Evidence map›Paper›PMID 35188804›Full record

SynthesisJCO precision oncology2022

Utility of Perioperative Measurement of Cell-Free DNA and Circulating Tumor DNA in Informing the Prognosis of GI Cancers: A Systematic Review.

Phillip J Hsu, Khushboo Singh, Ankit Dhiman, Hunter D D Witmer, Chuan He, Oliver S Eng, Daniel V T Catenacci, Mitchell C Posner, Kiran K Turaga

Open access · greenAbstract readSystematic Review
In one paragraph

Synthesis in JCO precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

9 authors at 1 institution in 1 country.

Phillip J HsuDepartment of Surgery, University of Chicago, Chicago, IL.
Khushboo SinghDepartment of Surgery, University of Chicago, Chicago, IL.
Ankit DhimanDepartment of Surgery, University of Chicago, Chicago, IL.ORCID 0000-0003-3086-2587
Hunter D D WitmerDepartment of Surgery, University of Chicago, Chicago, IL.ORCID 0000-0003-0008-8658
Chuan HeDepartment of Chemistry, University of Chicago, Chicago, IL.
Oliver S EngDepartment of Surgery, University of Chicago, Chicago, IL.
Daniel V T CatenacciDepartment of Medicine, University of Chicago, Chicago, IL.
Mitchell C PosnerDepartment of Surgery, University of Chicago, Chicago, IL.
Kiran K TuragaDepartment of Surgery, University of Chicago, Chicago, IL.
University of Chicago · US

Funding

MEDICAL SCIENTIST TRAININGT32GM007281 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 1985 to 2022
$32.1M
NIGMS NIH HHS T32 GM007281
6 · The paper itself

Abstract

purposeCurrent surveillance imaging and tumor markers lack sensitivity for the early detection of recurrence in GI cancers. This study critically evaluates the current literature on the role of sequential measurement of circulating tumor DNA (ctDNA) before and after curative resection in informing recurrence.

methodsA systematic search using a predefined, registered protocol was conducted for studies published between January 2010 and May 2020. Included studies described patients with GI cancers treated with curative-intent surgical resection and measurement of ctDNA both before and after surgery. Patients were divided into three groups on the basis of the presence or absence of ctDNA at these time points. The primary outcome was recurrence-free survival (RFS).

resultsThe search yielded 3,873 articles; five met the inclusion criteria and collectively evaluated 57 patients. Pooled median RFS was 62 months (interquartile range 19 to not reached). Although median RFS was not reached in group 1 (- to -) or group 2 (+ to -), median RFS in group 3 (+ to +) was 15 months (interquartile range 9.6-60.4 months). Cox hazard ratio was 4.46 (95% CI, 1.17 to 16.99;

conclusionDetectable ctDNA, either preoperatively or postoperatively, and its persistence after curative surgery are associated with a greater risk of recurrence and decreased RFS in GI cancers. Thus, perioperative measurement of ctDNA may be a useful postoperative risk stratification tool and guide additional therapies.

Indexed as

Cell-Free Nucleic AcidsCirculating Tumor DNAGastrointestinal NeoplasmsBiomarkers, TumorHumansPrognosisBiomarkers, TumorCell-Free Nucleic AcidsCirculating Tumor DNA

Identifiers

PMID35188804
PMCPMC8984241
OpenAlexW4212954032

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.