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      Emerging strategies to overcome resistance to third-generation EGFR inhibitors

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          Abstract

          Epidermal growth factor receptor (EGFR), the receptor for members of the epidermal growth factor family, regulates cell proliferation and signal transduction; moreover, EGFR is related to the inhibition of tumor cell proliferation, angiogenesis, invasion, metastasis, and apoptosis. Therefore, EGFR has become an important target for the treatment of cancer, including non-small cell lung cancer, head and neck cancer, breast cancer, glioma, cervical cancer, and bladder cancer. First- to third-generation EGFR inhibitors have shown considerable efficacy and have significantly improved disease prognosis. However, most patients develop drug resistance after treatment. The challenge of overcoming intrinsic and acquired resistance in primary and recurrent cancer mediated by EGFR mutations is thus driving the search for alternative strategies in the design of new therapeutic agents. In view of resistance to third-generation inhibitors, understanding the intricate mechanisms of resistance will offer insight for the development of more advanced targeted therapies. In this review, we discuss the molecular mechanisms of resistance to third-generation EGFR inhibitors and review recent strategies for overcoming resistance, new challenges, and future development directions.

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          Pembrolizumab plus Chemotherapy in Metastatic Non–Small-Cell Lung Cancer

          First-line therapy for advanced non-small-cell lung cancer (NSCLC) that lacks targetable mutations is platinum-based chemotherapy. Among patients with a tumor proportion score for programmed death ligand 1 (PD-L1) of 50% or greater, pembrolizumab has replaced cytotoxic chemotherapy as the first-line treatment of choice. The addition of pembrolizumab to chemotherapy resulted in significantly higher rates of response and longer progression-free survival than chemotherapy alone in a phase 2 trial.
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            Atezolizumab for First-Line Treatment of Metastatic Nonsquamous NSCLC

            The cancer-cell-killing property of atezolizumab may be enhanced by the blockade of vascular endothelial growth factor-mediated immunosuppression with bevacizumab. This open-label, phase 3 study evaluated atezolizumab plus bevacizumab plus chemotherapy in patients with metastatic nonsquamous non-small-cell lung cancer (NSCLC) who had not previously received chemotherapy.
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              Pembrolizumab plus Chemotherapy for Squamous Non–Small-Cell Lung Cancer

              Standard first-line therapy for metastatic, squamous non-small-cell lung cancer (NSCLC) is platinum-based chemotherapy or pembrolizumab (for patients with programmed death ligand 1 [PD-L1] expression on ≥50% of tumor cells). More recently, pembrolizumab plus chemotherapy was shown to significantly prolong overall survival among patients with nonsquamous NSCLC.
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                Author and article information

                Contributors
                ouyangliang@scu.edu.cn
                yuxiwang@scu.edu.cn
                weimi003@scu.edu.cn
                Journal
                J Hematol Oncol
                J Hematol Oncol
                Journal of Hematology & Oncology
                BioMed Central (London )
                1756-8722
                15 July 2022
                15 July 2022
                2022
                : 15
                : 94
                Affiliations
                [1 ]GRID grid.13291.38, ISNI 0000 0001 0807 1581, Department of Respiratory and Critical Care Medicine, Targeted Tracer Research and Development Laboratory, Institute of Respiratory Health, Innovation Center of Nursing Research, Nursing Key Laboratory of Sichuan Province, West China Hospital, , Sichuan University, ; Chengdu, 610041 China
                [2 ]GRID grid.267301.1, ISNI 0000 0004 0386 9246, Department of Pharmaceutical Sciences, College of Pharmacy, , University of Tennessee Health Science Center, ; Memphis, TN 38163 USA
                [3 ]GRID grid.13291.38, ISNI 0000 0001 0807 1581, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, and Collaborative Innovation Center of Biotherapy, , Sichuan University, ; Chengdu, 610041 China
                [4 ]GRID grid.13291.38, ISNI 0000 0001 0807 1581, Precision Medicine Key Laboratory of Sichuan Province and Precision Medicine Research Center, West China Hospital, , Sichuan University, ; Chengdu, 610041 China
                [5 ]Tianfu Jincheng Laboratory, Chengdu, 610041 China
                Article
                1311
                10.1186/s13045-022-01311-6
                9287895
                35840984
                77647dac-4006-46f0-b8d2-667f2092afeb
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 23 March 2022
                : 28 June 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 82037718
                Award ID: 81922064
                Award ID: 22177083
                Funded by: West China Nursing Discipline Development Special Fund Project, Sichuan University
                Award ID: HXHL21011
                Award ID: HXHL21011
                Award ID: HXHL21011
                Award ID: HXHL21011
                Award ID: HXHL21011
                Award ID: HXHL21011
                Award ID: HXHL21011
                Award ID: HXHL21011
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2022

                Oncology & Radiotherapy
                epidermal growth factor receptor (egfr),drug resistance,inhibitors,structure–activity relationship,tyrosine kinase,cancer

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