Literature DB >> 30227419

Controversies among Cancer Registry Participants, Genomic Researchers, and Institutional Review Boards about Returning Participants' Genomic Results.

Karen L Edwards1, Deborah Goodman2, Catherine O Johnson2, Lari Wenzel2, Celeste Condit3, Deborah Bowen4.   

Abstract

OBJECTIVES: Genomic information will increasingly be used to aid in the prevention, diagnosis, and treatment of disease. Several national initiatives are paving the way for this new reality, while also promoting new models of participant-engaged research. We compare the opinions of research participants in a cancer registry, human genetic researchers, and institutional review board (IRB) professionals about the return of individual-level genetic results (ROR).
METHODS: Online surveys were administered to participants in a cancer registry (n = 450) and overlapping questions were compared to our previous online national surveys of human genetic researchers (n = 351) and IRB professionals (n = 208).
RESULTS: The majority of respondents agreed that researchers have an obligation to return individual results when they would affect a participant's health. While 77% of registry participants favored ROR if the researcher feels the participant might be interested in the results, only 30% of the IRB professionals and 25% of the genetic researchers agreed with this statement.
CONCLUSIONS: Significant differences emerged between the stakeholder groups in several ROR scenarios. Policies that are acceptable to participants, researchers and IRBs, and that ensure human subject protections and facilitate research are needed.
© 2018 S. Karger AG, Basel.

Entities:  

Keywords:  Cancer; Genomics; Precision medicine; Research participant perspective; Return of results

Mesh:

Year:  2018        PMID: 30227419      PMCID: PMC7833045          DOI: 10.1159/000490235

Source DB:  PubMed          Journal:  Public Health Genomics        ISSN: 1662-4246            Impact factor:   2.000


  27 in total

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3.  Informed consent and genomic incidental findings: IRB chair perspectives.

Authors:  Christian M Simon; Janet K Williams; Laura Shinkunas; Debra Brandt; Sandra Daack-Hirsch; Martha Driessnack
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4.  Communication of biobanks' research results: what do (potential) participants want?

Authors:  Tineke M Meulenkamp; Sjef K Gevers; Jasper A Bovenberg; Gerard H Koppelman; Astrid van Hylckama Vlieg; Ellen M A Smets
Journal:  Am J Med Genet A       Date:  2010-10       Impact factor: 2.802

5.  Disclosure of incidental findings in cancer genomic research: investigators' perceptions on obligations and barriers.

Authors:  E Kleiderman; D Avard; A Besso; S Ali-Khan; G Sauvageau; J Hébert
Journal:  Clin Genet       Date:  2014-12-09       Impact factor: 4.438

6.  "I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.

Authors:  Anne Townsend; Shelin Adam; Patricia H Birch; Zoe Lohn; Francois Rousseau; Jan M Friedman
Journal:  Am J Med Genet A       Date:  2012-08-17       Impact factor: 2.802

7.  Communicating the results of clinical research to participants: attitudes, practices, and future directions.

Authors:  David I Shalowitz; Franklin G Miller
Journal:  PLoS Med       Date:  2008-05-13       Impact factor: 11.069

8.  Public preferences for the return of research results in genetic research: a conjoint analysis.

Authors:  Juli Murphy Bollinger; John F P Bridges; Ateesha Mohamed; David Kaufman
Journal:  Genet Med       Date:  2014-05-22       Impact factor: 8.822

9.  IRB perspectives on the return of individual results from genomic research.

Authors:  Lynn G Dressler; Sondra Smolek; Roselle Ponsaran; Janell M Markey; Helene Starks; Nancy Gerson; Susan Lewis; Nancy Press; Eric Juengst; Georgia L Wiesner
Journal:  Genet Med       Date:  2012-01-05       Impact factor: 8.822

10.  Researchers' views on informed consent for return of secondary results in genomic research.

Authors:  Paul S Appelbaum; Abby Fyer; Robert L Klitzman; Josue Martinez; Erik Parens; Yuan Zhang; Wendy K Chung
Journal:  Genet Med       Date:  2014-12-11       Impact factor: 8.822

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  6 in total

1.  Return of individual research results from genomic research: A systematic review of stakeholder perspectives.

Authors:  Danya F Vears; Joel T Minion; Stephanie J Roberts; James Cummings; Mavis Machirori; Mwenza Blell; Isabelle Budin-Ljøsne; Lorraine Cowley; Stephanie O M Dyke; Clara Gaff; Robert Green; Alison Hall; Amber L Johns; Bartha M Knoppers; Stephanie Mulrine; Christine Patch; Eva Winkler; Madeleine J Murtagh
Journal:  PLoS One       Date:  2021-11-08       Impact factor: 3.240

Review 2.  Views on genomic research result delivery methods and informed consent: a review.

Authors:  Danya F Vears; Joel T Minion; Stephanie J Roberts; James Cummings; Mavis Machirori; Madeleine J Murtagh
Journal:  Per Med       Date:  2021-04-06       Impact factor: 2.512

3.  Stakeholder Perspectives on Returning Nonactionable Apolipoprotein L1 (APOL1) Genetic Results to African American Research Participants.

Authors:  Kathleen M West; Kerri L Cavanaugh; Erika Blacksher; Stephanie M Fullerton; Ebele M Umeukeje; Bessie Young; Wylie Burke
Journal:  J Empir Res Hum Res Ethics       Date:  2021-12-06       Impact factor: 1.978

4.  Researchers' perspectives on return of individual genetics results to research participants: a qualitative study.

Authors:  Erisa Sabakaki Mwaka; Deborah Ekusai Sebatta; Joseph Ochieng; Ian Guyton Munabi; Godfrey Bagenda; Deborah Ainembabazi; David Kaawa-Mafigiri
Journal:  Glob Bioeth       Date:  2021-03-09

5.  Perspectives and ethical considerations for return of genetics and genomics research results: a qualitative study of genomics researchers in Uganda.

Authors:  Joseph Ochieng; Betty Kwagala; John Barugahare; Erisa Mwaka; Deborah Ekusai-Sebatta; Joseph Ali; Nelson K Sewankambo
Journal:  BMC Med Ethics       Date:  2021-11-19       Impact factor: 2.652

6.  Perspectives on returning individual and aggregate genomic research results to study participants and communities in Kenya: a qualitative study.

Authors:  Isaac Kisiangani; Shukri F Mohamed; Catherine Kyobutungi; Paulina Tindana; Anita Ghansah; Michele Ramsay; Gershim Asiki
Journal:  BMC Med Ethics       Date:  2022-03-18       Impact factor: 2.834

  6 in total

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