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Liquid biopsy for KRAS, NRAS and BRAF mutation testing in advanced colorectal cancer patients: the Argentinean experience.

Leandro GüttleinMaría R LucaFederico EstesoCristóbal FresnoJavier MarianiMercedes Otero PizarroEsteban BrestSolange StarapoliKevin KreimbergPaula TevesAndrea Mendoza BertelliMaría R GirottiRuben SalanovaJuan Manuel O'Connor
Published in: Future oncology (London, England) (2022)
Objective: To analyze the frequency of KRAS, NRAS and BRAF hotspot mutations in circulating tumor DNA (ctDNA) from patients with metastatic colorectal cancer (mCRC). Methods: Observational, descriptive and retrospective study in mCRC patients with available ctDNA-based genotype of KRAS , NRAS and BRAF . Results: The frequencies of plasma mutations for KRAS , NRAS and BRAF were 34% (± 7), 4% (± 3) and 4% (± 3), respectively. Median overall survival of plasma-tested RAS/BRAF -mutated patients was 26.6 months (95% CI: 14.4-not estimable [NE]), while RAS/BRAF wild-type patients did not reach the median survival during follow-up. Median progression-free survival for RAS/BRAF wild-type and RAS/BRAF -mutated patients was 12 (95% CI: 7-NE) and 4 months (95% CI: 4-NE), respectively. Conclusion: Our work supports the utility of KRAS , NRAS and BRAF analysis in liquid biopsy from mCRC patients.
Keyphrases
  • wild type
  • end stage renal disease
  • circulating tumor
  • ejection fraction
  • chronic kidney disease
  • newly diagnosed
  • prognostic factors
  • metastatic colorectal cancer
  • free survival
  • patient reported