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Value of Information of Secondary dAta in ONCOGEnetics (VISAGE-ONCO)

2021年7月12日 更新者:Centre Georges Francois Leclerc

VISAGE-ONCO study is a qualitative transversal study aiming to identify and describe processes and mechanisms that explain in cancerology the feelings and experience of patients and health professionals with regard to the possibility of having access to secondary findings generated by the use High-speed exome sequencing . Semi-structured interviews will be conducted with patients and health professionals to answer this aims from 2 situations.

The first situation is in the context of the standard practice for theranostic purposes, where somatic and constitutional analysis of the various genes involved in carcinogenesis is carried out systematically in parallel. Patients are informed that the analysis of these genes may reveal the existence of a genetic predisposition to another type of cancer than the one for which patients have consulted, with a risk for themselves or their relatives, which could modify their management. This targeted information on genetic predisposition genes to cancer is therefore provided as part of standard management for theranostic purposes, but without any detailed exploration of the reasons why patients wanted to be informed.

The second situation is in the framework exome analysis position in the strategy of genetic redisposition factors identification in early-onset cancer study (EX²TRICAN NCT04141462) where all the genes identified in human pathology are part of the analysis. Patients have the possibility of accessing a result concerning a gene that may or may not be linked to a hereditary cancer risk if patients have ticked off in the consent form the wish to be informed.

Therefore, two distinct questions arise:

  • That of understanding the wish of patients to be given back actionable data which can be identified in a fortuitous way within the framework of standard management for theranostic purposes and in EX²TRICAN, by taking into account the fact that these data can constitute an opportunity for the patient in terms of management; but patients also constitute a risk of transmission for they relatives, and a psychological risk by the anxiety generated;
  • The wish to have access - or not - to data which are not actively sought today within the framework of standard care for theranostic purposes and in EX²TRICAN (genetic alterations increasing the risk of cardiovascular or metabolic diseases), but which could be proposed in a systematic way in the future because of their actionable character.

研究概览

地位

招聘中

研究类型

观察性的

注册 (预期的)

70

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

  • 姓名:Sandrine DABAKUYO, PHD
  • 电话号码:33 0345348067
  • 邮箱sdabakuyo@cgfl.fr

学习地点

      • Dijon、法国
        • 招聘中
        • Centre Georges François Leclerc
        • 接触:
        • 接触:
        • 首席研究员:
          • François GHIRINGHELLI, PU-PH

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Patients with cancer who will undergo exomes analysis

描述

Inclusion Criteria:

Standard care patients for theranostic goal

  • Histological or cytological evidence of a diagnosis of metastatic or locally advanced solid tumor
  • Tumor material available and usable for the analyses required by the study
  • Request for genetic analysis to be performed at the initiation of the 1st or 2nd line of treatment
  • Normal biological parameters
  • Life expectancy ≥ 6 months
  • Performance status ≤ 1
  • Social security affiliation
  • Who have received information and agreed to participate

Patient from EX²TRICAN study

  • Histological or cytological evidence of a diagnosis of metastatic or locally advanced solid tumor
  • Having cancer before age 40
  • Patient affiliated to social security
  • Availability of a tumor sample if secondary functional studies are required
  • Availability of the 2 parents when the trio approach is required
  • Availability of affected relatives
  • Who have received information and agreed to participate

Health professional

  • To be oncologist or geneticist or genetic counselor and able to be inform, prescribe and transmit the results of secondary data
  • Working at university hospital center of dijon or cancerology center Georges Francois Leclerc at Dijon
  • Who have received information and agreed to participate

Exclusion Criteria:

Standard care patients for theranostic goal

  • History of Human immunodeficiency virus infection
  • History of Hepatitis B virus /Hepatitis C virus infection
  • To be pregnant or likely to be or breastfeeding disorders psychiatric

Patient from EX²TRICAN study

  • Minor index cases
  • Disorders psychiatric

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:其他
  • 时间观点:横截面

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Patient's experience through semi-structured interviews
大体时间:1 day (during the interview)
Patients were asked during a semi-structured interview, to understand their feelings and experience ith regard to the possibility of having access to secondary findings
1 day (during the interview)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2019年12月9日

初级完成 (预期的)

2022年6月9日

研究完成 (预期的)

2022年12月9日

研究注册日期

首次提交

2021年6月28日

首先提交符合 QC 标准的

2021年7月12日

首次发布 (实际的)

2021年7月22日

研究记录更新

最后更新发布 (实际的)

2021年7月22日

上次提交的符合 QC 标准的更新

2021年7月12日

最后验证

2021年7月1日

更多信息

与本研究相关的术语

其他研究编号

  • 2019-A02303-54

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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