Evidence map›Paper›PMID 31527859›Full record

ArticleEuropean journal of human genetics : EJHG2020

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

Jude E Cléophat, Ana Marin, Sylvie Pelletier, Yann Joly, Pierre Gagnon, Alberte Déry, Jocelyne Chiquette, Bruno Gagnon, Louis Roy, Vasiliki Bitzas and 2 more

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

12 authors.

Jude E CléophatCHU de Québec-Laval University Research Center, Oncology Division, Quebec City, QC, Canada.
Ana MarinFaculty of Medicine and Health Sciences, Sherbrooke University, Sherbrooke, QC, Canada.
Sylvie PelletierCHU de Québec-Laval University Research Center, Oncology Division, Quebec City, QC, Canada.
Yann JolyCenter of Genomics and Policy, McGill University, Montreal, QC, Canada.ORCID http://orcid.org/0000-0002-8775-2322
Pierre GagnonCHU de Québec-Laval University Research Center, Oncology Division, Quebec City, QC, Canada.
Alberte DéryQuebec Palliative Care Association, Granby, QC, Canada.
Jocelyne ChiquetteCHU de Québec-Laval University Research Center, Oncology Division, Quebec City, QC, Canada.
Bruno GagnonCHU de Québec-Laval University Research Center, Oncology Division, Quebec City, QC, Canada.
Louis RoyCHU de Québec-Laval University, Quebec City, QC, Canada.
Vasiliki BitzasJewish General Hospital, Palliative Care Unit, Montreal, QC, Canada.
Hermann NabiCHU de Québec-Laval University Research Center, Oncology Division, Quebec City, QC, Canada.
Michel DorvalCHU de Québec-Laval University Research Center, Oncology Division, Quebec City, QC, Canada. michel.dorval@crchudequebec.ulaval.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AttitudeGenetic TestingMedical History TakingAdultFamilyFemaleFocus GroupsGenetic Predisposition to DiseaseHumansMaleMiddle AgedNeoplasmsPalliative Care

Identifiers

PMID31527859
PMCPMC6974613

What OpenQuestion holds

Textmetadata
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.