2014
DOI: 10.1200/jco.2014.32.15_suppl.1526
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EGFR mutation screening in non-small cell lung cancer: Results from an access program in Brazil.

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Cited by 4 publications
(3 citation statements)
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“…Some efforts have been made to compile data on the frequency of molecular abnormalities in Brazilian patients ( Table 2 ). 40 - 48 Overall, the data suggest that the frequency of EGFR mutations is lower in Brazil (approximately 25%) than in Asia but higher than in White populations in North America and Europe ( Figure 3 ), confirming findings from other Latin American countries. 49 It has been speculated that the ethnic background could be responsible for the distinct molecular profile seen in these instances, perhaps due to the characteristic genetic admixture seen in Brazilians, inherited from European, African, and Native American ancestors.…”
Section: Molecular Testingsupporting
confidence: 76%
“…Some efforts have been made to compile data on the frequency of molecular abnormalities in Brazilian patients ( Table 2 ). 40 - 48 Overall, the data suggest that the frequency of EGFR mutations is lower in Brazil (approximately 25%) than in Asia but higher than in White populations in North America and Europe ( Figure 3 ), confirming findings from other Latin American countries. 49 It has been speculated that the ethnic background could be responsible for the distinct molecular profile seen in these instances, perhaps due to the characteristic genetic admixture seen in Brazilians, inherited from European, African, and Native American ancestors.…”
Section: Molecular Testingsupporting
confidence: 76%
“…The estimated number of new cases was published by INCA (the National Cancer Institute of Brazil). 2 The proportion of patients with the disease at an advanced stage and who were in a clinical condition to be able to receive first-line treatment was estimated based on the 2014 National Lung Cancer Audit in the United Kingdom and the European study of real-world treatment data published by Moro-Sibilot et al 16,17 The proportion of patients with activation of mutations in the EGFR gene was extracted from the largest database available in the literature. 18…”
Section: Estimation Of the Number Of Eligible Patientsmentioning
confidence: 99%
“…A prevalência das alterações nos genes EGFR e ALK em pacientes com CPNPC foi retirada de estudos brasileiros, sendo 25,5% e 4%, respectivamente (Pontes et al, 2014;Gomes et al, 2015).…”
Section: Dados Epidemiológicosunclassified