Around 50–60% of Asian www.selleckchem.com/products/VX-680(MK-0457).html patients and 20–30% of Western patients with adenocarcinomas are expected to carry

activating EGFR mutations, while a negligible proportion of patients with other lung cancer histology are expected to carry such mutations. Therefore, the EGFR mutation detection rate can be estimated from the clinical and demographic parameters, including race and histology, of the study subjects. If we assume that 50% of Asian adenocarcinoma patients carry EGFR mutations, the expected detection rate in an Asian study population comprising 80% adenocarcinoma patients should be 40%. In this context, the results of several previous studies suggesting that the EGFR mutation test in cfDNA might be equivalent to that in tissue exceed the expected learn more rate of EGFR positivity. Hence, it is difficult

to accept these although the tests used in those studies are highly sensitive and always performed with the utmost precision. In addition, other reports published detection rates around 20% [26, 27], which is similar to our report, and still EGFR mutation testing in cfDNA has not been introduced in clinical practice in spite of such promising results over several years. Therefore, more data are required to evaluate the suitability of the cfDNA test and assess whether it can replace the traditional tumor tissue test. Table 5 Previous reports on LY2603618 mw EGFR mutation test from circulating free DNA Year Authors Subjects DNA concentration Mutation test Detection rate 2006 Kimura H, et al. [16] Asian 70 ng/mL (range, 0–1720 ng/mL) SARMS 48.1% (13/27) Female : 37% Nonsmoker : N/A ADC : 85% ORR : 33% 2008 Maheswaran S, et al. [24] Western N/A SARMS 39% (7/18)

EGFR mutant patients 2009 He C, et al. [29] Asian N/A Mutant-enriched PCR 49.3% (66/134) Female : 37% Nonsmoker : 53% ADC : 75% 2009 Bai H, et al. [28] Asian N/A dHPLC 34.3% (79/230) Female : 46% Nonsmoker : 55% ADC : 74% ORR : 36% (37/102) 2009 Mack PC, et al. [26] Western/Asian : 96/4% 2.3 ng/μL (range, 1–9 ng/μL ) SARMS 20% (10/49) Female : 56% Nonsmoker : 53% ADC : 67% 2009 Kuang Y, et al. [25] Western Grape seed extract 52.3 ng/μL (range, 10–163 ng/μL ) SARMS and WAVE/Surveyor 54% (29/54) Female : 81.5% Whole genome amplification Nonsmoker : N/A ADC : N/A ORR : 56% 2010 Brevet M, et al. [31] Western N/A Mass spectrometry genotyping assay (Sequenom) and mutant-enriched PCR Whole genome amplification 23.2% (10/31) Female : 52% Nonsmoker : 45% ADC : 97% 2010 Jian G, et al. [27] Asian N/A Taqman PCR 23.2% (13/56) Female : 46% Nonsmoker : 58% ADC : 78% ORR : 30% 2011 Jiang B, et al. [30] Asian Minimum 4 ng/μL (range, 11–66 ng/μL ) Mutant-enriched PCR 31% (18/58) Female : 31% Nonsmoker : 38% ADC : 72% 2011 Taniguchi K, et al. [32] Asian N/A BEAMing 72.7% (32/44) EGFR mutant patients This study Kim HR, et al. Asian 8.6 ng/μL PNA-based PCR clamping 16.