Evidence map›Paper›PMID 34865066›Full record

ArticleJournal of the National Cancer Institute2022

Next Step for Global Adolescent and Young Adult Oncology: A Core Patient-Centered Outcome Set.

Olga Husson, Bryce B Reeve, Anne-Sophie Darlington, Christabel K Cheung, Samantha Sodergren, Winette T A van der Graaf, John M Salsman

Open access · greenAbstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% of its field
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. A conceptual model of cancer care and lived experiences in adolescents and young adults with cancer: results from the multi-national European STRONG AYA project.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
  3. Article
  4. Review
  5. Patient-Reported Quality of Life at Diagnosis in Adolescent and Young Adults With Cancer.Journal of the National Comprehensive Cancer Network : JNCCN · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
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

7 authors at 6 institutions in 3 countries.

Olga HussonDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0002-1387-8686
Bryce B ReeveDepartment of Population Health Sciences, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-6709-8714
Anne-Sophie DarlingtonSchool of Health Sciences, University of Southampton, Southampton, UK.
Christabel K CheungSchool of Social Work, University of Maryland, Baltimore, MD, USA.ORCID 0000-0003-0721-7053
Samantha SodergrenSchool of Health Sciences, University of Southampton, Southampton, UK.
Winette T A van der GraafDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0001-7549-3338
John M SalsmanDepartment of Social Sciences and Health Policy, Wake Forest School of Medicine, Wake Forest Baptist Comprehensive Cancer Center, Winston Salem, NC, USA.ORCID 0000-0003-2317-4006
University of Southampton · GBAtrium Health Wake Forest Baptist · USDuke University · USErasmus MC · NLInstitute of Cancer Research · GBUniversity of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The relatively small number of cancers in the adolescent and young adult (AYA) age group, those aged 15-39 years, does not appropriately reflect the personal and societal costs of cancer in this population, as reflected in the potential years of life lost or saved, the decreased productivity and health-related quality of life due to the impact of the disease during formative years, and long-term complications or disabilities. Improvements in care and outcomes for AYAs with cancer require collaboration among different stakeholders at different levels (patients, caregivers, health-care professionals, researchers, industry, and policymakers). Development of a Core Outcome Set (COS), an agreed minimum set of outcomes that should be measured globally in research and routine clinical practice-specifically for AYAs with cancer-with outcomes that are well defined based on the perspective of those who are affected and assessed with validated measures, is urgently required. A globally implemented COS for AYAs with cancer will facilitate better pooling of research data and the implementation of high-quality health-care registries, which by benchmarking not only nationally but also internationally, may ultimately improve the value of the care given to these underserved young cancer patients. We reflect on the need to develop a COS for AYAs with cancer, the arenas of application, and the challenges of implementing an age-specific COS in research and clinical practice.

Indexed as

NeoplasmsQuality of LifeAdolescentCaregiversHumansMedical OncologyPatient-Centered CareYoung Adult

Identifiers

PMID34865066
PMCPMC9002284
OpenAlexW4200333226

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.