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Clinical utility of liquid biopsy and integrative genomic profiling in early-stage and oligometastatic cancer patients treated with radiotherapy.
Cifuentes, Guadalupe A; Santiago, Adrián; Méndez Blanco, Lucía; Fueyo, María; López Martínez, Esther; Soria, Raquel; Martín López, Irene; Cucarella Beltrán, Pepa; Pardo-Coto, Pablo; Rodriguez-Rubi, David; Urquilla, Karla; Durán, Noelia S; Álvarez, Rebeca; Lago, Claudia G; Otero, Andrea; Diñeiro, Marta; Capín, Raquel; Cadiñanos, Juan; Cabanillas, Rubén.
Affiliation
  • Cifuentes GA; Laboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
  • Santiago A; Laboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
  • Méndez Blanco L; Servicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
  • Fueyo M; Servicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
  • López Martínez E; Servicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
  • Soria R; Servicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
  • Martín López I; Laboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
  • Cucarella Beltrán P; Servicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
  • Pardo-Coto P; Oncología Médica, Centro Médico de Asturias, Oviedo, Asturias, Spain.
  • Rodriguez-Rubi D; Oncología Médica, Centro Médico de Asturias, Oviedo, Asturias, Spain.
  • Urquilla K; Servicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
  • Durán NS; Laboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
  • Álvarez R; Laboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
  • Lago CG; Laboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
  • Otero A; Área de Medicina de Precisión, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
  • Diñeiro M; Laboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
  • Capín R; Laboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
  • Cadiñanos J; Laboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain. jcb@imoma.es.
  • Cabanillas R; Área de Medicina de Precisión, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain. ruben.cabanillas@cprecisionc.com.
Br J Cancer ; 128(5): 857-876, 2023 03.
Article in En | MEDLINE | ID: mdl-36550207
ABSTRACT

BACKGROUND:

Liquid biopsy and Integrative Genomic Profiling (IGP) are yet to be implemented into routine Radiation Oncology. Here we assess the utility of germline, tumour and circulating cell-free DNA-based genomic analyses for the clinical management of early-stage and oligometastatic cancer patients treated by precision radiotherapy.

METHODS:

We performed germline, tissue- and liquid biopsy NGS panels on 50 early-stage/oligometastatic cancer patients undergoing radiotherapy. We also monitored ctDNA variants in serial liquid biopsies collected during radiotherapy and follow-up and evaluated the clinical utility of such comprehensive approach.

RESULTS:

The integration of different genomic studies revealed that only 1/3 of the liquid biopsy variants are of tumour origin. Altogether, 55 tumour variants (affecting 3/4 of the patients) were considered potentially actionable (for treatment and prognosis), whereas potential follow-up biomarkers were identified in all cases. Germline cancer-predisposing variants were present in three patients, which would have not been eligible for hereditary cancer testing according to clinical guidelines. The presence of detectable ctDNA variants before radiotherapy was associated with progression-free survival both in oligometastatic patients and in those with early-stage.

CONCLUSIONS:

IGP provides both valuable and actionable information for personalised decision-making in Radiation Oncology.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Radiation Oncology / Circulating Tumor DNA / Neoplasms Type of study: Guideline / Prognostic_studies Limits: Humans Language: En Journal: Br J Cancer Year: 2023 Document type: Article Affiliation country: Spain

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Radiation Oncology / Circulating Tumor DNA / Neoplasms Type of study: Guideline / Prognostic_studies Limits: Humans Language: En Journal: Br J Cancer Year: 2023 Document type: Article Affiliation country: Spain