Evidence map›Paper›PMID 27852040›Full record

Trial reportOncotarget2017

Clinical validation of prospective liquid biopsy monitoring in patients with wild-type RAS metastatic colorectal cancer treated with FOLFIRI-cetuximab.

Rodrigo A Toledo, Antonio Cubillo, Estela Vega, Elena Garralda, Rafael Alvarez, Lisardo U de la Varga, Jesús R Pascual, Gema Sánchez, Francesca Sarno, Susana H Prieto and 4 more

Abstract readClinical Trial
In one paragraph

Trial report in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
–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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  9. Circulating Tumor DNA to Drive Treatment in Metastatic Colorectal Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Review
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  11. Evaluation ofCells · 2023
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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

14 authors.

Rodrigo A ToledoCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Antonio CubilloCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Estela VegaCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Elena GarraldaCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Rafael AlvarezCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Lisardo U de la VargaCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Jesús R PascualCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Gema SánchezCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Francesca SarnoCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Susana H PrietoLaboratorio de Dianas Terapeúticas, Madrid, Spain.
Sofía PereaCentro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain.
Pedro P Lopéz-CasasSpanish National Cancer Research Centre (CNIO), Madrid, Spain.
Fernando López-RíosLaboratorio de Dianas Terapeúticas, Madrid, Spain.
Manuel HidalgoSpanish National Cancer Research Centre (CNIO), Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer genomics and translational medicine rely on the molecular profiling of patient's tumor obtained during surgery or biopsy. Alternatively, blood is a less invasive source of tumor DNA shed, amongst other ways, as cell-free DNA (cfDNA). Highly-sensitive assays capable to detect cancer genetic events from patient's blood plasma became popularly known as liquid biopsy (LqB). Importantly, retrospective studies including small number of selected patients with metastatic colorectal cancer (mCRC) patients treated with anti-EGFR therapy have shown LqB capable to detect the acquired clonal mutations in RAS genes leading to therapy resistance. However, the usefulness of LqB in the real-life clinical monitoring of these patients still lack additional validation on controlled studies. In this context, we designed a prospective LqB clinical trial to monitor newly diagnosed KRAS wild-type (wt) mCRC patients who received a standard FOLFIRI-cetuximab regimen. We used BEAMing technique for evaluate cfDNA mutations in KRAS, NRAS, BRAF, and PIK3CA in twenty-five patients during a 2-y period. A total of 2,178 cfDNA mutation analyses were performed and we observed that: a) continued wt circulating status was correlated with a prolonged response; b) smoldering increases in mutant cfDNA were correlated with acquired resistance; while c) mutation upsurge/explosion anticipated a remarkable clinical deterioration. The current study provides evidences, obtained for the first time in an unbiased and prospective manner, that reinforces the utility of LqB for monitoring mCRC patients.

Indexed as

Antineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCamptothecinCetuximabClass I Phosphatidylinositol 3-KinasesColorectal NeoplasmsDNA Mutational AnalysisFemaleFluorouracilGTP PhosphohydrolasesHumansLeucovorinLiquid BiopsyMaleMembrane ProteinsNeoplasm MetastasisAntineoplastic Agents, ImmunologicalBRAF protein, humanCamptothecinCetuximabClass I Phosphatidylinositol 3-KinasesFluorouracilGTP PhosphohydrolasesKRAS protein, humanLeucovorinMembrane ProteinsNRAS protein, humanPIK3CA protein, humanProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)ras Proteinsanti-EGFRcetuximabcfDNAcolorectal cancerliquid biopsy

Identifiers

PMID27852040
PMCPMC5471055

What OpenQuestion holds

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Registered trials

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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.