Literature DB >> 31527859

What do cancer patients' relatives think about addressing cancer family history and performing genetic testing in palliative care?

Jude E Cléophat1,2,3, Ana Marin4,5,6, Sylvie Pelletier1, Yann Joly7, Pierre Gagnon1,3,8, Alberte Déry9, Jocelyne Chiquette1,3,5,10, Bruno Gagnon1,3,10, Louis Roy5, Vasiliki Bitzas11, Hermann Nabi1,3,10,12, Michel Dorval13,14,15,16.   

Abstract

Palliative care may be an opportunity to discuss cancer family history and familial cancer risks with patients' relatives. It may also represent the last opportunity to collect, from dying patients, clinical data and biospecimens that will inform cancer risk assessment and prevention in their surviving relatives. This study aims to explore the perspectives of cancer patients' relatives about cancer heritability, addressing cancer family history, and performing genetic testing in palliative care settings. Thirteen first-degree relatives of cancer patients who died in palliative care participated in the study. Two focus groups were conducted and transcribed verbatim. Two independent coders conducted a thematic content analysis. The themes included: (1) Knowledge of cancer heritability; (2) Experiences and expectations regarding cancer family history discussions, and (3) Views on genetic testing in palliative care patients and DNA biobanking. Participants seemed aware that cancer family history is a potential risk factor for developing the disease. They considered the palliative care period an inappropriate moment to discuss cancer heritability. They also did not consider palliative care providers as appropriate resources to consult for such matters as they are not specialized in this field. Participants welcomed DNA biobanking and genetic testing conducted at the palliative care patients' request. Cancer occurrence within families raises concerns among relatives about cancer heritability, but the palliative care period is not considered the most appropriate moment to address this issue. However, discussions about the risk to cancer patients' relatives might need to be considered on a case-by-case basis.

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Year:  2019        PMID: 31527859      PMCID: PMC6974613          DOI: 10.1038/s41431-019-0505-3

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  22 in total

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Authors:  Alison Metcalfe; Rachel Pumphrey; Collette Clifford
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2.  The qualitative content analysis process.

Authors:  Satu Elo; Helvi Kyngäs
Journal:  J Adv Nurs       Date:  2008-04       Impact factor: 3.187

3.  A model for patient-direct screening and referral for familial cancer risk.

Authors:  Kristin B Niendorf; Melissa A Geller; Rachel Isaksson Vogel; Timothy R Church; Anna Leininger; Angela Bakke; Robert D Madoff
Journal:  Fam Cancer       Date:  2016-10       Impact factor: 2.375

4.  Physicians' current practices and opportunities for DNA banking of dying patients with cancer.

Authors:  John M Quillin; Joann N Bodurtha; Laura A Siminoff; Thomas J Smith
Journal:  J Oncol Pract       Date:  2011-05       Impact factor: 3.840

5.  Caring for families with a family history of cancer: why concerns about genetic predisposition are missing from the palliative agenda.

Authors:  Alison Kate Lillie; Collette Clifford; Alison Metcalfe
Journal:  Palliat Med       Date:  2011-01-12       Impact factor: 4.762

6.  The Role of Palliative Medicine in Assessing Hereditary Cancer Risk.

Authors:  Mohammed S Abusamaan; John Martin Quillin; Oluwafemi Owodunni; Oluwabunmi Emidio; In Guk Kang; Brandon Yu; Brittany Ma; Lauryn Bailey; Rab Razzak; Thomas J Smith; Joann N Bodurtha
Journal:  Am J Hosp Palliat Care       Date:  2018-05-29       Impact factor: 2.500

7.  High-Risk Palliative Care Patients' Knowledge and Attitudes about Hereditary Cancer Testing and DNA Banking.

Authors:  John M Quillin; Oluwabunmi Emidio; Brittany Ma; Lauryn Bailey; Thomas J Smith; In Guk Kang; Brandon J Yu; Oluwafemi Patrick Owodunni; Mohammed Abusamaan; Rab Razzak; Joann N Bodurtha
Journal:  J Genet Couns       Date:  2017-12-04       Impact factor: 2.537

8.  Qualitative research. Introducing focus groups.

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Journal:  BMJ       Date:  1995-07-29

9.  Mainstreaming genetics in palliative care: barriers and suggestions for clinical genetic services.

Authors:  A Dearing; N Taverner
Journal:  J Community Genet       Date:  2017-11-20

Review 10.  The current state of cancer family history collection tools in primary care: a systematic review.

Authors:  Nadeem Qureshi; June C Carroll; Brenda Wilson; Pasqualina Santaguida; Judith Allanson; Melissa Brouwers; Parminder Raina
Journal:  Genet Med       Date:  2009-07       Impact factor: 8.822

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  3 in total

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2.  Approaching discussions about genetics with palliative patients and their families: a qualitative exploration with genetic health professionals.

Authors:  Stephanie White; Erin Turbitt; Jane L Phillips; Chris Jacobs
Journal:  Eur J Hum Genet       Date:  2022-09-05       Impact factor: 5.351

3.  Demographic and socioeconomic trends in DNA banking utilization in the USA.

Authors:  Joshua Prudent; Esthermarie Lopez; Donna Dorshorst; Hannah C Cox; Joann N Bodurtha
Journal:  J Community Genet       Date:  2021-06-29
  3 in total

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