Clinical outcomes of Atezolizumab Therapy for Previously-Treated Advanced-Stage Non-Small Cell Lung Cancer: A Real-World Study in Taiwan

被引:1
|
作者
Wu, Shang -Gin [1 ,2 ]
Chiang, Chi-Lu [3 ,4 ,5 ]
Wang, Chin -Chou [6 ]
Hung, Jen-Yu [7 ,8 ,9 ]
Hsia, Te-Chun [10 ,11 ]
Kuo, Chih-Hsi [12 ]
Shih, Jin-Yuan [1 ]
机构
[1] Natl Taiwan Univ, Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[2] Natl Taiwan Univ, Canc Ctr, Dept Internal Med, Taipei, Taiwan
[3] Taipei Vet Gen Hosp, Dept Chest Med, Taipei, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Sch Med, Taipei, Taiwan
[5] Natl Yang Ming Chiao Tung Univ, Inst Clin Med, Taipei, Taiwan
[6] Chang Gung Univ, Chang Gung Mem Hosp, Kaohsiung Med Ctr, Dept Med,Coll Med,Div Pulm & Critical Care Med, Kaohsiung, Taiwan
[7] Kaohsiung Med Univ, Kaohsiung Municipal Ta Tung Hosp, Dept Internal Med, Kaohsiung, Taiwan
[8] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Internal Med, Div Pulm & Crit Care Med, Kaohsiung, Taiwan
[9] Kaohsiung Med Univ, Coll Med, Fac Med, Kaohsiung, Taiwan
[10] China Med Univ, Dept Internal Med, Div Pulm & Crit Care Med, Taichung, Taiwan
[11] China Med Univ Hosp, Taichung, Taiwan
[12] Chang Gung Univ, Chang Gung Mem Hosp, Dept Thorac Med, Coll Med,Div Lung Canc & Intervent Bronchoscopy, Taipei, Taiwan
来源
JOURNAL OF CANCER | 2022年 / 13卷 / 09期
关键词
Atezolizumab; Epidermal growth factor receptor mutation; Non-small-cell lung cancer; Tyrosine kinase inhibitor; Osimertinib; Immune checkpoint inhibitor; TO-LYMPHOCYTE RATIO; NSCLC; IMMUNOTHERAPY; ASSOCIATION; COMBINATION; DURVALUMAB; GEFITINIB; DOCETAXEL; NIVOLUMAB; EFFICACY;
D O I
10.7150/jca.74617
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immune checkpoint inhibitors (ICIs) are the standard treatment for non-small-cell lung cancer (NSCLC). We assessed the clinical prognostic factors in NSCLC patients receiving atezolizumab as a second- or later-line (2L+) treatment. Data were retrospectively collected for NSCLC patients treated with atezolizumab from July 2017 to June 2019 at six medical centers in Taiwan. Clinical characteristics, treatment course and responses of patients were recorded. A total of 128 NSCLC patients received 2L+ atezolizumab, and the outcomes included a response rate of 10.2%, median progression-free survival (mPFS) of 3.5 months, and median overall survival (mOS) of 10.7 months. Eleven patients who had received osimertinib treatment before atezolizumab had a shorter mPFS (2.3 versus 3.5 months; p = 0.002) and mOS (4.8 versus 11.2 months; p < 0.001) than those without prior osimertinib treatment. Even for the subgroup of patients with EGFR-mutant non-squamous NSCLC, prior osimertinib was still associated with shorter PFS (2.3 versus 4.1 months; p = 0.006) and OS (4.8 versus 11.7 months; p < 0.001). Multivariate analysis revealed that prior osimertinib treatment correlated with not only shorter PFS (hazard ratio [HR]: 2.94; 95% confidence interval [CI], 1.34-6.47; p = 0.007) but also shorter OS (HR, 3.55; 95% CI, 1.57???8.03; p = 0.002). Patients with prior ICIs treatment (HR, 3.18; p = 0.002) or poor performance status (HR, 2.70; p = 0.001) had shorter OS. In conclusion, osimertinib treatment before atezolizumab therapy was associated with a shorter PFS and a poor prognosis in NSCLC patients in real-world settings. Further studies with larger sample sizes are needed to validate these observations.
引用
收藏
页码:2922 / 2932
页数:11
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