Sep 2026· International Journal of Particle Therapy· Vol 22, pp. 101963· 0 citations· 73 references
Medicine
TL;DR
Evidence supporting the use of hypofractionated PT re-RT remains limited but encouraging, and identifying predictors of toxicity and treatment response is essential to guide future research and to establish this approach as a viable option for selected patients.
Abstract
Aim Re-irradiation (re-RT) with hypofractionated proton therapy (PT) may be a treatment option in selected cases. Aim is to provide a critical overview of the state of the art. Methods PRISMA-compliant systematic review was performed on 2nd October 2025. All tumor sites were considered, provided that re-RT was performed with dose/fraction>2Gy(RBE) in adults. Oncological and toxicity outcomes were retrieved. Results Twelve original research works were identified. The total number of patients treated with hypofractionated PT re-RT was 478. The majority of patients were treated for recurrent tumors of either the gastrointestinal (GI) region (n = 143) or the lung (n = 123). The majority of the published series refers to data derived from retrospective and monoinstitutional experiences. Most patients were treated for recurrent tumors of either the gastrointestinal (GI) region (n = 143) or the lung (n = 123). Median sample size was 32 (interquartile range: 26-46, range: 14-83). Moderate hypofractionation (< 5 Gy(RBE)/fraction) was the most frequent schedule. All included studies had a radical intent. Overall, 2 year overall survival ranged from 8.4% (head & neck) to 87.5% (liver). The rate of severe side effects remained relevant. Of note, clinical outcomes and toxicity profiles were highly heterogeneous among the different tumor sites. Therefore, in the setting of re-RT with PT, conclusive data on the efficacy and toxicity profile of hypofractionated schedules could not be provided yet. Re-RT remains a personalized approach in almost all settings of tumor recurrence. Conclusion Evidence supporting the use of hypofractionated PT re-RT remains limited but encouraging. Identifying predictors of toxicity and treatment response is essential to guide future research and to establish this approach as a viable option for selected patients.
Pancreatic re-RT is feasible and may offer promising local control and time off chemotherapy for selected patients, and improvements in RT delivery with online adaptive therapy may further minimize toxicity.
Helen X. Hou, Hannah J. Roberts, P. Pathak et al.· American Journal of Clinical...· 0 citations
Objective To evaluate the efficacy and safety of low-dose hypofractionated radiotherapy (LDHRT) for liver metastases when combined with immunotherapy. Methods Patients with liver metastases receiving immunotherapy were enrolled in this study at Changzhou Second People’s Hospital from January 2019 to May 2025 (Ethics Ap...
Lan-Qun Qin, Yan-Shuang Wei, Li Tao et al.· OncoTargets and Therapy· 0 citations
Purpose Recurrent or second primary head and neck cancer (rsHNC) presents a radiotherapeutic challenge due to limited tolerance of previously irradiated tissues. These patients could benefit from dose painting (DP), which focuses on delivering maximal dose to areas of high tumor burden while respecting dose constraints...
E. Dale, M. Evensen, C. D. Amdal et al.· Frontiers in Oncology· 0 citations
BACKGROUND AND PURPOSE
Managing locally recurrent soft tissue sarcomas (STS) following prior radiation therapy remains challenging due to the lack of retreatment options and heightened risk of treatment-associated toxicity. Brachytherapy enables delivery of highly localized radiation with rapid dose fall-off and may se...
Ashwin Subramaniam, William Jin, B. Rich et al.· Brachytherapy· 0 citations
Introduction Lung cancer is commonly treated with stereotactic body radiotherapy (SBRT) and hypofractionated RT (HFRT). Delivering these ablative regimens with proton beam therapy (PBT) may yield dosimetric and clinical advantages, particularly for high-risk cases. We evaluated safety and efficacy of SBRT/HFRT PBT for...
Alexander J. Allen, C. B. Simone, Kai Sun et al.· Clinical and Translational R...· 0 citations
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