Evidence map›Paper›PMID 27381741›Full record

ArticleJournal of the National Cancer Institute2016

Beyond Composite Endpoints Analysis: Semicompeting Risks as an Underutilized Framework for Cancer Research.

Ina Jazić, Deborah Schrag, Daniel J Sargent, Sebastien Haneuse

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Recurrence and Postoperative Death in Patients with Colorectal Cancer: A New Perspective via Semi-competing Risk Framework.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
  6. Review
  7. High-Dimensional Survival Analysis: Methods and Applications.Annual review of statistics and its application · 2023
    Article
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  9. Article
  10. Article
  11. Review
  12. Article
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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

4 authors at 3 institutions in 1 country.

Ina JazićDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA (IJ, SH); Division of Population Sciences, Dana Farber Cancer Institute, Boston, MA (DS); Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN (DJS) ijazic@fas.harvard.edu.
Deborah SchragDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA (IJ, SH); Division of Population Sciences, Dana Farber Cancer Institute, Boston, MA (DS); Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN (DJS).
Daniel J SargentDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA (IJ, SH); Division of Population Sciences, Dana Farber Cancer Institute, Boston, MA (DS); Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN (DJS).
Sebastien HaneuseDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA (IJ, SH); Division of Population Sciences, Dana Farber Cancer Institute, Boston, MA (DS); Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN (DJS).
Harvard University · USDana-Farber Cancer Institute · USMayo Clinic · US

Funding

Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
Training Grant in Quantitative Sciences for Cancer ResearchT32CA009337 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI QUACKENBUSH, JOHN, TRIPPA, LORENZO · 1986 to 2025
$12.3M
Clustered semi-competing risks analysis in quality of end-of-life care studiesR01CA181360 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI HANEUSE, SEBASTIEN · 2014 to 2017
$1.8M
Partnerships Between Medicaid, Tumor Registries & Cancer Control ResearchersK05CA169384 · NCI · DANA-FARBER CANCER INST · PI SCHRAG, DEBORAH · 2012 to 2016
$586k
NCI NIH HHS K05 CA169384NCI NIH HHS R01 CA181360NCI NIH HHS T32 CA009337NCI NIH HHS U10 CA180882
6 · The paper itself

Abstract

backgroundComposite endpoints (CEP), such as progression-free survival, are commonly used in cancer research. Notwithstanding their popularity, however, CEP analyses suffer from a number of drawbacks, especially when death is combined with a nonterminal event (ie, progression or recurrence), exemplifying the semicompeting risks setting. We investigated the semicompeting risks framework as a complementary analysis strategy that avoids certain drawbacks of CEPs.

methodsThe illness-death model under the semicompeting risks framework was compared with standard analysis approaches: CEP analyses and (separate) univariate analyses for each component endpoint. Data from a previously published phase III randomized clinical trial in metastatic colon cancer including 1419 participants in the N9741 trial (conducted between 1997 and 2003) were used to determine the impact of the loss of information associated with combining multiple endpoints, as well as of ignoring the potentially informative role of death. A simulation study was conducted to further explore these issues.

resultsFailure to account for critical features of semicompeting risks data can lead to potentially severely misleading conclusions. Advantages of semicompeting risks analyses include a clear delineation of treatment effects on both events, the ability to draw conclusions about a patient's joint risk of the two events, and an assessment of the dependence between the two event types.

conclusionsEmbedding and analyzing component outcomes in the semicompeting risks framework, either as a supplement or alternative to CEP analyses, represents an important, underutilized, and feasible opportunity for cancer research.

Indexed as

DeathDisease ProgressionModels, StatisticalAntineoplastic Combined Chemotherapy ProtocolsBiomedical ResearchClinical Trials as TopicColorectal NeoplasmsComputer SimulationDisease-Free SurvivalEndpoint DeterminationHumansNeoplasm MetastasisRisk Assessment

Identifiers

PMID27381741
PMCPMC5241896
OpenAlexW2472030246

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.