Evidence map›Paper›PMID 39467291›Full record

ArticleAnnals of internal medicine2024

Projected Impact and Cost-Effectiveness of Novel Molecular Blood-Based or Stool-Based Screening Tests for Colorectal Cancer.

Uri Ladabaum, Ajitha Mannalithara, Robert E Schoen, Jason A Dominitz, David Lieberman

Erratum issuedAbstract read
In one paragraph

Article in Annals of internal medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Novel Liquid Biopsy in Gastrointestinal Cancers.Journal of gastroenterology and hepatology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. A Blood-Based Test for Colorectal Cancer Screening.HCA healthcare journal of medicine · 2025
    Article
  13. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Uri LadabaumDivision of Gastroenterology and Hepatology and Department of Medicine, Stanford University School of Medicine, Stanford, California (U.L., A.M.).ORCID 0000-0002-9328-4545
Ajitha MannalitharaDivision of Gastroenterology and Hepatology and Department of Medicine, Stanford University School of Medicine, Stanford, California (U.L., A.M.).ORCID 0000-0001-9810-1069
Robert E SchoenDivision of Gastroenterology, Hepatology and Nutrition, and Department of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania (R.E.S.).ORCID 0000-0001-7153-2766
Jason A DominitzVeterans Administration Puget Sound Health Care System, Seattle; and Division of Gastroenterology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington (J.A.D.).ORCID 0000-0002-8070-7086
David LiebermanDivision of Gastroenterology and Hepatology, Oregon Health and Sciences University, Portland, Oregon (D.L.).

Funding

Blood-Based Testing for Advanced AdenomaU01CA271884 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROBERT E. SCHOEN, Cristian Tomasetti · 2022 to 2026
$4.6M
NCI NIH HHS U01 CA271884
6 · The paper itself

Abstract

backgroundCell-free DNA blood tests (cf-bDNA) and next-generation stool tests could change colorectal cancer (CRC) screening.

objectiveTo estimate the clinical and economic impacts of novel CRC screening tests.

designCost-effectiveness analysis using MOSAIC (Model of Screening and Surveillance for Colorectal Cancer). DATA SOURCES: Published data. TARGET POPULATION: Average-risk persons. TIME HORIZON: Ages 45 to 100 years. PERSPECTIVE: Health sector.

interventionNovel versus established CRC screening tests. OUTCOME MEASURES: Incidence and mortality of CRC, quality-adjusted life-years (QALYs), costs. RESULTS OF BASE-CASE ANALYSIS: For colonoscopy every 10 years, annual fecal immunochemical test (FIT), and triennial next-generation multitarget stool DNA, FIT-RNA, cf-bDNA (Guardant Shield), or cf-bDNA (Freenome), the relative rates (RRs) and 95% uncertainty intervals (UIs) versus no screening for CRC incidence were 0.21 (0.19 to 0.22), 0.29 (0.27 to 0.31), 0.33 (0.32 to 0.36), 0.32 (0.30 to 0.34), 0.58 (0.55 to 0.61) and 0.58 (0.55 to 0.60), respectively; the RRs for CRC death were 0.19 (0.17 to 0.20), 0.25 (0.23 to 0.27), 0.28 (0.27 to 0.30), 0.28 (0.26 to 0.30), 0.44 (0.42 to 0.47), and 0.46 (0.44 to 0.49), respectively. The cf-bDNA test (Shield; list price $1495) cost $89 600 ($74 800 to $102 300) per QALY gained versus no screening; alternatives were less costly and more effective. RESULTS OF SENSITIVITY ANALYSIS: Incremental costs exceeded incremental benefits when novel test intervals were shortened to 2 or 1 years. The cf-bDNA test matched FIT's impact on CRC mortality at 1.35 (1.30 to 1.40)-fold FIT's uptake rate, assuming equal colonoscopy follow-up. If persons who accept colonoscopy or stool tests shifted to cf-bDNA, CRC deaths increased. This adverse effect was overcome if every 3 such substitutions were counterbalanced by cf-bDNA uptake by 2 or more persons refusing alternatives, assuming equal colonoscopy follow-up. LIMITATION: Longitudinal test-specific participation patterns are unknown.

conclusionFirst-generation cf-bDNA tests may deliver net benefit or harm, depending on the balance between achieving screening in persons who decline alternatives versus substituting cf-bDNA for more effective alternatives. PRIMARY FUNDING SOURCE: The Gorrindo Family Fund.

Indexed as

ColonoscopyColorectal NeoplasmsCost-Benefit AnalysisEarly Detection of CancerFecesOccult BloodQuality-Adjusted Life YearsAgedAged, 80 and overCell-Free Nucleic AcidsFemaleHumansIncidenceMaleMass ScreeningMiddle AgedCell-Free Nucleic Acids

Identifiers

PMID39467291
PMCPMC12302969

What OpenQuestion holds

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LicenceTDM
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.