COVID-19 vaccination uptake and safety profile among germline BRCA1 and BRCA2 pathogenic variant carriers in Singapore.

IF 2 4区 医学 Q3 ONCOLOGY Hereditary Cancer in Clinical Practice Pub Date : 2023-04-12 DOI:10.1186/s13053-023-00248-2
Zewen Zhang, Nur Diana Binte Ishak, Frances Victoria Fajardo Que, Zi Yang Chua, Sock Hoai Chan, Jianbang Chiang, Joanne Ngeow Yuen Yie
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Abstract

Background: Although Singapore is one of the highest vaccinated countries in the world, vaccine hesitancy remains in a subpopulation, including individuals with cancer predisposition syndromes. At the Cancer Genetics Service National Cancer Centre Singapore, we see patients with germline genetic alterations, most being BRCA1/2 pathogenic/likely pathogenic variant (PV/LPV) carriers. While reported safe for cancer patients, there are limited studies addressing the safety profile and outcomes of COVID-19 vaccination among individuals with germline PV/LPV in cancer predisposition genes such as BRCA1/2. This study aims to evaluate the outcomes of COVID-19 vaccination among germline PV/LPV carriers in BRCA1/2.

Methods: We conducted a phone call survey of COVID-19 vaccination uptake and toxicity in a prospective cohort of 189 participants with germline BRCA1/2 PV/LPV between 1st Sept 2021 and 30th Sept 2021. We collected demographics data including gender, race, age, history of cancer, types of cancer, and number of cancers. Statistical difference in baseline demographics between responders with history of cancer and those without were assessed using Chi-square, Fisher's exact and independent t-test analysis. Logistic regression was used to evaluate effect of demographics on the occurrence of post-vaccination side effects.

Results: Among 189 BRCA1/2 PV/LPV carriers responded, 97 carried PV/LPV in BRCA1 and 92 in BRCA2. Majority were vaccinated (89.5%) and had completed the two-dose vaccine schedule, with 7 (4.1%) received only one dose. The most common post-vaccination side effects was myalgia (56.5%) followed by fever (40.2%), headache (16.3%) and fatigue (11.2%). There were no major severe side events. Evaluation by logistic regression showed that the occurrence of side effects was not affected by PV/LPV gene (BRCA1 or BRCA2), gender, race, age or history of cancer.

Conclusion: The post-vaccination side effects profile among individuals with germline PV/LPV in BRCA1/2 is consistent with the Singaporean general population, hence recommendations for COVID-19 vaccination for these individuals should not differ from non-carriers and should be encouraged by their healthcare providers.

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新加坡种系BRCA1和BRCA2致病变异携带者的COVID-19疫苗接种情况和安全性
背景:虽然新加坡是世界上疫苗接种率最高的国家之一,但在一个亚人群中,包括有癌症易感综合征的个体,仍然存在疫苗犹豫。在新加坡国家癌症中心癌症遗传服务中心,我们看到有生殖系遗传改变的患者,大多数是BRCA1/2致病性/可能致病性变异(PV/LPV)携带者。虽然有报道称对癌症患者是安全的,但在BRCA1/2等癌症易感基因中携带种系PV/LPV的个体中,关于COVID-19疫苗接种的安全性和结果的研究有限。本研究旨在评估BRCA1/2种系PV/LPV携带者接种COVID-19疫苗的结果。方法:我们在2021年9月1日至2021年9月30日期间,对189名生殖系BRCA1/2 PV/LPV患者进行了COVID-19疫苗接种摄取和毒性的电话调查。我们收集了人口统计数据,包括性别、种族、年龄、癌症病史、癌症类型和癌症数量。有癌症病史和没有癌症病史的应答者的基线人口统计学差异使用卡方、Fisher精确和独立t检验分析进行评估。采用Logistic回归评价人口统计学因素对疫苗接种后副反应发生的影响。结果:189名BRCA1/2 PV/LPV携带者中,97名BRCA1携带者和92名BRCA2携带者携带PV/LPV。大多数(89.5%)接种了两剂疫苗,7人(4.1%)只接种了一剂疫苗。接种疫苗后最常见的副作用是肌痛(56.5%),其次是发热(40.2%)、头痛(16.3%)和疲劳(11.2%)。没有严重的副反应。经logistic回归评估,副作用的发生与PV/LPV基因(BRCA1或BRCA2)、性别、种族、年龄或癌症史无关。结论:BRCA1/2种系PV/LPV个体的疫苗接种后副作用与新加坡普通人群一致,因此对这些个体的COVID-19疫苗接种建议不应与非携带者不同,应得到其医疗保健提供者的鼓励。
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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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