Anti-thymocyte globulin could improve the outcome of allogeneic hematopoietic stem cell transplantation in patients with highly aggressive T-cell tumors

The early experiment result in our hospital showed that anti-thymocyte globulin (ATG) inhibited the proliferation of lymphoid tumor cells in the T-cell tumors. We used the ATG as the part of the conditioning regimen and to evaluate the long-term anti-leukemia effect, the safety and complication in t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Blood cancer journal (New York) 2015-07, Vol.5 (7), p.e332-e332
Hauptverfasser: Yang, J, Cai, Y, Jiang, J L, Wan, L P, Yan, S K, Wang, C
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e332
container_issue 7
container_start_page e332
container_title Blood cancer journal (New York)
container_volume 5
creator Yang, J
Cai, Y
Jiang, J L
Wan, L P
Yan, S K
Wang, C
description The early experiment result in our hospital showed that anti-thymocyte globulin (ATG) inhibited the proliferation of lymphoid tumor cells in the T-cell tumors. We used the ATG as the part of the conditioning regimen and to evaluate the long-term anti-leukemia effect, the safety and complication in the patients with highly aggressive T-cell lymphomas. Twenty-three patients were enrolled into this study. At the time of transplant, six patients reached first or subsequent complete response, three patients had a partial remission and 14 patients had relapsed or primary refractory disease. The conditioning regimen consisted of ATG, total body irradiation, toposide and cyclophosphamide. The complete remission rate after transplant was 95.7%. At a median follow-up time of 25 months, 16 (69.6%) patients are alive and free from diseases, including nine patients in refractory and progressive disease. Seven patients died after transplant, five from relapse and two from treatment-related complications. The incidence of grades II–IV acute graft-vs-host disease (GvHD) was 39.1%. The maximum cumulative incidence of chronic GvHD was 30%. The most frequent and severe conditioning-related toxicities observed in 8 out of 23 patients were grades III/IV infections during cytopenia. Thus, ATG-based conditioning is a feasible and effective alternative for patients with highly aggressive T-cell tumors.
doi_str_mv 10.1038/bcj.2015.54
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4526780</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4037746961</sourcerecordid><originalsourceid>FETCH-LOGICAL-c446t-4b95b5943d6f1d5be641183eb3211747b0384fd2ee018ff13dbdbb048f63a8ba3</originalsourceid><addsrcrecordid>eNptkUFrFTEUhYMottSu3EvApZ1nMpNkMhuhFKtCwU1dh2TmzkwemWRMMpX3T_y5prxanmA294b75ZxLDkJvKdlR0siPpt_vakL5jrMX6LwmjFW8kfzlSX-GLlPak3K4oB3tXqOzWtQN6bg4R7-vfbZVng9L6A8Z8OSC2Zz1uA-bG7Bd1hgeAOcZcNhyH5ZSR6ydCxN4sD2eYdE5rMFCLreUYcE9OIdz1D6tTvussw0eF8m1dOBzwr9snvFsp9kdsJ6mCCnZYnJfHV9uS4jpDXo1apfg8qleoB-3n-9vvlZ33798u7m-q3rGRK6Y6bjhHWsGMdKBGxCMUtmAaWpKW9aa8klsHGoAQuU40mYwgzGEyVE0WhrdXKBPR911MwsMfVkwaqfWaBcdDypoq_6deDurKTwoxmvRSlIE3j8JxPBzg5TVPmzRl50VbSWTQnStKNSHI9XHkFKE8dmBEvWYpCpJqsckFWeFfne61DP7N7cCXB2BVEZ-gnhi-h-9P7SgrWk</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1784866976</pqid></control><display><type>article</type><title>Anti-thymocyte globulin could improve the outcome of allogeneic hematopoietic stem cell transplantation in patients with highly aggressive T-cell tumors</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Springer Nature OA Free Journals</source><source>Nature Free</source><source>PubMed Central</source><creator>Yang, J ; Cai, Y ; Jiang, J L ; Wan, L P ; Yan, S K ; Wang, C</creator><creatorcontrib>Yang, J ; Cai, Y ; Jiang, J L ; Wan, L P ; Yan, S K ; Wang, C</creatorcontrib><description>The early experiment result in our hospital showed that anti-thymocyte globulin (ATG) inhibited the proliferation of lymphoid tumor cells in the T-cell tumors. We used the ATG as the part of the conditioning regimen and to evaluate the long-term anti-leukemia effect, the safety and complication in the patients with highly aggressive T-cell lymphomas. Twenty-three patients were enrolled into this study. At the time of transplant, six patients reached first or subsequent complete response, three patients had a partial remission and 14 patients had relapsed or primary refractory disease. The conditioning regimen consisted of ATG, total body irradiation, toposide and cyclophosphamide. The complete remission rate after transplant was 95.7%. At a median follow-up time of 25 months, 16 (69.6%) patients are alive and free from diseases, including nine patients in refractory and progressive disease. Seven patients died after transplant, five from relapse and two from treatment-related complications. The incidence of grades II–IV acute graft-vs-host disease (GvHD) was 39.1%. The maximum cumulative incidence of chronic GvHD was 30%. The most frequent and severe conditioning-related toxicities observed in 8 out of 23 patients were grades III/IV infections during cytopenia. Thus, ATG-based conditioning is a feasible and effective alternative for patients with highly aggressive T-cell tumors.</description><identifier>ISSN: 2044-5385</identifier><identifier>EISSN: 2044-5385</identifier><identifier>DOI: 10.1038/bcj.2015.54</identifier><identifier>PMID: 26230956</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/100 ; 692/67 ; 692/699/1541/1990/291/1621/1916 ; Adolescent ; Adult ; Antilymphocyte Serum - therapeutic use ; Antineoplastic Agents - therapeutic use ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Child ; Combined Modality Therapy ; Disease-Free Survival ; Female ; Hematology ; Hematopoietic Stem Cell Transplantation ; Humans ; Kaplan-Meier Estimate ; Lymphoma, T-Cell - mortality ; Lymphoma, T-Cell - pathology ; Lymphoma, T-Cell - therapy ; Male ; Middle Aged ; Oncology ; Original ; original-article ; Prospective Studies ; Transplantation, Homologous ; Treatment Outcome ; Young Adult</subject><ispartof>Blood cancer journal (New York), 2015-07, Vol.5 (7), p.e332-e332</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Jul 2015</rights><rights>Copyright © 2015 Macmillan Publishers Limited 2015 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-4b95b5943d6f1d5be641183eb3211747b0384fd2ee018ff13dbdbb048f63a8ba3</citedby><cites>FETCH-LOGICAL-c446t-4b95b5943d6f1d5be641183eb3211747b0384fd2ee018ff13dbdbb048f63a8ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526780/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526780/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,27907,27908,41103,42172,51559,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26230956$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, J</creatorcontrib><creatorcontrib>Cai, Y</creatorcontrib><creatorcontrib>Jiang, J L</creatorcontrib><creatorcontrib>Wan, L P</creatorcontrib><creatorcontrib>Yan, S K</creatorcontrib><creatorcontrib>Wang, C</creatorcontrib><title>Anti-thymocyte globulin could improve the outcome of allogeneic hematopoietic stem cell transplantation in patients with highly aggressive T-cell tumors</title><title>Blood cancer journal (New York)</title><addtitle>Blood Cancer Journal</addtitle><addtitle>Blood Cancer J</addtitle><description>The early experiment result in our hospital showed that anti-thymocyte globulin (ATG) inhibited the proliferation of lymphoid tumor cells in the T-cell tumors. We used the ATG as the part of the conditioning regimen and to evaluate the long-term anti-leukemia effect, the safety and complication in the patients with highly aggressive T-cell lymphomas. Twenty-three patients were enrolled into this study. At the time of transplant, six patients reached first or subsequent complete response, three patients had a partial remission and 14 patients had relapsed or primary refractory disease. The conditioning regimen consisted of ATG, total body irradiation, toposide and cyclophosphamide. The complete remission rate after transplant was 95.7%. At a median follow-up time of 25 months, 16 (69.6%) patients are alive and free from diseases, including nine patients in refractory and progressive disease. Seven patients died after transplant, five from relapse and two from treatment-related complications. The incidence of grades II–IV acute graft-vs-host disease (GvHD) was 39.1%. The maximum cumulative incidence of chronic GvHD was 30%. The most frequent and severe conditioning-related toxicities observed in 8 out of 23 patients were grades III/IV infections during cytopenia. Thus, ATG-based conditioning is a feasible and effective alternative for patients with highly aggressive T-cell tumors.</description><subject>13/100</subject><subject>692/67</subject><subject>692/699/1541/1990/291/1621/1916</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Antilymphocyte Serum - therapeutic use</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Child</subject><subject>Combined Modality Therapy</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Hematology</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Lymphoma, T-Cell - mortality</subject><subject>Lymphoma, T-Cell - pathology</subject><subject>Lymphoma, T-Cell - therapy</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Original</subject><subject>original-article</subject><subject>Prospective Studies</subject><subject>Transplantation, Homologous</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>2044-5385</issn><issn>2044-5385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkUFrFTEUhYMottSu3EvApZ1nMpNkMhuhFKtCwU1dh2TmzkwemWRMMpX3T_y5prxanmA294b75ZxLDkJvKdlR0siPpt_vakL5jrMX6LwmjFW8kfzlSX-GLlPak3K4oB3tXqOzWtQN6bg4R7-vfbZVng9L6A8Z8OSC2Zz1uA-bG7Bd1hgeAOcZcNhyH5ZSR6ydCxN4sD2eYdE5rMFCLreUYcE9OIdz1D6tTvussw0eF8m1dOBzwr9snvFsp9kdsJ6mCCnZYnJfHV9uS4jpDXo1apfg8qleoB-3n-9vvlZ33798u7m-q3rGRK6Y6bjhHWsGMdKBGxCMUtmAaWpKW9aa8klsHGoAQuU40mYwgzGEyVE0WhrdXKBPR911MwsMfVkwaqfWaBcdDypoq_6deDurKTwoxmvRSlIE3j8JxPBzg5TVPmzRl50VbSWTQnStKNSHI9XHkFKE8dmBEvWYpCpJqsckFWeFfne61DP7N7cCXB2BVEZ-gnhi-h-9P7SgrWk</recordid><startdate>20150731</startdate><enddate>20150731</enddate><creator>Yang, J</creator><creator>Cai, Y</creator><creator>Jiang, J L</creator><creator>Wan, L P</creator><creator>Yan, S K</creator><creator>Wang, C</creator><general>Nature Publishing Group UK</general><general>Springer Nature B.V</general><general>Nature Publishing Group</general><scope>C6C</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20150731</creationdate><title>Anti-thymocyte globulin could improve the outcome of allogeneic hematopoietic stem cell transplantation in patients with highly aggressive T-cell tumors</title><author>Yang, J ; Cai, Y ; Jiang, J L ; Wan, L P ; Yan, S K ; Wang, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-4b95b5943d6f1d5be641183eb3211747b0384fd2ee018ff13dbdbb048f63a8ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>13/100</topic><topic>692/67</topic><topic>692/699/1541/1990/291/1621/1916</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Antilymphocyte Serum - therapeutic use</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Child</topic><topic>Combined Modality Therapy</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Hematology</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Lymphoma, T-Cell - mortality</topic><topic>Lymphoma, T-Cell - pathology</topic><topic>Lymphoma, T-Cell - therapy</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Original</topic><topic>original-article</topic><topic>Prospective Studies</topic><topic>Transplantation, Homologous</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, J</creatorcontrib><creatorcontrib>Cai, Y</creatorcontrib><creatorcontrib>Jiang, J L</creatorcontrib><creatorcontrib>Wan, L P</creatorcontrib><creatorcontrib>Yan, S K</creatorcontrib><creatorcontrib>Wang, C</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Blood cancer journal (New York)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, J</au><au>Cai, Y</au><au>Jiang, J L</au><au>Wan, L P</au><au>Yan, S K</au><au>Wang, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-thymocyte globulin could improve the outcome of allogeneic hematopoietic stem cell transplantation in patients with highly aggressive T-cell tumors</atitle><jtitle>Blood cancer journal (New York)</jtitle><stitle>Blood Cancer Journal</stitle><addtitle>Blood Cancer J</addtitle><date>2015-07-31</date><risdate>2015</risdate><volume>5</volume><issue>7</issue><spage>e332</spage><epage>e332</epage><pages>e332-e332</pages><issn>2044-5385</issn><eissn>2044-5385</eissn><abstract>The early experiment result in our hospital showed that anti-thymocyte globulin (ATG) inhibited the proliferation of lymphoid tumor cells in the T-cell tumors. We used the ATG as the part of the conditioning regimen and to evaluate the long-term anti-leukemia effect, the safety and complication in the patients with highly aggressive T-cell lymphomas. Twenty-three patients were enrolled into this study. At the time of transplant, six patients reached first or subsequent complete response, three patients had a partial remission and 14 patients had relapsed or primary refractory disease. The conditioning regimen consisted of ATG, total body irradiation, toposide and cyclophosphamide. The complete remission rate after transplant was 95.7%. At a median follow-up time of 25 months, 16 (69.6%) patients are alive and free from diseases, including nine patients in refractory and progressive disease. Seven patients died after transplant, five from relapse and two from treatment-related complications. The incidence of grades II–IV acute graft-vs-host disease (GvHD) was 39.1%. The maximum cumulative incidence of chronic GvHD was 30%. The most frequent and severe conditioning-related toxicities observed in 8 out of 23 patients were grades III/IV infections during cytopenia. Thus, ATG-based conditioning is a feasible and effective alternative for patients with highly aggressive T-cell tumors.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26230956</pmid><doi>10.1038/bcj.2015.54</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2044-5385
ispartof Blood cancer journal (New York), 2015-07, Vol.5 (7), p.e332-e332
issn 2044-5385
2044-5385
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4526780
source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Springer Nature OA Free Journals; Nature Free; PubMed Central
subjects 13/100
692/67
692/699/1541/1990/291/1621/1916
Adolescent
Adult
Antilymphocyte Serum - therapeutic use
Antineoplastic Agents - therapeutic use
Biomedical and Life Sciences
Biomedicine
Cancer Research
Child
Combined Modality Therapy
Disease-Free Survival
Female
Hematology
Hematopoietic Stem Cell Transplantation
Humans
Kaplan-Meier Estimate
Lymphoma, T-Cell - mortality
Lymphoma, T-Cell - pathology
Lymphoma, T-Cell - therapy
Male
Middle Aged
Oncology
Original
original-article
Prospective Studies
Transplantation, Homologous
Treatment Outcome
Young Adult
title Anti-thymocyte globulin could improve the outcome of allogeneic hematopoietic stem cell transplantation in patients with highly aggressive T-cell tumors
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T08%3A07%3A10IST&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=Anti-thymocyte%20globulin%20could%20improve%20the%20outcome%20of%20allogeneic%20hematopoietic%20stem%20cell%20transplantation%20in%20patients%20with%20highly%20aggressive%20T-cell%20tumors&rft.jtitle=Blood%20cancer%20journal%20(New%20York)&rft.au=Yang,%20J&rft.date=2015-07-31&rft.volume=5&rft.issue=7&rft.spage=e332&rft.epage=e332&rft.pages=e332-e332&rft.issn=2044-5385&rft.eissn=2044-5385&rft_id=info:doi/10.1038/bcj.2015.54&rft_dat=%3Cproquest_pubme%3E4037746961%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=1784866976&rft_id=info:pmid/26230956&rfr_iscdi=true