Abstract

Background: Biobanks play a critical role in cancer research by providing high quality biological samples for research. However, the availability of tumor samples in single research institutions is often limited, especially for rare cancers. In order to facilitate the search for samples scattered among different Belgian institutions, a nationwide virtual tumorbank project was launched and is operational since February 2012. The Belgian Virtual Tumorbank (BVT) network encompasses the tumor biobanks from eleven Belgian university hospitals that collect and store residual human tumor samples locally and is coordinated by the Belgian Cancer Registry.Materials and Methods: A web application was developed and consists of two modules. The registration module (BVTr) centralizes the tumor sample data from the local partner biobanks. The catalog module (BVTc) allows researchers to trace the tumor samples in the 11 tumor biobanks. The BVTc contains patient, medical and technical data, but excludes identifying information to ensure privacy of individuals. Automatic and manual controls guarantee high quality data on the samples requested by scientists for research purposes in oncology. A major advantage of the BVT network is that the available data can be linked to the data of the Belgian Cancer Registry for quality control purposes.Results: Currently, more than 92,000 registrations are available in the catalog. Twenty-seven percent of the residual primary tumor samples originate from breast tissue, but also less frequent localisations such as head and neck (4%), male genital organs (1.7%), and urinary tract (1%) are available. In addition to the residual tumor tissue samples, also other available material can be stored and registered by the local biobanks. The most common type is corresponding normal tissue (19%).Other frequently available materials are plasma, blood, serum, DNA, and buffy coat. Even PBMCs, RNA, cytology, and urine are available in some cases.Discussion and Conclusion: The BVT catalog is a valuable source of information for oncology research and the ultimate goal is to promote multidisciplinary cancer research (i.e., pathogenesis, disease prediction, prevention, diagnosis, treatment, and prognosis) for the benefit of all cancer patients.

Highlights

  • Cancer registration in Belgium has evolved from a number of regional initiatives in the late nineties toward a national and centralized population based cancer registry with a firm legal basis

  • The national virtual tumorbank has been set up in order to facilitate the search for samples scattered among different Belgian institutions

  • The central database (BVTr) allows centralization of patient, technical and oncological data of human residual samples stored locally in a harmonized and standardized way while the catalog (BVTc) enables researchers to localize the samples required for their oncology research

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Summary

Introduction

Cancer registration in Belgium has evolved from a number of regional initiatives in the late nineties toward a national and centralized population based cancer registry with a firm legal basis. In addition to describing cancer incidence and survival, the BCR is involved in clinical registration projects [13, 14], in the evaluation of quality of care in oncology [15], in the registration of all tissue samples taken for early diagnosis and screening for breast, colorectal and cervical cancer [16] and in the centralization of the data on residual human tumor samples stored in local biobanks for scientific research purposes. The Belgian Virtual Tumorbank (BVT) network encompasses the tumor biobanks from eleven Belgian university hospitals that collect and store residual human tumor samples locally and is coordinated by the Belgian Cancer Registry

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