Carfilzomib-Induced Tumor Lysis Syndrome and Biventricular Heart Failure in a Patient With Multiple Myeloma
Farhan Azad1, Ross Moyer1, Clive J Miranda1
1Internal Medicine, University at Buffalo, Buffalo, USA.
Abstract:
Carfilzomib is a proteasome inhibitor (PI) used in multiple myeloma (MM) that is resistant to other therapies. Despite its efficacy and potency, carfilzomib has been associated with kidney injuries, cardiovascular toxic effects, and hematological adverse events. Tumor lysis syndrome (TLS) following the use of PIs in MM, a malignancy not known to cause TLS, has seldom been reported. We present a case of a patient with a known diagnosis of MM who received prior therapy including bortezomib, a first-generation PI, developing worsening heart failure and new onset TLS days after the administration of carfilzomib.
Insights
Carfilzomib, a proteasome inhibitor, can cause tumor lysis syndrome (TLS) and heart failure in multiple myeloma patients. This rare complication highlights the need for careful monitoring during treatment.
Area of Science:
- Oncology
- Pharmacology
Background:
- Multiple myeloma (MM) is a hematological malignancy.
- Proteasome inhibitors (PIs) like carfilzomib are used to treat refractory MM.
- Carfilzomib is associated with known toxicities, including cardiovascular and renal effects.
Observation:
- A patient with MM, previously treated with bortezomib, received carfilzomib.
- The patient developed worsening heart failure and new-onset tumor lysis syndrome (TLS).
- TLS is a rare complication of PI therapy in MM.
Findings:
- Carfilzomib administration preceded the onset of TLS and cardiac complications.
- This case suggests a potential link between carfilzomib and TLS in MM.
- The development of TLS in MM treated with PIs is an underreported event.
Implications:
- Clinicians should be vigilant for TLS in MM patients receiving carfilzomib.
- Further investigation into the mechanisms of PI-induced TLS is warranted.
- This case underscores the importance of monitoring for rare adverse events during novel cancer therapy.
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