Fear of cancer recurrence in breast cancer survivors carrying a BRCA1 or 2 genetic mutation : a cross-sectional study.

IF 2 4区 医学 Q3 ONCOLOGY
Alexandra Michel, Michel Dorval, Jocelyne Chiquette, Josée Savard
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Abstract

Background: Fear of cancer recurrence (FCR) affects virtually all patients who have been treated for cancer, to varying degrees. Breast cancer survivors who carry a BRCA1 or BRCA2 gene mutation are at high risk of cancer recurrence. No study has yet assessed FCR specifically in this population.

Objectives: This cross-sectional study, conducted in women who were treated for breast cancer and carrying a BRCA1/2 mutation, aimed to: (1) assess the mean level of FCR and estimate the proportion of patients with clinical levels of FCR; (2) examine the relationships between FCR and selected psychological variables (e.g., avoidance, intolerance to uncertainty) and quality of life; (3) explore whether FCR levels vary as a function of the past preventive treatment received; and (4) to assess the associations between FCR and the presence of decisional conflict or regret regarding the various preventive options.

Method: Participants were recruited through an e-mail sent to an oncogenetic network mailing list (Réseau ROSE). Participants were asked to complete a battery of questionnaires online assessing FCR and other psychological and quality of life variables.

Results: A total of 89 women completed the survey. Most participants had undergone a preventive mastectomy (62.9%) and a preventive salpingo-oophorectomy (75.3%) at the time of the study. The mean Fear of Cancer Recurrence Inventory-severity score was 16.8, which exceeds the clinical cut-off score of 13, and 70.8% of the participants showed a clinical level of FCR. FCR was significantly associated with higher levels of anxiety and depression, and higher avoidance and intolerance of uncertainty, but not with quality of life. No significant difference was observed on the total FCR score between women who had received preventive surgery (mastectomy and/or salpingo-oophorectomy) and those considering it, and those not considering it. The association was significant between higher FRC scores and greater decisional conflicts and regrets about choosing to undergo preventive surgery.

Conclusion: These data suggest that FCR is a significant problem for breast cancer survivors carrying a BRCA1/2 genetic mutation, even after undergoing a prophylactic surgery. This highlights the importance of providing these women with specific psychological intervention focusing on FCR.

携带 BRCA1 或 2 基因突变的乳腺癌幸存者对癌症复发的恐惧:一项横断面研究。
背景:对癌症复发的恐惧(FCR)在不同程度上影响着几乎所有接受过癌症治疗的患者。携带 BRCA1 或 BRCA2 基因突变的乳腺癌幸存者是癌症复发的高危人群。目前还没有研究专门对这一人群的 FCR 进行评估:这项横断面研究以接受过乳腺癌治疗且携带 BRCA1/2 基因突变的女性为对象,旨在(目的:这项横断面研究的对象是接受过乳腺癌治疗且携带 BRCA1/2 基因突变的女性,旨在:(1)评估 FCR 的平均水平,并估计临床水平 FCR 患者的比例;(2)研究 FCR 与选定的心理变量(如回避、不耐受不确定性)和生活质量之间的关系;(3)探讨 FCR 水平是否随过去接受的预防性治疗而变化;以及(4)评估 FCR 与在各种预防性选择中是否存在决策冲突或遗憾之间的关联:通过向肿瘤基因网络邮件列表(Réseau ROSE)发送电子邮件的方式招募参与者。参与者需在线完成一系列问卷,评估FCR及其他心理和生活质量变量:共有 89 名妇女完成了调查。大多数参与者在调查时已接受了预防性乳房切除术(62.9%)和预防性输卵管切除术(75.3%)。对癌症复发的恐惧清单-严重程度的平均得分为 16.8 分,超过了 13 分的临床临界值,70.8% 的参与者显示出了 FCR 的临床水平。FCR 与较高程度的焦虑和抑郁、较高程度的回避和对不确定性的不容忍明显相关,但与生活质量无关。接受过预防性手术(乳房切除术和/或输卵管切除术)的妇女、考虑接受手术的妇女和未考虑接受手术的妇女在 FCR 总分上没有明显差异。FCR得分越高,选择接受预防性手术时的决策冲突和后悔程度就越大,两者之间存在明显关联:这些数据表明,对于携带 BRCA1/2 基因突变的乳腺癌幸存者来说,即使接受了预防性手术,FCR 仍是一个重要问题。这凸显了为这些妇女提供以 FCR 为重点的特定心理干预的重要性。
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来源期刊
CiteScore
3.10
自引率
5.90%
发文量
38
审稿时长
>12 weeks
期刊介绍: Hereditary Cancer in Clinical Practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. Cancer genetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. With the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. Topics covered by the journal include but are not limited to: Original research articles on any aspect of inherited predispositions to cancer. Reviews of inherited cancer predispositions. Application of molecular and cytogenetic analysis to clinical decision making. Clinical aspects of the management of hereditary cancers. Genetic counselling issues associated with cancer genetics. The role of registries in improving health care of patients with an inherited predisposition to cancer.
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