Medical management of pancreatic cancer: from personalization to broadening treatment strategies.

Journal: Cancer treatment reviews
Published Date:

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the most heterogeneous and deadly cancers. This review examines recently implemented strategies to integrate predictive tools and targeted therapies to improve treatments personalization and patient outcomes. Predictive transcriptomic signatures based on machine learning should optimize first-line chemotherapy selection, while organoid-based chemo-profiling could help late-line or non-standard treatments, particularly when transcriptomic signatures are unavailable to guide therapeutic decisions. Liquid biopsies enable real-time, non-invasive monitoring of tumour progression and resistance. Targeted therapies, even limited to a small subset of PDAC patients, exploit specific molecular vulnerabilities and several of those are under clinical evaluation to join PDAC armamentarium. Given PDAC's biological complexity, a multimodal approach combining predictive tools, functional testing, and molecularly-guided therapies is required to progress. Implementing those strategies in routine practice, combined with technological and clinical advances should enhance the precision, accessibility, and effectiveness of personalized PDAC treatment, as well as expand therapeutic options with new targets.

Authors

  • Nelson Dusetti
    Centre de Recherche en Cancérologie de Marseille (CRCM), INSERM U1068, Institut Paoli-Calmettes, Aix Marseille Université, CNRS UMR 7258, Marseille, France.
  • Jean Baptiste Bachet
    Dpt of Gastroenterology, Pitié-Salpêtrière Hospital - Sorbonne Universités, Paris, France.
  • Brice Chanez
    Medical Oncology Department, Institut Paoli-Calmettes, Marseille, France.
  • Cindy Neuzillet
    Medical oncology, Institut Curie, Paris, France.
  • Louis de Mestier
    Université Paris Cité, Dpt of Pancreatology - FHU MOSAIC, Beaujon Hospital, INSERM U1149, Clichy, France.
  • Nicolas Williet
    Department of Hepato-Gastroenterology and Gastrointestinal Oncology, University Institute of Cancerology and Hematology of Saint-Etienne (ICHUSE), Saint-Etienne, France.
  • Nicolas Frauhoffer
    Cancer Research Center of Marseille (CRCM), INSERM U1068, CNRS UMR 7258, Aix-Marseille University and Paoli-Calmettes Institut, Marseille, France.
  • Remy Nicolle
    Université Paris Cité, FHU MOSAIC, Centre de Recherche sur l'Inflammation (CRI), INSERM, U1149, CNRS, ERL 8252, F-75018, Paris, France.
  • Alice Boilève
    Gustave Roussy, INSERM U1279, Villejuif, France; Paris Saclay University, Orsay, France; Gustave Roussy, Department of Medical Oncology, Villejuif, France.
  • Anthony Turpin
    Department of Oncology, Lille University Hospital, Lille, France; CNRS UMR9020, INSERM UMR1277, Lille University, Pasteur Institut, Lille, France.
  • Raphaël Rodriguez
    Curie Institut, CNRS, INSERM, PSL Paris University, Paris, France.
  • Jérôme Cros
    Service d'anesthésie pédiatrique, Hôpital des Enfants, Limoges, France.
  • Juan Iovanna
    Centre de Recherche en Cancérologie de Marseille (CRCM), INSERM U1068, Institut Paoli-Calmettes, Aix Marseille Université, CNRS UMR 7258, Marseille, France.
  • Pascal Hammel
    Dpt of Medical oncology, Paul Brousse Hospital, Villejuif, France.