Pneumonitis in advanced non-small-cell lung cancer patients treated with EGFR tyrosine kinase inhibitor: Meta-analysis of 153 cohorts with 15,713 patients Meta-analysis of incidence and risk factors of EGFR-TKI pneumonitis in NSCLC

被引:68
作者
Suh, Chong Hyun [1 ,2 ]
Park, Hye Sun [3 ,4 ]
Kim, Kyung Won [1 ,2 ]
Pyo, Junhee [5 ]
Hatabu, Hiroto [3 ,4 ]
Nishino, Mizuki [3 ,4 ]
机构
[1] Univ Ulsan, Asan Med Ctr, Dept Radiol, Coll Med, 86 Asanbyeongwon Gil, Seoul 138736, South Korea
[2] Univ Ulsan, Asan Med Ctr, Res Inst Radiol, Coll Med, 86 Asanbyeongwon Gil, Seoul 138736, South Korea
[3] Brigham & Womens Hosp, Dept Radiol, 450 Brookline Ave, Boston, MA 02215 USA
[4] Harvard Med Sch, Dana Farber Canc Inst, 450 Brookline Ave, Boston, MA 02215 USA
[5] Univ Utrecht, WHO Collaborating Ctr Pharmaceut Policy & Regulat, Dept Pharmaceut Sci, Univ Weg 99, NL-3584 CG Utrecht, Netherlands
关键词
EGFR tyrosine kinase inhibitor; Pneumonitis; Non-small-cell lung cancer; Meta-analysis; PHASE-II TRIAL; FACTOR RECEPTOR MUTATIONS; CHEMOTHERAPY-NAIVE PATIENTS; SINGLE-AGENT GEFITINIB; ERBB FAMILY BLOCKER; HIGH-DOSE GEFITINIB; TIVANTINIB ARQ 197; JAPANESE PATIENTS; OPEN-LABEL; ELDERLY-PATIENTS;
D O I
10.1016/j.lungcan.2018.06.032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Pneumonitis is a significant toxicity of EGFR tyrosine kinase inhibitors (EGFR-TKI) in non-small-cell lung cancer (NSCLC) patients. We studied the incidence of pneumonitis in clinical trials of EGFR-TKI published in 2003-2017, and performed subgroups analyses to identity predisposing factors. Methods: Ovid-MEDLINE and EMBASE search up to 4/17/17 using the keywords, "erlotinib", "gefitinib", "afatinib", "osimertinib", and "lung cancer", resulted in a total of 153 eligible trial cohorts with 15,713 advanced NSCLC patients treated with EGFR-TKI. The pooled incidence of all-grade, high-grade, and grade 5 pneumonitis was obtained. Subgroup analyses were performed with meta-regression using study-level covariates. Results: Among the patients without prior exposure to EGFR-TKI, the overall incidence was 1.12% (95% CI:0.79-1.58%) for all-grade, 0.61% (95% CI:0.40-0.93%) for high-grade, and 0.20% (95% CI:0.11-0.38%) for grade 5 pneumonitis. The incidence was significantly higher in Japanese studies compared to studies of non Japan origin, for all-grade (4.77% vs. 0.55%, p < 0.001), high grade (2.49% vs. 0.37%, p < 0.001), and grade 5 pneumonitis (1.00% vs. 0.18%, p < 0.001). Multivariate analyses demonstrated higher odds of pneumonitis in Japanese studies for all-grade (odds ratio [OR]: 5.04; 95% p < 0.001), high-grade (OR: 4.45; 95% p < 0.001), and grade 5 pneumonitis (OR: 4.55; 95% CI:2.20-9.44, p < 0.001) compared to others, after adjusting for types of EGFR-TKI and lines of therapy. In patients with EGFR retreatment analyzed separately, the pooled incidence was 1.13% (95% CI:0.40-3.15%) for all-grade, 0.49% (95% CI:0.21-1.11%) for high-grade, and 0.16% (95% CI:0.04-0.65%) for grade 5 pneumonitis. Conclusions: The overall incidence of EGFR-TKI pneumonitis was 1.12% in patients without prior exposure to EGFR-TKI, and 1.13% in EGFR-TKI retreatment group. The cohorts from Japan had significantly higher incidence of pneumonitis, providing insights for further mechanistic studies.
引用
收藏
页码:60 / 69
页数:10
相关论文
共 169 条
[1]   A randomized phase II study comparing erlotinib versus erlotinib with alternating chemotherapy in relapsed non-small-cell lung cancer patients: the NVALT-10 study† [J].
Aerts, J. G. ;
Codrington, H. ;
Lankheet, N. A. G. ;
Burgers, S. ;
Biesma, B. ;
Dingemans, A. -M. C. ;
Vincent, A. D. ;
Dalesio, O. ;
Groen, H. J. M. ;
Smit, E. F. .
ANNALS OF ONCOLOGY, 2013, 24 (11) :2860-2865
[2]   Phase II Study of Afatinib as Third-Line Treatment for Patients in Korea With Stage IIIB/IV Non-Small Cell Lung Cancer Harboring Wild-Type EGFR [J].
Ahn, Myung-Ju ;
Kim, Sang-We ;
Cho, Byoung-Chul ;
Ahn, Jin Seok ;
Lee, Dae Ho ;
Sun, Jong-Mu ;
Massey, Dan ;
Kim, Miyoung ;
Shi, Yang ;
Park, Keunchil .
ONCOLOGIST, 2014, 19 (07) :702-703
[3]   A Phase II Study of Erlotinib as Initial Treatment for Patients with Stage IIIB-IV Non-small Cell Lung Cancer [J].
Akerley, Wallace ;
Boucher, Kenneth M. ;
Bentz, Joel S. ;
Arbogast, Kylee ;
Walters, Theodore .
JOURNAL OF THORACIC ONCOLOGY, 2009, 4 (02) :214-219
[4]   Predictive factors for interstitial lung disease, antitumor response, and survival in non-small-cell lung cancer patients treated with gefitinib [J].
Ando, M ;
Okamoto, I ;
Yamamoto, N ;
Takeda, K ;
Tamura, K ;
Seto, T ;
Ariyoshi, Y ;
Fukuoka, M .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (16) :2549-2556
[5]   A phase II trial of gefitinib as first-line therapy for advanced non-small cell lung cancer with epidermal growth factor receptor mutations [J].
Asahina, H. ;
Yamazaki, K. ;
Kinoshita, I. ;
Sukoh, N. ;
Harada, M. ;
Yokouchi, H. ;
Ishida, T. ;
Ogura, S. ;
Kojima, T. ;
Okamoto, Y. ;
Fujita, Y. ;
Dosaka-Akita, H. ;
Isobe, H. ;
Nishimura, M. .
BRITISH JOURNAL OF CANCER, 2006, 95 (08) :998-1004
[6]   Phase II Study of Gefitinib Readministration in Patients with Advanced Non-Small Cell Lung Cancer and Previous Response to Gefitinib [J].
Asahina, Hajime ;
Oizumi, Satoshi ;
Inoue, Akira ;
Kinoshita, Ichiro ;
Ishida, Takashi ;
Fujita, Yuka ;
Sukoh, Noriaki ;
Harada, Masao ;
Maemondo, Makoto ;
Saijo, Yasuo ;
Dosaka-Akita, Hirotoshi ;
Isobe, Hiroshi ;
Nukiwa, Toshihiro ;
Nishimura, Masaharu .
ONCOLOGY, 2010, 79 (5-6) :423-429
[7]   Gefitinib as First-line Treatment in Elderly Epidermal Growth Factor Receptor-mutated Patients With Advanced Lung Adenocarcinoma: Results of a Nagano Lung Cancer Research Group Study [J].
Asami, Kazuhiro ;
Koizumi, Tomonobu ;
Hirai, Kazuya ;
Ameshima, Shingo ;
Tsukadaira, Akihiro ;
Morozumi, Nobutoshi ;
Morikawa, Akio ;
Atagi, Shinji ;
Kawahara, Masaaki .
CLINICAL LUNG CANCER, 2011, 12 (06) :387-392
[8]   Nested Case Control Study of Proteomic Biomarkers for Interstitial Lung Disease in Japanese Patients With Non-Small-Cell Lung Cancer Treated With Erlotinib: A Multicenter Phase IV Study (JO21661) [J].
Atagi, Shinji ;
Katakami, Nobuyuki ;
Yoshioka, Hiroshige ;
Fukuoka, Masahiro ;
Kudoh, Shoji ;
Ogiwara, Atsushi ;
Imai, Masato ;
Ueda, Masamichi ;
Matsui, Shigeyuki .
CLINICAL LUNG CANCER, 2013, 14 (04) :407-417
[9]   Phase 2 trial of erlotinib with or without PF-3512676 (CPG 7909, a Toll-like receptor 9 agonist) in patients with advanced recurrent EGFR-positive non-small cell lung cancer [J].
Belani, Chandra P. ;
Nemunaitis, John J. ;
Chachoua, Abraham ;
Eisenberg, Peter D. ;
Raez, Luiz E. ;
Cuevas, J. Daniel ;
Mather, Cecile B. ;
Benner, Rebecca J. ;
Meech, Sandra J. .
CANCER BIOLOGY & THERAPY, 2013, 14 (07) :557-563
[10]   Phase II study of everolimus-erlotinib in previously treated patients with advanced non-small-cell lung cancer [J].
Besse, B. ;
Leighl, N. ;
Bennouna, J. ;
Papadimitrakopoulou, V. A. ;
Blais, N. ;
Traynor, A. M. ;
Soria, J. -C. ;
Gogov, S. ;
Miller, N. ;
Jehl, V. ;
Johnson, B. E. .
ANNALS OF ONCOLOGY, 2014, 25 (02) :409-415