Domaradzki Jan, Czekajewska Justyna, Walkowiak Dariusz
Department of Social Sciences and Humanities, Poznań University of Medical Sciences, Poznań, Poland.
Department of Organization and Management in Health Care, Poznań University of Medical Sciences, Poznań, Poland.
Med Sci Monit. 2024 Jun 13;30:e944263. doi: 10.12659/MSM.944263.
BACKGROUND Biobanks are legally regulated entities that acquire, store, prepare, preserve, test, analyze, and distribute defined biological material and related information and data from human sources. This study aimed to evaluate trust, support and willingness to donate personal data and tissue samples for biobanking from cancer patients attending oncology departments in Poznań, Poland. MATERIAL AND METHODS This study utilized data from questionnaire-based survey conducted from February to June 2023 among 548 patients from 2 Poznań hospitals equipped with oncology treatment units. The survey employed convenience sampling. Statistical analysis was carried out using JASP 0.18.3 and PQStat1.8.6., with significance levels set at 0.05. Descriptive statistics and logistic regression were utilized to present the results. RESULTS 92.2% of cancer patients supported the establishment of cancer research biobank in Poland, and 93.1% declared the willingness to share their cancer tissues for research purposes. Patients' willingness to donate was associated with biomedical research conducted by biobanks and types of biobank institutions. Most patients were willing to donate for research on cancer, genetic and autoimmune diseases or dementia, but were reluctant to participate in research on sexual identity, intelligence, aggression and for-profit research. Patients were willing to donate to biobanks managed by medical universities, public institutions, clinical hospitals and national biobanks but not to foreign and private biobanks. CONCLUSIONS Although patients' support for cancer biobank is high it is not unconditional as their willingness to participate in cancer-related research is associated with types of biomedical research conducted by biobanks and different types of biobank institutions.
背景 生物样本库是依法监管的实体,用于获取、存储、制备、保存、检测、分析和分发来自人类的特定生物材料以及相关信息和数据。本研究旨在评估波兰波兹南肿瘤科室癌症患者对为生物样本库捐赠个人数据和组织样本的信任度、支持度和意愿。
材料与方法 本研究利用了2023年2月至6月在波兹南两家设有肿瘤治疗科室的医院对548名患者进行的问卷调查数据。该调查采用便利抽样。使用JASP 0.18.3和PQStat1.8.6进行统计分析,显著性水平设定为0.05。采用描述性统计和逻辑回归来呈现结果。
结果 92.2%的癌症患者支持在波兰建立癌症研究生物样本库,93.1%的患者表示愿意为研究目的分享他们的癌组织。患者的捐赠意愿与生物样本库开展的生物医学研究以及生物样本库机构类型有关。大多数患者愿意为癌症、遗传和自身免疫性疾病或痴呆症研究捐赠,但不愿参与关于性取向、智力、攻击性和营利性研究。患者愿意向由医科大学、公共机构、临床医院和国家生物样本库管理的生物样本库捐赠,但不愿向外国和私人生物样本库捐赠。
结论 尽管患者对癌症生物样本库的支持度很高,但并非无条件支持,因为他们参与癌症相关研究的意愿与生物样本库开展的生物医学研究类型和不同类型的生物样本库机构有关。