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A Novel Adverse Event Associated with Olaparib Therapy in a Patient with Metastatic Breast Cancer
Megan Wheelden1, Leah Cream1, Jeffrey Sivik2
1Department of Medicine, Division of Hematology/Oncology, Penn State Hershey Medical Center, Hershey, PA, USA.
Abstract:
Olaparib was first FDA approved for use in women with advanced ovarian cancer and germline BRCA mutations. Based on the results of subsequent research, the use of this drug has been expanded to patients with metastatic breast cancer with germline BRCA mutation. With the use of a relatively new medication and a larger patient population eligible for therapy, monitoring for novel adverse events associated with therapy is important. This case represents a patient with metastatic breast cancer and germline BRCA2 mutation who developed erythema nodosum after initiation of therapy with olaparib capsules. Her characteristic rash appeared shortly after starting olaparib and recurred after restarting olaparib an additional two times. She was treated with short courses of prednisone therapy with or without holding olaparib with resolution of her rash. The patient was later restarted on olaparib capsules 200 mg twice daily, and she more recently has been maintained on olaparib tablets 300 mg twice daily. On both regimens, the patient experienced only attenuated episodes of erythema nodosum that have not required cessation of therapy or steroid therapy.
Insights
Olaparib, a PARP inhibitor, can cause erythema nodosum in patients with metastatic breast cancer and BRCA2 mutations. This adverse event may be managed with dose adjustments and short-term steroid therapy.
Area of Science:
- Oncology
- Pharmacology
- Dermatology
Background:
- Olaparib is FDA-approved for ovarian and metastatic breast cancer with germline BRCA mutations.
- Expanded use necessitates monitoring for novel adverse events.
- PARP inhibitors represent a significant advancement in targeted cancer therapy.
Observation:
- A patient with metastatic breast cancer and a germline BRCA2 mutation developed erythema nodosum.
- The rash appeared shortly after initiating olaparib and recurred upon re-challenge.
- Erythema nodosum is a rare but notable adverse event associated with olaparib therapy.
Findings:
- The patient's erythema nodosum resolved with prednisone therapy and/or temporary olaparib discontinuation.
- Subsequent olaparib re-initiation at adjusted doses (capsules and tablets) resulted in attenuated erythema nodosum episodes.
- The patient was able to continue olaparib therapy without requiring cessation or steroid treatment.
Implications:
- This case highlights erythema nodosum as a potential adverse event of olaparib in BRCA-mutated breast cancer.
- Management strategies involving dose modification and short-term corticosteroids may allow for continued olaparib treatment.
- Further research into the mechanisms and management of olaparib-induced skin reactions is warranted.
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