HUSLAB, Department of Pathology, University of Helsinki and Helsinki University Hospital, Haartmaninkatu 3, Helsinki, Finland.
Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Tukholmankatu 8, Helsinki, Finland.
Virchows Arch. 2020 Feb;476(2):273-283. doi: 10.1007/s00428-019-02625-6. Epub 2019 Aug 5.
Finnish hospital-integrated biobanks administer millions of formalin-fixed paraffin-embedded tissue samples collected within the clinical diagnostics. According to the Finnish Biobank Act, these samples can be coupled with patients' clinical follow-up data and the data retrieved from national health registries. We collected a nationwide pulmonary carcinoid tumour series from Finnish biobanks to study prognostic factors as well as to explore how the number of tumours found in the Finnish biobanks corresponds to the number of tumours registered by the Finnish Cancer Registry (FCR). Finnish biobanks identified 88% of the tumours registered by the FCR and were able to deliver 63%. The main reasons for lacking samples were paucity of resected primary tumour tissue, incompatible primary diagnosis, and the absence of tissue blocks in the archives. The main bottleneck in the sample application process was retrieving patient data. Altogether, we received 224 tumour samples with appropriate patient data and identified six prognostic factors for shorter disease-specific survival: age over 56 years at the time of diagnosis, tumour size over 2.5 cm, atypical histology, Ki-67 proliferation index higher than 2.5%, hilar/mediastinal lymph node involvement at the time of diagnosis, and the presence of metastatic disease. In conclusion, the Finnish biobank infrastructure offers excellent opportunities for tissue-based research. However, to be able to develop the biobank operations further, involving more medical knowledge in the sample and data acquisition process is a necessity. Also, when working with tissue samples collected over decades, histological expertise is essential for re-evaluation and re-classification of the samples.
芬兰的医院整合生物库管理着数以百万计的临床诊断中收集的福尔马林固定石蜡包埋组织样本。根据《芬兰生物库法》,这些样本可以与患者的临床随访数据以及从国家健康登记处检索到的数据相结合。我们从芬兰的生物库中收集了一个全国性的肺类癌肿瘤系列,以研究预后因素,并探讨芬兰生物库中发现的肿瘤数量与芬兰癌症登记处(FCR)登记的肿瘤数量之间的关系。芬兰生物库识别出了 FCR 登记的肿瘤中的 88%,并能够提供其中的 63%。缺乏样本的主要原因是切除的原发性肿瘤组织不足、原发性诊断不兼容以及档案中没有组织块。样本应用过程中的主要瓶颈是检索患者数据。总的来说,我们收到了 224 份有适当患者数据的肿瘤样本,并确定了六个与疾病特异性生存时间较短相关的预后因素:诊断时年龄超过 56 岁、肿瘤大小超过 2.5 厘米、非典型组织学、Ki-67 增殖指数高于 2.5%、诊断时肺门/纵隔淋巴结受累以及存在转移性疾病。总之,芬兰的生物库基础设施为基于组织的研究提供了极好的机会。然而,为了能够进一步发展生物库业务,在样本和数据采集过程中涉及更多的医学知识是必要的。此外,在处理几十年来收集的组织样本时,对于重新评估和重新分类样本,组织学专业知识是必不可少的。