The effectiveness of afatinib in patients with lung adenocarcinoma harboring complex epidermal growth factor receptor mutation

被引:22
作者
Wu, Shang-Gin [1 ,2 ,3 ]
Yu, Chong-Jen [1 ,2 ]
Yang, James Chih-Hsin [2 ,4 ,5 ]
Shih, Jin-Yuan [1 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Internal Med, 7 Chung Shan South Rd, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Med, Taipei, Taiwan
[3] Natl Taiwan Univ, Dept Internal Med, Ctr Canc, Taipei, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Oncol, Taipei, Taiwan
[5] Natl Taiwan Univ, Grad Inst Oncol, Canc Res Ctr, Taipei, Taiwan
关键词
afatinib; complex mutation; EGFRmutation; lung adenocarcinoma; progression-free survival; TYROSINE KINASE INHIBITORS; UNCOMMON EGFR MUTATIONS; MALIGNANT PLEURAL EFFUSION; GEFITINIB TREATMENT; OPEN-LABEL; EXON; 18; CANCER; MULTICENTER; RESISTANCE; PATTERNS;
D O I
10.1177/1758835920946156
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and aims: Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs) are effective against classicalEGFRmutations in lung cancer. However, their effectiveness and the prognosis of lung cancer patients with complexEGFRmutations are not well delineated. Therefore, we aimed to investigate the treatment effectiveness of different EGFR TKIs in patients with complexEGFRmutations. Patients and methods: From 2005 to 2020, we collected lung adenocarcinoma tissue samples forEGFRmutation analysis using direct Sanger sequencing. Patients withEGFRmutations treated with EGFR TKIs as first-line treatment were enrolled. Clinical characteristics,EGFRmutation status, treatment response, progression-free survival (PFS), and overall survival (OS) were analyzed. Results: Among 2675 patients withEGFRmutations, 239 (8.9%) had complexEGFRmutations, of whom 125 received EGFR TKI treatment as first-line treatment. Multivariate analysis revealed that afatinib was a more favorable factor for PFS than gefitinib [hazard ratio (HR), 2.01; 95% confidence interval (CI), 1.11-3.62] and erlotinib (HR, 2.61; 95% CI, 1.31-5.22), especially in patients with uncommon mutation patterns. Afatinib treatment as first-line treatment was also associated with longer OS compared with erlotinib (HR, 2.48; 95% CI, 1.20-5.12). Classical mutation pattern was associated with longer PFS (p = 0.001) and OS (p = 0.020). Secondary T790M was detected in 22 of 52 (42.3%) patients who had re-biopsied tissue samples after acquiring resistance to EGFR TKIs. There was no significant difference in secondary T790M formation after acquired resistance to the three EGFR TKIs (p = 0.261). Furthermore, three (5.8%) patients had small-cell lung cancer transformation. Conclusion: Afatinib is an effective first-line treatment for patients with lung adenocarcinoma harboring complexEGFRmutations, especially those with uncommon mutation patterns.
引用
收藏
页数:17
相关论文
共 67 条
  • [1] [Anonymous], 2018, ONCOLOGY TIMES, V40, P18
  • [2] EGFR Exon 20 Insertion Mutations in Lung Adenocarcinomas: Prevalence, Molecular Heterogeneity, and Clinicopathologic Characteristics
    Arcila, Maria E.
    Nafa, Khedoudja
    Chaft, Jamie E.
    Rekhtman, Natasha
    Lau, Christopher
    Reva, Boris A.
    Zakowski, Maureen F.
    Kris, Mark G.
    Ladanyi, Marc
    [J]. MOLECULAR CANCER THERAPEUTICS, 2013, 12 (02) : 220 - 229
  • [3] Astaras C, 2020, HEAL TIMES ONCOL HEM, V3, P10, DOI DOI 10.36000/HBT.OH.2020.03.01
  • [4] Efficacy of EGFR tyrosine kinase inhibitors in patients with EGFR-mutated non-small cell lung cancer except both exon 19 deletion and exon 21 L858R: A retrospective analysis in Korea
    Baek, Jin Ho
    Sun, Jong-Mu
    Min, Young Joo
    Cho, Eun Kyung
    Cho, Byoung Chul
    Kim, Joo-Hang
    Ahn, Myung-Ju
    Park, Keunchil
    [J]. LUNG CANCER, 2015, 87 (02) : 148 - 154
  • [5] Sensitivities to various epidermal growth factor receptor-tyrosine kinase inhibitors of uncommon epidermal growth factor receptor mutations L861Q and S768I: What is the optimal epidermal growth factor receptor-tyrosine kinase inhibitor?
    Banno, Eri
    Togashi, Yosuke
    Nakamura, Yu
    Chiba, Masato
    Kobayashi, Yoshihisa
    Hayashi, Hidetoshi
    Terashima, Masato
    de Velasco, Marco A.
    Sakai, Kazuko
    Fujita, Yoshihiko
    Mitsudomi, Tetsuya
    Nishio, Kazuto
    [J]. CANCER SCIENCE, 2016, 107 (08) : 1134 - 1140
  • [6] Rare EGFR exon 18 and exon 20 mutations in non-small-cell lung cancer on 10 117 patients: a multicentre observational study by the French ERMETIC-IFCT network
    Beau-Faller, M.
    Prim, N.
    Ruppert, A. -M.
    Nanni-Metellus, I.
    Lacave, R.
    Lacroix, L.
    Escande, F.
    Lizard, S.
    Pretet, J. -L
    Rouquette, I.
    de Cremoux, P.
    Solassol, J.
    de Fraipont, F.
    Bieche, I.
    Cayre, A.
    Favre-Guillevin, E.
    Tomasini, P.
    Wislez, M.
    Besse, B.
    Legrain, M.
    Voegeli, A. -C.
    Baudrin, L.
    Morin, F.
    Zalcman, G.
    Quoix, E.
    Blons, H.
    Cadranel, J.
    [J]. ANNALS OF ONCOLOGY, 2014, 25 (01) : 126 - 131
  • [7] Clinical Outcomes of EGFR Exon 20 Insertion Mutations in Advanced Non-small Cell Lung Cancer in Korea
    Byeon, Seonggyu
    Kim, Youjin
    Lim, Sung Won
    Cho, Jang Ho
    Park, Sehoon
    Lee, Jiyun
    Sun, Jong-Mu
    Choi, Yoon-La
    Lee, Se-Hoon
    Ahn, Jin Seok
    Park, Keunchil
    Ahn, Myung-Ju
    [J]. CANCER RESEARCH AND TREATMENT, 2019, 51 (02): : 623 - 631
  • [8] Distinctive activation patterns in constitutively active and gefitinib-sensitive EGFR mutants
    Chen, YR
    Fu, YN
    Lin, CH
    Yang, ST
    Hu, SF
    Chen, YT
    Tsai, SF
    Huang, SF
    [J]. ONCOGENE, 2006, 25 (08) : 1205 - 1215
  • [9] EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations:: one-third of doublets occur at five pairs of amino acids
    Chen, Z.
    Feng, J.
    Saldivar, J-S
    Gu, D.
    Bockholt, A.
    Sommer, S. S.
    [J]. ONCOGENE, 2008, 27 (31) : 4336 - 4343
  • [10] Efficacy of irreversible EGFR-TKIs for the uncommon secondary resistant EGFR mutations L747S, D761Y, and T854A
    Chiba, Masato
    Togashi, Yosuke
    Bannno, Eri
    Kobayashi, Yoshihisa
    Nakamura, Yu
    Hayashi, Hidetoshi
    Terashima, Masato
    De Velasco, Marco A.
    Sakai, Kazuko
    Fujita, Yoshihiko
    Mitsudomi, Tetsuya
    Nishio, Kazuto
    [J]. BMC CANCER, 2017, 17