richard</creator><creator>Popat, Uday</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><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9376-9377</orcidid></search><sort><creationdate>20150801</creationdate><title>Hematopoietic Progenitor Cell Harvesting Is Feasible after Treatment with Brentuximab Vedotin in CD30+ Lymphoma Patients Who Received Multiple Prior Lines of Treatment</title><author>Afable, Manuel ; Caimi, Paolo F ; Hosing, Chitra ; de Lima, Marcos ; Khouri, Issa ; William, Basem M ; Nieto, Yago ; Cooper, Brenda W ; Anderlini, Paolo ; Gerson, Stanton L ; Lazarus, Hillard M ; Champlin, Richard ; Popat, Uday</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c580t-54581510bbc09edce252fe37002cd75b837bfb6ea3e800d315a39db3d21f26ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Autologous transplantation</topic><topic>Brentuximab</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Hematopoietic Stem Cell Transplantation - methods</topic><topic>Hodgkin Disease - therapy</topic><topic>Humans</topic><topic>Immunoconjugates - administration &amp; dosage</topic><topic>Immunoconjugates - therapeutic use</topic><topic>Ki-1 Antigen - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mobilization</topic><topic>Retrospective Studies</topic><topic>Stem Cells - metabolism</topic><topic>Transplantation Conditioning - methods</topic><topic>Young Adult</topic><toplevel>online_resources</toplevel><creatorcontrib>Afable, Manuel</creatorcontrib><creatorcontrib>Caimi, Paolo F</creatorcontrib><creatorcontrib>Hosing, Chitra</creatorcontrib><creatorcontrib>de Lima, Marcos</creatorcontrib><creatorcontrib>Khouri, Issa</creatorcontrib><creatorcontrib>William, Basem M</creatorcontrib><creatorcontrib>Nieto, Yago</creatorcontrib><creatorcontrib>Cooper, Brenda W</creatorcontrib><creatorcontrib>Anderlini, Paolo</creatorcontrib><creatorcontrib>Gerson, Stanton L</creatorcontrib><creatorcontrib>Lazarus, Hillard M</creatorcontrib><creatorcontrib>Champlin, Richard</creatorcontrib><creatorcontrib>Popat, Uday</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biology of blood and marrow transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Afable, Manuel</au><au>Caimi, Paolo F</au><au>Hosing, Chitra</au><au>de Lima, Marcos</au><au>Khouri, Issa</au><au>William, Basem M</au><au>Nieto, Yago</au><au>Cooper, Brenda W</au><au>Anderlini, Paolo</au><au>Gerson, Stanton L</au><au>Lazarus, Hillard M</au><au>Champlin, Richard</au><au>Popat, Uday</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hematopoietic Progenitor Cell Harvesting Is Feasible after Treatment with Brentuximab Vedotin in CD30+ Lymphoma Patients Who Received Multiple Prior Lines of Treatment</atitle><jtitle>Biology of blood and marrow transplantation</jtitle><addtitle>Biol Blood Marrow Transplant</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>21</volume><issue>8</issue><spage>1529</spage><epage>1531</epage><pages>1529-1531</pages><issn>1083-8791</issn><eissn>1523-6536</eissn><abstract>Abstract Brentuximab vedotin (BV), an antibody-drug conjugate that targets CD30, induces high response rates in CD30+ lymphoid malignancies. It is unknown if BV use affects procurement of autologous CD34+ stem cells and hematopoietic engraftment after autologous stem cell transplantation (ASCT). We examined 42 patients treated with BV before mobilization. Median times from diagnosis to transplantation, from initial BV treatment to transplantation, and from last BV treatment to stem cell collection were 21 months (range, 10 to 210), 5 months (range, 1.5 to 16.8), and 30 days (range, 2 to 280), respectively. Mobilization was successful on the first attempt in 38 patients (90.4%). The median number of infused CD34+ cells was 5.46 × 106 /kg (range, 1.65 to 54.78 × 106 /kg). The median times to neutrophil and platelet engraftment were 10 (range, 9 to 13), and 10.5 days (range, 7 to 35), respectively. BV before high-dose chemotherapy–ASCT did not adversely affect peripheral blood stem cell mobilization and subsequent engraftment in a cohort of heavily pretreated patients with CD30+ lymphomas.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25937397</pmid><doi>10.1016/j.bbmt.2015.04.022</doi><tpages>3</tpages><orcidid>https://orcid.org/0000-0001-9376-9377</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1083-8791
ispartof Biology of blood and marrow transplantation, 2015-08, Vol.21 (8), p.1529-1531
issn 1083-8791
1523-6536
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4830276
source MEDLINE; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adolescent
Adult
Aged
Autologous transplantation
Brentuximab
Female
Hematology, Oncology and Palliative Medicine
Hematopoietic Stem Cell Transplantation - methods
Hodgkin Disease - therapy
Humans
Immunoconjugates - administration & dosage
Immunoconjugates - therapeutic use
Ki-1 Antigen - metabolism
Male
Middle Aged
Mobilization
Retrospective Studies
Stem Cells - metabolism
Transplantation Conditioning - methods
Young Adult
title Hematopoietic Progenitor Cell Harvesting Is Feasible after Treatment with Brentuximab Vedotin in CD30+ Lymphoma Patients Who Received Multiple Prior Lines of Treatment
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T10%3A08%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hematopoietic%20Progenitor%20Cell%20Harvesting%20Is%20Feasible%20after%20Treatment%20with%20Brentuximab%20Vedotin%20in%20CD30+%20Lymphoma%20Patients%20Who%20Received%20Multiple%20Prior%20Lines%20of%20Treatment&rft.jtitle=Biology%20of%20blood%20and%20marrow%20transplantation&rft.au=Afable,%20Manuel&rft.date=2015-08-01&rft.volume=21&rft.issue=8&rft.spage=1529&rft.epage=1531&rft.pages=1529-1531&rft.issn=1083-8791&rft.eissn=1523-6536&rft_id=info:doi/10.1016/j.bbmt.2015.04.022&rft_dat=%3Cproquest_pubme%3E1697213737%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1697213737&rft_id=info:pmid/25937397&rft_els_id=1_s2_0_S1083879115002992&rfr_iscdi=true