Allogeneic stem cell transplantation as part of front line therapy for Mantle cell lymphoma

Summary Mantle cell lymphoma (MCL) is an aggressive form of non‐Hodgkin lymphoma that remains incurable for the majority of patients. Allogeneic stem cell transplantation (alloSCT) produces long‐term disease‐free remissions for around 30–40% patients, however it is reserved for the treatment of rela...

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Veröffentlicht in:British journal of haematology 2019-03, Vol.184 (6), p.999-1005
Hauptverfasser: Rule, Simon, Cook, Gordon, Russell, Nigel H., Hunter, Ann, Robinson, Stephen, Morley, Nick, Sureda, Anna, Patrick, Pip, Clifton‐Hadley, Laura, Adedayo, Toyin, Kirkwood, Amy, Peggs, Karl S.
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container_end_page 1005
container_issue 6
container_start_page 999
container_title British journal of haematology
container_volume 184
creator Rule, Simon
Cook, Gordon
Russell, Nigel H.
Hunter, Ann
Robinson, Stephen
Morley, Nick
Sureda, Anna
Patrick, Pip
Clifton‐Hadley, Laura
Adedayo, Toyin
Kirkwood, Amy
Peggs, Karl S.
description Summary Mantle cell lymphoma (MCL) is an aggressive form of non‐Hodgkin lymphoma that remains incurable for the majority of patients. Allogeneic stem cell transplantation (alloSCT) produces long‐term disease‐free remissions for around 30–40% patients, however it is reserved for the treatment of relapsed disease. This study examined the use of front line transplantation for young patients in an attempt to improve outcomes. Twenty‐five patients received an alloSCT using BEAM [BCNU (carmustine), etoposide, cytarabine, melphalan)‐Campath conditioning following permissive induction therapy from both related and unrelated donors. This was a multi‐centre prospective trial. Twenty‐four of 25 patients engrafted with no non‐relapse mortality events by day 100. With a median follow‐up of 60·5 months, there have been six deaths (3 from MCL). The progression‐free survival (PFS) and overall survival were 68% and 80% at 2 years and 56% and 76% at 5 years. PFS was very similar for both sibling and unrelated transplants and there was no difference in PFS between patients with respect to remission status prior to transplantation. Nine (38%) patients experienced acute graft‐versus‐host disease (GVHD) and 14 (58%) experienced chronic GVHD, of which 8 were extensive. Front line alloSCT is feasible but should only be considered for patients at high risk of early progression following conventional therapy.
doi_str_mv 10.1111/bjh.15723
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Allogeneic stem cell transplantation (alloSCT) produces long‐term disease‐free remissions for around 30–40% patients, however it is reserved for the treatment of relapsed disease. This study examined the use of front line transplantation for young patients in an attempt to improve outcomes. Twenty‐five patients received an alloSCT using BEAM [BCNU (carmustine), etoposide, cytarabine, melphalan)‐Campath conditioning following permissive induction therapy from both related and unrelated donors. This was a multi‐centre prospective trial. Twenty‐four of 25 patients engrafted with no non‐relapse mortality events by day 100. With a median follow‐up of 60·5 months, there have been six deaths (3 from MCL). The progression‐free survival (PFS) and overall survival were 68% and 80% at 2 years and 56% and 76% at 5 years. PFS was very similar for both sibling and unrelated transplants and there was no difference in PFS between patients with respect to remission status prior to transplantation. Nine (38%) patients experienced acute graft‐versus‐host disease (GVHD) and 14 (58%) experienced chronic GVHD, of which 8 were extensive. Front line alloSCT is feasible but should only be considered for patients at high risk of early progression following conventional therapy.</description><identifier>ISSN: 0007-1048</identifier><identifier>EISSN: 1365-2141</identifier><identifier>DOI: 10.1111/bjh.15723</identifier><identifier>PMID: 30560573</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; clinical trials ; Cytarabine ; Etoposide ; Female ; Graft-versus-host reaction ; Hematology ; Hematopoietic Stem Cell Transplantation - methods ; Humans ; Induction therapy ; Lymphoma ; Lymphoma, Mantle-Cell - pathology ; Lymphoma, Mantle-Cell - therapy ; Lymphoma, Non-Hodgkin - pathology ; Lymphoma, Non-Hodgkin - therapy ; Male ; Mantle cell lymphoma ; Medical treatment ; Melphalan ; Middle Aged ; non‐Hodgkin lymphoma ; Patients ; Remission ; Stem cell transplantation ; Stem cells ; Transplantation ; Transplantation Conditioning - methods ; Transplantation, Homologous - methods ; Transplants &amp; implants</subject><ispartof>British journal of haematology, 2019-03, Vol.184 (6), p.999-1005</ispartof><rights>2018 British Society for Haematology and John Wiley &amp; Sons Ltd</rights><rights>2018 British Society for Haematology and John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2019 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4543-f1a6c8182c50b293403720ae2c36820994b4d63cc911884d490f1924c5f52393</citedby><cites>FETCH-LOGICAL-c4543-f1a6c8182c50b293403720ae2c36820994b4d63cc911884d490f1924c5f52393</cites><orcidid>0000-0001-8937-6351</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbjh.15723$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbjh.15723$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30560573$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rule, Simon</creatorcontrib><creatorcontrib>Cook, Gordon</creatorcontrib><creatorcontrib>Russell, Nigel H.</creatorcontrib><creatorcontrib>Hunter, Ann</creatorcontrib><creatorcontrib>Robinson, Stephen</creatorcontrib><creatorcontrib>Morley, Nick</creatorcontrib><creatorcontrib>Sureda, Anna</creatorcontrib><creatorcontrib>Patrick, Pip</creatorcontrib><creatorcontrib>Clifton‐Hadley, Laura</creatorcontrib><creatorcontrib>Adedayo, Toyin</creatorcontrib><creatorcontrib>Kirkwood, Amy</creatorcontrib><creatorcontrib>Peggs, Karl S.</creatorcontrib><title>Allogeneic stem cell transplantation as part of front line therapy for Mantle cell lymphoma</title><title>British journal of haematology</title><addtitle>Br J Haematol</addtitle><description>Summary Mantle cell lymphoma (MCL) is an aggressive form of non‐Hodgkin lymphoma that remains incurable for the majority of patients. Allogeneic stem cell transplantation (alloSCT) produces long‐term disease‐free remissions for around 30–40% patients, however it is reserved for the treatment of relapsed disease. This study examined the use of front line transplantation for young patients in an attempt to improve outcomes. Twenty‐five patients received an alloSCT using BEAM [BCNU (carmustine), etoposide, cytarabine, melphalan)‐Campath conditioning following permissive induction therapy from both related and unrelated donors. This was a multi‐centre prospective trial. Twenty‐four of 25 patients engrafted with no non‐relapse mortality events by day 100. With a median follow‐up of 60·5 months, there have been six deaths (3 from MCL). The progression‐free survival (PFS) and overall survival were 68% and 80% at 2 years and 56% and 76% at 5 years. PFS was very similar for both sibling and unrelated transplants and there was no difference in PFS between patients with respect to remission status prior to transplantation. Nine (38%) patients experienced acute graft‐versus‐host disease (GVHD) and 14 (58%) experienced chronic GVHD, of which 8 were extensive. Front line alloSCT is feasible but should only be considered for patients at high risk of early progression following conventional therapy.</description><subject>Adult</subject><subject>Aged</subject><subject>clinical trials</subject><subject>Cytarabine</subject><subject>Etoposide</subject><subject>Female</subject><subject>Graft-versus-host reaction</subject><subject>Hematology</subject><subject>Hematopoietic Stem Cell Transplantation - methods</subject><subject>Humans</subject><subject>Induction therapy</subject><subject>Lymphoma</subject><subject>Lymphoma, Mantle-Cell - pathology</subject><subject>Lymphoma, Mantle-Cell - therapy</subject><subject>Lymphoma, Non-Hodgkin - pathology</subject><subject>Lymphoma, Non-Hodgkin - therapy</subject><subject>Male</subject><subject>Mantle cell lymphoma</subject><subject>Medical treatment</subject><subject>Melphalan</subject><subject>Middle Aged</subject><subject>non‐Hodgkin lymphoma</subject><subject>Patients</subject><subject>Remission</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Transplantation</subject><subject>Transplantation Conditioning - methods</subject><subject>Transplantation, Homologous - methods</subject><subject>Transplants &amp; 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Cook, Gordon ; Russell, Nigel H. ; Hunter, Ann ; Robinson, Stephen ; Morley, Nick ; Sureda, Anna ; Patrick, Pip ; Clifton‐Hadley, Laura ; Adedayo, Toyin ; Kirkwood, Amy ; Peggs, Karl S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4543-f1a6c8182c50b293403720ae2c36820994b4d63cc911884d490f1924c5f52393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Aged</topic><topic>clinical trials</topic><topic>Cytarabine</topic><topic>Etoposide</topic><topic>Female</topic><topic>Graft-versus-host reaction</topic><topic>Hematology</topic><topic>Hematopoietic Stem Cell Transplantation - methods</topic><topic>Humans</topic><topic>Induction therapy</topic><topic>Lymphoma</topic><topic>Lymphoma, Mantle-Cell - pathology</topic><topic>Lymphoma, Mantle-Cell - therapy</topic><topic>Lymphoma, Non-Hodgkin - pathology</topic><topic>Lymphoma, Non-Hodgkin - therapy</topic><topic>Male</topic><topic>Mantle cell lymphoma</topic><topic>Medical treatment</topic><topic>Melphalan</topic><topic>Middle Aged</topic><topic>non‐Hodgkin lymphoma</topic><topic>Patients</topic><topic>Remission</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>Transplantation</topic><topic>Transplantation Conditioning - methods</topic><topic>Transplantation, Homologous - methods</topic><topic>Transplants &amp; implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rule, Simon</creatorcontrib><creatorcontrib>Cook, Gordon</creatorcontrib><creatorcontrib>Russell, Nigel H.</creatorcontrib><creatorcontrib>Hunter, Ann</creatorcontrib><creatorcontrib>Robinson, Stephen</creatorcontrib><creatorcontrib>Morley, Nick</creatorcontrib><creatorcontrib>Sureda, Anna</creatorcontrib><creatorcontrib>Patrick, Pip</creatorcontrib><creatorcontrib>Clifton‐Hadley, Laura</creatorcontrib><creatorcontrib>Adedayo, Toyin</creatorcontrib><creatorcontrib>Kirkwood, Amy</creatorcontrib><creatorcontrib>Peggs, Karl S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>British journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rule, Simon</au><au>Cook, Gordon</au><au>Russell, Nigel H.</au><au>Hunter, Ann</au><au>Robinson, Stephen</au><au>Morley, Nick</au><au>Sureda, Anna</au><au>Patrick, Pip</au><au>Clifton‐Hadley, Laura</au><au>Adedayo, Toyin</au><au>Kirkwood, Amy</au><au>Peggs, Karl S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Allogeneic stem cell transplantation as part of front line therapy for Mantle cell lymphoma</atitle><jtitle>British journal of haematology</jtitle><addtitle>Br J Haematol</addtitle><date>2019-03</date><risdate>2019</risdate><volume>184</volume><issue>6</issue><spage>999</spage><epage>1005</epage><pages>999-1005</pages><issn>0007-1048</issn><eissn>1365-2141</eissn><abstract>Summary Mantle cell lymphoma (MCL) is an aggressive form of non‐Hodgkin lymphoma that remains incurable for the majority of patients. Allogeneic stem cell transplantation (alloSCT) produces long‐term disease‐free remissions for around 30–40% patients, however it is reserved for the treatment of relapsed disease. This study examined the use of front line transplantation for young patients in an attempt to improve outcomes. Twenty‐five patients received an alloSCT using BEAM [BCNU (carmustine), etoposide, cytarabine, melphalan)‐Campath conditioning following permissive induction therapy from both related and unrelated donors. This was a multi‐centre prospective trial. Twenty‐four of 25 patients engrafted with no non‐relapse mortality events by day 100. With a median follow‐up of 60·5 months, there have been six deaths (3 from MCL). The progression‐free survival (PFS) and overall survival were 68% and 80% at 2 years and 56% and 76% at 5 years. PFS was very similar for both sibling and unrelated transplants and there was no difference in PFS between patients with respect to remission status prior to transplantation. Nine (38%) patients experienced acute graft‐versus‐host disease (GVHD) and 14 (58%) experienced chronic GVHD, of which 8 were extensive. Front line alloSCT is feasible but should only be considered for patients at high risk of early progression following conventional therapy.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>30560573</pmid><doi>10.1111/bjh.15723</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-8937-6351</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
clinical trials
Cytarabine
Etoposide
Female
Graft-versus-host reaction
Hematology
Hematopoietic Stem Cell Transplantation - methods
Humans
Induction therapy
Lymphoma
Lymphoma, Mantle-Cell - pathology
Lymphoma, Mantle-Cell - therapy
Lymphoma, Non-Hodgkin - pathology
Lymphoma, Non-Hodgkin - therapy
Male
Mantle cell lymphoma
Medical treatment
Melphalan
Middle Aged
non‐Hodgkin lymphoma
Patients
Remission
Stem cell transplantation
Stem cells
Transplantation
Transplantation Conditioning - methods
Transplantation, Homologous - methods
Transplants & implants
title Allogeneic stem cell transplantation as part of front line therapy for Mantle cell lymphoma
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