Evidence map›Paper›PMID 34410976›Full record

ArticleIn vivo (Athens, Greece)

RAS Mutational Status in Advanced Colorectal Adenocarcinoma Treated With Anti-angiogenics: Preliminary Experience With Liquid Biopsy.

Belén García DE Santiago, Miriam López-Gómez, Pedro David Delgado-López, Ana Jiménez Gordo, Fernando Neria, Israel John Thuissard-Vasallo, César Gómez-Raposo, Francisco Zambrana Tevar, Juan Moreno-Rubio, Alicia Martínez Hernández and 2 more

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 34% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Cancers · 2022
    Article
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

12 authors at 4 institutions in 1 country.

Belén García DE SantiagoDepartment of Pharmacy, Infanta Sofía University Hospital, FIIB HUIS HHEN, Madrid, Spain; belengsantiago@yahoo.es.
Miriam López-GómezDepartment of Oncology, Infanta Sofía University Hospital, FIIB HUIS HHEN, Madrid, Spain.
Pedro David Delgado-LópezDepartment of Neurosurgery, Burgos University Hospital, Burgos, Spain.
Ana Jiménez GordoDepartment of Oncology, Infanta Sofía University Hospital, FIIB HUIS HHEN, Madrid, Spain.
Fernando NeriaFaculty of Biomedical Science and Health, Universidad Europea, Madrid, Spain.
Israel John Thuissard-VasalloFaculty of Biomedical Science and Health, Universidad Europea, Madrid, Spain.
César Gómez-RaposoDepartment of Oncology, Infanta Sofía University Hospital, FIIB HUIS HHEN, Madrid, Spain.
Francisco Zambrana TevarDepartment of Oncology, Infanta Sofía University Hospital, FIIB HUIS HHEN, Madrid, Spain.
Juan Moreno-RubioClinical Oncology Group, IMDEA Food Institute, CEI UAM+CSIC, Madrid, Spain.
Alicia Martínez HernándezDepartment of Pharmacy, Infanta Sofía University Hospital, FIIB HUIS HHEN, Madrid, Spain.
Irene IglesiasDepartment of Pharmacology, Pharmacognosy and Botany, Faculty of Pharmacy, Complutense University Madrid, Madrid, Spain.
Enrique CasadoDepartment of Oncology, Infanta Sofía University Hospital, FIIB HUIS HHEN, Madrid, Spain.
Hospital Universitario Infanta Sofía · ESUniversidad Europea de Madrid · ESMadrid Institute for Advanced Studies · ESUniversidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo determinate molecular changes in the downstream epidermal growth factor receptor signaling pathway using serial liquid biopsies in patients with metastatic colorectal tumors (mCRC) under anti-angiogenic treatment. PATIENTS AND

methodsDetermination of RAS mutation in primary tissue samples from colorectal tumors was performed in the 23 patients included in the study at diagnosis using quantitative-polymerase chain reaction. Sequential mutations were studied in circulating tumor (ct) DNA obtained from plasma samples.

resultsTwenty-three patients with RAS-mutated primary tumors were included. In the first ctDNA determination, 17 of these patients were found to have wild-type RAS status. Remarkably, three out of these 17 wild-type cases changed to RAS-mutated in subsequent ctDNA assays.

conclusionSerial liquid biopsies in patients with mCRC might be a useful tool for identifying changes in the RAS mutation status in patients who had undergone previous anti-angiogenic therapy. The understanding of these changes might help to better define the landscape of mCRC and be the path to future randomized studies.

Indexed as

AdenocarcinomaCirculating Tumor DNAColorectal NeoplasmsHumansLiquid BiopsyMutationCirculating Tumor DNAanti-angiogenic therapiescirculating tumor DNAColorectal cancerliquid biopsyRAS mutations

Identifiers

PMID34410976
PMCPMC8408740
OpenAlexW3194778165

What OpenQuestion holds

Textmetadata
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.