Real-world treatment patterns of metastatic non-small cell lung cancer patients receiving epidermal growth factor receptor tyrosine kinase inhibitors

被引:13
作者
Shenolikar, Rahul [1 ]
Liu, Sizhu [1 ]
Shah, Anne [1 ]
Tse, Jenny
Cao, Yao
Near, Aimee
机构
[1] AstraZeneca, Gaithersburg, MD USA
关键词
metastasis; non-small cell lung cancer; target therapy; tyrosine kinase inhibitors; 1ST-LINE TREATMENT; OPEN-LABEL; CHEMOTHERAPY; ERLOTINIB; AFATINIB; MULTICENTER; MUTATIONS; GEFITINIB;
D O I
10.1002/cam4.4918
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Several epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKI) have been approved for first-line (1L) treatment of EGFR-mutated metastatic non-small cell lung cancer (mNSCLC) in the United States (US). Real-world analyses of 1L treatment patterns with EGFR TKIs, including the third-generation EGFR TKI osimertinib which was most recently approved in 2018, are still sparse. Methods This retrospective observational study used data from IQVIA's prescription claims (LRx) and medical claims (Dx) databases. mNSCLC patients newly treated with any EGFR TKI in the 1L setting were identified from January 1, 2015 to April 30, 2020; the first date of EGFR TKI (third-generation osimertinib, first-generation [erlotinib, gefitinib], or second-generation [afatinib, dacomitinib]) was the index date. Treatment patterns were reported in the cohorts stratified by 1L EGFR TKI. Results A total of 2505 patients were included in the study (982 osimertinib, 1060 first-generation, and 463 second-generation EGFR TKI). Beginning in 2018, osimertinib became the most common 1L EGFR TKI (66.7%) and in early 2020, it accounted for 90.6% of 1L EGFR TKIs. Nearly all patients (>97%) were treated with 1L EGFR TKI monotherapy. Patients with 1L osimertinib had longer treatment duration compared to patients with 1L first- or second-generation EGFR TKI (median months: 17.8 vs. 8.7 vs. 10.5, respectively; log-rank test for comparisons with osimertinib p < 0.0001) over median follow-up times of 9.8, 20.5, and 19.3 months. 32.5% and 36.3% of the first- and second-generation EGFR TKI cohorts, respectively, had evidence of 2L treatment. Osimertinib monotherapy accounted for the majority of 2L treatments (58.3%/60.7%) and 11.3%/8.9% had 2L chemotherapy or immuno-oncology therapy following 1L first- or second-generation EGFR TKI. Conclusion In this real-world study of a US claims database, 1L treatment duration was longer with osimertinib compared with other EGFR TKIs. Future studies with longer follow-up are recommended to understand treatment patterns after progression on EGFR TKIs.
引用
收藏
页码:159 / 169
页数:11
相关论文
共 38 条
[1]  
[Anonymous], 2021, REF PERM NCCN CLIN P
[2]   Measures of follow-up in time-to-event studies: Why provide them and what should they be? [J].
Betensky, Rebecca A. .
CLINICAL TRIALS, 2015, 12 (04) :403-408
[3]   Analysis of time-to-treatment discontinuation of targeted therapy, immunotherapy, and chemotherapy in clinical trials of patients with non-small-cell lung cancer [J].
Blumenthal, G. M. ;
Gong, Y. ;
Kehl, K. ;
Mishra-Kalyani, P. ;
Goldberg, K. B. ;
Khozin, S. ;
Kluetz, P. G. ;
Oxnard, G. R. ;
Pazdur, R. .
ANNALS OF ONCOLOGY, 2019, 30 (05) :830-838
[4]   EGFR mutation testing and treatment decisions in patients progressing on first- or second-generation epidermal growth factor receptor tyrosine kinase inhibitors [J].
Chiang, Anne C. ;
Fernandes, Ancilla W. ;
Pavilack, Melissa ;
Wu, Jennifer W. ;
Laliberte, Francois ;
Duh, Mei Sheng ;
Chehab, Nabil ;
Subramanian, Janakiraman .
BMC CANCER, 2020, 20 (01)
[5]   Preclinical Comparison of the Blood-brain barrier Permeability of Osimertinib with Other EGFR TKIs [J].
Colclough, Nicola ;
Chen, Kan ;
Johnstrom, Peter ;
Strittmatter, Nicole ;
Yan, Yumei ;
Wrigley, Gail L. ;
Schou, Magnus ;
Goodwin, Richard ;
Varnas, Katarina ;
Adua, Sally J. ;
Zhao, Minghui ;
Nguyen, Don X. ;
Maglennon, Gareth ;
Barton, Peter ;
Atkinson, James ;
Zhang, Lin ;
Janefeldt, Annika ;
Wilson, Joanne ;
Smith, Aaron ;
Takano, Akihiro ;
Arakawa, Ryosuke ;
Kondrashov, Mikhail ;
Malmquist, Jonas ;
Revunov, Evgeny ;
Vazquez-Romero, Ana ;
Moein, Mohammad Mahdi ;
Windhorst, Albert D. ;
Karp, Natasha A. ;
Finlay, M. Raymond, V ;
Ward, Richard A. ;
Yates, James W. T. ;
Smith, Paul D. ;
Farde, Lars ;
Cheng, Zack ;
Cross, Darren A. E. .
CLINICAL CANCER RESEARCH, 2021, 27 (01) :189-201
[6]   Chemotherapy and Survival Benefit in Elderly Patients With Advanced Non-Small-Cell Lung Cancer [J].
Davidoff, Amy J. ;
Tang, Mei ;
Seal, Brian ;
Edelman, Martin J. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (13) :2191-2197
[7]  
FDA, 2018, FDA APPR DAC MET NON
[8]  
Food and Drug Administration, 2018, FDA APPR OS 1 LIN TR
[9]   Phase III study comparing bevacizumab plus erlotinib to erlotinib in patients with untreated NSCLC harboring activating EGFR mutations: NEJ026. [J].
Furuya, Naoki ;
Fukuhara, Tatsuro ;
Saito, Haruhiro ;
Watanabe, Kana ;
Sugawara, Shunichi ;
Iwasawa, Shunichiro ;
Tsunezuka, Yoshio ;
Yamaguchi, Ou ;
Okada, Morihito ;
Yoshimori, Kouzou ;
Nakachi, Ichiro ;
Gemma, Akihiko ;
Azuma, Koichi ;
Hagiwara, Koichi ;
Nukiwa, Toshihiro ;
Morita, Satoshi ;
Kobayashi, Kunihiko ;
Maemondo, Makoto .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
[10]   Factors Associated with Adherence to and Treatment Duration of Erlotinib Among Patients with Non-Small Cell Lung Cancer [J].
Hess, Lisa M. ;
Louder, Anthony ;
Winfree, Katherine ;
Zhu, Yajun E. ;
Oton, Ana B. ;
Nair, Radhika .
JOURNAL OF MANAGED CARE & SPECIALTY PHARMACY, 2017, 23 (06) :643-652