The impact of EGFR T790M mutation status following the development of Osimertinib resistance on the efficacy of Osimertinib in non-small cell lung cancer: A meta-analysis

被引:1
作者
Guo, Liuxian [1 ,2 ]
Zhou, Guojin [1 ,2 ]
Huang, Min [2 ]
Tang, Kejing [1 ]
Xu, Jing [3 ]
Chen, Jie [1 ,4 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Pharm, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Sch Pharmaceut Sci, E-132 Waihuandong Rd, Guangzhou, Peoples R China
[3] Southern Med Univ, Dermatol Hosp, Dept Pharm, Guangzhou, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Pharm, Guangzhou 510080, Peoples R China
关键词
drug resistance; EGFR T790M mutation; meta-analysis; non-small cell lung cancer; Osimertinib; CIRCULATING TUMOR DNA; NEWCASTLE-OTTAWA SCALE; GENOMIC LANDSCAPE; PLASMA; NSCLC; TKI; MECHANISMS; THERAPY; QUALITY;
D O I
10.1111/crj.13748
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
BackgroundPrevious studies have suggested that loss of the EGFR T790M gene mutation may contribute to the development of resistance to Osimertinib in non-small cell lung cancer (NSCLC).AimsThis study aims to assess the relationship between the clinical effectiveness of Osimertinib in NSCLC patients and the T790M mutation status following resistance to Osimertinib and examine differences between plasma and tissue tests and between Asian and non-Asian groups.MethodsThe PubMed, Web of Science, Cochrane, and EMBASE databases were comprehensively searched for studies on the association between T790M mutation status and the efficacy of Osimertinib between January 2014 and November 2023. Meta-analysis was carried out using Review Manager 5.4 software.ResultsAfter evaluating 2727 articles, a total of 14 studies were included in the final analysis. Positive correlations between EGFR T790M mutation status after Osimertinib resistance and longer PFS (HR: 0.44, 95% CI: 0.30-0.66), longer OS (HR: 0.3, 95% CI: 0.10-0.86), longer TTD (HR: 0.69, 95% CI: 0.45-1.07), and improved clinical outcomes including PFS and TTD subgroups (HR: 0.58, 95% CI: 0.47-0.73) were observed. Subgroup analysis revealed that, compared with the blood tests, the results of the T790M mutation tests by the tissue are more significant (HR: 0.24, 95% CI: 0.11-0.52 for tissue tests; HR: 0.47, 95% CI: 0.22-1.00 for plasma tests), and the PFS of Osimertinib were similar for Asian and non-Asian patients (HR: 0.46, 95% CI: 0.31-0.68 for Asians; HR: 0.12, 95% CI: 0.01-1.27 for non-Asians).ConclusionsPersistence of the T790M gene mutation after the development of Osimertinib resistance is associated with higher therapeutic benefits of Osimertinib in NSCLC patients. The results of tissue detection are more significant than those of plasma detection. Persistence of the T790M gene mutation after the development of Osimertinib resistance is associated with higher therapeutic benefits of Osimertinib in NSCLC patients. The results of tissue detection are more significant than those of plasma detection. Furthermore, Asian patients were found to experience similar benefits from Osimertinib treatment as non-Asian patients. image
引用
收藏
页数:14
相关论文
共 69 条
[1]   Analyses of CNS Response to Osimertinib in Patients with T790M-Positive Advanced NSCLC from ASTRIS Korean Subset, Open-Label Real-World Study [J].
Ahn, Beung-Chul ;
Kim, Jee Hung ;
Pyo, Kyoung-Ho ;
Lim, Sun Min ;
Hong, Min Hee ;
Kim, Hye Ryun ;
Cho, Byoung Chul .
CANCERS, 2021, 13 (15)
[2]   A Phase II Study of Osimertinib in Patients with Advanced-Stage Non-Small Cell Lung Cancer following Prior Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor (EGFR TKI) Therapy with EGFR and T790M Mutations Detected in Plasma Circulating Tumour DNA (PLASMA Study) [J].
Ang, Yvonne L. E. ;
Zhao, Xiaotian ;
Reungwetwattana, Thanyanan ;
Cho, Byoung-Chul ;
Liao, Bin-Chi ;
Yeung, Rebecca ;
Loong, Herbert H. ;
Kim, Dong-Wan ;
Yang, James Chih-Hsin ;
Lim, Sun Min ;
Ahn, Myung-Ju ;
Lee, Se-Hoon ;
Suwatanapongched, Thitiporn ;
Kongchauy, Kanchaporn ;
Ou, Qiuxiang ;
Yu, Ruoying ;
Tai, Bee Choo ;
Goh, Boon Cher ;
Mok, Tony S. K. ;
Soo, Ross A. .
CANCERS, 2023, 15 (20)
[3]   Rebiopsy of Lung Cancer Patients with Acquired Resistance to EGFR Inhibitors and Enhanced Detection of the T790M Mutation Using a Locked Nucleic Acid-Based Assay [J].
Arcila, Maria E. ;
Oxnard, Geoffrey R. ;
Nafa, Khedoudja ;
Riely, Gregory J. ;
Solomon, Stephen B. ;
Zakowski, Maureen F. ;
Kris, Mark G. ;
Pao, William ;
Miller, Vincent A. ;
Ladanyi, Marc .
CLINICAL CANCER RESEARCH, 2011, 17 (05) :1169-1180
[4]   High ratio of T790M to EGFR activating mutations correlate with the osimertinib response in non-small-cell lung cancer [J].
Ariyasu, Ryo ;
Nishikawa, Shingo ;
Uchibori, Ken ;
Oh-hara, Tomoko ;
Yoshizawa, Takahiro ;
Dotsu, Yosuke ;
Koyama, Junji ;
Saiki, Masafumi ;
Sonoda, Tomoaki ;
Kitazono, Satoru ;
Yanagitani, Noriko ;
Horiike, Atsushi ;
Inase, Naohiko ;
Kasahara, Kazuo ;
Nishio, Makoto ;
Katayama, Ryohei .
LUNG CANCER, 2018, 117 :1-6
[5]   Evolution and clinical impact of co-occurring genetic alterations in advanced-stage EGFR-mutant lung cancers [J].
Blakely, Collin M. ;
Watkins, Thomas B. K. ;
Wu, Wei ;
Gini, Beatrice ;
Chabon, Jacob J. ;
McCoach, Caroline E. ;
McGranahan, Nicholas ;
Wilson, Gareth A. ;
Birkbak, Nicolai J. ;
Olivas, Victor R. ;
Rotow, Julia ;
Maynard, Ashley ;
Wang, Victoria ;
Gubens, Matthew A. ;
Banks, Kimberly C. ;
Lanman, Richard B. ;
Caulin, Aleah F. ;
St John, John ;
Cordero, Anibal R. ;
Giannikopoulos, Petros ;
Simmons, Andrew D. ;
Mack, Philip C. ;
Gandara, David R. ;
Husain, Hatim ;
Doebele, Robert C. ;
Riess, Jonathan W. ;
Diehn, Maximilian ;
Swanton, Charles ;
Bivona, Trever G. .
NATURE GENETICS, 2017, 49 (12) :1693-+
[6]   Tackling Osimertinib Resistance in EGFR-Mutant Non-Small Cell Lung Cancer [J].
Blaquier, Juan Bautista ;
Ortiz-Cuaran, Sandra ;
Ricciuti, Biagio ;
Mezquita, Laura ;
Cardona, Andres Felipe ;
Recondo, Gonzalo .
CLINICAL CANCER RESEARCH, 2023, 29 (18) :3579-3591
[7]   From the beginning to resistance: Study of plasma monitoring and resistance mechanisms in a cohort of patients treated with osimertinib for advanced T790M-positive NSCLC [J].
Bordi, Paola ;
Del Re, Marzia ;
Minari, Roberta ;
Rofi, Eleonora ;
Buti, Sebastiano ;
Restante, Giuliana ;
Squadrilli, Anna ;
Crucitta, Stefania ;
Casartelli, Chiara ;
Gnetti, Letizia ;
Azzoni, Cinzia ;
Bottarelli, Lorena ;
Petrini, Iacopo ;
Cosenza, Agnese ;
Ferri, Leonarda ;
Rapacchi, Elena ;
Danesi, Romano ;
Tiseo, Marcello .
LUNG CANCER, 2019, 131 :78-85
[8]   Applications of cell-free circulating tumor DNA detection in EGFR mutant lung cancer [J].
Bulbul, Ajaz ;
Leal, Alessandro ;
Husain, Hatim .
JOURNAL OF THORACIC DISEASE, 2020, 12 (05) :2877-2882
[9]   Comparison between Three Different Techniques for the Detection of EGFR Mutations in Liquid Biopsies of Patients with Advanced Stage Lung Adenocarcinoma [J].
Casula, Milena ;
Pisano, Marina ;
Paliogiannis, Panagiotis ;
Colombino, Maria ;
Sini, Maria Cristina ;
Zinellu, Angelo ;
Santeufemia, Davide ;
Manca, Antonella ;
Casula, Stefania ;
Tore, Silvia ;
Lobrano, Renato ;
Cossu, Antonio ;
Palmieri, Giuseppe .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (07)
[10]   Genomic Landscape of Primary Resistance to Osimertinib Among Hispanic Patients with EGFR-Mutant Non-Small Cell Lung Cancer (NSCLC): Results of an Observational Longitudinal Cohort Study [J].
Chamorro, Diego ;
Cardona, Andres F. ;
Rodriguez, July ;
Ruiz-Patino, Alejandro ;
Arrieta, Oscar A. ;
Moreno-Perez, Darwin ;
Rojas, Leonardo ;
Zatarain-Barron, Zyanya Lucia V. ;
Ardila, Dora ;
Viola, Lucia ;
Recondo, Gonzalo B. ;
Blaquier, Juan ;
Martin, Claudio ;
Raez, Luis ;
Samtani, Suraj ;
Ordonez-Reyes, Camila ;
Garcia-Robledo, Juan Esteban ;
Corrales, Luis ;
Sotelo, Carolina ;
Ricaurte, Luisa ;
Cuello, Mauricio ;
Mejia, Sergio ;
Jaller, Elvira ;
Vargas, Carlos ;
Carranza, Hernan ;
Otero, Jorge ;
Archila, Pilar ;
Bermudez, Maritza ;
Gamez, Tatiana ;
Russo, Alessandro ;
Malapelle, Umberto ;
Perez, Diego de Miguel ;
de Lima, Vladmir C. Cordeiro ;
Freitas, Helano ;
Saldahna, Erick ;
Rolfo, Christian ;
Rosell, Rafael .
TARGETED ONCOLOGY, 2023, 18 (03) :425-440