Abstract
Background: Patients with the heritable disease, Fanconi anemia (FA), have a 500-fold risk of developing head and neck squamous cell carcinomas (HNSCC). However, the use of conventional cytotoxic agents including radiation therapy and cisplatin-based chemotherapy is contraindicated in patients with FA due to underlying DNA repair defects. Methods/Results: We present a young FA patient with recurrent HNSCC and high-risk pathologic features treated with a therapeutic trial of chemoradiation. This novel strategy employs a gentle radiation dose and volume escalation with concurrent pembrolizumab. The patient completed the entire course of therapy with no treatment delays or interruptions. Conclusions: The FA patient population has a clear need for adjuvant treatment regimens given their predilection for HNSCC. A therapeutic trial may allow FA and other radiosensitive patients to trial radiation with the option to terminate treatment before any severe side effects occur and for some to complete a full course of treatment.
| Original language | English (US) |
|---|---|
| Pages (from-to) | E16-E22 |
| Journal | Head and Neck |
| Volume | 42 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 1 2020 |
All Science Journal Classification (ASJC) codes
- Otorhinolaryngology