Liquid Biopsy: The Challenges of a Revolutionary Approach in Oncology.

Journal: International journal of molecular sciences
Published Date:

Abstract

Liquid biopsy has gained attention in oncology as a non-invasive diagnostic tool, offering valuable insights into tumor biology through the analysis of circulating nucleic acid (cfDNA and cfRNA), circulating tumor cells (CTCs), extracellular vesicles (EVs), and tumor-educated platelets (TEPs). In this review, we summarize the clinical use of liquid biopsies in cancer now and look forward to its future, with a particular emphasis on some the methods used to isolate the liquid biopsy analytes. This technique provides real-time information on tumor dynamics, treatment response, and disease progression, with the potential for early diagnosis and personalized treatment. Despite its advantages, liquid biopsy faces several challenges, particularly in detecting analytes in early-stage cancers and evaluating the tumor molecular fraction. Tumor burden, molecular fraction, and the presence of subclones can impact the sensitivity and specificity of the analysis. Recent advancements in artificial intelligence (AI) have enhanced the diagnostic accuracy of liquid biopsy by integrating data, and multimodal approaches that combine multiple biomarkers such as ctDNA, CTCs, EVs, and TEPs show promise in providing a more comprehensive view of tumor characteristics. Liquid biopsy has the potential to revolutionize cancer care by providing rapid, non-invasive, and cost-effective diagnostics, enabling timely interventions and personalized treatment strategies.

Authors

  • Claudio Antonio Coppola
    Unità di Diagnostica Molecolare e Farmacogenetica, IRCCS Istituto Tumori "Giovanni Paolo II", 70124 Bari, Italy.
  • Simona De Summa
    Unità di Diagnostica Molecolare e Farmacogenetica, IRCCS Istituto Tumori "Giovanni Paolo II", 70124 Bari, Italy.
  • Giuseppina Matera
    Unità di Diagnostica Molecolare e Farmacogenetica, IRCCS Istituto Tumori "Giovanni Paolo II", 70124 Bari, Italy.
  • Brunella Pilato
    Unità di Diagnostica Molecolare e Farmacogenetica, IRCCS Istituto Tumori "Giovanni Paolo II", 70124 Bari, Italy.
  • Debora Traversa
    Unità di Diagnostica Molecolare e Farmacogenetica, IRCCS Istituto Tumori "Giovanni Paolo II", 70124 Bari, Italy.
  • Stefania Tommasi
    Unità di Diagnostica Molecolare e Farmacogenetica, IRCCS Istituto Tumori "Giovanni Paolo II", 70124 Bari, Italy.