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Les Mery

Researcher at International Agency for Research on Cancer

Publications -  13
Citations -  269

Les Mery is an academic researcher from International Agency for Research on Cancer. The author has contributed to research in topics: Cancer & Cancer registry. The author has an hindex of 6, co-authored 13 publications receiving 162 citations.

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A Global Cancer Surveillance Framework Within Noncommunicable Disease Surveillance: Making the Case for Population-Based Cancer Registries

TL;DR: A general framework for cancer surveillance is proposed that permits monitoring the core components of cancer control and communalities in approaches to the surveillance of other major NCDs as well as communicable diseases are examined.
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Leading Causes of Cancer Mortality - Caribbean Region, 2003-2013.

TL;DR: Several of the leading causes of cancer deaths in the Caribbean can be reduced through primary and secondary preventions, including prevention of exposure to risk factors, screening, early detection, and timely and effective treatment.
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Scaling Up the Surveillance of Childhood Cancer: A Global Roadmap

TL;DR: Based on their experience acquired at the International Agency for Research on Cancer in global cancer surveillance, this article reviewed crucial aspects to consider in the development of childhood cancer registration and presented their vision on how the Global Initiative for Cancer Registry Development can accelerate the measurement of the outcome of children with cancer.
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Resource requirements for cancer registration in areas with limited resources: Analysis of cost data from four low- and middle-income countries.

TL;DR: The results suggest that cancer registration involve substantial fixed costs and labor, and that partnership with other institutions is critical for the operation and sustainability of cancer registries in limited resource settings.
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Cancer registration for cancer control in Latin America: a status and progress report

TL;DR: Key elements for improving cancer surveillance in the region are outlined, including 1) involvement of local stakeholders and experts, 2) integration of cancer registries into existing surveillance systems, 3) improvement in data availability and quality, 4) enhanced communication and dissemination, and 5) better linkages between cancer Registries and cancer planning and cancer research.