Literature DB >> 31819920

Use and Patient-Reported Outcomes of Clinical Multigene Panel Testing for Cancer Susceptibility in the Multicenter Communication of Genetic Test Results by Telephone Study.

Michael J Hall1, Linda J Patrick-Miller2, Brian L Egleston1, Susan M Domchek3, Mary B Daly1, Pamela Ganschow4, Generosa Grana5, Olufunmilayo I Olopade2, Dominique Fetzer3, Amanda Brandt3, Rachelle Chambers6, Dana F Clark5, Andrea Forman1, Rikki Gaber4, Cassandra Gulden6, Janice Horte5, Jessica M Long3, Terra Lucas4, Shreshtha Madaan6, Kristin Mattie5, Danielle McKenna3, Susan Montgomery1, Sarah Nielsen6, Jacquelyn Powers3, Kim Rainey1, Christina Rybak1, Michelle Savage1, Christina Seelaus4, Jessica Stoll6, Jill E Stopfer3, Xinxin Shirley Yao5, Angela R Bradbury3.   

Abstract

PURPOSE: Multigene panels (MGPs) are increasingly being used despite questions regarding their clinical utility and no standard approach to genetic counseling. How frequently genetic providers use MGP testing and how patient-reported outcomes (PROs) differ from targeted testing (eg, BRCA1/2 only) are unknown.
METHODS: We evaluated use of MGP testing and PROs in participants undergoing cancer genetic testing in the multicenter Communication of Genetic Test Results by Telephone study (ClinicalTrials.gov identifier: ), a randomized study of telephone versus in-person disclosure of genetic test results. PROs included genetic knowledge, general and state anxiety, depression, cancer-specific distress, uncertainty, and satisfaction. Genetic providers offered targeted or MGP testing based on clinical assessment.
RESULTS: Since the inclusion of MGP testing in 2014, 395 patients (66%) were offered MGP testing. MGP testing increased over time from 57% in 2014 to 66% in 2015 (P = .02) and varied by site (46% to 78%; P < .01). Being offered MGP testing was significantly associated with not having Ashkenazi Jewish ancestry, having a history of cancer, not having a mutation in the family, not having made a treatment decision, and study site. After demographic adjustment, patients offered MGP testing had lower general anxiety (P = .04), state anxiety (P = .03), depression (P = .04), and uncertainty (P = .05) pre-disclosure compared with patients offered targeted testing. State anxiety (P = .05) and cancer-specific distress (P = .05) were lower at disclosure in the MGP group. There was a greater increase in change in uncertainty (P = .04) among patients who underwent MGP testing.
CONCLUSION: MGP testing was more frequently offered to patients with lower anxiety, depression, and uncertainty and was associated with favorable outcomes, with the exception of a greater increase in uncertainty compared with patients who had targeted testing. Addressing uncertainty may be important as MGP testing is increasingly adopted.

Entities:  

Year:  2018        PMID: 31819920      PMCID: PMC6901130          DOI: 10.1200/PO.18.00199

Source DB:  PubMed          Journal:  JCO Precis Oncol        ISSN: 2473-4284


  22 in total

1.  Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up.

Authors:  Anita Y Kinney; Laurie E Steffen; Barbara H Brumbach; Wendy Kohlmann; Ruofei Du; Ji-Hyun Lee; Amanda Gammon; Karin Butler; Saundra S Buys; Antoinette M Stroup; Rebecca A Campo; Kristina G Flores; Jeanne S Mandelblatt; Marc D Schwartz
Journal:  J Clin Oncol       Date:  2016-06-20       Impact factor: 44.544

2.  A brief assessment of concerns associated with genetic testing for cancer: the Multidimensional Impact of Cancer Risk Assessment (MICRA) questionnaire.

Authors:  David Cella; Chanita Hughes; Amy Peterman; Chih-Hung Chang; Beth N Peshkin; Marc D Schwartz; Lari Wenzel; Amy Lemke; Alfred C Marcus; Caryn Lerman
Journal:  Health Psychol       Date:  2002-11       Impact factor: 4.267

3.  Uptake, Results, and Outcomes of Germline Multiple-Gene Sequencing After Diagnosis of Breast Cancer.

Authors:  Allison W Kurian; Kevin C Ward; Ann S Hamilton; Dennis M Deapen; Paul Abrahamse; Irina Bondarenko; Yun Li; Sarah T Hawley; Monica Morrow; Reshma Jagsi; Steven J Katz
Journal:  JAMA Oncol       Date:  2018-08-01       Impact factor: 31.777

4.  Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial.

Authors:  Anita Y Kinney; Karin M Butler; Marc D Schwartz; Jeanne S Mandelblatt; Kenneth M Boucher; Lisa M Pappas; Amanda Gammon; Wendy Kohlmann; Sandra L Edwards; Antoinette M Stroup; Saundra S Buys; Kristina G Flores; Rebecca A Campo
Journal:  J Natl Cancer Inst       Date:  2014-11-05       Impact factor: 13.506

5.  Cancer genetics knowledge and beliefs and receipt of results in Ashkenazi Jewish individuals receiving counseling for BRCA1/2 mutations.

Authors:  Kimberly Kelly; Howard Leventhal; Monica Marvin; Deborah Toppmeyer; Jill Baran; Marvin Schwalb
Journal:  Cancer Control       Date:  2004 Jul-Aug       Impact factor: 3.302

6.  Gaps in Receipt of Clinically Indicated Genetic Counseling After Diagnosis of Breast Cancer.

Authors:  Steven J Katz; Kevin C Ward; Ann S Hamilton; M Chandler Mcleod; Lauren P Wallner; Monica Morrow; Reshma Jagsi; Sarah T Hawley; Allison W Kurian
Journal:  J Clin Oncol       Date:  2018-03-12       Impact factor: 50.717

7.  Cancer genetic counseling: communication and counselees' post-visit satisfaction, cognitions, anxiety, and needs fulfillment.

Authors:  Arwen H Pieterse; Alexandra M van Dulmen; Frits A Beemer; Jozien M Bensing; Margreet G E M Ausems
Journal:  J Genet Couns       Date:  2007-02-13       Impact factor: 2.537

8.  Known unknowns: building an ethics of uncertainty into genomic medicine.

Authors:  Ainsley J Newson; Samantha J Leonard; Alison Hall; Clara L Gaff
Journal:  BMC Med Genomics       Date:  2016-09-01       Impact factor: 3.063

9.  Predictors of next-generation sequencing panel selection using a shared decision-making approach.

Authors:  Eliza Courtney; Shao-Tzu Li; Tarryn Shaw; Yanni Chen; John Carson Allen; Joanne Ngeow
Journal:  NPJ Genom Med       Date:  2018-04-27       Impact factor: 8.617

10.  How do research participants perceive "uncertainty" in genome sequencing?

Authors:  Barbara B Biesecker; William Klein; Katie L Lewis; Tyler C Fisher; Martha Frances Wright; Leslie G Biesecker; Paul K Han
Journal:  Genet Med       Date:  2014-05-29       Impact factor: 8.822

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  6 in total

Review 1.  The role of genomics in global cancer prevention.

Authors:  Ophira Ginsburg; Paul Brennan; Patricia Ashton-Prolla; Anna Cantor; Daniela Mariosa
Journal:  Nat Rev Clin Oncol       Date:  2020-09-24       Impact factor: 66.675

2.  Knowledge and psychosocial impact of genetic counseling and multigene panel testing among individuals with ovarian cancer.

Authors:  Rachel A Pozzar; Fangxin Hong; Niya Xiong; Jill E Stopfer; Manan M Nayak; Meghan Underhill-Blazey
Journal:  Fam Cancer       Date:  2021-03-10       Impact factor: 2.375

Review 3.  Helping Patients Understand and Cope with BRCA Mutations.

Authors:  Sukh Makhnoon; Banu Arun; Isabelle Bedrosian
Journal:  Curr Oncol Rep       Date:  2022-03-18       Impact factor: 5.945

4.  Genetic risk assessment for hereditary renal cell carcinoma: Clinical consensus statement.

Authors:  Gennady Bratslavsky; Neil Mendhiratta; Michael Daneshvar; James Brugarolas; Mark W Ball; Adam Metwalli; Katherine L Nathanson; Phillip M Pierorazio; Ronald S Boris; Eric A Singer; Maria I Carlo; Mary B Daly; Elizabeth P Henske; Colette Hyatt; Lindsay Middleton; Gloria Morris; Anhyo Jeong; Vivek Narayan; W Kimryn Rathmell; Ulka Vaishampayan; Bruce H Lee; Dena Battle; Michael J Hall; Khaled Hafez; Michael A S Jewett; Christina Karamboulas; Sumanta K Pal; A Ari Hakimi; Alexander Kutikov; Othon Iliopoulos; W Marston Linehan; Eric Jonasch; Ramaprasad Srinivasan; Brian Shuch
Journal:  Cancer       Date:  2021-08-03       Impact factor: 6.860

Review 5.  First international workshop of the ATM and cancer risk group (4-5 December 2019).

Authors:  Fabienne Lesueur; Douglas F Easton; Anne-Laure Renault; Sean V Tavtigian; Jonine L Bernstein; Zsofia Kote-Jarai; Rosalind A Eeles; Dijana Plaseska-Karanfia; Lidia Feliubadaló; Banu Arun; Natalie Herold; Beatrix Versmold; Rita Katharina Schmutzler; Tú Nguyen-Dumont; Melissa C Southey; Leila Dorling; Alison M Dunning; Paola Ghiorzo; Bruna Samia Dalmasso; Eve Cavaciuti; Dorothée Le Gal; Nicholas J Roberts; Mev Dominguez-Valentin; Matti Rookus; Alexander M R Taylor; Alisa M Goldstein; David E Goldgar; Dominique Stoppa-Lyonnet; Nadine Andrieu
Journal:  Fam Cancer       Date:  2021-06-14       Impact factor: 2.375

6.  Randomized study of remote telehealth genetic services versus usual care in oncology practices without genetic counselors.

Authors:  Cara N Cacioppo; Brian L Egleston; Dominique Fetzer; Colleen Burke Sands; Syeda A Raza; Neeraja Reddy Malleda; Elisabeth McCarty Wood; India Rittenburg; Julianne Childs; David Cho; Martha Hosford; Tina Khair; Jamil Khatri; Lydia Komarnicky; Trina Poretta; Fahd Rahman; Satish Shah; Linda J Patrick-Miller; Susan M Domchek; Angela R Bradbury
Journal:  Cancer Med       Date:  2021-06-08       Impact factor: 4.452

  6 in total

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