Successful Treatment of Refractory Post-Transplant Lymphoproliferative Disorder With Chimeric Antigen Receptor T-Cell Therapy in a Heart Transplant Recipient.
Katherine HickmannRyan SweeneyChelsea PetersonKathleen FaringerMadeline RileyMark BunkerAzam HadiCyrus KhanYazan SamhouriPublished in: Journal of hematology (2024)
Post-transplant lymphoproliferative disorders (PTLDs) are opportunistic malignancies that complicate the success of hematopoietic stem cell or solid organ transplantation. These disorders often arise post-transplant due to the immunosuppression required for minimizing the risk of rejection of donor tissue. First-line treatment of these disorders includes limiting immunosuppression when permissible. Subsequent treatment includes the use of monoclonal anti-CD20 antibody (rituximab), and/or combination chemotherapy. Chimeric antigen receptor (CAR) T-cell therapy has revolutionized the treatment paradigm in many lymphoid malignancies. It is not approved for PTLD due to exclusion of PTLD patients from pivotal clinical trials. Also, its utilization post-transplant can be complex and multidisciplinary care is of utmost importance for successful administration of a potentially curative treatment. We present a 68-year-old patient with history of heart transplant for non-ischemic cardiomyopathy, diagnosed with PTLD that was refractory to treatment using current guidelines until successfully receiving CAR T-cell therapy.
Keyphrases
- cell therapy
- clinical trial
- heart failure
- mesenchymal stem cells
- epstein barr virus
- end stage renal disease
- stem cells
- randomized controlled trial
- squamous cell carcinoma
- palliative care
- oxidative stress
- chronic kidney disease
- diffuse large b cell lymphoma
- ischemia reperfusion injury
- ejection fraction
- quality improvement
- health insurance
- blood brain barrier
- patient reported outcomes
- affordable care act