Usefulness and Limitations of Rituximab in Managing Patients With Lymphoproliferative Disorder After Heart Transplantation

dc.contributor.authorSenechal, Mario
dc.contributor.authorCouture, Christian
dc.contributor.authorMorin, Joëlle
dc.contributor.authorLeblanc, Marie-Helene
dc.contributor.authorBourgault, Christine
dc.contributor.authorCantin, Bernard
dc.contributor.authorDemers, Sabrina
dc.date.accessioned2026-04-13T12:26:00Z
dc.date.issued2012-10
dc.description.abstractPosttransplant lymphoproliferative disorders remain an uncommon complication of heart transplant with a high mortality rate reported after conventional therapies. Four patients with posttransplant lymphoproliferative disorders, of whom 3 were CD20 positive, received intravenous dosages of rituximab, 375 mg/m2, weekly, for 6 ± 2 weeks. The overall response rate was 75% with 3 complete responses (CD20 positive) and 1 case of progressive disease (CD20 negative). Rituximab should be considered as a first-line therapy for patients with CD20 positive posttransplant lymphoproliferative disorders.
dc.identifier.citationExperimental and Clinical Transplantation, Cilt, 10, Sayı, 5, 2012 ss. 513-518en
dc.identifier.eissn2146-8427en
dc.identifier.issn1304-0855
dc.identifier.issue5en
dc.identifier.urihttps://hdl.handle.net/11727/14920
dc.identifier.volume10en
dc.language.isoen
dc.publisherBaşkent Üniversitesi
dc.sourceExperimental and Clinical Transplantationen
dc.subjectRituximab
dc.subjectLymphoma
dc.subjectHeart transplant
dc.subjectCD20
dc.titleUsefulness and Limitations of Rituximab in Managing Patients With Lymphoproliferative Disorder After Heart Transplantation
dc.typeCase Report

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