Evidence map›Paper›PMID 28176204›Full record

ArticleFamilial cancer2017

Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives.

Jessica Ezzell Hunter, Kathleen A Arnold, Jennifer E Cook, Jamilyn Zepp, Marian J Gilmore, Alan F Rope, James V Davis, Kellene M Bergen, Elizabeth Esterberg, Kristin R Muessig and 6 more

Open access · greenAbstract read
In one paragraph

Article in Familial cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Young-onset colorectal cancer.Nature reviews. Disease primers · 2023
    Review
  8. Article
  9. Review
  10. 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

16 authors at 5 institutions in 1 country.

Jessica Ezzell HunterCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA. Jessica.E.Hunter@kpchr.org.
Kathleen A ArnoldCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Jennifer E CookCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Jamilyn ZeppCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Marian J GilmoreCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Alan F RopeCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
James V DavisCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Kellene M BergenCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Elizabeth EsterbergCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Kristin R MuessigCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Susan K PetersonDepartment of Behavioral Science, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Sapna SyngalDana-Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Louise AchesonDepartments of Family Medicine and Community Health, Reproductive Biology, and Oncology, Case Western Reserve University, Cleveland, OH, USA.
Georgia WiesnerVanderbilt Hereditary Cancer Program, Department of Medicine, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, TN, USA.
Jacob ReissCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Katrina A B GoddardCenter for Health Research, Kaiser Permanente Northwest, 3800 N. Interstate Avenue, Portland, OR, 97229, USA.
Kaiser Permanente Center for Health Research · USCase Western Reserve University · USDana-Farber Brigham Cancer Center · USThe University of Texas MD Anderson Cancer Center · USVanderbilt University · US

Funding

Integrating Genetic Testing for Lynch Syndrome in a Managed Care SettingR01CA140377 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI GODDARD, KATRINA A. · 2011 to 2015
$2.8M
NCI NIH HHS R01 CA140377
6 · The paper itself

Abstract

Universal screening for Lynch syndrome (LS) among all cases of colorectal cancer (CRC) could increase the diagnosis of LS and reduce morbidity and mortality of LS-associated cancers. Given universal screening includes all patients, irrespective of high risk factors such early age at onset or family history of CRC, it is important to understand perspectives of all patients and not just those at high risk. As part of a study to assess the feasibility and implementation of universal screening, 189 patients newly diagnosed with CRC were surveyed about their interest in screening for LS and communication of results with at-risk family members. Overall, participants responded positively regarding screening for LS, with most wanting to know their genetic risks in general (86%) and risk of hereditary CRC (93%). Prior to receiving screening results, most participants stated they intended to share their screening results with parents (89%), siblings (96%), and children (96%). Of the 28 participants who received a positive LS screening result, 26 (93%) reported sharing their result with at least one first-degree family member. Interest in screening for LS and communication of screening results with family members was not associated with high risk factors. This study indicates that patients are interested in being screened for LS and that sharing information on the risk of LS with at-risk family members is not a significant barrier. These findings provide novel insight into patient perspectives about screening for LS and can guide successful implementation of universal screening programs.

Indexed as

AdultAgedAged, 80 and overColorectal NeoplasmsColorectal Neoplasms, Hereditary NonpolyposisFamilyFemaleGenetic Predisposition to DiseaseHumansMaleMass ScreeningMiddle AgedSurveys and QuestionnairesColorectal cancerGenetic screeningGenetic testingHNPCCLynch syndromeMicrosatellite instability

Identifiers

PMID28176204
PMCPMC5958898
OpenAlexW2586446971

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.