期刊论文详细信息
Cancer Genomics - Proteomics
Usefulness of Nanofluidic Digital PCR Arrays to Quantify T790M Mutation in EGFR-mutant Lung Adenocarcinoma
NAO HIROTA2  KYOHEI KABURAKI2  HAJIME OTSUKA1  YUJIRO TAKAI2  AKIRA IYODA1  SAKAE HOMMA2  TAKASHI MAKINO1  FUMIAKI ISHIDA2  NAOBUMI TOCHIGI3  GO SANO2  KAZUTOSHI SHIBUYA3  SUSUMU SAKAMOTO2  KEISHI SUGINO2  KAZUTOSHI ISOBE2  HIROSHI KOBAYASHI2  YOSHINOBU HATA1 
[1] Division Chest Surgery, Toho University School of Medicine, Tokyo, JapaDivision Chest Surgery, Toho University School of Medicine, Tokyo, JapaDivision Chest Surgery, Toho University School of Medicine, Tokyo, Japa;Division of Respiratory Medicine, Toho University School of Medicine, Tokyo, JapaDivision of Respiratory Medicine, Toho University School of Medicine, Tokyo, JapaDivision of Respiratory Medicine, Toho University School of Medicine, Tokyo, Japa;Department of Surgical Pathology, Toho University School of Medicine, Tokyo, JapaDepartment of Surgical Pathology, Toho University School of Medicine, Tokyo, JapaDepartment of Surgical Pathology, Toho University School of Medicine, Tokyo, Japa
关键词: Digital PCR;    non-small-cell lung cancer;    epidermal growth factor receptor tyrosine kinase inhibitor;    T790M;   
DOI  :  
来源: Delinasios GJ CO
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【 摘 要 】

Aim: The present pilot study assessed the usefulness of nanofluidic digital polymerase chain reaction (PCR) arrays in epidermal growth factor receptor (EGFR)-mutant lung adenocarcinoma after tyrosine kinase inhibitor (TKI) resistance. Patients and Methods: We enrolled 12 patients with primary lung adenocarcinoma with sensitive EGFR mutation-confirmed T790M status by re-biopsy after TKI resistance. Nanofluidic digital PCR arrays were used to quantify T790M in genomic DNA from the pre-treatment primary site and in serum cell-free DNA (cfDNA). Results: On digital PCR, quantified T790M at the pre-treatment primary site was higher in re-biopsy-positive T790M patients (n=4) than in re-biopsy-negative patients (n=8) (0.78%±0.36% vs. 0.07%±0.09%, p<0.01). T790M at the pre-treatment primary site correlated with progression-free survival (PFS) after gefitinib therapy (r=0.67, p=0.016). Conclusion: Use of digital PCR to quantify T790M at the primary site of EGFR-mutant lung adenocarcinoma predicted T790M emergence in re-biopsies after TKI resistance and PFS after gefitinib therapy.

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