The National Cancer Institute (NCI) is seeking capability statements from organizations regarding a contract for the collection and evaluation of human tissues, cells, and bio-fluids from donors with an epidemiologic profile. This initiative, managed by the Laboratory of Human Carcinogenesis, is intended to support molecular epidemiology studies focused on various cancers, including lung, breast, liver, and pancreatic cancer. The contractor will be tasked with recruiting participants, collecting biological specimens, processing epidemiological data, and ensuring compliance with ethical regulations.
The contract aims to continue and enhance previous efforts that started in 1996, shifting from tissue collection for experimental development to comprehensive case-control studies. Eligible organizations should respond by outlining their ability to meet the project's requirements, which include delivering viable tissues within three hours and maintaining data confidentiality. The anticipated contract period is five years, with considerations for small business set-asides. The notice encourages potential applicants, excluding the current provider, to demonstrate their qualifications and capabilities by submitting statements by February 18, 2025.
The draft Statement of Work outlines the objectives and tasks for a contractor supporting the Laboratory of Human Carcinogenesis (LHC) in researching the molecular epidemiology of human cancer. Key responsibilities include recruiting cancer cases and population-based controls, collecting and processing biological specimens, and maintaining ethical and legal approvals. The contractor is expected to accrue targeted cancer case numbers annually, covering various types including lung, liver, and pancreatic cancers, while also gathering demographic and medical data through structured questionnaires.
Biological samples must be handled and stored per regulatory standards, with regular reporting and data management requirements. The document emphasizes compliance with the Privacy Act and health regulations, as well as ensuring accessibility under Section 508 standards. Transition plans for phase-in and phase-out of contract activities, alongside extensive training requirements for personnel interacting with patients, are also detailed. Overall, this work underlines a significant commitment to advancing cancer research through meticulous data collection and specimen management.