A comprehensive comparison of third generation epidermal growth factor receptor tyrosine kinase inhibitors in the treatment efficacy and adverse events: A Bayesian meta-analysis

Jinyu Yu , Hanyu Wu , Lu Yang (MD) , Wei Liu , Baoshan Cao , Baosheng Liang , Yangchun Gu

Global Medical Genetics ›› 2025, Vol. 12 ›› Issue (03) : 100064

PDF (3926KB)
Global Medical Genetics ›› 2025, Vol. 12 ›› Issue (03) :100064 DOI: 10.1016/j.gmg.2025.100064
Research article
research-article
A comprehensive comparison of third generation epidermal growth factor receptor tyrosine kinase inhibitors in the treatment efficacy and adverse events: A Bayesian meta-analysis
Author information +
History +
PDF (3926KB)

Abstract

Background It is a challenge for clinicians to choose the optimal third generation EGFR-tyrosine kinase inhibitors (EGFR-TKIs) treatment for individual patients. In this meta-analysis we compare the efficacy of five third-generation EGFR-TKIs, as first-line and second-line therapies for non-small cell lung cancer (NSCLC) patients, and their adverse events (AEs).

Methods A Bayesian hierarchical network meta-analysis was conducted to evaluate the hazard ratios (HR) of first-line therapeutic effects and AEs for these third-generation EGFR-TKIs comparing with first-generation EGFR-TKIs. Additionally, a simple comparison analysis was conducted to evaluate second-line therapeutic effects.

Results All third-generation TKIs exhibited superior efficacy compared to Gefitinib in first-line treatment. Furmonertinib achieved the lowest HR in the exon 19 deletions subgroup (HR: 0.35; 95 % CI: 0.23-0.54), while Lazertinib showed the most favorable HR in the exon 21 L858R subgroup (HR: 0.44; 95 % CI: 0.28-0.70) and among patients with brain metastases (HR: 0.33; 95 % CI 0.18-0.59). In the second-line setting, Furmonertinib achieved the highest numerically objective response rate across the overall population (74.0 %; 95 % CI: 68.0-80.0 %) and all evaluated subgroups. Adverse event analysis showed that Furmonertinib had the lowest overall AE incidence, and Lazertinib had the lowest rate of high-grade (≥ grade 3) AEs.

Conclusions All third-generation EGFR-TKIs exhibited favorable efficacy in both first- and second-line settings. Differences in AE profiles were also noted.

Keywords

Non-small cell lung cancer / EGFR mutations / Third-generation TKIs / Efficacy / Adverse events

Cite this article

Download citation ▾
Jinyu Yu, Hanyu Wu, Lu Yang (MD), Wei Liu, Baoshan Cao, Baosheng Liang, Yangchun Gu. A comprehensive comparison of third generation epidermal growth factor receptor tyrosine kinase inhibitors in the treatment efficacy and adverse events: A Bayesian meta-analysis. Global Medical Genetics, 2025, 12(03): 100064 DOI:10.1016/j.gmg.2025.100064

登录浏览全文

4963

注册一个新账户 忘记密码

Appendix A. Supplementary material

Supplementary data associated with this article can be found in the online version at doi:10.1016/j.gmg.2025.100064.

References

[1]

Ferlay J., Ervik M., Lam F., Laversanne M., Colombet M., Mery L., et al. Global Cancer Observatory:Cancer today. Lyon, France: International Agency for Research on Cancer. Available from http://gco.iarc.who.int/today.accessed 2024-5-1. 2024.

[2]

B. Melosky, K. Kambartel, M. Häntschel, M. Bennetts, D.J. Nickens, J. Brinkmann, et al., Worldwide prevalence of epidermal growth factor receptor mutations in non-small cell lung cancer: a meta-analysis, Mol. Diagn. Ther. 26 (1) (2022) 7-18.

[3]

J.C. Soria, Y. Ohe, J. Vansteenkiste, T. Reungwetwattana, B. Chewaskulyong, K.H. Lee, et al., Osimertinib in untreated EGFR-mutated advanced non-small-cell lung cancer, N. Engl. J. Med 378 (2) (2018) 113-125.

[4]

Y. Cheng, Y. He, W. Li, H.L. Zhang, Q. Zhou, B. Wang, et al., Osimertinib versus comparator EGFR TKI as first-line treatment for EGFR-mutated advanced NSCLC: FLAURA China, a randomized study, Target Oncol. 16 (2) (2021) 165-176.

[5]

Y. Shi, G. Chen, X. Wang, Y. Liu, L. Wu, Y. Hao, et al., Furmonertinib (AST2818) versus gefitinib as first-line therapy for Chinese patients with locally advanced or metastatic EGFR mutation-positive non-small-cell lung cancer (FURLONG): a multicentre, double-blind, randomised phase 3 study, Lancet Respir. Med 10 (11) (2022) 1019-1028.

[6]

S. Lu, X. Dong, H. Jian, J. Chen, G. Chen, Y. Sun, et al., AENEAS: A Randomized Phase III Trial of Aumolertinib Versus Gefitinib as First-Line Therapy for Locally Advanced or MetastaticNon-Small-Cell Lung Cancer With EGFR Exon 19 Deletion or L858R Mutations, J. Clin. Oncol. 40 (27) (2022) 3162-3171.

[7]

T. Reungwetwattana, B.C. Cho, K.H. Lee, Y.K. Pang, C.H. Fong, J.H. Kang, et al., Lazertinib versus gefitinib tyrosine kinase inhibitors in treatment-naíve patients with EGFR-mutated advanced NSCLC: analysis of the asian subpopulation in LASER301, J. Thorac. Oncol. 18 (10) (2023) 1351-1361.

[8]

S. Lu, J. Zhou, H. Jian, L. Wu, Y. Cheng, Y. Fan, et al., Befotertinib (D-0316) versus icotinib as first-line therapy for patients with EGFR-mutated locally advanced or metastatic non-small-cell lung cancer: a multicentre, open-label, randomised phase 3 study. Lancet, Respir. Med 11 (10) (2023) 905-915.

[9]

B.C. Cho, B. Chewaskulyong, K.H. Lee, A. Dechaphunkul, V. Sriuranpong, F. Imamura, et al., Osimertinib versus Standard of Care EGFR TKI as First-Line Treatment in Patients with EGFRm Advanced NSCLC: FLAURA Asian Subset, J. Thorac. Oncol. 14 (1) (2019) 99-106.

[10]

S. Lu, Y. Zhang, G. Zhang, J. Zhou, S. Cang, Y. Cheng, et al., Efficacy and Safety of Befotertinib (D-0316) in Patients With EGFR T790M-Mutated NSCLC That Had Progressed After Prior EGFR Tyrosine Kinase Inhibitor Therapy: A Phase 2, Multicenter, Single-Arm, Open-Label Study, J. Thorac. Oncol. 17 (10) (2022) 1192-1204.

[11]

S. Lu, Q. Wang, G. Zhang, X. Dong, C.T. Yang, Y. Song, et al., Efficacy of aumolertinib (HS-10296) in patients with advanced EGFR T790M+ NSCLC: updated post-national medical products administration approval results from the APOLLO registrational trial, J. Thorac. Oncol. 17 (3) (2022) 411-422.

[12]

B.C. Cho, J.Y. Han, S.W. Kim, K.H. Lee, E.K. Cho, Y.G. Lee, et al., A phase 1/ 2 study of lazertinib 240 mg in patients with advanced EGFR T790M-Positive NSCLC after previous EGFR tyrosine kinase inhibitors, J. Thorac. Oncol. 17 (4) (2022) 558-567.

[13]

Y. Shi, X. Hu, S. Zhang, D. Lv, L. Wu, Q. Yu, et al., Efficacy, safety, and genetic analysis of furmonertinib (AST2818) in patients with EGFR T790M mutated non- small-cell lung cancer: a phase 2b, multicentre, single-arm, open-label study, Lancet Respir. Med 9 (8) (2021) 829-839.

[14]

T.S. Mok, Y.L. Wu, M.J. Ahn, M.C. Garassino, H.R. Kim, S.S. Ramalingam, et al., Osimertinib or platinum-pemetrexed in EGFR T790M-positive lung cancer, N. Engl. J. Med 376 (7) (2017) 629-640.

[15]

M.J. Ahn, C.M. Tsai, F.A. Shepherd, L. Bazhenova, L.V. Sequist, T. Hida, et al., Osimertinib in patients with T790M mutation-positive, advanced non-small cell lung cancer: Long-term follow-up from a pooled analysis of 2 phase 2 studies, Cancer 125 (6) (2019) 892-901.

[16]

M.Z.V. Nagasaka, S.M. Lim, M. Greco, F. Wu, S.I. Ou, Beyond osimertinib: the development of third-generation EGFR tyrosine kinase inhibitors for advanced EGFR+ NSCLC, J. Thorac. Oncol. 16 (2021) 740-763.

[17]

Cochrane Bias Methods Group and Cochrane Statistical Methods Group, 2019. RoB 2: A revised Cochrane risk-of-bias tool for randomized trials. Available at: 〈 https://methods.cochrane.org/bias/resources/rob-2-revised-cochrane-risk-bias-tool-randomized-trials〉 [Accessed 29 June 2024].

[18]

Wells G., Shea B., O’Connell J., Robertson J., Peterson V., Welch V., et al. The Newcastle- Ottawa scale (NOS) for assessing the quality of nonrandomised studies in meta-analysis. Available at 〈 https://www.ohri.ca/programs/clinical_epidemiology/oxford.asp〉 [Accessed 29 June 2024].

[19]

D.J. Lunn, A. Thomas, N. Best, D. Spiegelhalter, WinBUGS-a Bayesian modelling framework: concepts, structure, and extensibility, Stat. Comput. 10 (2000) 325-337.

[20]

V.M. Patil, V. Noronha, A. Joshi, A.B. Choughule, A. Bhattacharjee, R. Kumar, et al., Phase III study of gefitinib or pemetrexed with carboplatin in EGFR-mutated advanced lung adenocarcinoma, ESMO Open 2 (1) (2017) e000168.

[21]

Y.K. Shi, L. Wang, B.H. Han, W. Li, P. Yu, Y.P. Liu, et al., First-line icotinib versus cisplatin/pemetrexed plus pemetrexed maintenance therapy for patients with advanced EGFR mutation-positive lung adenocarcinoma (CONVINCE): a phase 3, open-label, randomized study, Ann. Oncol. 28 (10) (2017) 2443-2450.

[22]

B.C. Cho, S. Lu, E. Felip, A.I. Spira, N. Girard, J.S. Lee, et al., Amivantamab plus Lazertinib in Previously Untreated EGFR-Mutated Advanced NSCLC, N. Engl. J. Med 391 (16) (2024) 1486-1498.

[23]

C. Zhou, A. Xiong,OA02.04 a phase III study of rilertinib versus gefitinib as first-line therapy for patients with locally advanced or metastatic EGFR-mutated NSCLC, J. Thorac. Oncol. 19 (10) (2024) S11.

[24]

Zhou Q., Yu Y., Xing L., Cheng Y., Wang Y., Pan Y., et al. First-line zorifertinib for EGFR-mutant non-small cell lung cancer with central nervous system metastases: the phase 3 EVEREST trial. Med (New York, NY) 2024.

[25]

S.H. Lee, B.C. Cho, H. Hayashi, E. Felip, A.I. Spira, N. Girard, et al., OA02.05 lazertinib vs osimertinib in 1L EGFR-Mutant advanced NSCLC: a randomized, double-blind, exploratory analysis from MARIPOSA, J. Thorac. Oncol. 19 (10) (2024) S12.

[26]

S. Kim, Y. Heo, Y.-H. Lee, J.H. Kang, Are 19del and L858R really different disease entities? Future Oncol. 20 (23) (2024) 1689-1694.

[27]

T. Reungwetwattana, K. Nakagawa, B.C. Cho, M. Cobo, E.K. Cho, A. Bertolini, et al., CNS response to osimertinib versus standard epidermal growth factor receptor tyrosine kinase inhibitors in patients with untreated EGFR-mutated advanced non-small-cell lung cancer, J. Clin. Oncol. (2018) Jco2018783118.

[28]

S. Lu, X. Dong, H. Jian, J. Chen, G. Chen, Y. Sun, et al., Central nervous system efficacy of aumolertinib versus gefitinib in patients with untreated, EGFR- mutated, advanced non-small cell lung cancer: data from a randomized phase III trial (AENEAS), Cancer Commun. (Lond. ) 44 (9) (2024) 1005-1017.

[29]

Y. Shi, G. Chen, X. Wang, Y. Liu, L. Wu, Y. Hao, et al., Central nervous system efficacy of furmonertinib (AST2818) versus gefitinib as first-line treatment for EGFR-mutated NSCLC: results from the FURLONG study, J. Thorac. Oncol. 17 (11) (2022) 1297-1305.

[30]

R.A. Soo, B.C. Cho, J.H. Kim, M.J. Ahn, K.H. Lee, A. Zimina, et al., Central Nervous System Outcomes of Lazertinib Versus Gefitinib in EGFR-Mutated Advanced NSCLC: A LASER301 Subset Analysis, J. Thorac. Oncol. 18 (12) (2023) 1756-1766.

[31]

Y.L. Wu, M.J. Ahn, M.C. Garassino, J.Y. Han, N. Katakami, H.R. Kim, et al., CNS Efficacy of Osimertinib in Patients With T790M-Positive Advanced Non-Small- Cell Lung Cancer: Data From a Randomized Phase III Trial (AURA3), J. Clin. Oncol. 36 (26) (2018) 2702-2709.

[32]

X. Hu, S. Zhang, Z. Ma, J. Feng, L. Wu, D. Lv, et al., Central nervous system efficacy of furmonertinib (AST2818) in patients with EGFR T790M mutated non-small cell lung cancer: a pooled analysis from two phase 2 studies, BMC Med 21 (1) (2023) 164.

[33]

S. Park, M.H. Lee, M. Seong, S.T. Kim, J.H. Kang, B.C. Cho, et al., A phase II, multicenter, two cohort study of 160 mg osimertinib in EGFR T790M-positive non- small-cell lung cancer patients with brain metastases or leptomeningeal disease who progressed on prior EGFR TKI therapy, Ann. Oncol. 31 (10) (2020) 1397-1404.

[34]

J. Ma, L. Huang, C. Han, Expert consensus on the use of third-generation EGFR-TKIs in EGFR-mutated advanced non-small cell lung cancer with various T790M mutations post-resistance to first-/second-generation EGFR-TKIs, Ther. Adv. Med Oncol. 16 (2024) 17588359241289648.

[35]

Y. Zhang, M. Zhang, W. Cheng, S. Fang, Case report: Almonertinib in combination with bevacizumab for leptomeningeal metastases from epidermal growth factor receptor-mutation non-small cell lung cancer: Case series, Front Oncol. 12 (2022) 1040450.

[36]

Z.Q. Lu, J. Cai, X. Wang, J.P. Wei, Z.M. Zeng, L. Huang, et al., Osimertinib combined with bevacizumab for leptomeningeal metastasis from EGFR-mutation non- small cell lung cancer: A phase II single-arm prospective clinical trial, Thorac. Cancer 12 (2) (2021) 172-180.

[37]

H. Chen, S. Yang, L. Wang, Y. Wu, Y. Wu, S. Ma, et al., High-Dose Furmonertinib in Patients With EGFR-Mutated NSCLC and Leptomeningeal Metastases: A Prospective Real-World Study, J. Thorac. Oncol. (2024).

[38]

Consensus on Application of Third-generation EGFR-TKI in EGFR Mutated NSCLC (2022 Version), Zhongguo Fei Ai Za Zhi 25 (9) (2022) 627-641.

[39]

D.A. Cross, S.E. Ashton, S. Ghiorghiu, C. Eberlein, C.A. Nebhan, P.J. Spitzler, et al., AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer, Cancer Discov. 4 (9) (2014) 1046-1061.

[40]

J.C. Yang, D.R. Camidge, C.T. Yang, J. Zhou, R. Guo, C.H. Chiu, et al. Safety, efficacy, and pharmacokinetics of almonertinib (HS-10296) in pretreated patients with EGFR-mutated advanced NSCLC: a multicenter, open-label, phase 1 trial. J. Thorac. Oncol. 15 (12) (2020) 1907-1918.

[41]

Medicine specification of Befotertinib.〈 [cited]Available from: https://www.bettapharma.com/Contact/article/id/131〉. 2024

[42]

L. Han, X. Zhang, Z. Wang, X. Zhang, L. Zhao, W. Fu, et al., SH-1028, An Irreversible Third-Generation EGFR TKI, Overcomes T790M-Mediated Resistance in Non-Small Cell Lung Cancer, Front Pharm. 12 (2021) 665253.

[43]

Y. Shi, S. Zhang, X. Hu, J. Feng, Z. Ma, J. Zhou, et al. Safety, Clinical Activity, and Pharmacokinetics of Alflutinib (, AST2818) in Patients With Advanced NSCLC With EGFR T790M Mutation, J. Thorac. Oncol. 15 (6) (2020) 1015-1026.

[44]

J. Yun, M.H. Hong, S.Y. Kim, C.W. Park, S. Kim, M.R. Yun, et al., YH25448, an Irreversible EGFR-TKI with Potent Intracranial Activity in EGFR Mutant Non-Small Cell Lung Cancer, Clin. Cancer Res 25 (8) (2019) 2575-2587.

[45]

D.E. Heppner, F. Wittlinger, T.S. Beyett, T. Shaurova, D.A. Urul, B. Buckley, et al., Structural Basis for Inhibition of Mutant EGFR with Lazertinib (YH25448), ACS Med. Chem. Lett. 13 (12) (2022) 1856-1863.

[46]

Y. Zhang, Y. Zhang, W. Niu, X. Ge, F. Huang, J. Pang, et al., Experimental Study of Almonertinib Crossing the Blood-Brain Barrier in EGFR-Mutant NSCLC Brain Metastasis and Spinal Cord Metastasis Models, Front Pharm. 12 (2021) 750031.

[47]

P. Ballard, J.W. Yates, Z. Yang, D.W. Kim, J.C. Yang, M. Cantarini, et al., Preclinical Comparison of Osimertinib with Other EGFR-TKIs in EGFR-Mutant NSCLC Brain Metastases Models, and Early Evidence of Clinical Brain Metastases Activity, Clin. Cancer Res 22 (20) (2016) 5130-5140.

[48]

M.H. Hong, Y.J. Choi, H.K. Ahn, S.M. Lim, B. Keam, D.W. Kim, et al., Lazertinib in EGFR-Variant Non-Small Cell Lung Cancer With CNS Failure to Prior EGFR Tyrosine Kinase Inhibitors: A Nonrandomized Controlled Trial, JAMA Oncol. 10 (10) (2024) 1342-1351.

[49]

S. van Hoppe, A. Jamalpoor, J.J.M. Rood, E. Wagenaar, R.W. Sparidans, J.H. Beijnen, et al., Brain accumulation of osimertinib and its active metabolite AZ 5104 is restricted by ABCB1 (P-glycoprotein) and ABCG2 (breast cancer resistance protein), Pharmacol. Res. 146 (2019) 104297.

[50]

N. Colclough, K. Chen, P. Johnström, N. Strittmatter, Y. Yan, G.L. Wrigley, et al., Preclinical Comparison of the Blood-brain barrier Permeability of Osimertinib with Other EGFR TKIs, Clin. Cancer Res. 27 (1) (2021) 189-201.

[51]

C.-P. Wu, Y.-C. Li, M. Murakami, S.-H. Hsiao, Y.-C. Lee, Y.-H. Huang, et al., Furmonertinib, a third-generation EGFR tyrosine kinase inhibitor, overcomes multidrug resistance through inhibiting ABCB1 and ABCG 2 in cancer cells, Int. J. Mol. Sci. 24 (18) (2023) 13972.

[52]

E. Ishikawa, Y. Yokoyama, H. Chishima, H. Kasai, O. Kuniyoshi, M. Kimura, et al., Population pharmacokinetics, pharmacogenomics, and adverse events of osimertinib and its two active metabolites, AZ5104 and AZ7550, in Japanese patients with advanced non-small cell lung cancer: a prospective observational study, Investig. N. Drugs 41 (1) (2023) 122-133.

[53]

J. Ding, X. Ding, J. Zeng, X. Liu, Furmonertinib for EGFR-mutant advanced non-small cell lung cancer: a glittering diamond in the rough of EGFR-TKI, Front Pharm. 15 (2024) 1357913.

[54]

P. Parafianowicz, R. Krishan, B.D. Beutler, R.X. Islam, T. Singh, Myositis - A common but underreported adverse effect of osimertinib: case series and review of the literature, Cancer Treat. Res Commun. 25 (2020) 100254.

[55]

P.S. Malik, V. Noronha, D. Dabkara, V.K. Maddu, S. Rajappa, S. Limaye, et al., Safety of osimertinib in adult patients with metastatic epidermal growth factor receptor T790M mutation-positive non-small cell lung cancer: Results from a Phase IV study in India, Indian J. Cancer 59 (ement) (2022) S1-S10.

[56]

H. Zhang, K.K.W. To, Serum creatine kinase elevation following tyrosine kinase inhibitor treatment in cancer patients: Symptoms, mechanism, and clinical management, Clin. Transl. Sci. 17 (11) (2024) e70053.

[57]

Y. Jiang, Z. Su, Y. Lin, Y. Xiong, C. Li, J. Li, et al., Prognostic and predictive impact of creatine kinase level in non-small cell lung cancer treated with tyrosine kinase inhibitors, Transl. Lung Cancer Res 10 (9) (2021) 3771-3781.

[58]

X. Zhang, M. Zhang, X. Du, G. Zhang, Y. Niu, C. Wei, et al., Clinical efficacy and safety analysis of aumolertinib in real-world treatment of EGFR-mutated advanced non-small-cell lung cancer, Front Pharm. 15 (2024) 1331138.

[59]

F. Xiong, Y. Shen, T. Liu, Y. Zhang, X. Jiang, Osimerinib haematological toxicities in non-small cell lung cancer: a randomised controlled trials meta-analysis, BMJ Support Palliat. Care (2024).

[60]

P. Cheema, B.C. Cho, H. Freitas, M. Provencio, Y.M. Chen, S.W. Kim, et al., A real-world study of second or later-line osimertinib in patients with EGFR T790M- positive NSCLC: the final ASTRIS data, Future Oncol. 19 (1) (2023) 61-75.

[61]

Y. Hu, Y.P. Quan, Y.W. Duan, H. Li, J. Shen, N. Lin, et al., Aumolertinib effectively reduces clinical symptoms of an EGFR L858R-mutant non-small cell lung cancer case coupled with osimertinib-induced severe thrombocytopenia: a case report, Anticancer Drugs 34 (3) (2023) 455-459.

[62]

X. Tan, S. Chen, L. He, M. Huang, X. Zhang, Successful osimertinib rechallenge after severe thrombocytopenia caused by osimertinib combined with sitagliptin: a case report, Anticancer Drugs 34 (6) (2023) 791-796.

[63]

J.Y. Byun, A. Aiyeolemi, A. Qdaisat, C. Park, Association between epidermal growth factor receptor-tyrosine kinase inhibitors and venous thromboembolism among older patients with advanced non-small cell lung cancer, Cancer 130 (20) (2024) 3412-3425.

[64]

N. Girard, B.C. Cho, A.I. Spira, C.A. Shu, R.E. Sanborn, J.W. Neal, et al., Risk factors for venous thromboembolism (VTE) among patients with EGFR-mutated advanced non-small cell lung cancer (NSCLC) receiving amivantamab plus lazertinib versus either agent alone, J. Clin. Oncol. 41 (16_) (2023) 9137 -9137.

[65]

G. Zhou, L. Guo, J. Xu, K. Tang, J. Chen, Comparison of osimertinib plus bevacizumab against osimertinib alone in NSCLC harboring EGFR mutations: a systematic review and meta-analysis, Ther. Adv. Med Oncol. 16 (2024) 17588359241227677.

[66]

Q. Cui, Y. Hu, Q. Cui, D. Wu, Y. Mao, D. Ma, et al., Osimertinib Rechallenge With Bevacizumab vs. Chemotherapy Plus Bevacizumab in EGFR-Mutant NSCLC Patients With Osimertinib Resistance, Front Pharm. 12 (2021) 746707.

[67]

T. Jiang, X. Xu, X. Chen, N. Ding, Q. Hu, C. Zhou, et al., Osimertinib in combination with bevacizumab in EGFR-Mutated NSCLC with leptomeningeal metastases, Transl. Lung Cancer Res 9 (6) (2020) 2514-2517.

[68]

Q. Zhou, H.L. Zhang, L.Y. Jiang, Y.K. Shi, Y. Chen, J.M. Yu, et al., Real-world evidence of osimertinib in Chinese patients with EGFR T790M-positive non-small cell lung cancer: a subgroup analysis from ASTRIS study, J. Cancer Res Clin. Oncol. 149 (12) (2023) 10771-10780.

[69]

A. Gemma, M. Kusumoto, F. Sakai, M. Endo, T. Kato, Y. Saito, et al., Real-World Evaluation of Factors for Interstitial Lung Disease Incidence and Radiologic Characteristics in Patients With EGFR T790M-positive NSCLC Treated With Osimertinib in Japan, J. Thorac. Oncol. 15 (12) (2020) 1893-1906.

[70]

C. Iwai, T. Jo, T. Konishi, A. Fujita, N. Michihata, H. Matsui, et al., Interstitial Pneumonitis Following Sequential Administration of Programmed Death-1/ Programmed Death-Ligand 1 Inhibitors and Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitors For Non-Small Cell Lung Cancer: A Matched-Pair Cohort Study Using a Nationwide Inpatient Database, Clin. Lung Cancer 25 (6) (2024) e243-e251.

[71]

N. Okada, H. Hamano, K. Yagi, T. Niimura, F. Aizawa, M. Goda, et al., Effect of pre-treatment with EGFR-TKIs on immune checkpoint inhibitor-associated interstitial lung disease in lung cancer patients: Analysis using a Japanese claims database, Int J. Clin. Pharm. Ther. 62 (2) (2024) 69-76.

[72]

F. Kashizaki, H. Chen, A. Miyasaka, N. Tsuchiya, C. Yamada, S. Okazaki, et al., Safety of Readministration of EGFR-TKI After Onset of Interstitial Lung Disease in Advanced EGFR-Mutated NSCLC: A Systematic Review and Meta-Analysis, Clin. Lung Cancer 25 (1) (2024) e52-e57 e52.

[73]

Z. Qureshi, F. Altaf, A. Jamil, R. Siddique, Meta-analysis of Targeted Therapies in EGFR-mutated Non-Small Cell Lung Cancer: efficacy and safety of Osimertinib, Erlotinib, and Gefitinib as First-line Treatment, Am. J. Clin. Oncol. 48 (1) (2025) 44-54.

[74]

A. Liu, X. Wang, L. Wang, H. Zhuang, L. Xiong, X. Gan, et al., EGFR-TKIs or EGFR-TKIs combination treatments for untreated advanced EGFR-mutated NSCLC: a network meta-analysis, BMC Cancer 24 (1) (2024) 1390.

[75]

H.S. Zheng, X.Y. Qin, Y.Z. Zheng, X.P. Yang, J. Tan, W.J. Cai, et al., Addition of bevacizumab to EGFR tyrosine kinase inhibitors in advanced NSCLC: an updated systematic review and meta-analysis, Front Pharm. 14 (2023) 1238579.

[76]

T. Landre, J.B. Assié, K. Chouahnia, G. Des Guetz, J.B. Auliac, C. Chouaïd, First-line concomitant EGFR-TKI plus chemotherapy versus EGFR-TKI alone for advanced EGFR-mutated NSCLC: a meta-analysis of randomized phase III trials, Expert Rev. Anticanc 24 (8) (2024) 775-780.

[77]

J.Q. Yin, J. Huang, M. Ren, R. Tang, L.S. Xie, J.X. Xue, A Bayesian network meta-analysis of EGFR-tyrosine kinase inhibitor treatments in patients with EGFR mutation-positive non-small cell lung cancer, Cancer Pathog. Ther. 3 (2) (2025) 135-146.

[78]

Schünemann H.B.J., Guyatt G., Oxman A., editors. GRADE handbook for grading quality of evidence and strength of recommendations. The GRADE Working Group Updated October 2013.

[79]

A. Nikolakopoulou, J.P.T. Higgins, T. Papakonstantinou, A. Chaimani, C. Del Giovane, M. Egger, et al., CINeMA: An approach for assessing confidence in the results of a network meta-analysis, PLoS Med 17 (4) (2020) e1003082.

[80]

Georgia Salanti, Cinzia Del, Anna Giovane, et al., Evaluating the quality of evidence from a network meta-analysis, PloS One 9 (7) (2014) e99682.

[81]

GRADEpro GDT: GRADEpro Guideline Development Tool. McMaster University and Evidence Prime. p. Available from 〈 https://www.gradepro.org〉.

[82]

H. Viray, A.J. Piper-Vallillo, P. Widick, E. Academia, M. Shea, D. Rangachari, et al., A Real-World Study of Patient Characteristics and Clinical Outcomes in EGFR Mutated Lung Cancer Treated with First-Line Osimertinib: Expanding the FLAURA Trial Results into Routine Clinical Practice, Cancers (Basel) 16 (6) (2024).

Funding

the Peking University Third Hospital(Grant number BYSYFY2021050)

the Capital's Funds for Health Improvement and Research(Grant number 2024–1G-4251)

the Noncommunicable Chronic Diseases-National Science and Technology Major Project(Grant number 2023ZD0506600)

Beijing Science and Technology Innovation Medical Development Foundation(Grant number KC2021-JX-0186–25)

PDF (3926KB)

61

Accesses

0

Citation

Detail

Sections
Recommended

/