Comparison of detection methods of EGFR T790M mutations using plasma, serum, and tumor tissue in EGFR-TKI-resistant non-small cell lung cancer

被引:21
作者
Kobayashi, Keigo [1 ]
Naoki, Katsuhiko [1 ,2 ]
Manabe, Tadashi [1 ]
Masuzawa, Keita [1 ]
Hasegawa, Hanako [1 ]
Yasuda, Hiroyuki [1 ]
Kawada, Ichiro [1 ]
Soejima, Kenzo [1 ]
Betsuyaku, Tomoko [1 ]
机构
[1] Keio Univ, Sch Med, Dept Med, Div Pulm Med, Tokyo, Japan
[2] Kitasato Univ, Sch Med, Dept Resp Med, Tokyo, Kanagawa, Japan
关键词
EGFR; T790M mutation; liquid biopsy; COBAS ver2; PNA-LNA PCR clamp method; osimertinib; ACQUIRED-RESISTANCE; OPEN-LABEL; 1ST-LINE TREATMENT; RE-BIOPSY; PHASE-III; KINASE INHIBITORS; FREE DNA; CHEMOTHERAPY; GEFITINIB; ERLOTINIB;
D O I
10.2147/OTT.S161745
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Osimertinib, a third-generation epidermal growth factor receptor-tyrosine kinase inhibitor, exerts remarkable effects against EGFR T790M resistance mutation-positive non-small cell lung cancer. Identifying T790M mutation by re-biopsy is essential before prescribing osimertinib. Tissue biopsy is the golden standard for this purpose, but several factors limit its success rate. The liquid biopsy with blood, using circulating tumor DNA, has been an alternative method. However, the true biological meaning and equivalence of liquid biopsy and tumor biopsy are still under investigation. Especially, the usefulness of serum samples to detect T790M mutation is not yet been known. Patients and methods: We prospectively evaluated the sensitivity, specificity, and parallelism of the detection of EGFR mutations in tissue re-biopsy and liquid biopsy (plasma and serum), simultaneously, from June 2016 to May 2017. EGFR mutations in tumor re-biopsy were evaluated by COBAS ver2 and PNA-LNA PCR clamp method, and those in liquid biopsy were evaluated with COI3AS ver2. Results: Fifteen patients were enrolled. In 10 patients whose EGFR mutation was detected in liquid biopsy, the original EGFR mutation (exon 19 del or L858R) was detected in all patients. Detection of EGFR mutation by COBAS ver2 and by PNA-LNA method was almost the same in tissue re-biopsy. The detection rate of T790M was lower than that of the original EGFR mutation in liquid biopsy compared to that in tissue re-biopsy. The detection of T790M in serum exhibited a higher specificity (67%) and positive predictive value (50%) than that in plasma (50% and 40%, respectively). The detection sensitivity was similar in plasma and serum. Conclusion: Plasma, serum, and tissue genotyping can have complementary roles for detecting EGFR-T790M using COBAS ver2. Repeated tests with different samples and different methods may improve accuracy of T790M detection and will lead to the maximum benefit for the patient.
引用
收藏
页码:3335 / 3343
页数:9
相关论文
共 42 条
[21]   Large scale, prospective screening of EGFR mutations in the blood of advanced NSCLC patients to guide treatment decisions [J].
Mayo-de-las-Casas, C. ;
Jordana-Ariza, N. ;
Garzon-Ibanez, M. ;
Balada-Bel, A. ;
Bertran-Alamillo, J. ;
Viteri-Ramirez, S. ;
Reguart, N. ;
Munoz-Quintana, M. A. ;
Lianes-Barragan, P. ;
Camps, C. ;
Jantus, E. ;
Remon-Massip, J. ;
Calabuig, S. ;
Aguiar, D. ;
Gil, M. L. ;
Vinolas, N. ;
Santos-Rodriguez, A. K. ;
Majem, M. ;
Garcia-Pelaez, B. ;
Villatoro, S. ;
Perez-Rosado, A. ;
Monasterio, J. C. ;
Ovalle, E. ;
Catalan, M. J. ;
Campos, R. ;
Morales-Espinosa, D. ;
Martinez-Bueno, A. ;
Gonzalez-Cao, M. ;
Gonzalez, X. ;
Moya-Horno, I. ;
Sosa, A. E. ;
Karachaliou, N. ;
Rosell, R. ;
Molina-Vila, M. A. .
ANNALS OF ONCOLOGY, 2017, 28 (09) :2248-2255
[22]   Afatinib versus placebo for patients with advanced, metastatic non-small-cell lung cancer after failure of erlotinib, gefitinib, or both, and one or two lines of chemotherapy (LUX-Lung 1): a phase 2b/3 randomised trial [J].
Miller, Vincent A. ;
Hirsh, Vera ;
Cadranel, Jacques ;
Chen, Yuh-Min ;
Park, Keunchil ;
Kim, Sang-We ;
Zhou, Caicun ;
Su, Wu-Chou ;
Wang, Mengzhao ;
Sun, Yan ;
Heo, Dae Seog ;
Crino, Lucio ;
Tan, Eng-Huat ;
Chao, Tsu-Yi ;
Shahidi, Mehdi ;
Cong, Xiuyu Julie ;
Lorence, Robert M. ;
Yang, James Chih-Hsin .
LANCET ONCOLOGY, 2012, 13 (05) :528-538
[23]   Gefitinib versus cisplatin plus docetaxel in patients with non-small-cell lung cancer harbouring mutations of the epidermal growth factor receptor (WJTOG3405): an open label, randomised phase 3 trial [J].
Mitsudomi, Tetsuya ;
Morita, Satoshi ;
Yatabe, Yasushi ;
Negoro, Shunichi ;
Okamoto, Isamu ;
Tsurutani, Junji ;
Seto, Takashi ;
Satouchi, Miyako ;
Tada, Hirohito ;
Hirashima, Tomonori ;
Asami, Kazuhiro ;
Katakami, Nobuyuki ;
Takada, Minoru ;
Yoshioka, Hiroshige ;
Shibata, Kazuhiko ;
Kudoh, Shinzoh ;
Shimizu, Eiji ;
Saito, Hiroshi ;
Toyooka, Shinichi ;
Nakagawa, Kazuhiko ;
Fukuoka, Masahiro .
LANCET ONCOLOGY, 2010, 11 (02) :121-128
[24]   Emergence of epidermal growth factor receptor T790M mutation during chronic exposure to gefitinib in a non-small cell lung cancer cell line [J].
Ogino, Atsuko ;
Kitao, Hiroyuki ;
Hirano, Seiki ;
Uchida, Akiko ;
Ishiai, Masamichi ;
Kozuki, Toshiyuki ;
Takigawa, Nagio ;
Takata, Minoru ;
Kiura, Katsuyuki ;
Tanimoto, Mitsune .
CANCER RESEARCH, 2007, 67 (16) :7807-7814
[25]   Use of Research Biopsies in Clinical Trials: Are Risks and Benefits Adequately Discussed? [J].
Overman, Michael J. ;
Modak, Janhavi ;
Kopetz, Scott ;
Murthy, Ravi ;
Yao, James C. ;
Hicks, Marshall E. ;
Abbruzzese, James L. ;
Tam, Alda L. .
JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (01) :17-22
[26]   Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain [J].
Pao, W ;
Miller, VA ;
Politi, KA ;
Riely, GJ ;
Somwar, R ;
Zakowski, MF ;
Kris, MG ;
Varmus, H .
PLOS MEDICINE, 2005, 2 (03) :225-235
[27]   The APPLE Trial: Feasibility and Activity of AZD9291 (Osimertinib) Treatment on Positive PLasma T790M in EGFR-mutant NSCLC Patients. EORTC 1613 [J].
Remon, Jordi ;
Menis, Jessica ;
Hasan, Baktiar ;
Peric, Aleksandra ;
De Maio, Eleonora ;
Novello, Silvia ;
Reck, Martin ;
Berghmans, Thierry ;
Wasag, Bartosz ;
Besse, Benjamin ;
Dziadziuszko, Rafal .
CLINICAL LUNG CANCER, 2017, 18 (05) :583-588
[28]   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 [J].
Rosell, Rafael ;
Carcereny, Enric ;
Gervais, Radj ;
Vergnenegre, Alain ;
Massuti, Bartomeu ;
Felip, Enriqueta ;
Palmero, Ramon ;
Garcia-Gomez, Ramon ;
Pallares, Cinta ;
Miguel Sanchez, Jose ;
Porta, Rut ;
Cobo, Manuel ;
Garrido, Pilar ;
Longo, Flavia ;
Moran, Teresa ;
Insa, Amelia ;
De Marinis, Filippo ;
Corre, Romain ;
Bover, Isabel ;
Illiano, Alfonso ;
Dansin, Eric ;
de Castro, Javier ;
Milella, Michele ;
Reguart, Noemi ;
Altavilla, Giuseppe ;
Jimenez, Ulpiano ;
Provencio, Mariano ;
Angel Moreno, Miguel ;
Terrasa, Josefa ;
Munoz-Langa, Jose ;
Valdivia, Javier ;
Isla, Dolores ;
Domine, Manuel ;
Molinier, Olivier ;
Mazieres, Julien ;
Baize, Nathalie ;
Garcia-Campelo, Rosario ;
Robinet, Gilles ;
Rodriguez-Abreu, Delvys ;
Lopez-Vivanco, Guillermo ;
Gebbia, Vittorio ;
Ferrera-Delgado, Lioba ;
Bombaron, Pierre ;
Bernabe, Reyes ;
Bearz, Alessandra ;
Artal, Angel ;
Cortesi, Enrico ;
Rolfo, Christian ;
Sanchez-Ronco, Maria ;
Drozdowskyj, Ana .
LANCET ONCOLOGY, 2012, 13 (03) :239-246
[29]   Third generation EGFR TKIs in EGFR-mutated NSCLC: Where are we now and where are we going [J].
Russo, A. ;
Franchinaa, T. ;
Ricciardi, G. R. R. ;
Smiroldo, V. ;
Picciotto, M. ;
Zanghi, M. ;
Rolfo, C. ;
Adamo, V. .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2017, 117 :38-47
[30]   Rociletinib in EGFR-Mutated Non-Small-Cell Lung Cancer [J].
Sequist, L. V. ;
Soria, J-C ;
Goldman, J. W. ;
Wakelee, H. A. ;
Gadgeel, S. M. ;
Varga, A. ;
Papadimitrakopoulou, V. ;
Solomon, B. J. ;
Oxnard, G. R. ;
Dziadziuszko, R. ;
Aisner, D. L. ;
Doebele, R. C. ;
Galasso, C. ;
Garon, E. B. ;
Heist, R. S. ;
Logan, J. ;
Neal, J. W. ;
Mendenhall, M. A. ;
Nichols, S. ;
Piotrowska, Z. ;
Wozniak, A. J. ;
Raponi, M. ;
Karlovich, C. A. ;
Jaw-Tsai, S. ;
Isaacson, J. ;
Despain, D. ;
Matheny, S. L. ;
Rolfe, L. ;
Allen, A. R. ;
Camidge, D. R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (18) :1700-1709