Frontiers in Oncology (Aug 2024)

Is precision medicine the solution to improve organ preservation in laryngeal/hypopharyngeal cancer? A position paper by the Preserve Research Group

  • Davide Mattavelli,
  • Davide Mattavelli,
  • Gunnar Wichmann,
  • Davide Smussi,
  • Davide Smussi,
  • Alberto Paderno,
  • Maria Serrahima Plana,
  • Ricard Nin Mesia,
  • Micaela Compagnoni,
  • Alessandro Medda,
  • Susanna Chiocca,
  • Stefano Calza,
  • Yinxiu Zhan,
  • Carla Rognoni,
  • Rosanna Tarricone,
  • Rosanna Tarricone,
  • Erika Stucchi,
  • Erika Stucchi,
  • Luigi Lorini,
  • Cristina Gurizzan,
  • Ksenia Khelik,
  • Eivind Hovig,
  • Eivind Hovig,
  • Andreas Dietz,
  • Cesare Piazza,
  • Cesare Piazza,
  • Paolo Bossi,
  • Paolo Bossi

DOI
https://doi.org/10.3389/fonc.2024.1433333
Journal volume & issue
Vol. 14

Abstract

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In locally advanced (LA) laryngeal/hypopharyngeal squamous cell carcinoma (LHSCC), larynx preservation (LP) strategies aim at the cure of the disease while preserving a functional larynx, thus avoiding total laryngectomy and the associated impact on the quality of life. In the last decades, apart from transoral and open-neck organ preservation approaches, several non-surgical regimens have been investigated: radiotherapy alone, alternate, concurrent or sequential chemoradiation, and bioradiotherapy. Despite major progress, the identification of reliable and effective predictors for treatment response remains a clinical challenge. This review examines the current state of LP in LA-LHSCC and the need for predictive factors, highlighting the importance of the PRESERVE trial in addressing this gap. The PRESERVE trial represents a pivotal initiative aimed at finding the optimal therapy for laryngeal preservation specific to each patient through a retrospective analysis of data from previous LP trials and prospectively validating findings. The goal of the PRESERVE trial is to develop a comprehensive predictive classifier that integrates clinical, molecular, and multi-omics data, thereby enhancing the precision and efficacy of patient selection for LP protocols.

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