A total of 20 μl PCR reaction system included the following: 1x HotStarTaq buffer, 2.0 mM Mg2+, 0.2 mM dNTP, 0.2 μM of each primer, 1U HotStarTaq Polymerase (Qiagen), and 10ng DNA template. PCR reaction procedures were performed using 35 cycles of 15 sec at 94°C, 30 sec at 56°C, 1 min at 72°C and extension for 2 min at 72°C. Sequencing reactions were performed on an ABI3700 genetic analyzer

after PCR products were purified. Sequence variations were determined using Seqscape software (Applied Biosystems) with the KRAS and EGFR reference sequence (NM_004985 and NM_005228.3, National Center for Biotechnology Information). In order to avoid contamination during PCR steps, gloves and lab coats were worn at all times when AZD0156 mouse PCR is performed. Pipette tips with aerosol filters

were used to prevent microdroplets being injected into the PCR mixture. DNA sample preparation was done in a separate room from the area where PCR reaction mixes were prepared. Additionally negative control was also included during PCR procedure. Drug administration Five patients click here received gefitinib as first-line treatment after being identified to harbor EGFR-TKI sensitive mutations in mediastinal lymph nodes metastases obtained by mediastinoscope. One tablet of gefitinib (250 mg) was taken once daily at about the same time. Patients continued

the course uninterrupted until disease progression, intolerable toxicity or withdrawal of consent. All drugs were supplied by AstroZeneca. Assessment of response Baseline evaluation included medical history and physical examination, electrocardiogram, chest radiography, thorax CT scan and ultrasonography of the upper CA3 abdomen. Laboratory investigations included complete blood counts, urinalysis, renal function and liver function tests. Performance status was evaluated according to the Eastern Cooperative Oncology Group (ECOG) criteria. Patients were re-evaluated, using the same method at the end of the first and third months of therapy, and then every 3 months. Objective tumor response and its duration were assessed according to the RECIST criteria [27], and all responses ADAMTS5 were confirmed >28 days after the initial assessment of response. Statistical analysis McNemar’s test was used to compare the EGFR and KRAS mutation status between primary tumors and corresponding local lymph node metastases. Two-sided p values <0.05 were considered significant. Data evaluation was carried out with SPSS_13.0 statistical software. Results KRAS gene mutations in NSCLC primary tumors and corresponding local lymph node metastases KRAS mutations were detected in one primary tumor and seven lymph node metastases (Table 2).