Clinical predictors of response to EGFR-tyrosine kinase inhibitors in EGFR-mutated non-small cell lung cancer: A real-world multicentric cohort analysis from India

被引:18
|
作者
Garg, Avneet [1 ]
Batra, Ullas [2 ]
Choudhary, Priyanshu [2 ]
Jain, Deepali [3 ]
Khurana, Sachin [4 ]
Malik, Prabhat S. [4 ]
Muthu, Valliappan [5 ]
Prasad, K. T. [5 ]
Singh, Navneet [5 ]
Suri, Tejas [6 ]
Mohan, Anant [6 ]
机构
[1] Adesh Inst Med Sci & Res, Dept Pulm Med, Bhatinda, India
[2] Rajiv Gandhi Canc Inst & Res Ctr, Dept Med Oncol, New Delhi, India
[3] All India Inst Med Sci, Dept Pathol, New Delhi, India
[4] All India Inst Med Sci, Dept Med Oncol, New Delhi, India
[5] Postgrad Inst Med Educ & Res, Dept Pulm Med, Chandigarh, India
[6] All India Inst Med Sci, Dept Pulm Crit Care & Sleep Med, New Delhi, India
关键词
EGFR mutated NSCLC; TKI; PFS; GROWTH-FACTOR-RECEPTOR; ACQUIRED-RESISTANCE; 1ST-LINE TREATMENT; MUTATIONAL STATUS; PROGRESSION-FREE; TUMOR BURDEN; OPEN-LABEL; SURVIVAL; ADENOCARCINOMA; CHEMOTHERAPY;
D O I
10.1016/j.currproblcancer.2020.100570
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The development of various targeted therapies against Epidermal Growth Factor Receptor (EGFR) has been a major step in therapeutic advancements in lung cancer. However, the response to tyrosine kinase inhibitors (TKI) therapy in a real-world setting has not been well elucidated. Methods: As part of a retrospective analysis, patients with EGFR mutated non-small cell lung cancer at 4 tertiary care Institutions in North India between December 2007 and August 2018 were evaluated. The overall response rate, disease control rate, progression-free survival (PFS) and factors affecting PFS were analyzed. Results: A total of 483 patients were included, including 52.4% males, with mean (+/- SD) age of 56.7 (+/- 12.4) years. Majority (63.8%) had good performance status (Eastern Cooperative Oncology Group 0 or 1) and 77.4% were nonsmokers. Among the EGFR mutations, exon 19 deletion was the most common mutation detected (68.1%), followed by L858R mutation in exon 21 (26.9%). Extra-thoracic metastasis was present in 69.5% patients and majority of them had <= 2 metastatic sites (85.1%). TKIs were used as the first-line therapy in 64.8% patients, and gefitinib was the most frequently used TKI (67.3%), followed by erlotinib (26.7%). The overall response rate and disease control rate were 65.9% and 90.7% respectively. The median PFS was 9.3 months and brain was the exclusive site of progression in 18.0% patients. On univariate analysis, the factors that significantly affected PFS were, the number of metastatic sites and the type of EGFR mutation. On multivariate analysis, the number of metastatic sites was the only factor that affected the PFS [HR (95% CI): 2.5 (1.7-3.6); Pvalue <0.001]. Skin toxicity was the most common adverse event (32.3%), followed by involvement of the gastro-intestinal tract (22.5%). Conclusion: In this one of the largest multicentric Indian study of treatment outcomes in EGFR-mutated non-small cell lung cancer in a real-world setting, we found that increased tumor burden (number of metastatic sites > 2) was the only significant factor associated with a worse PFS. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页数:11
相关论文
共 50 条
  • [21] Nanomodified strategies to overcome EGFR-tyrosine kinase inhibitors resistance in non-small cell lung cancer
    Liao, Zi-Xian
    Huang, Kuo-Yen
    Kempson, Ivan M.
    Li, Hsin-Jung
    Tseng, S. -Ja
    Yang, Pan-Chyr
    JOURNAL OF CONTROLLED RELEASE, 2020, 324 : 482 - 492
  • [22] The efficacy of EGFR-tyrosine kinase inhibitor in non-small cell lung cancer patients with synchronous brain metastasis: a real-world study
    Choi, Jin-Hyuk
    Choi, Yong Won
    Lee, Hyun Woo
    Kang, Seok Yun
    Jeong, Geum Sook
    Ahn, Mi Sun
    Oh, Young-Taek
    Noh, O. Kyu
    Kim, Se-Hyuk
    Roh, Tae Hoon
    Sheen, Seung Soo
    KOREAN JOURNAL OF INTERNAL MEDICINE, 2022, 37 (02): : 434 - 443
  • [23] CLINICAL ANALYSIS OF AFATINIB IN EGFR-TYROSINE KINASE INHIBITOR NAIVE PATIENTS WITH NON-SMALL CELL LUNG CANCER HABORING EGFR MUTATIONS
    Nasu, Shingo
    Takata, So
    Masuhiro, Kentaro
    Morita, Satomu
    Iwata, Kaori
    Ryota, Noriko
    Okada, Yukari
    Tokuoka, Yoshie
    Ueda, Yuki
    Kumode, Akinori
    Usui, Naoko
    Tanaka, Ayako
    Shiroyama, Takayuki
    Morishita, Naoko
    Suzuki, Hidekazu
    Okamoto, Norio
    Hirashima, Tomonori
    RESPIROLOGY, 2017, 22 : 114 - 114
  • [24] Real-world utilization of EGFR TKIs and prognostic factors for survival in EGFR-mutated non-small cell lung cancer patients with brain metastases
    Yu, Xiaoqing
    Sheng, Jiamin
    Pan, Guoqiang
    Fan, Yun
    INTERNATIONAL JOURNAL OF CANCER, 2021, 149 (05) : 1121 - 1128
  • [25] Furmonertinib treatment in patients with EGFR-mutated non-small cell lung cancer and leptomeningeal metastases: A real-world study
    Chen, H.
    Wang, L.
    Wu, Y.
    Wu, Y.
    Ma, S.
    Sen, Y.
    Zhen, H.
    Mo, Y.
    Zhang, C.
    Wang, Q.
    ANNALS OF ONCOLOGY, 2023, 34 : S1697 - S1697
  • [26] Efficacy of Tyrosine Kinase Inhibitors in EGFR Mutated Non-Small Cell Lung Cancer with Leptomeningeal Metastases
    Flippot, R.
    Auclin, E.
    Biondani, P.
    Le Rhun, E.
    Adam, J.
    Planchard, D.
    Caramella, C.
    Le Pechoux, C.
    Lacroix, L.
    Gazzah, A.
    Mezquita, L.
    Besse, B.
    JOURNAL OF THORACIC ONCOLOGY, 2018, 13 (10) : S467 - S467
  • [27] Tyrosine kinase inhibitors for EGFR- and ALK-mutated non-small cell lung cancer
    Thompson, Jonathan R.
    Menon, Smitha P.
    Dy, Grace K.
    ADMET AND DMPK, 2016, 4 (03): : 186 - 211
  • [28] Erratum to: Different efficacy of EGFR tyrosine kinase inhibitors and prognosis in patients with subtypes of EGFR-mutated advanced non-small cell lung cancer: a meta-analysis
    Huan Wang
    Jing Huang
    Xiaojin Yu
    Shuhua Han
    Xing Yan
    Siqing Sun
    Xiaoli Zhu
    Journal of Cancer Research and Clinical Oncology, 2014, 140 : 1911 - 1911
  • [29] Adjuvant EGFR tyrosine kinase inhibitors for patients with resected EGFR-mutated non-small-cell lung cancer: a network meta-analysis
    Tian, Wentao
    Tan, Nuopei
    Ke, Jiawen
    Zou, Ji'an
    Liu, Xiaohan
    Pan, Yue
    Zeng, Yue
    Peng, Yurong
    Wu, Fang
    FUTURE ONCOLOGY, 2022, 18 (21) : 2695 - 2708
  • [30] Leptomeningeal carcinomatosis from EGFR-mutated non-small cell lung cancer
    Iuchi, T.
    Shingyoji, M.
    Setoguchi, T.
    Yoshida, Y.
    Ashinuma, H.
    Hasegawa, Y.
    Sakaida, T.
    ANNALS OF ONCOLOGY, 2017, 28