2018
DOI: 10.1200/cci.17.00052
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Status of Lung Cancer Data Collection in Europe

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Cited by 5 publications
(3 citation statements)
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“…Stage I disease is ideally treated with surgical resection, preferentially video-assisted thoracoscopic surgery lobectomy; the best outcomes are associated with an R0 resection [4,[36][37][38][39]. Despite this, surgery rates have fallen in Europe and the U.S. in recent years (but not in England and Wales) [40,41]. Where MDTs are currently employed in surgical decision making, two possible explanations for this decline arise: an MDT might conclude that surgery is clinically inappropriate based on patient characteristics (such as comorbidities) and recommend other treatments [15]; alternatively, patients who are borderline unfit or unwilling to undergo surgery may choose a less invasive treatment option.…”
Section: Stage I Nsclc: Surgery Versus Sbrtmentioning
confidence: 99%
“…Stage I disease is ideally treated with surgical resection, preferentially video-assisted thoracoscopic surgery lobectomy; the best outcomes are associated with an R0 resection [4,[36][37][38][39]. Despite this, surgery rates have fallen in Europe and the U.S. in recent years (but not in England and Wales) [40,41]. Where MDTs are currently employed in surgical decision making, two possible explanations for this decline arise: an MDT might conclude that surgery is clinically inappropriate based on patient characteristics (such as comorbidities) and recommend other treatments [15]; alternatively, patients who are borderline unfit or unwilling to undergo surgery may choose a less invasive treatment option.…”
Section: Stage I Nsclc: Surgery Versus Sbrtmentioning
confidence: 99%
“…Also, only a minority of cancer registries can provide sufficient data for the calculation of parameters necessary for the assessment of outcomes and quality of care [69]. • In a 2015 survey, only 6 countries -Denmark, Germany, Hungary, the Netherlands, Slovenia, and United Kingdomreported a lung cancer data collection, or audit, programme in addition to a cancer registry [70,71]. The creation of a pan-European dataset is a significant challenge but will expose variation in practice, identify best practices, show where improvement is needed, and guide investment in resources.…”
Section: Cancer Registration and Data Availabilitymentioning
confidence: 99%
“…Several international data-sharing networks have recently emerged to help researchers get access to clinical and genomic data in genomic cancer medicine. For examples, international networks such as PCORnet, 6 OHDSI Research Network, 7 GENIE, 8 BRCA Exchange from GA4GH7, 9 CancerLinQ, 10 ORIEN, 11 and ICGC ARGO, 12 and European networks such as Europe lung cancer data collection 13 and the German Cancer Consortium (DKTK) 14 are some important initiatives in this field. Although such initiatives are interesting, access to full data is restricted to consortium members or lacks relevant clinical information to link genomic alterations with clinical benefit under specific drugs.…”
Section: Introductionmentioning
confidence: 99%