Evidence map›Paper›PMID 41438484›Full record

ArticleAdvances in radiation oncology2026

Boron Neutron Capture Therapy in Recurrent High-Grade Gliomas: Safety, Efficacy, and Pharmacokinetics From a Multicenter, Dose-Escalation Phase 1 Trial.

Woohyoung Kim, Jae-Sung Park, Jin-Ho Song, Heon Yoo, Kawngwoo Park, Hyun Ju Kim, Dong-Won Shin, Sung Uk Lee, Stephen Ahn, Seunggyun Ha and 5 more

Abstract read
In one paragraph

Article in Advances in radiation oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Woohyoung KimDepartment of Clinical Development, DAWONMEDAX CO, Ltd, Incheon, Republic of Korea.
Jae-Sung ParkDepartment of Neurosurgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Jin-Ho SongDepartment of Radiation Oncology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Heon YooDepartment or Neuro-Oncology Clinic, National Cancer Center, Goyang, Republic of Korea.
Kawngwoo ParkDepartment of Neurosurgery, Gachon University Gil Medical Center, Incheon, Republic of Korea.
Hyun Ju KimDepartment of Radiation Oncology, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of Korea.
Dong-Won ShinDepartment of Neurosurgery, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of Korea.
Sung Uk LeeCenter for Proton Therapy, National Cancer Center, Goyang, Republic of Korea.
Stephen AhnDepartment of Neurosurgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Seunggyun HaDivision of Nuclear Medicine, Department of Radiology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
JunGyu YiMedical Device Division, DAWONMEDAX CO, Ltd, Incheon, Republic of Korea.
Kwan ChoDAWONMEDAX CO, Ltd, Incheon, Republic of Korea.
Hyo Jung SeoDepartment of Nuclear Medicine, BNCT Center, Incheon, Republic of Korea.
Hyung-Seok LimAsan Medical Center, Department of Clinical Pharmacology and Therapeutics, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Gi-Taek YeeDepartment of Radiation Oncology, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Boron neutron capture therapy (BNCT) is an advanced radiation therapy delivering highly selective tumor cell destruction via localized fission reactions. This phase 1 study evaluated the safety and efficacy of BNCT using [B-10]L-4-boronophenylalanine (BPA) in patients with recurrent high-grade gliomas, mostly glioblastomas. Methods and Materials: A 3 + 3 dose-escalation design was used to determine the maximum tolerated dose of BNCT across 3 planned cohorts (D Results: Six patients were treated between December 2022 and January 2024: 3 in the 9 Gy-Eq and 3 in the 11 Gy-Eq cohort. No DLTs or grade ≥4 TEAEs occurred. Two patients experienced grade 3 TEAEs (brain edema, seizure). Common adverse events were alopecia, aphasia, brain edema, and seizures. One serious adverse event (grade 3 seizure) was reported. Median follow-up was 9.03 months. Median progression-free survival was 1.87 months by response assessment in neuro-oncology; not reached by modified response assessment in neuro-oncology. Objective response was not observed. All patients survived to study completion; median OS not reached, maximum OS was 16.56 months. BPA pharmacokinetics were within expected ranges. The safety monitoring committee selected 11 Gy-Eq as the recommended phase 2 radiation dose, balancing tumoricidal effects with risks of necrosis and bevacizumab requirements. Conclusions: This study demonstrates the acceptable safety profile of BNCT and suggests potential survival benefits in recurrent high-grade glioma. However, given the limited sample size and follow-up period, extended observation is required to validate long-term efficacy and safety.

Identifiers

PMID41438484
PMCPMC12719081

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.