# Clinical outcomes of boron neutron capture therapy for unresectable oral cancer: a retrospective analysis

**Authors:** Yuki Yoshino, Satoshi Takeno, Teruhito Aihara, Naonori Hu, Akinori Sasaki, Kazuhiko Akita, Yasukazu Kanai, Mai Nojiri, Tsuyoshi Jinnin, Tetsuya Terada, Shinichi Haginomori, Keiji Nihei, Koji Ono

PMC · DOI: 10.3389/fonc.2026.1735487 · Frontiers in Oncology · 2026-02-13

## TL;DR

This study shows that boron neutron capture therapy (BNCT) is effective and safe for treating unresectable oral cancers that cannot be treated with standard radiation.

## Contribution

The study provides clinical evidence of BNCT's efficacy and safety in treating oral cancers unsuitable for definitive radiotherapy.

## Key findings

- BNCT achieved a 50% complete response rate in unresectable oral cancer patients.
- Severe oral mucositis occurred in 26% of patients, with predictors including high oral mucosal dose and dental metals.
- Two-year survival and disease control rates were 49% and 52%, respectively.

## Abstract

Surgery is the standard treatment for oral cancer but often causes functional and cosmetic problems, and reoperation is difficult. Radiotherapy (RT) is less effective, with reirradiation limited by normal tissue tolerance and salvage surgery after RT carrying high complication risks. Systemic therapy is used for local recurrence but yields poor outcomes, underscoring the need for better options. Boron neutron capture therapy (BNCT) is an established method that selectively delivers high tumor doses. This study evaluated BNCT efficacy and safety in unresectable oral cancers not amenable to definitive RT.

This retrospective study included oral cancer patients treated with BNCT between June 2020 and June 2024 under the Japanese public health insurance system. Primary endpoints were best treatment response and incidence of adverse events (AEs), particularly severe oral mucositis (Grade ≥ 3 by Common Terminology Criteria for AEs version 5). Predictors of severe oral mucositis were also examined. Secondary endpoints included overall survival (OS), locoregional control (LRC), and progression free survival (PFS).

Among 74 patients (follow-up period ≥3 months), the majority (73%) had recurrent cancer. The complete response rate was 50%. The major severe acute AE was severe oral mucositis (all Grade 3) in 26% of patients. The maximum oral mucosal dose and the number of dental metals were significant predictors of severe oral mucositis. The 2-year OS, LRC, and PFS rates were 49%, 52%, and 29%, respectively.

This study suggests that BNCT is an effective and safe treatment for unresectable oral cancers that cannot be definitively irradiated.

## Linked entities

- **Diseases:** oral cancer (MONDO:0023644)

## Full-text entities

- **Genes:** SLC7A5 (solute carrier family 7 member 5) [NCBI Gene 8140] {aka 4F2LC, CD98, D16S469E, E16, LAT1, MPE16}, TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}
- **Diseases:** Cancer (MESH:D009369), adrenal insufficiency (MESH:D000309), osteonecrosis (MESH:D010020), renal failure (MESH:D051437), Skin ulceration (MESH:D012883), BNCT (MESH:D016609), oral mucositis (MESH:D013280), N (MESH:C536108), AEs (MESH:D064420), LRC (MESH:D009364), head and neck cancer (MESH:D006258), metastases (MESH:D009362), hyperamylasemia (MESH:D034321), disease (MESH:D004194), PD (MESH:D010300), death (MESH:D003643), necrosis (MESH:D009336), Sepsis (MESH:D018805), squamous cell carcinoma (MESH:D002294), Kidney injury (MESH:D007674), mucositis (MESH:D052016), Hemorrhage (MESH:D006470), heart failure (MESH:D006333), laryngeal edema (MESH:D007819), non-oral cancers (MESH:D009062), pneumonia (MESH:D011014)
- **Chemicals:** 18F-fluorodeoxyglucose (MESH:D019788), metal (MESH:D008670), 10B (-), Boron (MESH:D001895)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945765/full.md

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Source: https://tomesphere.com/paper/PMC12945765