When it comes to projects that gather genomic data for population and biomedical studies, the lack of quality samples from the Middle East means that some groups are underrepresented. With a projected three-fold increase in the cancer rate between 2013 and 2050 in Egypt alone, this could have significant implications for the region in terms of personalized medicine.
For this reason, the non-governmental pediatric oncology organization Children’s Cancer Hospital-57357-Egypt (CCHE) established a Biorepository and Biospecimen Research Facility (CCHEBBR) to collect high-quality, clinically annotated, fit-for-all research biospecimens. Here Labib et al. (2015) offer a practical guide to the CCHEBBR’s development process, specifically highlighting how integrating the biorepository workflow with the established clinical hospital enables this development even with minimal resources.1
During the planning phase of biobank development, the team established an 8- to 10-member Biorepository Coordinating Committee (BCC) made up of professors active in stakeholder departments (research, surgical pathology, clinical pathology, surgery, pediatric oncology, radiotherapy and IT). They tasked this committee with organizing projects at the biobank, including the creation of and adherence to standard operating procedures (SOPs) and good laboratory practices.
They identified the following challenges particular to their region:
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lack of research culture in the community
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religion-based misconceptions
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lack of public trust, fear of being abused
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parent education levels
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patient privacy and sample coding
When it came to physical logistics, the team made the following choices:
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Space design |
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Electrical power and security |
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Equipment |
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Patient data safety and labeling |
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Software |
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Personnel and training |
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The BCC combed the existing literature when establishing SOPs for collection, processing and storage, and developed workflows for each specimen type that rely on significant cooperation with the central hospital. The authors indicate that adherence to these SOP workflows will be key to efficient, ethical management as well as sample distribution when that stage begins (five years from initial start-up). They revise and update these every six months.
Labib et al. report that recent monitoring efforts revealed that, for 5,438 patients over a 24-month period, 70.2% (n=3,812) supported biobanking and consented to donate for multipurpose research. The team credits this high acceptance rate, which required a cultural paradigm shift in many cases, to their team of research interviewers, who used clear, careful communication to address donor concerns and build public trust. They further attribute their general success to the way they tailored their SOPs to the existing infrastructure, enabling the team to standardize biobanking activities smoothly while minimizing costs.
The team plans to focus on four future projects:
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quality control
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biospecimen research
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biobanking microorganisms
- biobanking cell lines
Ultimately, the researchers believe that the development of a reliable biorepository like the CCHEBBR will have a two-fold impact: providing region-specific access to personalized medicine and advancing research toward the goal of finding a cure for cancer.
Reference
1. Labib, R. M. et al. (2015) “Biorepository for pediatric cancer with minimal resources: Meeting the challenges,” Biopreservation and Biobanking. doi: 10.1089/bio.2015.0004




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