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

Clara Pierini, Clara Mariano y Jelicich, Fabiola Bascuñán Acuña, María De San Martín, Aldana Casati, Cecilia Casullo, Marta Díaz Madero, Delfina Grennon Viel, Estefania Marzik, Gabriela Rodriguez, Victoria Viel Temperley
Ochomo Edwin Onyango, Philiph Tonui, Peter Itsura, Elkanah Omenge Orang'o, Kapten Muthoka, Sayo Loice, Benard Ochieng Samba, Barry Rosen, Patrick Loehrer, Susan Cu-Uvin
Annesha Chakraborti, Badira Cheriyalinkal Parambil, Venkata Rama Mohan Gollamudi, Maya Prasad, Siddhartha Laskar, Nehal Khanna, Jifmi Jose Manjali, Sajid Qureshi, Mukta Ramadwar, Poonam Panjwani, Akshay Baheti, Vasundhara Patil, Sneha Shah, Girish Chinnaswamy
Sandy Minck, Gerda Evans, Marie Lowe, Cindy Schultz-Ferguson, Catherine Woulfe, Kym Berchtenbreiter, Krysty Sullivan, Ann White, Lynette Moore, Susan Jarvis, Wendy V Ingman, Jennifer Stone
Md Foorquan Hashmi, Fiza Khan, Elen Baloyan, Liana Safaryan, Davit Zohrabyan, Gevorg Tamamyan, Samvel Bardakhchyan