Evidence map›Paper›PMID 28742791›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2017

Correlation Between Circulating Tumor DNA Levels and Response to Tyrosine Kinase Inhibitors (TKI) Treatment in Non-Small Cell Lung Cancer.

Zhangjing Wei, Wenyue Wang, Zitan Shu, Xue Zhou, Yanfang Zhang

Abstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Assessment ofArchives of medical science : AMS · 2020
    Article
  5. Article
  6. Article
  7. Circulating tumor DNA (ctDNA) in the era of personalized cancer therapy.Journal of diabetes and metabolic disorders · 2018
    Review
  8. 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

5 authors.

Zhangjing WeiDepartment of Diagnostic Medicine, JingMen No. 1 People's Hospital, JingMen, Hubei, China (mainland).
Wenyue WangDepartment of Department of Gynecology and Obstetrics, Shayang People's Hospital, JingMen, Hubei, China (mainland).
Zitan ShuDepartment of Diagnostic Medicine, JingMen No. 1 People's Hospital, JingMen, Hubei, China (mainland).
Xue ZhouDepartment of Diagnostic Medicine, JingMen No. 1 People's Hospital, JingMen, Hubei, China (mainland).
Yanfang ZhangDepartment of Diagnostic Medicine, Shengli Oilfield Central Hospital, Dongying, Shandong, China (mainland).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Clinical monitoring of EGFR-positive NSCLC patients is important to gauge treatment response. The current study addresses the usage of circulating tumor DNA (ctDNA) as a prognostic marker during treatment of first-generation TKIs. MATERIAL AND METHODS Serial samplings of peripheral blood from 200 EGFR-positive NSCLC patients were taken. Baseline ctDNA quantification was conducted by digital droplet PCR before TKI treatment was administered and compared to primary biopsies. Thereafter blood sampling at different treatment cycles were measured and assessed for its prognostic and predictive value. RESULTS ctDNA was successfully detected in a number of patients and overall concordance rate was 84%. Importantly, we observed a strong correlation to ctDNA increase with disease progression using radiographic scans. In addition to survival analysis, we noted patients with the largest ctDNA variations had worst outcome. A significant number of EGFR patients during treatment developed a secondary mutation T790M and this cohort had worst survival outcome as well. CONCLUSIONS Our study demonstrated a highly associative relation of ctDNA to NSCLC patients during treatment that can be utilized to gauge treatment response. CtDNA is an attractive means compared with conventional core needle biopsies and presents new methods for accurately profiling NSCLC disease progression.

Indexed as

AgedBiomarkers, TumorCarcinoma, Non-Small-Cell LungCirculating Tumor DNADisease ProgressionDrug Resistance, NeoplasmErbB ReceptorsFemaleGenes, erbB-1HumansLung NeoplasmsMaleMiddle AgedMutationPrognosisProtein Kinase InhibitorsBiomarkers, TumorCirculating Tumor DNAErbB ReceptorsProtein Kinase InhibitorsProtein-Tyrosine Kinases

Identifiers

PMID28742791
PMCPMC5540003

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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.