Evidence map›Paper›PMID 42240135›Full record

ArticleClinical pharmacology and therapeutics2026

Systematic Evaluation of Data and Trial Fitness for Oncology Trial Emulation: Empirical Findings from the CARE Initiative.

Natalie Levy, Paige Sheridan, Ulka Campbell, David Lenis, Inish O'Doherty, Adina Estrin, Nileesa Gautam, Monica Iyer, Sarah McDonald, Andrew Belli and 33 more

Abstract read
In one paragraph

Article in Clinical pharmacology and therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

43 authors.

Natalie LevyAetion, Inc, New York, New York, USA.ORCID 0000-0002-6828-8237
Paige SheridanAetion, Inc, New York, New York, USA.ORCID 0000-0002-2099-6760
Ulka CampbellAetion, Inc, New York, New York, USA.ORCID 0000-0002-3503-8178
David LenisAetion, Inc, New York, New York, USA.ORCID 0000-0001-8697-1737
Inish O'DohertyAetion, Inc, New York, New York, USA.ORCID 0000-0001-9958-5333
Adina EstrinAetion, Inc, New York, New York, USA.ORCID 0000-0001-8866-2911
Nileesa GautamAetion, Inc, New York, New York, USA.ORCID 0009-0002-3643-433X
Monica IyerAetion, Inc, New York, New York, USA.ORCID 0009-0003-1656-8370
Sarah McDonaldAetion, Inc, New York, New York, USA.
Andrew BelliCOTA Healthcare, New York, New York, USA.
Gillis CarriganCenter for Observational Research, Amgen, San Francisco, California, USA.ORCID 0000-0002-7973-3607
K Arnold ChanTriNetX, LLC, Cambridge, Massachusetts, USA.ORCID 0000-0001-8161-1986
James ChenTempus, Chicago, Illinois, USA.
Victoria ChiaCenter for Observational Research, Amgen, San Francisco, California, USA.ORCID 0000-0001-5980-3308
Neil DhopeshwarkarTriNetX, LLC, Cambridge, Massachusetts, USA.ORCID 0000-0001-6305-256X
Joy EckertReagan-Udall Foundation for the Food and Drug Administration, Washington, DC, USA.ORCID 0009-0001-7603-953X
Laura FernandesCOTA Healthcare, New York, New York, USA.ORCID 0000-0002-5986-3885
Joel GreshockJohnson and Johnson, New Brunswick, New Jersey, USA.ORCID 0000-0001-6567-4266
Rachele Hendricks-SturrupDuke-Margolis Center for Health Policy, Washington, DC, USA.ORCID 0000-0002-3390-2583
Jenny HuangGilead Sciences, Foster City, California, USA.
XiaoLong JiaoPfizer, New York City, New York, USA.
Sajan KhoslaAstraZeneca, Gaithersburg, Maryland, USA.ORCID 0000-0002-5114-1968
Orsolya LunacsekBayer, Whippany, NJ, USA.ORCID 0000-0003-4872-9813
Lynn McRoyPfizer, New York City, New York, USA.
Yanina NatanzonConcertAI, Cambridge, Massachusetts, USA.ORCID 0000-0002-9302-0304
Osayi OvbiosaAbbVie, North Chicago, Illinois, USA.ORCID 0000-0003-1869-9908
Nelson PaceAbbVie, North Chicago, Illinois, USA.ORCID 0000-0002-4548-0912
Simone PinheiroAbbVie, North Chicago, Illinois, USA.ORCID 0000-0002-9360-1379
Megan ReesLoopback Analytics, Dallas, Texas, USA.
Jennifer RiderConcertAI, Cambridge, Massachusetts, USA.ORCID 0000-0002-2637-6036
Mothaffar Fahed RimawiBaylor College of Medicine, Houston, Texas, USA.ORCID 0000-0002-4284-5656
Travis RobinsonLoopback Analytics, Dallas, Texas, USA.
Carla Rodriguez-WatsonReagan-Udall Foundation for the Food and Drug Administration, Washington, DC, USA.ORCID 0000-0003-4898-1613
Chithra SangliTempus, Chicago, Illinois, USA.ORCID 0009-0000-1234-7122
Khaled SarsourJohnson and Johnson, New Brunswick, New Jersey, USA.
Sebastian SchneeweissDivision of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0003-2575-467X
Mark ShapiroxCures, Oakland, California, USA.
Mark StewartFriends of Cancer Research, Washington, DC, USA.ORCID 0000-0002-4847-0736
Aliki TaylorGilead Sciences, Foster City, California, USA.ORCID 0000-0002-4863-9810
C K WangCOTA Healthcare, New York, New York, USA.
Shirley WangDivision of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0001-7761-7090
Yiduo ZhangAstraZeneca, Gaithersburg, Maryland, USA.
Ann MadsenAetion, Inc, New York, New York, USA.ORCID 0000-0002-9206-708X

Funding

AbbVieAmgenAstraZenecaBayerGilead SciencesJohnson & JohnsonPfizer
6 · The paper itself

Abstract

The Coalition to Advance Real-World Evidence through Randomized Controlled Trial Emulation (CARE) Initiative seeks to advance understanding of when real-world data (RWD) can generate valid treatment effectiveness estimates by emulating completed oncology randomized controlled trials (RCTs). A prerequisite for meaningful RCT emulation insights is the identification and use of RWD with sufficient fitness to satisfy RCT-specific data elements. We conducted a systematic, multi-stage feasibility assessment of six commercially available US electronic health record-based RWD sources across 23 candidate oncology RCTs. Each potential RCT-RWD combination was first screened for availability of the RCT indication, outcomes, and sample size ≥ 1.5-times enrollment for each trial arm. Combinations passing this screen underwent more detailed evaluation of RCT design elements including eligibility criteria, outcomes, and potential confounders. Each data element was rated with respect to availability, missingness, and validity. Final feasibility determination was informed by ratings of essential element capture and refined sample size estimates. Of 54 candidate RCT-RWD combinations assessed, nine advanced to detailed feasibility assessment and three were selected for emulation protocol development. Fit-for-emulation constraints included complex eligibility criteria, biomarker requirements, performance status requirements, and outcome ascertainment. These findings highlight the importance of systematic feasibility evaluation before conducting emulations and may inform data selection for future RWD studies in oncology. Data fitness for oncology RCT emulation could be improved by linking high-quality, oncology-specific RWD sources to broader EHR and claims data sources or through customized data abstraction.

Indexed as

Medical OncologyNeoplasmsRandomized Controlled Trials as TopicResearch DesignElectronic Health RecordsFeasibility StudiesHumansSample SizeTreatment Outcome

Identifiers

PMID42240135
PMCPMC13337134

What OpenQuestion holds

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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.