Efficacy and safety of regimens used for the treatment of multicentric Castleman disease: A systematic review
Objectives Treatment options for multicentric Castleman disease (MCD) remain limited. The only FDA‐approved drug is siltuximab for idiopathic MCD (iMCD), but the response rate with siltuximab is less than 50%. We performed a systematic review to examine the efficacy and safety of various regimens us...
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Veröffentlicht in: | European journal of haematology 2022-10, Vol.109 (4), p.309-320 |
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container_title | European journal of haematology |
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creator | Rehman, Mohammad Ebad Ur Chattaraj, Asmi Neupane, Karun Rafae, Abdul Saeed, Sajeel Basit, Jawad Ibrahim, Atif Khouri, Jack Mukherjee, Sudipto Anwer, Faiz |
description | Objectives
Treatment options for multicentric Castleman disease (MCD) remain limited. The only FDA‐approved drug is siltuximab for idiopathic MCD (iMCD), but the response rate with siltuximab is less than 50%. We performed a systematic review to examine the efficacy and safety of various regimens used for the treatment of MCD.
Methods
A database search on PubMed, Embase, Cochrane, Web of Science, and Clinicaltrials.gov using the terms “Castleman disease,” “treatment outcome,” and “patient safety” was done.
Results and Conclusions
Results from a randomized controlled trial and an extension study highlighted the efficacy and long‐term safety of siltuximab for iMCD; other trials showed tocilizumab to be a suitable alternative. A recent trial reported high response rates with thalidomide in iMCD patients. Promising results were reported for bortezomib in relapsed/ refractory MCD. For human herpesvirus‐8 (HHV8)‐associated MCD, rituximab along with doxorubicin therapy followed by maintenance with zidovudine and valganciclovir is the most effective therapy. A single‐arm trial has highlighted the potential role of tocilizumab in HHV8‐MCD. Data for these regimens are limited and mostly comprise nonrandomized trials. Further research on emerging agents could have a major impact on the treatment of this rare disease. |
doi_str_mv | 10.1111/ejh.13823 |
format | Article |
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Treatment options for multicentric Castleman disease (MCD) remain limited. The only FDA‐approved drug is siltuximab for idiopathic MCD (iMCD), but the response rate with siltuximab is less than 50%. We performed a systematic review to examine the efficacy and safety of various regimens used for the treatment of MCD.
Methods
A database search on PubMed, Embase, Cochrane, Web of Science, and Clinicaltrials.gov using the terms “Castleman disease,” “treatment outcome,” and “patient safety” was done.
Results and Conclusions
Results from a randomized controlled trial and an extension study highlighted the efficacy and long‐term safety of siltuximab for iMCD; other trials showed tocilizumab to be a suitable alternative. A recent trial reported high response rates with thalidomide in iMCD patients. Promising results were reported for bortezomib in relapsed/ refractory MCD. For human herpesvirus‐8 (HHV8)‐associated MCD, rituximab along with doxorubicin therapy followed by maintenance with zidovudine and valganciclovir is the most effective therapy. A single‐arm trial has highlighted the potential role of tocilizumab in HHV8‐MCD. Data for these regimens are limited and mostly comprise nonrandomized trials. Further research on emerging agents could have a major impact on the treatment of this rare disease.</description><identifier>ISSN: 0902-4441</identifier><identifier>EISSN: 1600-0609</identifier><identifier>DOI: 10.1111/ejh.13823</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Bortezomib ; Castleman disease ; Castleman's disease ; Clinical trials ; Doxorubicin ; HHV8 ; IL‐6 ; lymphadenopathy ; Patient safety ; Patients ; Rare diseases ; Rituximab ; Safety ; siltuximab ; Systematic review ; Thalidomide ; Zidovudine</subject><ispartof>European journal of haematology, 2022-10, Vol.109 (4), p.309-320</ispartof><rights>2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2953-6a0119a8fd361d30e07d1194f87e91558e5f9d32aa6ad39f867ab89b1a28d1813</citedby><cites>FETCH-LOGICAL-c2953-6a0119a8fd361d30e07d1194f87e91558e5f9d32aa6ad39f867ab89b1a28d1813</cites><orcidid>0000-0003-4113-3304 ; 0000-0001-6914-7439</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%2Fejh.13823$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fejh.13823$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Rehman, Mohammad Ebad Ur</creatorcontrib><creatorcontrib>Chattaraj, Asmi</creatorcontrib><creatorcontrib>Neupane, Karun</creatorcontrib><creatorcontrib>Rafae, Abdul</creatorcontrib><creatorcontrib>Saeed, Sajeel</creatorcontrib><creatorcontrib>Basit, Jawad</creatorcontrib><creatorcontrib>Ibrahim, Atif</creatorcontrib><creatorcontrib>Khouri, Jack</creatorcontrib><creatorcontrib>Mukherjee, Sudipto</creatorcontrib><creatorcontrib>Anwer, Faiz</creatorcontrib><title>Efficacy and safety of regimens used for the treatment of multicentric Castleman disease: A systematic review</title><title>European journal of haematology</title><description>Objectives
Treatment options for multicentric Castleman disease (MCD) remain limited. The only FDA‐approved drug is siltuximab for idiopathic MCD (iMCD), but the response rate with siltuximab is less than 50%. We performed a systematic review to examine the efficacy and safety of various regimens used for the treatment of MCD.
Methods
A database search on PubMed, Embase, Cochrane, Web of Science, and Clinicaltrials.gov using the terms “Castleman disease,” “treatment outcome,” and “patient safety” was done.
Results and Conclusions
Results from a randomized controlled trial and an extension study highlighted the efficacy and long‐term safety of siltuximab for iMCD; other trials showed tocilizumab to be a suitable alternative. A recent trial reported high response rates with thalidomide in iMCD patients. Promising results were reported for bortezomib in relapsed/ refractory MCD. For human herpesvirus‐8 (HHV8)‐associated MCD, rituximab along with doxorubicin therapy followed by maintenance with zidovudine and valganciclovir is the most effective therapy. A single‐arm trial has highlighted the potential role of tocilizumab in HHV8‐MCD. Data for these regimens are limited and mostly comprise nonrandomized trials. Further research on emerging agents could have a major impact on the treatment of this rare disease.</description><subject>Bortezomib</subject><subject>Castleman disease</subject><subject>Castleman's disease</subject><subject>Clinical trials</subject><subject>Doxorubicin</subject><subject>HHV8</subject><subject>IL‐6</subject><subject>lymphadenopathy</subject><subject>Patient safety</subject><subject>Patients</subject><subject>Rare diseases</subject><subject>Rituximab</subject><subject>Safety</subject><subject>siltuximab</subject><subject>Systematic review</subject><subject>Thalidomide</subject><subject>Zidovudine</subject><issn>0902-4441</issn><issn>1600-0609</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp10MtqGzEUBmARGojrZpE3EHTTLibRZUYjdReMWycEuknW4mR0FMvMxZU0DfP2UequCtVG6OfT4fATcsXZNS_nBg_7ay61kGdkxRVjFVPMfCArZpio6rrmF-RjSgfGmDC8XZFh633ooFsojI4m8JgXOnka8SUMOCY6J3TUT5HmPdIcEXKJ8zsZ5j6Hrjxi6OgGUu5xgJG6kBASfqO3NC0pl6yoMu93wNdP5NxDn_Dy770mT9-3j5td9fDzx93m9qHqhGlkpYBxbkB7JxV3kiFrXQlqr1s0vGk0Nt44KQAUOGm8Vi08a_PMQWjHNZdr8uU09xinXzOmbIeQOux7GHGakxVKi1YrIZtCP_9DD9Mcx7KdFS0XqlU1N0V9PakuTilF9PYYwwBxsZzZ9-JtKd7-Kb7Ym5N9DT0u_4d2e787_XgDgNCEUw</recordid><startdate>202210</startdate><enddate>202210</enddate><creator>Rehman, Mohammad Ebad Ur</creator><creator>Chattaraj, Asmi</creator><creator>Neupane, Karun</creator><creator>Rafae, Abdul</creator><creator>Saeed, Sajeel</creator><creator>Basit, Jawad</creator><creator>Ibrahim, Atif</creator><creator>Khouri, Jack</creator><creator>Mukherjee, Sudipto</creator><creator>Anwer, Faiz</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4113-3304</orcidid><orcidid>https://orcid.org/0000-0001-6914-7439</orcidid></search><sort><creationdate>202210</creationdate><title>Efficacy and safety of regimens used for the treatment of multicentric Castleman disease: A systematic review</title><author>Rehman, Mohammad Ebad Ur ; Chattaraj, Asmi ; Neupane, Karun ; Rafae, Abdul ; Saeed, Sajeel ; Basit, Jawad ; Ibrahim, Atif ; Khouri, Jack ; Mukherjee, Sudipto ; Anwer, Faiz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2953-6a0119a8fd361d30e07d1194f87e91558e5f9d32aa6ad39f867ab89b1a28d1813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Bortezomib</topic><topic>Castleman disease</topic><topic>Castleman's disease</topic><topic>Clinical trials</topic><topic>Doxorubicin</topic><topic>HHV8</topic><topic>IL‐6</topic><topic>lymphadenopathy</topic><topic>Patient safety</topic><topic>Patients</topic><topic>Rare diseases</topic><topic>Rituximab</topic><topic>Safety</topic><topic>siltuximab</topic><topic>Systematic review</topic><topic>Thalidomide</topic><topic>Zidovudine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rehman, Mohammad Ebad Ur</creatorcontrib><creatorcontrib>Chattaraj, Asmi</creatorcontrib><creatorcontrib>Neupane, Karun</creatorcontrib><creatorcontrib>Rafae, Abdul</creatorcontrib><creatorcontrib>Saeed, Sajeel</creatorcontrib><creatorcontrib>Basit, Jawad</creatorcontrib><creatorcontrib>Ibrahim, Atif</creatorcontrib><creatorcontrib>Khouri, Jack</creatorcontrib><creatorcontrib>Mukherjee, Sudipto</creatorcontrib><creatorcontrib>Anwer, Faiz</creatorcontrib><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rehman, Mohammad Ebad Ur</au><au>Chattaraj, Asmi</au><au>Neupane, Karun</au><au>Rafae, Abdul</au><au>Saeed, Sajeel</au><au>Basit, Jawad</au><au>Ibrahim, Atif</au><au>Khouri, Jack</au><au>Mukherjee, Sudipto</au><au>Anwer, Faiz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy and safety of regimens used for the treatment of multicentric Castleman disease: A systematic review</atitle><jtitle>European journal of haematology</jtitle><date>2022-10</date><risdate>2022</risdate><volume>109</volume><issue>4</issue><spage>309</spage><epage>320</epage><pages>309-320</pages><issn>0902-4441</issn><eissn>1600-0609</eissn><abstract>Objectives
Treatment options for multicentric Castleman disease (MCD) remain limited. The only FDA‐approved drug is siltuximab for idiopathic MCD (iMCD), but the response rate with siltuximab is less than 50%. We performed a systematic review to examine the efficacy and safety of various regimens used for the treatment of MCD.
Methods
A database search on PubMed, Embase, Cochrane, Web of Science, and Clinicaltrials.gov using the terms “Castleman disease,” “treatment outcome,” and “patient safety” was done.
Results and Conclusions
Results from a randomized controlled trial and an extension study highlighted the efficacy and long‐term safety of siltuximab for iMCD; other trials showed tocilizumab to be a suitable alternative. A recent trial reported high response rates with thalidomide in iMCD patients. Promising results were reported for bortezomib in relapsed/ refractory MCD. For human herpesvirus‐8 (HHV8)‐associated MCD, rituximab along with doxorubicin therapy followed by maintenance with zidovudine and valganciclovir is the most effective therapy. A single‐arm trial has highlighted the potential role of tocilizumab in HHV8‐MCD. Data for these regimens are limited and mostly comprise nonrandomized trials. Further research on emerging agents could have a major impact on the treatment of this rare disease.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/ejh.13823</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4113-3304</orcidid><orcidid>https://orcid.org/0000-0001-6914-7439</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bortezomib Castleman disease Castleman's disease Clinical trials Doxorubicin HHV8 IL‐6 lymphadenopathy Patient safety Patients Rare diseases Rituximab Safety siltuximab Systematic review Thalidomide Zidovudine |
title | Efficacy and safety of regimens used for the treatment of multicentric Castleman disease: A systematic review |
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