In conclusion, universal screening is good value for money and, together with near-universal screening (age-targeted screening for individuals <70 years), it should be proposed to decision-makers as a potential LS screening program. We agree with Grosse that context matters, and this is why each individual health system should select the most suitable model and adapt it for its own requirements. The challenges of LS screening will be to reach all CRC patients affected by LS, inform and test as many relatives as possible, offer effective surveillance interventions to reduce cancer morbidity and mortality among mutation carriers, and thus effectively maximize the health status of the population with the available resources.

Universal screening of Lynch syndrome is ready for implementation / DI MARCO, Marco; D'Andrea, E.; Villari, P.. - In: GENETICS IN MEDICINE. - ISSN 1098-3600. - (2019), pp. 1-2. [10.1038/s41436-018-0027-3]

Universal screening of Lynch syndrome is ready for implementation

Di Marco M.;D'Andrea E.;Villari P.
2019

Abstract

In conclusion, universal screening is good value for money and, together with near-universal screening (age-targeted screening for individuals <70 years), it should be proposed to decision-makers as a potential LS screening program. We agree with Grosse that context matters, and this is why each individual health system should select the most suitable model and adapt it for its own requirements. The challenges of LS screening will be to reach all CRC patients affected by LS, inform and test as many relatives as possible, offer effective surveillance interventions to reduce cancer morbidity and mortality among mutation carriers, and thus effectively maximize the health status of the population with the available resources.
2019
cost-benefit analysis; humans; colorectal neoplasms, hereditary nonpolyposis; mass screening
01 Pubblicazione su rivista::01f Lettera, Nota
Universal screening of Lynch syndrome is ready for implementation / DI MARCO, Marco; D'Andrea, E.; Villari, P.. - In: GENETICS IN MEDICINE. - ISSN 1098-3600. - (2019), pp. 1-2. [10.1038/s41436-018-0027-3]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1304729
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