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
Hauptverfasser: Rehman, Mohammad Ebad Ur, Chattaraj, Asmi, Neupane, Karun, Rafae, Abdul, Saeed, Sajeel, Basit, Jawad, Ibrahim, Atif, Khouri, Jack, Mukherjee, Sudipto, Anwer, Faiz
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container_end_page 320
container_issue 4
container_start_page 309
container_title European journal of haematology
container_volume 109
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
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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 &amp; Sons A/S. 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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. 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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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