The study of primary and acquired resistance to first-line osimertinib to improve the outcome of EGFR-mutated advanced Non-small cell lung cancer patients: the challenge is open for new therapeutic strategies

被引:29
作者
Ferro, Alessandra [1 ]
Marinato, Gian Marco [1 ,2 ]
Mulargiu, Cristiana [1 ,2 ]
Marino, Monica [1 ,2 ]
Pasello, Giulia [1 ,2 ]
Guarneri, Valentina [1 ,2 ]
Bonanno, Laura [1 ,2 ,3 ]
机构
[1] IRCCS, Veneto Inst Oncol IOV, Med Oncol 2, Padua, Italy
[2] Univ Padua, Dept Surg Oncol & Gastroenterol, Padua, Italy
[3] Via Gattamelata 64, I-35128 Padua, Italy
关键词
Epidermal growth factor receptor; Non -small cell lung cancer; Osimertinib; Targeted therapy; Cancer resistance mechanism; Personalized medicine; GROWTH-FACTOR RECEPTOR; TYROSINE KINASE INHIBITORS; TEPOTINIB PLUS OSIMERTINIB; MET AMPLIFICATION METAMP; OPEN-LABEL; ADVANCED NSCLC; GENETIC ALTERATIONS; CLINICAL-FEATURES; MUTATIONS; ADENOCARCINOMA;
D O I
10.1016/j.critrevonc.2024.104295
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The development of targeted therapy in epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC) patients has radically changed their clinical perspectives. Current first-line standard treatment for advanced disease is commonly considered third-generation tyrosine kinase inhibitors (TKI), osimertinib. The study of primary and acquired resistance to front-line osimertinib is one of the main burning issues to further improve patients' outcome. Great heterogeneity has been depicted in terms of duration of clinical benefit and pattern of progression and this might be related to molecular factors including subtypes of EGFR mutations and concomitant genetic alterations. Acquired resistance can be categorized into two main classes: EGFR-dependent and EGFR-independent mechanisms and specific pattern of progression to first-line osimertinib have been demonstrated. The purpose of the manuscript is to provide a comprehensive overview of literature about molecular resistance mechanisms to first-line osimertinib, from a clinical perspective and therefore in relationship to emerging therapeutic approaches.
引用
收藏
页数:19
相关论文
共 213 条
[1]   Targeting BRAF Activation as Acquired Resistance Mechanism to EGFR Tyrosine Kinase Inhibitors in EGFR-Mutant Non-Small-Cell Lung Cancer [J].
Aboubakar Nana, Frank ;
Ocak, Sebahat .
PHARMACEUTICS, 2021, 13 (09)
[2]  
Ahn MJ, 2022, J THORAC ONCOL, V17, pS469, DOI 10.1016/j.jtho.2022.07.823
[3]  
Ahn S, 2016, J PATHOL TRANSL MED, V50, P258
[4]   Efficacy of Osimertinib Plus Bevacizumab vs Osimertinib in Patients With EGFR T790M-Mutated Non-Small Cell Lung Cancer Previously Treated With Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitor West Japan Oncology Group 8715L Phase 2 Randomized Clinical Trial [J].
Akamatsu, Hiroaki ;
Toi, Yukihiro ;
Hayashi, Hidetoshi ;
Fujimoto, Daichi ;
Tachihara, Motoko ;
Furuya, Naoki ;
Otani, Sakiko ;
Shimizu, Junichi ;
Katakami, Nobuyuki ;
Azuma, Koichi ;
Miura, Naoko ;
Nishino, Kazumi ;
Hara, Satoshi ;
Teraoka, Shunsuke ;
Morita, Satoshi ;
Nakagawa, Kazuhiko ;
Yamamoto, Nobuyuki .
JAMA ONCOLOGY, 2021, 7 (03) :386-394
[5]   Histomolecular Resistance Mechanisms to First-Line Osimertinib in EGFR-Mutated Advanced Non-Small Cell Lung Cancer: A Multicentric Retrospective French Study [J].
Akli, Assya ;
Girard, Nicolas ;
Fallet, Vincent ;
Rousseau-Bussac, Gaelle ;
Gounant, Valerie ;
Friard, Sylvie ;
Tredaniel, Jean ;
Dujon, Cecile ;
Wislez, Marie ;
Duchemann, Boris ;
Giroux-Leprieur, Etienne .
TARGETED ONCOLOGY, 2022, 17 (06) :675-682
[6]  
[Anonymous], 2018, FDA approves osimertinib for first-line treatment of metastatic NSCLC with most common EGFR mutations press release
[7]   EGFR Exon 20 Insertion Mutations in Lung Adenocarcinomas: Prevalence, Molecular Heterogeneity, and Clinicopathologic Characteristics [J].
Arcila, Maria E. ;
Nafa, Khedoudja ;
Chaft, Jamie E. ;
Rekhtman, Natasha ;
Lau, Christopher ;
Reva, Boris A. ;
Zakowski, Maureen F. ;
Kris, Mark G. ;
Ladanyi, Marc .
MOLECULAR CANCER THERAPEUTICS, 2013, 12 (02) :220-229
[8]   Immune checkpoint inhibitors in EGFR-mutant non-small cell lung cancer: A systematic review [J].
Attili, Ilaria ;
Passaro, Antonio ;
Corvaja, Carla ;
Aliaga, Pamela Trillo ;
Del Signore, Ester ;
Spitaleri, Gianluca ;
de Marinis, Filippo .
CANCER TREATMENT REVIEWS, 2023, 119
[9]   MET Exon 14 Mutations in Non-Small-Cell Lung Cancer Are Associated With Advanced Age and Stage-Dependent MET Genomic Amplification and c-Met Overexpression [J].
Awad, Mark M. ;
Oxnard, Geoffrey R. ;
Jackman, David M. ;
Savukoski, Daniel O. ;
Hall, Dimity ;
Shivdasani, Priyanka ;
Heng, Jennifer C. ;
Dahlberg, Suzanne E. ;
Anne, Pasi A. J. ;
Verma, Suman ;
Christensen, James ;
Hammerman, Peter S. ;
Sholl, Lynette M. .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (07) :721-+
[10]  
Bar J, 2022, J CLIN ONCOL, V40