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Carfilzomib: A cause of drug associated thrombotic microangiopathy
Ibrahim Qaqish1, Ilana M Schlam2, Harini A Chakkera1
1Department of Nephrology, Mayo Clinic Arizona, 5777 East Mayo Blvd, Phoenix, AZ 85054, USA.
Abstract:
Carfilzomib is a selective proteosome inhibitor approved for treatment of relapsed and refractory multiple myeloma. Recent reports have linked exposure to carfilzomib with development of thrombotic microangiopathy (TMA). We describe two cases of biopsy proven thrombotic microangiopathy that occurred after the initiation of carfilzomib (dosed at 32 mg/m(2) and 23 mg/m(2), respectively) for relapsed multiple myeloma. Both patients were managed with discontinuation of the drug, therapeutic plasma exchange (TPE) and supportive care. Hemoglobin, platelets and renal function did not improve with TPE. TMA resolved with creatinine returning to baseline several weeks after discontinuation of the drug. The outcomes suggest that TPE is not beneficial for treating carfilzomib-induced TMA.
Insights
Carfilzomib can cause thrombotic microangiopathy (TMA) in multiple myeloma patients. Discontinuing the drug, not therapeutic plasma exchange, led to TMA resolution.
Area of Science:
- Oncology
- Nephrology
- Hematology
Background:
- Carfilzomib is a proteasome inhibitor used for relapsed/refractory multiple myeloma.
- Thrombotic microangiopathy (TMA) has been anecdotally linked to carfilzomib exposure.
Observation:
- Two cases of biopsy-proven TMA are presented following carfilzomib initiation.
- Patients received carfilzomib at doses of 32 mg/m^2 and 23 mg/m^2.
- Management included drug discontinuation, therapeutic plasma exchange (TPE), and supportive care.
Findings:
- Therapeutic plasma exchange (TPE) did not improve hemoglobin, platelets, or renal function.
- TMA resolved with normalization of creatinine levels weeks after carfilzomib discontinuation.
- These outcomes suggest TPE is not beneficial for carfilzomib-induced TMA.
Implications:
- Carfilzomib-induced TMA may resolve with drug cessation alone.
- The role of TPE in managing this specific adverse event warrants reevaluation.
- Further research is needed to understand the mechanism and optimal treatment of carfilzomib-related TMA.
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