Taiwan Nationwide Study of First-Line ALK-TKI Therapy in ALK-Positive Lung Adenocarcinoma

被引:0
作者
Zheng, Zhe-Rong [1 ,2 ,3 ]
Wu, Jia-Jun [1 ,2 ,3 ]
Chiang, Chun-Ju [4 ,5 ]
Chen, Tzu-, I [6 ,7 ,8 ]
Chen, Kun-Chieh [1 ,2 ,3 ]
Chu, Cheng-Hsiang [1 ,2 ,3 ]
Lin, Sheng-Yi [9 ]
Yu, Sung-Liang [10 ,11 ]
Lee, Wen-Chung [4 ,5 ,12 ]
Liu, Tsang-Wu [13 ]
Chang, Gee-Chen [1 ,2 ,3 ,14 ]
机构
[1] Chung Shan Med Univ, Inst Med, 110,Sect 1,Jianguo N Rd, Taichung 402, Taiwan
[2] Chung Shan Med Univ, Sch Med, Taichung, Taiwan
[3] Chung Shan Med Univ Hosp, Dept Internal Med, Div Pulm Med, 110,Sect 1,Jianguo N Rd, Taichung 402, Taiwan
[4] Natl Taiwan Univ, Inst Epidemiol & Prevent Med, Coll Publ Hlth, 17,Xu Zhou Rd, Taipei 100, Taiwan
[5] Taiwan Canc Registry, Taipei, Taiwan
[6] Fu Jen Catholic Univ, Coll Med, Sch Med, Zhongzheng Rd,242062, New Taipei City 510, Taiwan
[7] Natl Inst Canc Res, Natl Hlth Res Inst, Tainan, Taiwan
[8] Asia Univ, Dept Healthcare Adm, Taichung, Taiwan
[9] Chung Shan Med Univ, Coll Med, Sch Med, Dept Anat, 110,Sect 1,Jianguo N Rd, Taichung 402, Taiwan
[10] Natl Taiwan Univ, Coll Med, Dept Clin Lab Sci & Med Biotechnol, 1,Changde St, Taipei 10048, Taiwan
[11] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei, Taiwan
[12] Natl Taiwan Univ, Inst Hlth Data Analyt & Stat, Coll Publ Hlth, Taipei, Taiwan
[13] Natl Inst Canc Res, Natl Hlth Res Inst, 35,Keyan Rd, Miaoli Cty 35053, Taiwan
[14] Natl Chung Hsing Univ, Inst Biomed Sci, Taichung, Taiwan
关键词
OPEN-LABEL; CANCER; CRIZOTINIB; SURVIVAL; LORLATINIB; SMOKING; CHEMOTHERAPY; INHIBITORS; MUTATIONS; ALECTINIB;
D O I
10.1007/s11523-024-01104-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The clinical outcomes of patients with anaplastic lymphoma kinase-positive (ALK+) advanced lung adenocarcinoma vary according to real-world data. Objective: In this study, we aimed to investigate the treatment discontinuation (TTD) and overall survival (OS) of patients with ALK+ advanced lung adenocarcinoma treated with first-line ALK-TKIs in Taiwan. Patients and methods: This retrospective study evaluated all advanced lung adenocarcinoma patients registered in the National Taiwan Cancer Registry from 2017 to 2020 who had ALK rearrangement and received ALK-TKI treatment, using data from Taiwan's National Health Insurance Research Database (NHIRD). The TKI treatment sequences were classified into first generation (G1: crizotinib), second generation (G2: ceritinib, alectinib, brigatinib), and third generation (G3: lorlatinib). Results: A total of 587 patients were analyzed, with a median age of 60.0 years, 91 (15.5%) aged >= 74 years, 293 (49.9%) female, 397 (67.6%) never smoked, and 534 (91.0%) with stage IV disease. Patients who received next-generation ALK-TKIs during the treatment course had longer median time to ALK-TKI TTD and OS. The TTD of the G1, G1+2, G1+2+3, G2, and G2+3 groups was 7.5 (5.4-11.1), 40.6 (29.4-not calculated (NC)), 50.3 (41.3-NC), 34.3 (29.2-43.0), and 36.3 (22.4-NC) months, respectively (p < 0.001). The median OS of the patients in the G1, G1+2, G1+2+3, G2, and G2+3 groups was 10.6 (7.5-14.6), not reached (NR) (NC-NC), NR (NC-NC), 43.0 (36.3-NC), and NR (30.3-NC) months, respectively (p < 0.001). Compared with treatment with crizotinib alone, the multivariate analysis revealed that treatment with next-generation TKIs was independently associated with longer TTD (G1+2 (hazard ratio (HR), 0.24; 95% CI 0.17-0.33; p < 0.001), G1+2+3 or G1+3 (HR, 0.17; 95% confidence interval (CI), 0.10-0.28; p < 0.001), G2 (HR, 0.26; 95% CI 0.19-0.36; p < 0.001), and G2+3 (HR, 0.25; 95% CI 0.14-0.44; p < 0.001)) and median OS (G12 (HR, 0.24; 95% CI 0.17-0.35; p < 0.001), G1+2+3 or G1+3 (HR, 0.09; 95% CI 0.04-0.21; p < 0.001), G2 (HR, 0.22; 95% CI 0.15-0.31; p < 0.001), and G2+3 (HR, 0.20; 95% CI 0.10-0.42; p < 0.001)). Conclusions: For patients with ALK+ NSCLC, treatments including next-generation ALK-TKIs were independently associated with longer survival outcomes.
引用
收藏
页码:941 / 955
页数:15
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