Publications by authors named "A Ortega-Franco"

Circulating tumor cells (CTCs) enumeration and molecular profiling hold promise in revolutionizing the management of solid tumors. Their understanding has evolved significantly over the past two decades, encompassing pivotal biological discoveries and clinical studies across various malignancies. While for some tumor types, such as breast, prostate, and colorectal cancer, CTCs are ready to enter clinical practice, for others, additional research is required.

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Background: Pembrolizumab is licensed for the treatment of pre-treated and PD-L1 positive non-small cell lung cancer (NSCLC), but response is heterogeneous. In this context, the Lung Immune Prognostic Index (LIPI) has been proposed as tool to prognosticate outcome.

Objective: To investigate the real-world efficacy and safety of pembrolizumab in pre-treated NSCLC patients and the clinical utility of LIPI for patients' selection.

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Article Synopsis
  • Circulating tumor DNA (ctDNA) is DNA from cancer cells found in the bloodstream, and liquid biopsy is a less invasive way to analyze this ctDNA, enabling the identification of cancer-specific genetic changes.
  • * This technology enhances cancer diagnostics by detecting early-stage diseases, understanding tumor diversity, and improving therapy decisions, including monitoring treatment response.
  • * Since gastrointestinal cancers are common and deadly, ctDNA offers a promising method for diagnosing and managing these tumors, potentially lowering the overall impact of cancer worldwide.
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The introduction of tyrosine kinase inhibitors (TKI) for the treatment of metastatic non-small cell lung cancer (NSCLC) harbouring sensitizing epidermal growth factor receptor (EGFR) gene mutations revolutionized the diagnostic and treatment algorithm of this subset of patients almost two decades ago. Since then, a number of trials have evaluated the role of TKI therapy in early-stage disease, with encouraging disease-free survival (DFS) results but lack of a survival advantage. ADAURA, a phase III trial evaluating 3 years of adjuvant osimertinib versus placebo in patients harbouring EGFR mutations with completely resected stage IB-IIIA NSCLC, recently reported a profound DFS benefit (hazard ratio 0.

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