Evidence map›Paper›PMID 41348983›Full record

ArticleJCO precision oncology2025

Clinical Utility of Multicancer Detection in Symptomatic Patients: A Decision-Making Perspective.

Giuliano Netto Flores Cruz, Keegan Korthauer

Abstract read
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Article in JCO precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Giuliano Netto Flores CruzCentre for Molecular Medicine and Therapeutics, British Columbia Children's Hospital Research Institute, Vancouver, Canada.ORCID 0000-0001-9122-8286
Keegan KorthauerCentre for Molecular Medicine and Therapeutics, British Columbia Children's Hospital Research Institute, Vancouver, Canada.ORCID 0000-0002-4565-1654

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThere is growing interest in multicancer detection (MCD) blood tests for diagnosing patients with cancer-related symptoms. However, recent studies suggest that MCD testing may not be sensitive enough to rule out cancer in the symptomatic population without retraining the underlying classifiers. On the basis of clinical guidelines for suspected cancer referral, here we cast these data into a formal diagnostic decision-making perspective to assess clinical utility.

methodsData were extracted from the SYMPLIFY study (ISRCTN10226380), which evaluated the performance of the Galleri test (GRAIL, LLC). The decision threshold for suspected cancer referral was extracted from the National Institute for Health and Care Excellence Guideline 12. Clinical utility was estimated using Bayesian decision curve analysis.

resultsFor the guideline-derived decision threshold of 3%, the Galleri MCD test avoided 18,005 unnecessary suspected cancer referrals per 100,000 symptomatic patients, with a 99.4% posterior probability of clinical utility. High probabilities of clinical utility were observed for gynecologic, lower GI, and upper GI referral pathways, avoiding between 25,414 and 62,501 unnecessary referrals per 100,000 symptomatic patients. The rapid diagnostic center and lung referral pathways showed negligible probabilities of clinical utility. The minimum diagnostic performance required for clinical utility varied significantly across referral pathways. The gynecologic pathway showed the lowest sensitivity requirement (under 30% for a highly specific test) and the lung pathway the highest (over 90% for any specificity level).

conclusionClinical utility of MCD testing for symptomatic patients in the United Kingdom varies substantially across referral pathways but is favorable for gynecologic and GI cancers. Future pathway-specific optimization of MCD tests must consider clinical utility explicitly and does not require retraining the underlying machine learning classifiers.

Indexed as

Clinical Decision-MakingNeoplasmsBayes TheoremFemaleHumansReferral and Consultation

Identifiers

PMID41348983
PMCPMC12685320

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