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. 2016 Oct 25;8(6):10637–10649. doi: 10.18632/oncotarget.12885

Table 5. The trends of BRAF mutations prevalence of micro PTCs from individual institutions.

Country City (State) Institution
(Reference)
Prevalence of BRAF mutations in micro PTCs
Period 1 Period 2 Period 3 Period 4 P
US Pittsburgh (PA) Univ. of Pittsburgh [14] 1974-1985
10/31(32.3%)
FMCA
1990-1992
3/16(18.8%)
FMCA
2000
4/17 (23.5%)
FMCA
2009
19/50(38%)
FMCA
NS
Poland Kielce Holycross Cancer Center [21] 2000-2004
45/90 (50%)
Three methods a
2005-2009
104/147 (70.7)
Three methods a
2010-2013
147/203 (72.4)
Three methodsa
0.001 b
Korea Seoul Samsung Medical Centre [26, 27] 2008-2009
253/396(63.9%)
DS
2010-2011
97/128(75.8%)
DS
0.013
China Tianjin Tianjin Medical Univ. Cancer Hospital [24, 25] 2001-2010
392/977(40.1%)
DS
2013-2014
1244/1984(62.7%)
DS
<0.001

Abbreviations: NS, not significant; DS, direct sequencing; FMCA, fluorescent melting curve analysis

a All analyses that were performed prior to 2013 by DS and allele-specific PCR (AS-PCR) were verified by quantitative Real time PCR (qPCR). In total, the authors used qPCR to analyze BRAF mutations in 705/723 PTCs (97.5%). The majority of samples were tested using the three methods (DS, AS-PCR and qPCR).

b P value for trend adjusted for age and sex