ecancermedicalscience

Short Communication

Cancer registries can provide evidence-based data to improve quality of care and prevent cancer deaths

28 Mar 2014
Christine Bouchardy, Elisabetta Rapiti, Simone Benhamou

Today, many countries are increasing their efforts to ensure that all cancer patients receive the best possible care. Population-based cancer registries have adapted their registration to collect additional clinical variables in order to provide clinicians with unbiased population data on cancer treatment and survival. Taking several examples of epidemiological cancer research performed at the Geneva Cancer Registry, we aim to illustrate how cancer registries oversee the treatment and outcomes of cancer patients in order to help clinicians continually improve quality of care and prevent cancer deaths in the population.

Related Articles

Patricia N Apenteng, Larry Akoko, Vihar Kotecha, Theresia Mwakyembe, Masumbuko Mwashambwa, Rukia Himid, Deo Hando, Charles Komba, Ally Mwanga, Peter Mbele, Paul Itule, Joshua Jackson, Mungeni Misidai, Cameron Gaskill, Doruk Ozgediz, Nathan Brand
Moushumi Suryavanshi, Prashant Mehta, Manoj Kumar, Saphalta Bhagmar, Vidit Kapoor, Dushyant Kumar, Sweta Mishra, Bhawna Chauhan
Maria Lucila González Donna, Eliza Ramirez Cabrera, Andrea Magali del Valle Ochelli, Lucia Ayala Albertini, Lucas Coradini, Verónica Alejandra Livieres Alayón, Iván Garrigoza Garcete, Cinthia Gauna Colas, Maria Luisa Cabañas León, Jabibi Noguera, Gladys Estigarribia, Alejandro Frydman, Carlos Palmes, Santiago Leguizamon, Matias Rodrigo Chacon, Federico Waisberg
Hafssa El Hilali, Nassiba Bahra, Sanae Guennouni, Chaymae Chbihi, Samia El Hakym, Diango Keita, Sara Nejjari, Abir Oufrid, Oumaima Siyouri, Lamiae Amaadour, Karima Oualla, Zineb Benbrahim, Touria Bouhafa, Nawfel Mellas, Samira El Fakir, Samia Arifi