AI Article Synopsis

  • Definitive concurrent chemoradiotherapy (CRT) is the primary treatment for advanced head and neck cancer, but it can lead to late radiation-induced side effects like brachial plexopathy (RIBP), affecting patients' quality of life.
  • A dosimetric study involving 30 HNC patients aimed to identify factors influencing radiation dose variations to the brachial plexus and evaluate RIBP occurrences during follow-up.
  • Results indicated that nodal stage and tumor location significantly affect radiation dose to the brachial plexus, with a 6.67% incidence of RIBP after a median follow-up of 17.9 months, highlighting the need to consider the brachial plexus as an organ at risk in

Article Abstract

Background: Definitive concurrent chemoradiotherapy (CRT) is the standard of care in advanced stages of head and neck cancer (HNC). With evident increase in survival rate there is also simultaneous increase in toxicity affecting the quality of life. One of the less researched late toxicity is radiation induced brachial plexopathy (RIBP). In this dosimetric study we intent to contour the brachial plexus (BP) as an organ at risk (OAR) and determine the factors that contribute to dose variations to BP, and clinically evaluate the patients for RIBP during follow-up using a questionnaire.

Materials And Methods: 30 patients with HNC planned for CRT from September 2020 to June 2022 were accrued. Patients were treated to a dose of 6600 cGy with intensity modulated radiotherapy using the simultaneous integrated boost technique. From the dose-volume histogram (DVH) statistics the BP volume, Dmax and other parameters like V66, V60 were assessed and was correlated with respect to primary tumour and nodal stage.

Results: On corelation, more than the T stage, the N stage and the primary location had a significant impact on the Dmax. With a median follow-up of 17.9 months, the incidence of RIBP was 6.67%. The 2-year disease free survival and the 2-year overall survival were 53.7% and 59.4%, respectively.

Conclusions: In oropharyngeal/hypopharyngeal primaries and in advanced nodal disease, BP receives higher doses contributing to RIBP. Primary tumor and nodal stage also impacted V60 and V66 of BP. Hence, contouring of BP as an OAR becomes imperative, and respecting the DVH parameters is essential.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11321783PMC
http://dx.doi.org/10.5603/rpor.101097DOI Listing

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