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May 31, 2026Radiation Oncology0 citationsOpen Access

High-dose stereotactic radiotherapy boost in the radical treatment of head and neck tumors

PPPaweł PolanowskiATAndrzej TukiendorfANAleksandra Nasiek

Key Points

  • The study evaluates the effectiveness and safety of high-dose stereotactic radiotherapy in the treatment of head and neck tumors.
  • Prospective, single-center trial with 28 patients having head and neck tumors.
  • Combining conventionally fractionated radiotherapy with a high-dose stereotactic boost of 8 to 18 Gy.
  • Registration on ClinicalTrials.gov (NCT06472570) and approval by local Bioethics Committee.
  • A complete response was observed in 25 patients (89%).
  • Positive surgical margins increased metastasis risk 18-fold (p = 0.015) and mortality risk 3-fold (p = 0.030).
  • Late toxicity increased after exceeding a biological effective dose of 143.33 Gy (p = 0.0148).

Abstract

The current results of head and neck cancer treatment remain suboptimal therefore, novel approaches are needed to improve its effectiveness. This prospective, single-center study aims to assess the results and safety of combining conventionally fractionated radiotherapy with a high-dose stereotactic radiotherapy boost in radical treatment. Twenty-eight patients with head and neck tumors of diverse localizations and histopathologies were recruited. The stereotactic boost was delivered to primary tumors or metastatic nodes up to 6 days before or after conventional radiotherapy. The boost doses ranged from 8 to 18 Gy. A complete response was observed in 25 patients (89%). The response did not depend on boost size or its timing within the regimen. Disease progression caused death in 5 cases. Positive surgical margins increased the risk of metastasis eighteenfold (p = 0.015) and mortality threefold (p = 0.030). A higher Zubrod performance status correlated with greater acute mucosal and skin toxicity. The most severe late complications were carotid blow-out syndrome (with actinomycosis coinfection) and brain necrosis. The risk of late toxicity increased after exceeding a biological effective dose of 143.33 Gy (p = 0.0148). A boost with a dose of 10 Gy represents a promising treatment option with permissible tolerance, with higher doses offering similar efficacy but greater late toxicity. The study protocol was approved by the local Bioethics Committee (KB/430 − 87/19) and registered on the ClinicalTrials.gov (NCT06472570) on 25 June 2024.

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Cite This Study

Polanowski et al. (2026) studied this question.

synapsesocial.com/papers/6a1bd0df5783ba022b6fc8bbhttps://doi.org/10.1186/s13014-026-02857-2
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