Evidence map›Paper›PMID 38732326›Full record

ArticleDiagnostics (Basel, Switzerland)2024

Advancing Evidence Generation for Circulating Tumor DNA: Lessons Learned from A Multi-Assay Study of Baseline Circulating Tumor DNA Levels across Cancer Types and Stages.

Brittany A McKelvey, Hillary S Andrews, Frederick L Baehner, James Chen, Carin R Espenschied, David Fabrizio, Vanessa Gorton, Claire Gould, Justin Guinney, Greg Jones and 10 more

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. 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

20 authors.

Brittany A McKelveyFriends of Cancer Research, Washington, DC 20036, USA.ORCID 0000-0001-9239-7153
Hillary S AndrewsFriends of Cancer Research, Washington, DC 20036, USA.ORCID 0000-0002-0177-2024
Frederick L BaehnerExact Sciences Corp., Madison, WI 53719, USA.
James ChenTempus AI, Inc., Chicago, IL 60654, USA.
Carin R EspenschiedGuardant Health, Inc., Redwood City, CA 94063, USA.ORCID 0000-0001-6108-7785
David FabrizioFoundation Medicine, Inc., Cambridge, MA 02141, USA.
Vanessa GortonPredicine, Hayward, CA 94545, USA.
Claire GouldBiodesix Inc., Louisville, CO 80027, USA.ORCID 0000-0001-8264-0463
Justin GuinneyTempus AI, Inc., Chicago, IL 60654, USA.
Greg JonesNeoGenomics Laboratories, Fort Myers, FL 33912, USA.ORCID 0000-0001-9652-0294
Xiangyang LvBurning Rock, Irvine, CA 92617, USA.
Michael S NahorskiNeoGenomics Laboratories, Fort Myers, FL 33912, USA.
Melanie R PalomaresExact Sciences Corp., Madison, WI 53719, USA.
Gary A PestanoBiodesix Inc., Louisville, CO 80027, USA.ORCID 0000-0002-7903-2552
Mark SausenPersonal Genome Diagnostics, Labcorp, Baltimore, MD 21224, USA.ORCID 0000-0002-2916-5269
Alain SilkTempus AI, Inc., Chicago, IL 60654, USA.
Nicole ZhangGuardant Health, Inc., Redwood City, CA 94063, USA.
Zhihong ZhangBurning Rock, Irvine, CA 92617, USA.
Mark D StewartFriends of Cancer Research, Washington, DC 20036, USA.
Jeff D AllenFriends of Cancer Research, Washington, DC 20036, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumor DNA (ctDNA) holds promise as a biomarker for predicting clinical responses to therapy in solid tumors, and multiple ctDNA assays are in development. However, the heterogeneity in ctDNA levels prior to treatment (baseline) across different cancer types and stages and across ctDNA assays has not been widely studied. Friends of Cancer Research formed a collaboration across multiple commercial ctDNA assay developers to assess baseline ctDNA levels across five cancer types in early- and late-stage disease. This retrospective study included eight commercial ctDNA assay developers providing summary-level de-identified data for patients with non-small cell lung cancer (NSCLC), bladder, breast, prostate, and head and neck squamous cell carcinoma following a common analysis protocol. Baseline ctDNA levels across late-stage cancer types were similarly detected, highlighting the potential use of ctDNA as a biomarker in these cancer types. Variability was observed in ctDNA levels across assays in early-stage NSCLC, indicative of the contribution of assay analytical performance and methodology on variability. We identified key data elements, including assay characteristics and clinicopathological metadata, that need to be standardized for future meta-analyses across multiple assays. This work facilitates evidence generation opportunities to support the use of ctDNA as a biomarker for clinical response.

Indexed as

biomarkercancerctDNA

Identifiers

PMID38732326
PMCPMC11083008

What OpenQuestion holds

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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.