Evidence map›Paper›PMID 35409133›Full record

ArticleInternational journal of molecular sciences2022

A Liquid Biopsy-Based Approach for Monitoring Treatment Response in Post-Operative Colorectal Cancer Patients.

Barbara Kinga Barták, Tamás Fodor, Alexandra Kalmár, Zsófia Brigitta Nagy, Sára Zsigrai, Krisztina Andrea Szigeti, Gábor Valcz, Péter Igaz, Magdolna Dank, István Takács and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  14. Liquid Biopsy by ctDNA in Liver Transplantation for Colorectal Cancer Liver Metastasis.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2023
    Article
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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

11 authors at 1 institution in 1 country.

Barbara Kinga BartákDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
Tamás FodorDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
Alexandra KalmárDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
Zsófia Brigitta NagyDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
Sára ZsigraiDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
Krisztina Andrea SzigetiDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
Gábor ValczDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
Péter IgazDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.ORCID 0000-0003-2192-554X
Magdolna DankDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
István TakácsDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
Béla MolnárDepartment of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.
Semmelweis University · HU

Funding

Higher Education Institutional Excellence Programme of the Ministry of Human Capacities in Hungary 0Hungarian National Research, Development and Innovation Office (NKFIH) NVKP_16-1-2016-0004
6 · The paper itself

Abstract

Monitoring the therapeutic response of colorectal cancer (CRC) patients is crucial to determine treatment strategies; therefore, we constructed a liquid biopsy-based approach for tracking tumor dynamics in non-metastatic (nmCRC) and metastatic (mCRC) patients (n = 55). Serial blood collections were performed during chemotherapy for measuring the amount and the global methylation pattern of cell-free DNA (cfDNA), the promoter methylation of SFRP2 and SDC2 genes, and the plasma homocysteine level. The average cfDNA amount was higher (p < 0.05) in nmCRC patients with recurrent cancer (30.4 ± 17.6 ng) and mCRC patients with progressive disease (PD) (44.3 ± 34.5 ng) compared to individuals with remission (13.2 ± 10.0 ng) or stable disease (12.5 ± 3.4 ng). More than 10% elevation of cfDNA from first to last sample collection was detected in all recurrent cases and 92% of PD patients, while a decrease was observed in most patients with remission. Global methylation level changes indicated a decline (75.5 ± 3.4% vs. 68.2 ± 8.4%), while the promoter methylation of SFRP2 and SDC2 and homocysteine level (10.9 ± 3.4 µmol/L vs. 13.7 ± 4.3 µmol/L) presented an increase in PD patients. In contrast, we found exact opposite changes in remission cases. Our study offers a more precise blood-based approach to monitor the treatment response to different chemotherapies than the currently used markers.

Indexed as

Cell-Free Nucleic AcidsColorectal NeoplasmsBiomarkers, TumorDNA MethylationHomocysteineHumansLiquid BiopsyNeoplasm Recurrence, LocalBiomarkers, TumorCell-Free Nucleic AcidsHomocysteinecell-free DNAcolorectal cancerDNA methylationhomocysteinetherapeutic response

Identifiers

PMID35409133
PMCPMC8998310
OpenAlexW4220662920

What OpenQuestion holds

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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.