Observational study of rebiopsy in EGFR-TKI-resistant patients with EGFR mutation-positive advanced NSCLC

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作者
Kenichi Koyama
Satoru Miura
Satoshi Watanabe
Satoshi Shoji
Jun Koshio
Yoshiki Hayashi
Daisuke Ishikawa
Ko Sato
Takao Miyabayashi
Masaaki Okajima
Takeshi Ota
Tomohiro Tanaka
Naoya Matsumoto
Hideyuki Kuriyama
Tetsuya Abe
Koichiro Nozaki
Kosuke Ichikawa
Rie Kondo
Hiroshi Tanaka
Toshiaki Kikuchi
机构
[1] Niigata Cancer Center Hospital,Department of Internal Medicine
[2] Niigata University Graduate School of Medical and Dental Sciences,Department of Respiratory Medicine and Infectious Diseases
[3] Nagaoka Red Cross Hospital,Department of Respiratory Medicine
[4] Nagaoka Chuo General Hospital,Department of Respiratory Medicine
[5] Niigata Prefectural Central Hospital,Department of Respiratory Medicine
[6] Niigata City General Hospital,Department of Respiratory Medicine
[7] Saiseikai Niigata Hospital,Department of Respiratory Medicine
[8] Shibata Hospital - Niigata Prefectural Hospital,Department of Respiratory Medicine
[9] Nishi Niigata Chuo Hospital,Department of Respiratory Medicine
[10] Sado General Hospital,Department of Respiratory Medicine
[11] Tsuruoka Municipal Shonai Hospital,Department of Respiratory Medicine
[12] Shinrakuen Hospital,Department of Respiratory Medicine
[13] Niigata Medical Center,Department of Respiratory Medicine
来源
Scientific Reports | / 12卷
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摘要
The identification of acquired resistance mutations has been essential in non-small-cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) active mutations. Rebiopsy plays a pivotal role in selecting the optimal treatment for patients who develop resistance to initial EGFR-tyrosine kinase inhibitors (EGFR-TKIs). This multicenter, observational study was conducted to investigate the details of rebiopsy in Japanese clinical practice. The primary endpoints were the implementation rate of rebiopsy and the concordance rate for T790M mutation detection between histological and cytological specimens using the cobas EGFR Mutation Test, version 2. One hundred ninety-four patients with EGFR-mutant NSCLC were enrolled, and 120 patients developed acquired resistance to EGFR-TKIs. The median age was 68 years (range 20–87), and 52.5% of the patients were women. Rebiopsy was performed in 109 patients, and the implementation rate of rebiopsy was 90.8%. The success rates of rebiopsy in the total, histology, cytology and liquid biopsy populations were 67.9%, 81.3%, 66.7% and 43.8%, respectively. The positive percent agreement and the negative percent agreement in the detection of the T790M mutation between the histological and cytological specimens were both 90.9%. Obtaining histological or cytological tissue samples at rebiopsy may contribute to improving the detection rate of the T790M mutation (trial registration number: UMIN000026019).
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  • [1] Lynch TJ(2004)Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib N. Engl. J. Med. 350 2129-2139
  • [2] Paez JG(2004)EGFR mutations in lung cancer: Correlation with clinical response to gefitinib therapy Science 304 1497-1500
  • [3] Maemondo M(2010)Gefitinib or chemotherapy for non-small-cell lung cancer with mutated EGFR N. Engl. J. Med. 362 2380-2388
  • [4] Mitsudomi T(2007)Mutations of the epidermal growth factor receptor gene and related genes as determinants of epidermal growth factor receptor tyrosine kinase inhibitors sensitivity in lung cancer Cancer Sci. 98 1817-1824
  • [5] Yatabe Y(2012)Erlotinib versus standard chemotherapy as first-line treatment for European patients with advanced EGFR mutation-positive non-small-cell lung cancer (EURTAC): A multicentre, open-label, randomised phase 3 trial Lancet Oncol. 13 239-246
  • [6] Rosell R(2011)Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): A multicentre, open-label, randomised, phase 3 study Lancet Oncol. 12 735-742
  • [7] Zhou C(2013)Phase III study of afatinib or cisplatin plus pemetrexed in patients with metastatic lung adenocarcinoma with EGFR mutations J. Clin. Oncol. 31 3327-3334
  • [8] Sequist LV(2014)Afatinib versus cisplatin plus gemcitabine for first-line treatment of Asian patients with advanced non-small-cell lung cancer harbouring EGFR mutations (LUX-Lung 6): An open-label, randomised phase 3 trial Lancet Oncol. 15 213-222
  • [9] Wu YL(2017)Systemic Therapy for Stage IV non-small-cell lung cancer: American society of clinical oncology clinical practice guideline update J. Clin. Oncol. 35 3484-3515
  • [10] Hanna N(2018)Metastatic non-small cell lung cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up Ann. Oncol. 29 iv192-iv237