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Notice Number: NOT-CA-06-002
Release Date: November 9, 2005
National Cancer Institute (NCI), (http://www.nci.nih.gov)
NIH is seeking input from the community.
This Request for Information (RFI) is for analysis and planning purposes only and should not be construed as a solicitation or as an obligation on the part of the Government. The Government does not intend to award a cooperative agreement, contract, or grant on the basis of responses to this RFI or otherwise pay for the preparation of any information submitted or for the Government's use of such information.
Cancer, with some exceptions, is a complex genetic disease in which mutations may contribute to its initiation and progression. Research has already identified a large number of mutations implicated in carcinogenesis, which has led to an understanding of many details underlying tumor development and progression. The successes of some newly introduced cancer drugs that act on known mutated proteins demonstrate that products of somatic genetic alterations are legitimate targets for therapy. However, given cancer's complexity, it is generally assumed that only a fraction of the molecular targets involved in carcinogenesis have been identified to date.
The complexity of cancer is perhaps best exemplified by the fact that there are many different human tumor types, each with distinct subgroups, and each presenting radically different scientific and clinical challenges. This heterogeneity arises, in part, from the fact that cancer genomes are dynamic and tumors are complex systems that are shaped by chromosome aberrations, nucleotide mutations, epigenetic phenomena, the cellular and biological context of the specific cancer, characteristics specific to the individual patient, and environmental influences. While certain similarities exist across cancer types, any effort to characterize the genomes of cancers in a comprehensive, systematic manner must address important questions related to heterogeneity.
In February 2005, the Directors of the National Cancer Institute (NCI) and the National Human Genome Research Institute (NHGRI) agreed to explore pursuing a 3-year pilot project, based on a recommendation in a recent National Cancer Advisory Board Biomedical Technology Subgroup Report (available at www.cancer.gov), to determine the feasibility of cataloging the genetic aberrations associated with a set of human cancers. Since cancer is a genetic disorder, in principle it should be possible to derive a complete catalog of mutations, and in some cases to determine other abnormalities. Once the information is known, a complete understanding of the functional consequences of these alterations can be used to develop and implement preventative or interventional strategies to eliminate and/or control cancer.
A comprehensive definition of molecular taxonomy for cancer is an ambitious endeavor. One of the important initial challenges is to identify which cancer(s) to study in the pilot project that will optimize the chance for initial success. Any investigator with biospecimen collections within the United States , or internationally, is encouraged to respond to the RFI and provide the information requested below. Please note that it would be very desirable if respondents provide a separate response for each significantly different cancer biorepository that they maintain.
With regard to any clinical protocols that were/are used, respondents should indicate whether or not the collection of biospecimens was or is being carried out in the context of a clinical trial. If clinical trials were or are involved, please indicate whether or not:
Further, with regard to any clinical protocols that might have been or are still being followed, respondents should, if possible, indicate whether or not:
With regard to any annotation of biospecimens, respondents should, if possible, indicate whether or not:
With regard to the contents of each biorepository , respondents should provide, if possible, the following details:
Further, with regard to the contents of each biorepository , respondents should, if possible, describe:
With regard to standard operating, quality control, and quality assurance procedures , respondents should, if possible, indicate whether or not:
The goal of this RFI is to identify and gather data about the characteristics of existing human tumor repositories. The information gathered from this process will help distinguish the key features of biospecimen collections that could meet the needs of the pilot cancer genome characterization project. The NCI welcomes any additional information the respondent wishes to submit, such as details of repository contents, collection procedures, biorepository management procedures, and human subjects protocols. Please attach such information as appendices to the main response.
The document should not be longer than five pages. It would be helpful if the data are provided in a tabular form. To assist you, we have provided two options for providing information directly through the CGAP web site ( cgap.nci.nih.gov) . The response deadline is 8 weeks from the publication of this announcement; therefore, the closing date is January 12, 2006 . If you choose to not fill out the form on the CGAP web site, please submit your responses to us either via mail or e-mail using the addresses shown below:
Daniela S. Gerhard, Ph.D.
Office of Cancer Genomics
National Cancer Institute
31 Center Drive , Room 31A07
Bethesda , MD 20892
Administrative Program Assistant
Weekly TOC for this Announcement
NIH Funding Opportunities and Notices
Office of Extramural
National Institutes of Health (NIH)
9000 Rockville Pike
Bethesda, Maryland 20892
Department of Health
and Human Services (HHS)
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