Charged particle radiotherapy for thyroid cancer. A systematic review
The role of external beam radiotherapy (EBRT) in thyroid cancer (TC) remains contentious due to limited data. Retrospective studies suggest adjuvant EBRT benefits high-risk differentiated thyroid cancer (DTC) and limited-stage anaplastic thyroid carcinoma (ATC), enhancing locoregional control and pr...
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Veröffentlicht in: | Critical reviews in oncology/hematology 2024-10, Vol.202, p.104463, Article 104463 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The role of external beam radiotherapy (EBRT) in thyroid cancer (TC) remains contentious due to limited data. Retrospective studies suggest adjuvant EBRT benefits high-risk differentiated thyroid cancer (DTC) and limited-stage anaplastic thyroid carcinoma (ATC), enhancing locoregional control and progression-free survival when combined with surgery and chemotherapy. Intensity-modulated radiotherapy (IMRT) and particle therapy (PT), including protons, carbon ions, and Boron Neutron Capture Therapy (BNCT), represent advances in TC treatment. Following PRISMA guidelines, we reviewed 471 studies from January 2002 to January 2024, selecting 14 articles (10 preclinical, 4 clinical). Preclinical research focused on BNCT in ATC mouse models, showing promising local control rates. Clinical studies explored proton, neutron, or photon radiotherapy, reporting favorable outcomes and manageable toxicity. While PT shows promise supported by biological rationale, further research is necessary to clarify its role and potential combination with systemic treatments in TC management.
•Thyroid cancer (TC) presents diverse subtypes with varying characteristics.•Treatment relies on surgery, radioactive iodine, and other modalities.•Article explores particle radiotherapy's role, especially boron neutron capture therapy (BNCT).•Reviewed studies encompass preclinical and clinical trials.•Particle therapy shows potential, requiring further research for optimal integration into TC management. |
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ISSN: | 1040-8428 1879-0461 1879-0461 |
DOI: | 10.1016/j.critrevonc.2024.104463 |