Autologous hematopoietic stem cell transplantation in patients with refractory Crohn’s disease
Background & Aims: Crohn’s disease (CD) is an immunologically mediated inflammatory disease of the gastrointestinal tract. Due to a high morbidity and/or an increase in mortality in refractory cases, a new treatment approach is needed. In theory, maximum immune ablation by autologous hematopoiet...
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Veröffentlicht in: | Gastroenterology (New York, N.Y. 1943) N.Y. 1943), 2005-03, Vol.128 (3), p.552-563 |
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creator | Oyama, Yu Craig, Robert M. Traynor, Ann E. Quigley, Kathleen Statkute, Laisvyde Halverson, Amy Brush, Mary Verda, Larissa Kowalska, Barbara Krosnjar, Nela Kletzel, Morris Whitington, Peter F. Burt, Richard K. |
description | Background & Aims:
Crohn’s disease (CD) is an immunologically mediated inflammatory disease of the gastrointestinal tract. Due to a high morbidity and/or an increase in mortality in refractory cases, a new treatment approach is needed. In theory, maximum immune ablation by autologous hematopoietic stem cell transplantation (HSCT) can induce a remission.
Methods:
We conducted a phase 1 HSCT study in 12 patients with refractory CD. Candidates were younger than 60 years of age with a Crohn’s Disease Activity Index (CDAI) of 250–400 despite conventional therapies including infliximab. Peripheral blood stem cells were mobilized with cyclophosphamide and granulocyte colony-stimulating factor and CD34
+ enriched. The immune ablative (conditioning) regimen consisted of 200 mg/kg cyclophosphamide and 90 mg/kg equine antithymocyte globulin.
Results:
The procedure was well tolerated with anticipated cytopenias, neutropenic fever, and disease-related fever, diarrhea, anorexia, nausea, and vomiting. The median days for neutrophil and platelet engraftment were 9.5 (range, 8–11) and 9 (range, 9–18), respectively. The initial median CDAI was 291 (range, 250–358). Symptoms and CDAI improved before hospital discharge, whereas radiographic and colonoscopy findings improved gradually over months to years following HSCT. Eleven of 12 patients entered a sustained remission defined by a CDAI ≤150. After a median follow-up of 18.5 months (range, 7–37 months), only one patient has developed a recurrence of active CD, which occurred 15 months after HSCT.
Conclusions:
Autologous HSCT may be performed safely and has a marked salutary effect on CD activity. A randomized study will be needed to confirm the efficacy of this therapy. |
doi_str_mv | 10.1053/j.gastro.2004.11.051 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67508583</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0016508504021560</els_id><sourcerecordid>67508583</sourcerecordid><originalsourceid>FETCH-LOGICAL-c406t-d1c26adebf1e025490e238605ebf45f16f7806f6c4a4b622c1fa9e9cf47912183</originalsourceid><addsrcrecordid>eNp9kMFO3DAQhq2Kqiy0b1BVPnFLmHFib3JBQitakJB6ac-u15mwXiVxsL0gbn0NXq9PUq92JW6cZjT6559_Psa-IpQIsrrclg8mpuBLAVCXiCVI_MAWKEVTAKA4YYtcVCGhkafsLMYtALRVg5_YKcqlklULC_bnepf84B_8LvINjSb52TtKzvKYaOSWhoGnYKY4D2ZKJjk_cTfxOXc0pcifXdrwQH0wNvnwwlfBb6Z_f18j71wkE-kz-9ibIdKXYz1nv7_f_FrdFvc_f9ytru8LW4NKRYdWKNPRukcCIesWSFSNApkntexR9csGVK9sbeq1EsJib1pqbV8vWxTYVOfs4uA7B_-4o5j06OI-vpkoP6fVcg-iqbKwPght8DHm6HoObjThRSPoPVm91Qeyek9WI-pMNq99O_rv1iN1b0tHlFlwdRBQ_vLJUdDRZkaWOhfIJt159_6F_04yjxg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67508583</pqid></control><display><type>article</type><title>Autologous hematopoietic stem cell transplantation in patients with refractory Crohn’s disease</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>Alma/SFX Local Collection</source><creator>Oyama, Yu ; Craig, Robert M. ; Traynor, Ann E. ; Quigley, Kathleen ; Statkute, Laisvyde ; Halverson, Amy ; Brush, Mary ; Verda, Larissa ; Kowalska, Barbara ; Krosnjar, Nela ; Kletzel, Morris ; Whitington, Peter F. ; Burt, Richard K.</creator><creatorcontrib>Oyama, Yu ; Craig, Robert M. ; Traynor, Ann E. ; Quigley, Kathleen ; Statkute, Laisvyde ; Halverson, Amy ; Brush, Mary ; Verda, Larissa ; Kowalska, Barbara ; Krosnjar, Nela ; Kletzel, Morris ; Whitington, Peter F. ; Burt, Richard K.</creatorcontrib><description>Background & Aims:
Crohn’s disease (CD) is an immunologically mediated inflammatory disease of the gastrointestinal tract. Due to a high morbidity and/or an increase in mortality in refractory cases, a new treatment approach is needed. In theory, maximum immune ablation by autologous hematopoietic stem cell transplantation (HSCT) can induce a remission.
Methods:
We conducted a phase 1 HSCT study in 12 patients with refractory CD. Candidates were younger than 60 years of age with a Crohn’s Disease Activity Index (CDAI) of 250–400 despite conventional therapies including infliximab. Peripheral blood stem cells were mobilized with cyclophosphamide and granulocyte colony-stimulating factor and CD34
+ enriched. The immune ablative (conditioning) regimen consisted of 200 mg/kg cyclophosphamide and 90 mg/kg equine antithymocyte globulin.
Results:
The procedure was well tolerated with anticipated cytopenias, neutropenic fever, and disease-related fever, diarrhea, anorexia, nausea, and vomiting. The median days for neutrophil and platelet engraftment were 9.5 (range, 8–11) and 9 (range, 9–18), respectively. The initial median CDAI was 291 (range, 250–358). Symptoms and CDAI improved before hospital discharge, whereas radiographic and colonoscopy findings improved gradually over months to years following HSCT. Eleven of 12 patients entered a sustained remission defined by a CDAI ≤150. After a median follow-up of 18.5 months (range, 7–37 months), only one patient has developed a recurrence of active CD, which occurred 15 months after HSCT.
Conclusions:
Autologous HSCT may be performed safely and has a marked salutary effect on CD activity. A randomized study will be needed to confirm the efficacy of this therapy.</description><identifier>ISSN: 0016-5085</identifier><identifier>EISSN: 1528-0012</identifier><identifier>DOI: 10.1053/j.gastro.2004.11.051</identifier><identifier>PMID: 15765390</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Crohn Disease - physiopathology ; Crohn Disease - therapy ; Female ; Hematopoietic Stem Cell Transplantation - adverse effects ; Humans ; Male ; Pilot Projects ; Recurrence ; Remission Induction ; Survival Analysis ; Treatment Outcome</subject><ispartof>Gastroenterology (New York, N.Y. 1943), 2005-03, Vol.128 (3), p.552-563</ispartof><rights>2005 American Gastroenterological Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-d1c26adebf1e025490e238605ebf45f16f7806f6c4a4b622c1fa9e9cf47912183</citedby><cites>FETCH-LOGICAL-c406t-d1c26adebf1e025490e238605ebf45f16f7806f6c4a4b622c1fa9e9cf47912183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0016508504021560$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15765390$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oyama, Yu</creatorcontrib><creatorcontrib>Craig, Robert M.</creatorcontrib><creatorcontrib>Traynor, Ann E.</creatorcontrib><creatorcontrib>Quigley, Kathleen</creatorcontrib><creatorcontrib>Statkute, Laisvyde</creatorcontrib><creatorcontrib>Halverson, Amy</creatorcontrib><creatorcontrib>Brush, Mary</creatorcontrib><creatorcontrib>Verda, Larissa</creatorcontrib><creatorcontrib>Kowalska, Barbara</creatorcontrib><creatorcontrib>Krosnjar, Nela</creatorcontrib><creatorcontrib>Kletzel, Morris</creatorcontrib><creatorcontrib>Whitington, Peter F.</creatorcontrib><creatorcontrib>Burt, Richard K.</creatorcontrib><title>Autologous hematopoietic stem cell transplantation in patients with refractory Crohn’s disease</title><title>Gastroenterology (New York, N.Y. 1943)</title><addtitle>Gastroenterology</addtitle><description>Background & Aims:
Crohn’s disease (CD) is an immunologically mediated inflammatory disease of the gastrointestinal tract. Due to a high morbidity and/or an increase in mortality in refractory cases, a new treatment approach is needed. In theory, maximum immune ablation by autologous hematopoietic stem cell transplantation (HSCT) can induce a remission.
Methods:
We conducted a phase 1 HSCT study in 12 patients with refractory CD. Candidates were younger than 60 years of age with a Crohn’s Disease Activity Index (CDAI) of 250–400 despite conventional therapies including infliximab. Peripheral blood stem cells were mobilized with cyclophosphamide and granulocyte colony-stimulating factor and CD34
+ enriched. The immune ablative (conditioning) regimen consisted of 200 mg/kg cyclophosphamide and 90 mg/kg equine antithymocyte globulin.
Results:
The procedure was well tolerated with anticipated cytopenias, neutropenic fever, and disease-related fever, diarrhea, anorexia, nausea, and vomiting. The median days for neutrophil and platelet engraftment were 9.5 (range, 8–11) and 9 (range, 9–18), respectively. The initial median CDAI was 291 (range, 250–358). Symptoms and CDAI improved before hospital discharge, whereas radiographic and colonoscopy findings improved gradually over months to years following HSCT. Eleven of 12 patients entered a sustained remission defined by a CDAI ≤150. After a median follow-up of 18.5 months (range, 7–37 months), only one patient has developed a recurrence of active CD, which occurred 15 months after HSCT.
Conclusions:
Autologous HSCT may be performed safely and has a marked salutary effect on CD activity. A randomized study will be needed to confirm the efficacy of this therapy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Crohn Disease - physiopathology</subject><subject>Crohn Disease - therapy</subject><subject>Female</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>Humans</subject><subject>Male</subject><subject>Pilot Projects</subject><subject>Recurrence</subject><subject>Remission Induction</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><issn>0016-5085</issn><issn>1528-0012</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFO3DAQhq2Kqiy0b1BVPnFLmHFib3JBQitakJB6ac-u15mwXiVxsL0gbn0NXq9PUq92JW6cZjT6559_Psa-IpQIsrrclg8mpuBLAVCXiCVI_MAWKEVTAKA4YYtcVCGhkafsLMYtALRVg5_YKcqlklULC_bnepf84B_8LvINjSb52TtKzvKYaOSWhoGnYKY4D2ZKJjk_cTfxOXc0pcifXdrwQH0wNvnwwlfBb6Z_f18j71wkE-kz-9ibIdKXYz1nv7_f_FrdFvc_f9ytru8LW4NKRYdWKNPRukcCIesWSFSNApkntexR9csGVK9sbeq1EsJib1pqbV8vWxTYVOfs4uA7B_-4o5j06OI-vpkoP6fVcg-iqbKwPght8DHm6HoObjThRSPoPVm91Qeyek9WI-pMNq99O_rv1iN1b0tHlFlwdRBQ_vLJUdDRZkaWOhfIJt159_6F_04yjxg</recordid><startdate>20050301</startdate><enddate>20050301</enddate><creator>Oyama, Yu</creator><creator>Craig, Robert M.</creator><creator>Traynor, Ann E.</creator><creator>Quigley, Kathleen</creator><creator>Statkute, Laisvyde</creator><creator>Halverson, Amy</creator><creator>Brush, Mary</creator><creator>Verda, Larissa</creator><creator>Kowalska, Barbara</creator><creator>Krosnjar, Nela</creator><creator>Kletzel, Morris</creator><creator>Whitington, Peter F.</creator><creator>Burt, Richard K.</creator><general>Elsevier Inc</general><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>20050301</creationdate><title>Autologous hematopoietic stem cell transplantation in patients with refractory Crohn’s disease</title><author>Oyama, Yu ; Craig, Robert M. ; Traynor, Ann E. ; Quigley, Kathleen ; Statkute, Laisvyde ; Halverson, Amy ; Brush, Mary ; Verda, Larissa ; Kowalska, Barbara ; Krosnjar, Nela ; Kletzel, Morris ; Whitington, Peter F. ; Burt, Richard K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-d1c26adebf1e025490e238605ebf45f16f7806f6c4a4b622c1fa9e9cf47912183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Crohn Disease - physiopathology</topic><topic>Crohn Disease - therapy</topic><topic>Female</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Humans</topic><topic>Male</topic><topic>Pilot Projects</topic><topic>Recurrence</topic><topic>Remission Induction</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oyama, Yu</creatorcontrib><creatorcontrib>Craig, Robert M.</creatorcontrib><creatorcontrib>Traynor, Ann E.</creatorcontrib><creatorcontrib>Quigley, Kathleen</creatorcontrib><creatorcontrib>Statkute, Laisvyde</creatorcontrib><creatorcontrib>Halverson, Amy</creatorcontrib><creatorcontrib>Brush, Mary</creatorcontrib><creatorcontrib>Verda, Larissa</creatorcontrib><creatorcontrib>Kowalska, Barbara</creatorcontrib><creatorcontrib>Krosnjar, Nela</creatorcontrib><creatorcontrib>Kletzel, Morris</creatorcontrib><creatorcontrib>Whitington, Peter F.</creatorcontrib><creatorcontrib>Burt, Richard K.</creatorcontrib><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>Gastroenterology (New York, N.Y. 1943)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oyama, Yu</au><au>Craig, Robert M.</au><au>Traynor, Ann E.</au><au>Quigley, Kathleen</au><au>Statkute, Laisvyde</au><au>Halverson, Amy</au><au>Brush, Mary</au><au>Verda, Larissa</au><au>Kowalska, Barbara</au><au>Krosnjar, Nela</au><au>Kletzel, Morris</au><au>Whitington, Peter F.</au><au>Burt, Richard K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autologous hematopoietic stem cell transplantation in patients with refractory Crohn’s disease</atitle><jtitle>Gastroenterology (New York, N.Y. 1943)</jtitle><addtitle>Gastroenterology</addtitle><date>2005-03-01</date><risdate>2005</risdate><volume>128</volume><issue>3</issue><spage>552</spage><epage>563</epage><pages>552-563</pages><issn>0016-5085</issn><eissn>1528-0012</eissn><abstract>Background & Aims:
Crohn’s disease (CD) is an immunologically mediated inflammatory disease of the gastrointestinal tract. Due to a high morbidity and/or an increase in mortality in refractory cases, a new treatment approach is needed. In theory, maximum immune ablation by autologous hematopoietic stem cell transplantation (HSCT) can induce a remission.
Methods:
We conducted a phase 1 HSCT study in 12 patients with refractory CD. Candidates were younger than 60 years of age with a Crohn’s Disease Activity Index (CDAI) of 250–400 despite conventional therapies including infliximab. Peripheral blood stem cells were mobilized with cyclophosphamide and granulocyte colony-stimulating factor and CD34
+ enriched. The immune ablative (conditioning) regimen consisted of 200 mg/kg cyclophosphamide and 90 mg/kg equine antithymocyte globulin.
Results:
The procedure was well tolerated with anticipated cytopenias, neutropenic fever, and disease-related fever, diarrhea, anorexia, nausea, and vomiting. The median days for neutrophil and platelet engraftment were 9.5 (range, 8–11) and 9 (range, 9–18), respectively. The initial median CDAI was 291 (range, 250–358). Symptoms and CDAI improved before hospital discharge, whereas radiographic and colonoscopy findings improved gradually over months to years following HSCT. Eleven of 12 patients entered a sustained remission defined by a CDAI ≤150. After a median follow-up of 18.5 months (range, 7–37 months), only one patient has developed a recurrence of active CD, which occurred 15 months after HSCT.
Conclusions:
Autologous HSCT may be performed safely and has a marked salutary effect on CD activity. A randomized study will be needed to confirm the efficacy of this therapy.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15765390</pmid><doi>10.1053/j.gastro.2004.11.051</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Crohn Disease - physiopathology Crohn Disease - therapy Female Hematopoietic Stem Cell Transplantation - adverse effects Humans Male Pilot Projects Recurrence Remission Induction Survival Analysis Treatment Outcome |
title | Autologous hematopoietic stem cell transplantation in patients with refractory Crohn’s disease |
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