Evidence map›Paper›PMID 24997220›Full record

Trial reportContemporary clinical trials2014

Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes.

Carlos J Gallego, Caroline S Bennette, Patrick Heagerty, Bryan Comstock, Martha Horike-Pyne, Fuki Hisama, Laura M Amendola, Robin L Bennett, Michael O Dorschner, Peter Tarczy-Hornoch and 9 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Contemporary clinical trials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
–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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Article
  9. Article
  10. Is "incidental finding" the best term?: a study of patients' preferences.Genetics in medicine : official journal of the American College of Medical Genetics · 2017
    Article
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  12. 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

19 authors.

Carlos J GallegoDivision of Medical Genetics, University of Washington, 1705 NE Pacific Street, K253, Box 357720, Seattle, WA 98195-7720, United States; Pharmaceutical Outcomes Research and Policy Program, University of Washington, 1959 NE Pacific Street, Health Sciences Building, Room H-375, Box 357630, Seattle, WA 98195-7630, United States. Electronic address: carlosjg@uw.edu.
Caroline S BennettePharmaceutical Outcomes Research and Policy Program, University of Washington, 1959 NE Pacific Street, Health Sciences Building, Room H-375, Box 357630, Seattle, WA 98195-7630, United States. Electronic address: cb11@u.washington.edu.
Patrick HeagertyDepartment of Biostatistics, University of Washington, F-600, Health Sciences Building, Box 357232, Seattle, WA 98195-7232, United States. Electronic address: heagerty@uw.edu.
Bryan ComstockDepartment of Biostatistics, University of Washington, F-600, Health Sciences Building, Box 357232, Seattle, WA 98195-7232, United States. Electronic address: bac4@uw.edu.
Martha Horike-PyneDivision of Medical Genetics, University of Washington, 1705 NE Pacific Street, K253, Box 357720, Seattle, WA 98195-7720, United States. Electronic address: mjpyne@u.washington.edu.
Fuki HisamaDivision of Medical Genetics, University of Washington, 1705 NE Pacific Street, K253, Box 357720, Seattle, WA 98195-7720, United States. Electronic address: fmh2@uw.edu.
Laura M AmendolaDivision of Medical Genetics, University of Washington, 1705 NE Pacific Street, K253, Box 357720, Seattle, WA 98195-7720, United States. Electronic address: lauraa7@uw.edu.
Robin L BennettDivision of Medical Genetics, University of Washington, 1705 NE Pacific Street, K253, Box 357720, Seattle, WA 98195-7720, United States. Electronic address: robinb@uw.edu.
Michael O DorschnerDepartment of Psychiatry and Behavioral Sciences, University of Washington, VAPSHCS GRECC S-182, 1660 S. Columbian Way, Seattle, WA 98108, United States. Electronic address: mod@uw.edu.
Peter Tarczy-HornochDepartment of Biomedical Informatics and Medical Education, University of Washington, Box 358047, United States. Electronic address: pth@u.washington.edu.
William M GradyClinical Research Division, Fred Hutchinson Cancer Research Center, Division of Gastroenterology, University of Washington, 1100 Fairview Ave. N., Box 19024, Mailstop D4-100, Seattle, WA 98109, United States. Electronic address: wgrady@fhcrc.org.
S Malia FullertonDepartment of Bioethics and Humanities, University of Washington, 1959 NE Pacific Street, A204 Health Sciences Center, Box 357120, Seattle, WA 98195, United States. Electronic address: smfllrtn@u.washington.edu.
Susan B TrinidadDepartment of Bioethics and Humanities, University of Washington, 1959 NE Pacific Street, A204 Health Sciences Center, Box 357120, Seattle, WA 98195, United States. Electronic address: sbtrini@uw.edu.
Dean A RegierCanadian Centre for Applied Research in Cancer Control, BC Cancer Agency, 2nd Floor, BC Cancer Research Centre, 675 West 10th Avenue, Vancouver, BC V5Z 1L3, Canada. Electronic address: dregier@bccrc.ca.
Deborah A NickersonDepartment of Genome Sciences, University of Washington, 3720 15th Avenue NE, Foege Building S-250, Box 355065, Seattle, WA 98195, United States. Electronic address: debnick@u.washington.edu.
Wylie BurkeDepartment of Bioethics and Humanities, University of Washington, 1959 NE Pacific Street, A204 Health Sciences Center, Box 357120, Seattle, WA 98195, United States. Electronic address: wburke@u.washington.edu.
Donald L PatrickDepartment of Health Services, University of Washington, Seattle, 4333 Brooklyn Ave NE, Rm 14-101, Box 359455, Seattle, WA 98195-9455, United States. Electronic address: donald@u.washington.edu.
Gail P JarvikDivision of Medical Genetics, University of Washington, 1705 NE Pacific Street, K253, Box 357720, Seattle, WA 98195-7720, United States. Electronic address: pair@uw.edu.
David L VeenstraPharmaceutical Outcomes Research and Policy Program, University of Washington, 1959 NE Pacific Street, Health Sciences Building, Room H-375, Box 357630, Seattle, WA 98195-7630, United States. Electronic address: veenstra@uw.edu.

Funding

Clinical sequencing in cancer: Clinical ethical and technological studiesU01HG006507 · NHGRI · UNIVERSITY OF WASHINGTON · PI JARVIK, GAIL PAIRITZ · 2012 to 2016
$10.6M
Biobehavioral Cancer Prevention and Control Training ProgramR25CA092408 · NCI · UNIVERSITY OF WASHINGTON · PI PATRICK, DONALD LEE · 2001 to 2015
$7.1M
CSER RoRC Centralized Support Coordinating CenterU01HG007307 · NHGRI · UNIVERSITY OF WASHINGTON · PI BURKE, WYLIE G., JARVIK, GAIL PAIRITZ · 2013 to 2016
$3.6M
UW Patient-Centered Outcomes Research Career Development Program (K12)K12HS021686 · AHRQ · UNIVERSITY OF WASHINGTON · PI SULLIVAN, SEAN D · 2012 to 2013
$902k
AHRQ HHS K12 HS021686NCI NIH HHS R25 CA092408NHGRI NIH HHS U01 HG0006507NHGRI NIH HHS U01 HG006507NHGRI NIH HHS U01 HG007307NHGRI NIH HHS U01HG007307
6 · The paper itself

Abstract

Whole exome and whole genome sequencing are applications of next generation sequencing transforming clinical care, but there is little evidence whether these tests improve patient outcomes or if they are cost effective compared to current standard of care. These gaps in knowledge can be addressed by comparative effectiveness and patient-centered outcomes research. We designed a randomized controlled trial that incorporates these research methods to evaluate whole exome sequencing compared to usual care in patients being evaluated for hereditary colorectal cancer and polyposis syndromes. Approximately 220 patients will be randomized and followed for 12 months after return of genomic findings. Patients will receive findings associated with colorectal cancer in a first return of results visit, and findings not associated with colorectal cancer (incidental findings) during a second return of results visit. The primary outcome is efficacy to detect mutations associated with these syndromes; secondary outcomes include psychosocial impact, cost-effectiveness and comparative costs. The secondary outcomes will be obtained via surveys before and after each return visit. The expected challenges in conducting this randomized controlled trial include the relatively low prevalence of genetic disease, difficult interpretation of some genetic variants, and uncertainty about which incidental findings should be returned to patients. The approaches utilized in this study may help guide other investigators in clinical genomics to identify useful outcome measures and strategies to address comparative effectiveness questions about the clinical implementation of genomic sequencing in clinical care.

Indexed as

ExomeResearch DesignAdenomatous Polyposis ColiColorectal NeoplasmsColorectal Neoplasms, Hereditary NonpolyposisComparative Effectiveness ResearchCost-Benefit AnalysisGenetic Predisposition to DiseaseHigh-Throughput Nucleotide SequencingHumansPrecision MedicineSequence Analysis, DNAComparative effectiveness researchGenomicsNext generation sequencingOutcomes researchRandomized clinical trialWhole exome sequencing

Identifiers

PMID24997220
PMCPMC4175052

What OpenQuestion holds

Textmetadata
LicenceTDM
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.