Document Type
Article
Publication Date
12-2-2021
Abstract
T-cell PTLDs are lymphoid proliferations that develop in recipients of SOT or allogeneic HSCT. They carry an extremely poor prognosis with a reported median survival of only 6 months. The infrequency with which they are encountered makes treatment a challenge due to the lack of prospective trials to guide management. The significantly higher risk of morbidity and mortality in T-cell PTLD, compared to B-cell PTLD, underscores the challenge of treating these patients and the need for new therapeutic options. Brentuximab vedotin, an ADC targeting CD30, is FDA-approved in combination with CHP as front-line treatment for patients with CD30 expressing PTCL. Herein we report a case of CD30-positive T-cell PTLD that was successfully treated with BV-CHP, suggesting the added value of the addition of BV to chemotherapy, contributing to our patient's long and ongoing progression-free survival. To our knowledge, this is the first documented case of successful treatment using BV-CHP for a CD30-positive, EBV-negative, late T-cell PTLD.
Recommended Citation
Hong, Jennifer; Johnson, William T; Kartan, Saritha; Gonsalves, Anitha S; Fenkel, Jonathan M.; Gong, Jerald Z.; and Porcu, Pierluigi, "Durable Response to Brentuximab Vedotin Plus Cyclophosphamide, Doxorubicin, and Prednisone (BV-CHP) in a Patient with CD30-Positive PTCL Arising as a Post-Transplant Lymphoproliferative Disorder (PTLD)" (2021). Department of Medical Oncology Faculty Papers. Paper 167.
https://jdc.jefferson.edu/medoncfp/167
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
PubMed ID
34940065
Language
English
Included in
Gastroenterology Commons, Oncology Commons, Pathology Commons
Comments
This article is the author’s final published version in Current Oncology, Volume 28, Issue 6, December 2021, Pages 5067-5072.
The published version is available at https://doi.org/10.3390/curroncol28060426. Copyright © Hong et al.