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• W2893147130 abstract "Background: Cancer registration is a systematic process of data collection of adequate data about patient with confirmed cancer, followed by processing and dissemination of reports to allow understanding of magnitude and pattern of cancer in certain covered population. Alexandria Cancer Registry (ACR) is a well-established central hospital based cancer registry from university hospitals, hospitals of ministry of public health, medical care organization and health insurance hospitals to cover more than 90% of diagnosed cases with cancer. Data are collected active and passive ways. Data abstracts include: age, gender, residence, occupation, date of first diagnosis and contact address of the patient together with items about mode of diagnosis, site, laterality, topography, histology, lymph node affections, modality of treatment and health status during the last visit. Cancer registrars in ACR attended several continuous training activities in abstracting, case ascertainment and TNM coding to allow competence, reliability and accuracy of data through intimate supervision from pathologists, oncologists, surgeons and radiologists in the registry board. Data manipulation and analysis are routinely by CanReg5.0 software. The last report in 2015, shows a total of 4550 confirmed cases have been registered, with a male to female ratio 1:1.1. The report adopted the guidelines of IACR-WHO. The report shows the frequency of cases by systems, age and gender, followed by affected organs within each system. The most affected system was connective tissues and soft tissue including female breast cancer. The second most affected system was gastrointestinal system. Primary hepatocellular carcinoma replaced urinary bladder as the first most frequent cancer among males with young age presentation. As a data bank, several research activities has been done in ACR in the form of case control studies in collaboration with IARC and Mario Negri Institute, Milan, Italy. Screening for colorectal cancer started with University of Alabama at Birmingham. Several interesting findings will be displayed, discussed and explained during the presentation. Conclusion: The appropriate data quality of cancer patients in cancer registry along with the catalog guided biologic repositories are considered as initial pillar to establish a biobank and allowed us to join International Biobank (IBB) and BCNet in IARC to accelerate global understanding of causes of cancer and joining a framework of other members will allow exchange of knowledge and upscale levels of cancer prevention." @default.
• W2893147130 created "2018-10-05" @default.
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• W2893147130 date "2018-10-01" @default.
• W2893147130 modified "2023-09-26" @default.
• W2893147130 title "A 30 Years’ Experience in Cancer Prevention From Alexandria, Egypt" @default.
• W2893147130 doi "https://doi.org/10.1200/jgo.18.87200" @default.
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