Recommendations for Implementing Lung Cancer Screening with Low-Dose Computed Tomography in Europe
- PMID: 32599792
- PMCID: PMC7352874
- DOI: 10.3390/cancers12061672
Recommendations for Implementing Lung Cancer Screening with Low-Dose Computed Tomography in Europe
Abstract
Lung cancer screening (LCS) with low-dose computed tomography (LDCT) was demonstrated in the National Lung Screening Trial (NLST) to reduce mortality from the disease. European mortality data has recently become available from the Nelson randomised controlled trial, which confirmed lung cancer mortality reductions by 26% in men and 39-61% in women. Recent studies in Europe and the USA also showed positive results in screening workers exposed to asbestos. All European experts attending the "Initiative for European Lung Screening (IELS)"-a large international group of physicians and other experts concerned with lung cancer-agreed that LDCT-LCS should be implemented in Europe. However, the economic impact of LDCT-LCS and guidelines for its effective and safe implementation still need to be formulated. To this purpose, the IELS was asked to prepare recommendations to implement LCS and examine outstanding issues. A subgroup carried out a comprehensive literature review on LDCT-LCS and presented findings at a meeting held in Milan in November 2018. The present recommendations reflect that consensus was reached.
Keywords: computed tomography; consensus; implementation; low dose; lung cancer; mortality; reduction; screening; statement.
Conflict of interest statement
G.V. has financial relationships with Medtronic, Ab Medica, and Johnson & Johnson outside the submitted work. D.B. has a financial relationship with Astra Zeneca, C.H. is inventor of the patents owned by Cornell Research Foundation (CRF), she has divested herself of all royalties arising. She is also the President of the Early Diagnosis and Treatment Research Foundation. M.O. reports grants from the Royal Dutch Academy of Sciences, from the Netherlands Organisation of Scientific Research, and from the Netherlands Organisation for Health Research and Development. HJDK reports personal fees from the University of Zurich/Astra Zeneca, outside the submitted work; he is PI of the Horison 2020 EU Study 4-in-the-lung-run. J.K.F. reports financial relationship with AstraZeneca, Epigenomics; NUCLEIX Ltd., from iDNA, grants from Janssen Research & Development, LLC, outside the submitted work. J.J.Z. reports financial relationship with VisionGate. C.R. reports grants from AIRC. G.R. reports personal fees from Scanlan International. W.R. reports grants from Medical University of Gdańsk, outside the submitted work; he has a patent “A profile of blood protein markers as a test for the detection of lung cancer issued”. G.V.S. reports personal fees from Eli Lilly, Roche, AstraZeneca, MSD, Takeda. M.T. reports to have developed the PLCOm2012 lung cancer risk prediction model, which is mentioned in the article. The model is open access and available free of charge to non-commercial users. For commercial users licensing has been assigned to Brock University. To date, M.C.T. has not received any money for use of the PLCOm2012 model. S.S. reports grants and other from Varian Medical Systems, grants from ViewRay Inc, grants and personal fees from Astra Zeneca, personal fees from MSD, personal fees from Celgene, outside the submitted work. S.N. reports personal fees from Astra Zeneca, BI, MSD, Takeda, Pfizer, Roche, BMS, Abbvie, Eli Lilly, Bayer. S.G., S.I., J.S., L.F.N., M.V.I., P.N., R.L.M., P.N., L.B., N.T., R.Y., A.R., G.F., K.B., C.v.d.A., L.B., D.C., J.P.V.M., P.M., Z.S., G.P. declare no competing interests.
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