
HOSPITAL DE CANCER DE BARRETOS
HOSPITAL DE CANCER DE BARRETOS
2 Projects, page 1 of 1
Open Access Mandate for Publications and Research data assignment_turned_in Project2019 - 2022Partners:HOSPITAL DE CANCER DE BARRETOS, University of the Republic, TSU, MINISTRY OF HEALTH, KLINIKUM DER UNIVERSITAET ZU KOELN +24 partnersHOSPITAL DE CANCER DE BARRETOS,University of the Republic,TSU,MINISTRY OF HEALTH,KLINIKUM DER UNIVERSITAET ZU KOELN,El Bosque University,TUMS,CLB,WOMEN S ASSOCIATION OF EDUCATION AND FIGHT AGAINST CANCER,MINISTRY OF HEALTH,HOSPITAL DE CANCER DE BARRETOS,ICO,Hospital A.C. Camarg,Hospital A.C. Camarg,University of Glasgow,University of the Republic,IARC,UBA,Charles University,TSU,UBA,GERMAN CANCER RESEARCH CENTER,KLINIKUM DER UNIVERSITAET ZU KOELN,GERMAN CANCER RESEARCH CENTER,UNITO,TUMS,WOMEN S ASSOCIATION OF EDUCATION AND FIGHT AGAINST CANCER,University of Bristol,El Bosque UniversityFunder: European Commission Project Code: 825771Overall Budget: 3,996,230 EURFunder Contribution: 3,153,450 EURWorldwide, more than 550,000 new cases of head and neck cancer (HNC) occur each year, resulting in approximately 300,000 deaths annually. It is the 6th most common cancer in both Europe and South America. A major reason for the high mortality rate for this cancer is the late stage of diagnosis for many patients. Accurate assessment of the prognosis of HNC cases also allows for appropriate treatment decisions. HEADSpAcE will bring together a consortium of 15 partners with a long and successful record of collaboration in HNC. The impact of HEADSpAcE will be to understand reasons for late diagnosis and reduce the proportion of HNC that are diagnosed at a very late stage. It will identify the most appropriate fashion for diagnosis cancer caused by human papilloma virus, and also provide genomic evidence of strong predictors of prognosis that will have the potential to improve care and reduce treatment related morbidity. We will also develop guidelines for implementation into clinical care.
more_vert Open Access Mandate for Publications and Research data assignment_turned_in Project2019 - 2023Partners:URV, HOSPITAL DE CANCER DE BARRETOS, University of Cuenca, HOSPITAL DE CANCER DE BARRETOS, NOVA +9 partnersURV,HOSPITAL DE CANCER DE BARRETOS,University of Cuenca,HOSPITAL DE CANCER DE BARRETOS,NOVA,LABMAN,MicroLIQUID (Spain),FHG,LABMAN,UGhent,CONSORCIO DE INVESTIGACION SOBRE VIH SIDA TB CISIDAT,University of Cuenca,MicroLIQUID (Spain),CONSORCIO DE INVESTIGACION SOBRE VIH SIDA TB CISIDATFunder: European Commission Project Code: 825747Overall Budget: 3,999,310 EURFunder Contribution: 3,301,990 EURCervical cancer is the 4th most common cancer in women worlThe ELEVATE project sets a multidisciplinary team comprising manufactures and experts from Europe and the Community of Latin American and Caribbean States, to improve the global adequacy and coverage of cervical cancer screening, particularly to specific populations of women that by not being regularly screened (hard-to-reach populations) are at higher-risk to develop cervical cancer. Although Cervical cancer is still the fourth most common cancer in women worldwide, with up to 85% of the burden occurring in developing countries, preventive vaccination against human papillomavirus and early detection of precancer in screening programs has shown to be successful in reducing cancer incidence and mortality.1–3 However, different challenges hamper a global implementation of such programs and are in the base of women’s non-attendance to screening. This highlights the lack of reflection of ethnic, cultural and resource differences from different populations in current cervical cancer screening. In ELEVATE it is proposed to conduct social science investigations to identify hard-to-reach women in Belgium, Brazil, Ecuador and Portugal, to address their barriers to screening and to design strategies to make primary screening more accessible to them, and therefore, contribute to reduce the global burden of cervical cancer. This will be complemented with fundamental and technological research to develop an efficient and marketable test for the combined genomic and proteomic detection of high-risk HPV infections in those populations. The test will be made portable, low-cost, compatible with self-sampling, point-of-care and generate rapid and easy-to-understand results, without relying on electrical outlets or trained health personnel. Integrant part of the proposal is also to infer and disseminate the societal, economic implications of the developed strategies using a hard-to-reach community-based participatory research.
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