Treatment patterns, testing practices, and outcomes in the pre-FLAURA era for patients with EGFR mutation-positive advanced NSCLC: a retrospective chart review (REFLECT)

被引:6
作者
Addeo, Alfredo [2 ]
Hochmair, Maximilian [1 ]
Janzic, Urska [3 ]
Dudnik, Elizabeth [4 ]
Charpidou, Andriani [5 ]
Pluzannski, Adam [6 ]
Ciuleanu, Tudor [7 ,8 ]
Donev, Ivan Shterev [9 ]
Elbaz, Judith [10 ]
Aaroe, Jorgen [11 ]
Ott, Rene [12 ]
Peled, Nir [13 ,14 ]
机构
[1] Karl Landsteiner Inst Lung Res & Pulm Oncol, Dept Resp & Crit Care Med, Klin Floridsdorf, Brunner Str 68, A-1210 Vienna, Austria
[2] Geneva Univ Hosp, Med Oncol, Geneva, Switzerland
[3] Univ Clin Resp & Allerg Dis Golnik, Med Oncol Dept, Golnik, Slovenia
[4] Rabin Med Ctr, Clalit Hlth Serv, Davidoff Canc Ctr, Petah Tiqwa, Israel
[5] Natl & Kapodistrian Univ Athens, Dept Internal Med 3, Oncol Unit, Athens, Greece
[6] Maria Sklodowska Curie Natl Res Inst Oncol, Dept Lung Canc & Chest Tumors, Warsaw, Poland
[7] Prof Dr Ion Chiricuta Oncol Inst, Med Oncol Dept, Cluj Napoca, Romania
[8] Iuliu Hatieganu Univ Med & Pharm, Cluj Napoca, Romania
[9] MHAT Nadezhda, Dept Med Oncol, Sofia, Bulgaria
[10] AstraZeneca Israel, Oncol, Hod Hasharon, Israel
[11] AstraZeneca Nordic, Oncol, Oslo, Norway
[12] AstraZeneca AG, OBU Europe, Zug, Switzerland
[13] Soroka Canc Ctr, Beer Sheva, Israel
[14] Hebrew Univ Jerusalem, Shaare Zedek Canc Ctr, Jerusalem, Israel
关键词
attrition; EGFR T790M testing; EGFR-TKI; NSCLC; real-world evidence; CELL LUNG-CANCER; TYROSINE KINASE INHIBITOR; ACQUIRED-RESISTANCE; T790M MUTATION; OPEN-LABEL; PHASE-III; MULTICENTER; OSIMERTINIB; TKI; ADENOCARCINOMA;
D O I
10.1177/17588359211059874
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: For epidermal growth factor receptor mutation-positive (EGFRm) non-small-cell lung cancer (NSCLC), EGFR-tyrosine kinase inhibitors (EGFR-TKIs) are the preferred first-line (1 L) treatment in the advanced setting. Osimertinib, a third-generation EGFR-TKI, received full approval in 2017 for second-line (2 L) treatment of EGFR T790M-positive NSCLC. The REFLECT study characterizes real-world treatment/testing patterns, attrition rates, and outcomes in patients with EGFRm advanced NSCLC treated with 1 L first-/second-generation (1G/2G) EGFR-TKIs before 1 L osimertinib approval. Methods: Retrospective chart review (NCT04031898) of European/Israeli adults with EGFRm unresectable locally advanced/metastatic NSCLC, initiating 1 L 1G/2G EGFR-TKIs 01/01/15-30/06/18 (index date). Results: In 896 patients (median follow-up of 21.5 months), the most frequently initiated 1 L EGFR-TKI was afatinib (45%). Disease progression was reported in 81%, including 10% (86/896) who died at 1 L. By the end of study, most patients discontinued 1 L (85%), of whom 33% did not receive 2 L therapy. From index, median 1 L real-world progression-free survival was 13.0 (95% confidence interval (CI): 12.3-14.1) months; median overall survival (OS) was 26.2 (95% CI: 23.6-28.4) months. 71% of patients with 1 L progression were tested for T790M; 58% were positive. Of those with T790M, 95% received osimertinib in 2 L or later. Central nervous system (CNS) metastases were recorded in 22% at index, and 15% developed CNS metastases during treatment (median time from index 13.5 months). Median OS was 19.4 months (95% CI: 17.1-22.1) in patients with CNS metastases at index, 24.8 months (95% CIs not available) with CNS metastases diagnosed during treatment, and 30.3 months (95% CI: 27.1, 33.8) with no CNS metastases recorded. Conclusion: REFLECT is a large real-world study describing treatment patterns prior to 1 L osimertinib availability for EGFRm advanced NSCLC. Given the attrition rates highlighted in the study and the impact of CNS progression on outcomes, offering a 1 L EGFR-TKI with CNS penetration may improve patient outcomes in this treatment setting.
引用
收藏
页数:11
相关论文
共 35 条
[1]  
Akamatsu H, 2017, ANN ONCOL, V28, P128
[2]   Rebiopsy of Lung Cancer Patients with Acquired Resistance to EGFR Inhibitors and Enhanced Detection of the T790M Mutation Using a Locked Nucleic Acid-Based Assay [J].
Arcila, Maria E. ;
Oxnard, Geoffrey R. ;
Nafa, Khedoudja ;
Riely, Gregory J. ;
Solomon, Stephen B. ;
Zakowski, Maureen F. ;
Kris, Mark G. ;
Pao, William ;
Miller, Vincent A. ;
Ladanyi, Marc .
CLINICAL CANCER RESEARCH, 2011, 17 (05) :1169-1180
[3]   Postoperative stereotactic radiosurgery compared with whole brain radiotherapy for resected metastatic brain disease (NCCTG N107C/CEC.3): a multicentre, randomised, controlled, phase 3 trial [J].
Brown, Paul D. ;
Ballman, Karla V. ;
Cerhan, Jane H. ;
Anderson, S. Keith ;
Carrero, Xiomara W. ;
Whitton, Anthony C. ;
Greenspoon, Jeffrey ;
Parney, Ian F. ;
Laack, Nadia N. I. ;
Ashman, Jonathan B. ;
Bahary, Jean-Paul ;
Hadjipanayis, Costas G. ;
Urbanic, James J. ;
Barker, Fred G., II ;
Farace, Elana ;
Khuntia, Deepak ;
Giannini, Caterina ;
Buckner, Jan C. ;
Galanis, Evanthia ;
Roberge, David .
LANCET ONCOLOGY, 2017, 18 (08) :1049-1060
[4]   Real-world EGFR testing in patients with stage IIIB/IV non-small-cell lung cancer in North China: A multicenter, non-interventional study [J].
Cheng, Ying ;
Wang, Yan ;
Zhao, Jun ;
Liu, Yunpeng ;
Gao, Hongjun ;
Ma, Kewei ;
Zhang, Shucai ;
Xin, Hua ;
Liu, Jiwei ;
Han, Chengbo ;
Zhu, Zhitu ;
Wang, Yan ;
Chen, Jun ;
Wen, Fugang ;
Li, Junling ;
Zhang, Jie ;
Zheng, Zhendong ;
Dai, Zhaoxia ;
Piao, Hongmei ;
Li, Xiaoling ;
Li, Yinyin ;
Zhong, Min ;
Ma, Rui ;
Zhuang, Yongzhi ;
Xu, Yuqing ;
Qu, Zhuohui ;
Yang, Haibo ;
Pan, Chunxia ;
Yang, Fan ;
Zhang, Daxin ;
Li, Bing .
THORACIC CANCER, 2018, 9 (11) :1461-1469
[5]   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)
[6]  
Colclough N., CLIN CANCER RES, V2020, P189
[7]   AZD9291, an Irreversible EGFR TKI, Overcomes T790M-Mediated Resistance to EGFR Inhibitors in Lung Cancer [J].
Cross, Darren A. E. ;
Ashton, Susan E. ;
Ghiorghiu, Serban ;
Eberlein, Cath ;
Nebhan, Caroline A. ;
Spitzler, Paula J. ;
Orme, Jonathon P. ;
Finlay, M. Raymond V. ;
Ward, Richard A. ;
Mellor, Martine J. ;
Hughes, Gareth ;
Rahi, Amar ;
Jacobs, Vivien N. ;
Brewer, Monica Red ;
Ichihara, Eiki ;
Sun, Jing ;
Jin, Hailing ;
Ballard, Peter ;
Al-Kadhimi, Katherine ;
Rowlinson, Rachel ;
Klinowska, Teresa ;
Richmond, Graham H. P. ;
Cantarini, Mireille ;
Kim, Dong-Wan ;
Ranson, Malcolm R. ;
Pao, William .
CANCER DISCOVERY, 2014, 4 (09) :1046-1061
[8]   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 [J].
Garg, Avneet ;
Batra, Ullas ;
Choudhary, Priyanshu ;
Jain, Deepali ;
Khurana, Sachin ;
Malik, Prabhat S. ;
Muthu, Valliappan ;
Prasad, K. T. ;
Singh, Navneet ;
Suri, Tejas ;
Mohan, Anant .
CURRENT PROBLEMS IN CANCER, 2020, 44 (03)
[9]   Therapy for Stage IV Non-Small-Cell Lung Cancer With Driver Alterations: ASCO and OH (CCO) Joint Guideline Update [J].
Hanna, Nasser H. ;
Robinson, Andrew G. ;
Temin, Sarah ;
Baker, Sherman, Jr. ;
Brahmer, Julie R. ;
Ellis, Peter M. ;
Gaspar, Laurie E. ;
Haddad, Rami Y. ;
Hesketh, Paul J. ;
Jain, Dharamvir ;
Jaiyesimi, Ishmael ;
Johnson, David H. ;
Leighl, Natasha B. ;
Moffitt, Pamela R. ;
Phillips, Tanyanika ;
Riely, Gregory J. ;
Rosell, Rafael ;
Schiller, Joan H. ;
Schneider, Bryan J. ;
Singh, Navneet ;
Spigel, David R. ;
Tashbar, Joan ;
Masters, Gregory .
JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (09) :1040-1091
[10]  
Isobe H, 2017, LUNG CANCER-TARGETS, V8, P191, DOI 10.2147/LCTT.S140491