Evidence map›Paper›PMID 41941752›Full record

ArticleJournal of the National Cancer Institute2026

Common sense oncology values to action: a patient-led framework for randomized clinical trial design.

Michelle L Tregear, Haydeé C Verduzco-Aguirre, Brian Shkabari, Rachel Koven, Henry Scowcroft, Viji Venkatash, Michael D Brundage, Runcie C W Chidebe, Elizabeth A Eisenhauer, Bishal Gyawali and 3 more

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 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

13 authors.

Michelle L TregearNational Breast Cancer Coalition, Washington, DC, United States.
Haydeé C Verduzco-AguirreDepartment of Hemato-Oncology, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Mexico.
Brian ShkabariDivision of Cancer Care and Epidemiology, Sinclair Cancer Research Institute, Kingston, ON, Canada.ORCID 0009-0002-3623-1399
Rachel KovenPatient and Family Advisory Council, Southeast Regional Cancer Program, Kingston Health Sciences Centre, Kingston, ON, Canada.
Henry ScowcroftIndependent Communications Consultant and Patient Advocate, United Kingdom.
Viji VenkatashThe Max Foundation, Mumbai, India.
Michael D BrundageDivision of Cancer Care and Epidemiology, Sinclair Cancer Research Institute, Kingston, ON, Canada.ORCID 0000-0002-5104-0497
Runcie C W ChidebeProject PINK BLUE- Health and Psychological Trust Centre, Abuja, Nigeria.ORCID 0000-0002-6025-776X
Elizabeth A EisenhauerDepartment of Oncology, Queen's University, Kingston, ON, Canada.ORCID 0009-0006-1410-7820
Bishal GyawaliDivision of Cancer Care and Epidemiology, Sinclair Cancer Research Institute, Kingston, ON, Canada.ORCID 0000-0001-7444-8594
Bhawna SirohiVedanta Medical Research Foundation-Balco Medical Centre, Raipur, India.ORCID 0000-0001-8093-1531
Christopher M BoothDivision of Cancer Care and Epidemiology, Sinclair Cancer Research Institute, Kingston, ON, Canada.ORCID 0000-0002-1353-3653
Christopher G C A JacksonDepartment of Medicine, University of Otago, Dunedin, New Zealand.ORCID 0000-0001-6150-709X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRandomized controlled trials are the foundation of oncology drug development, yet increasing concern exists that some prioritize regulatory approval over outcomes that matter to patients. The Common Sense Oncology (CSO) initiative was founded to reorient research toward patient-valued endpoints. The CSO Patient Priorities Working Group sought to codevelop a pragmatic, patient-centered framework articulating values and actions to guide the design, conduct, and reporting of oncology randomized controlled trials.

methodsA multiphase, mixed-methods process included literature review, thematic analysis, and international stakeholder engagement. Eight focus groups were held between April 2024 and January 2025 with 131 participants across 7 countries, including people with lived cancer experience, advocates, clinicians, and trialists. Feedback from surveys and structured discussions-quantitative ratings and qualitative insights-informed iterative framework refinement.

resultsThe final framework defines 9 core values with associated actions: meaningful research question, patient partnerships, informed consent, meaningful benefit, generalizability, optimal comparator arm, minimal participant burden, timely feedback of results, and clear dissemination. All values received high endorsement (median 8-9 on a 9-point numeric rating scale [from 1 (least important) to 9 (most important)]). Qualitative analysis emphasized meaningful endpoints, transparent communication, equitable inclusion, fair compensation, and plain-language consent.

conclusionsThe CSO Values to Action Framework provides a validated, internationally informed structure for trialists, ethics boards, funders, and advocates. It offers a practical tool to align oncology research with what matters most to patients, promoting more ethical, inclusive, and relevant clinical trials.

Indexed as

Medical OncologyNeoplasmsRandomized Controlled Trials as TopicResearch DesignFocus GroupsHumansInformed ConsentPatient Participation

Identifiers

PMID41941752
PMCPMC13549713

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.