Evidence map›Paper›PMID 36550207›Full record

ArticleBritish journal of cancer2023

Clinical utility of liquid biopsy and integrative genomic profiling in early-stage and oligometastatic cancer patients treated with radiotherapy.

Guadalupe A Cifuentes, Adrián Santiago, Lucía Méndez Blanco, María Fueyo, Esther López Martínez, Raquel Soria, Irene Martín López, Pepa Cucarella Beltrán, Pablo Pardo-Coto, David Rodriguez-Rubi and 9 more

Abstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Ovarian Cancer Diagnosis and Prognosis Based on Cell-Free DNA Methylation.Cancer control : journal of the Moffitt Cancer Center
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Guadalupe A CifuentesLaboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.ORCID 0000-0002-0042-0051
Adrián SantiagoLaboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
Lucía Méndez BlancoServicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
María FueyoServicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
Esther López MartínezServicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
Raquel SoriaServicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
Irene Martín LópezLaboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
Pepa Cucarella BeltránServicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
Pablo Pardo-CotoOncología Médica, Centro Médico de Asturias, Oviedo, Asturias, Spain.
David Rodriguez-RubiOncología Médica, Centro Médico de Asturias, Oviedo, Asturias, Spain.
Karla UrquillaServicio de Oncología Radioterápica, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA, Oviedo, Asturias, Spain.
Noelia S DuránLaboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
Rebeca ÁlvarezLaboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
Claudia G LagoLaboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
Andrea OteroÁrea de Medicina de Precisión, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
Marta DiñeiroLaboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
Raquel CapínLaboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain.
Juan CadiñanosLaboratorio de Medicina Molecular, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain. jcb@imoma.es.ORCID 0000-0001-7561-7759
Rubén CabanillasÁrea de Medicina de Precisión, Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA), Oviedo, Asturias, Spain. ruben.cabanillas@cprecisionc.com.ORCID 0000-0003-3084-7766

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLiquid 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.

methodsWe 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.

resultsThe 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.

conclusionsIGP provides both valuable and actionable information for personalised decision-making in Radiation Oncology.

Indexed as

Circulating Tumor DNANeoplasmsRadiation OncologyBiomarkers, TumorGenomicsHumansLiquid BiopsyMutationBiomarkers, TumorCirculating Tumor DNA

Identifiers

PMID36550207
PMCPMC9977775

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.