Volume 69, Issue 2 , Pages 475-482, 1 October 2007
Boron Neutron Capture Therapy in the Treatment of Locally Recurred Head and Neck Cancer
Purpose
Head and neck carcinomas that recur locally after conventional irradiation pose a difficult therapeutic problem. We evaluated safety and efficacy of boron neutron capture therapy (BNCT) in the treatment of such cancers.
Methods and Materials
Twelve patients with inoperable, recurred, locally advanced (rT3, rT4, or rN2) head and neck cancer were treated with BNCT in a prospective, single-center Phase I-II study. Prior treatments consisted of surgery and conventionally fractionated photon irradiation to a cumulative dose of 56–74 Gy administered with or without concomitant chemotherapy. Tumor responses were assessed using the RECIST (Response Evaluation Criteria in Solid Tumors) criteria and adverse effects using the National Cancer Institute common toxicity grading v3.0. Intravenously administered boronophenylalanine-fructose (BPA-F, 400 mg/kg) was used as the boron carrier. Each patient was scheduled to be treated twice with BNCT.
Results
Ten patients received BNCT twice; 2 were treated once. Ten (83%) patients responded to BNCT, and 2 (17%) had tumor growth stabilization for 5.5 and 7.6 months. The median duration of response was 12.1 months; six responses were ongoing at the time of analysis or death (range, 4.9–19.2 months). Four (33%) patients were alive without recurrence with a median follow-up of 14.0 months (range, 12.8–19.2 months). The most common acute adverse effects were mucositis, fatigue, and local pain; 2 patients had a severe (Grade 3) late adverse effect (xerostomia, 1; dysphagia, 1).
Conclusions
Boron neutron capture therapy is effective and safe in the treatment of inoperable, locally advanced head and neck carcinomas that recur at previously irradiated sites.
Boron neutron capture therapy, Radiotherapy, Head and neck cancer, Positron emission tomography, Boronophenylalanine
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Presented at the 12th International Congress on Neutron Capture Therapy, Takamatsu, Kagawa, Japan, October 9–13, 2006.
Supported by grants from the Academy of Finland and Helsinki University Central Hospital research funds. L.K., T.S., H.K., J.C., M. Kortesniemi, J.U.-S., S.S., and M. Kouri have received financial compensation from Boneca Corporation Ltd for the work done to treat BNCT patients. H.J. has received financial compensation from Boneca Corporation Ltd for consultations. H.K. is an employee of Boneca Corporation Ltd.
PII: S0360-3016(07)00555-X
doi:10.1016/j.ijrobp.2007.03.039
© 2007 Elsevier Inc. All rights reserved.
Volume 69, Issue 2 , Pages 475-482, 1 October 2007
