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Assessment of postoperative circulating tumour DNA to predict early recurrence in patients with stage I-III right-sided colon cancer: prospective observational study.
Lygre, Kristin B; Forthun, Rakel B; Høysæter, Trude; Hjelle, Sigrun M; Eide, Geir E; Gjertsen, Bjørn T; Pfeffer, Frank; Hovland, Randi.
Afiliação
  • Lygre KB; Department of Gastrointestinal Surgery, Haraldsplass Deaconess Hospital, Bergen, Norway.
  • Forthun RB; Department of Gastrointestinal Surgery, Haukeland University Hospital, Bergen, Norway.
  • Høysæter T; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Hjelle SM; Department of Medicine, Haukeland University Hospital, Bergen, Norway.
  • Eide GE; Section for Cancer Genomics, Haukeland University Hospital, Bergen, Norway.
  • Gjertsen BT; Section for Cancer Genomics, Haukeland University Hospital, Bergen, Norway.
  • Pfeffer F; Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
  • Hovland R; Department of Medicine, Haukeland University Hospital, Bergen, Norway.
BJS Open ; 8(1)2024 Jan 03.
Article em En | MEDLINE | ID: mdl-38242575
ABSTRACT

BACKGROUND:

Right-sided colon cancer (RCC) differs in mutation profile and risk of recurrence compared to distal colon cancer. Circulating tumour DNA (ctDNA) present after surgery can identify patients with residual disease after curative surgery and predict risk of early recurrence.

METHODS:

This is a prospective observational biomarker trial with exploration of ctDNA in 50 non-metastatic RCC patients for which oncological right-sided colectomy was performed. Blood samples were collected preoperatively, within 1 month post surgery, 3 months (not mandatory), 6 months and every 6 months thereafter. Plasma cell free DNA and/or tumour was investigated for cancer-related mutations by the next-generation sequencing (NGS) panel AVENIO surveillance specifically designed for ctDNA analysis. Detected mutations were quantified using digital droplet PCR (ddPCR) for follow-up. Recurrence-free survival was explored.

RESULTS:

50 patients were recruited. Somatic cancer-related mutations were detected in 47/50 patients. ddPCR validated results from NGS for 27/34 (plasma) and 72/72 samples (tumour). Preoperative ctDNA was detected in 31/47 of the stage I/III patients and the majority of ctDNA positive patients showed reduction of ctDNA after surgery (27/31). ctDNA-positive patients at first postoperative sample had high recurrence risk compared to patients without measurable ctDNA (adjusted hazard ratio 172.91; 95% c.i. 8.70 to 3437.24; P 0.001).

CONCLUSION:

ctDNA was detectable in most patients with non-metastatic RCC before surgery. Positive postoperative ctDNA was strongly associated with early recurrence. Detectable postoperative ctDNA is a prognostic factor with high (100%) positive predictive value for recurrence in this cohort of non-metastatic RCC. CLINICAL TRIAL REGISTRATION ClinicalTrials.gov ID NCT03776591.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Neoplasias do Colo / DNA Tumoral Circulante / Neoplasias Renais Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: BJS Open Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Neoplasias do Colo / DNA Tumoral Circulante / Neoplasias Renais Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: BJS Open Ano de publicação: 2024 Tipo de documento: Article