Atezolizumab in patients with advanced non -small cell lung cancer and history of asymptomatic, treated brain metastases: Exploratory analyses of the phase III OAK study

被引:136
作者
Gadgeel, Shirish M. [1 ]
Lukas, Rimas, V [2 ]
Goldschmidt, Jerome [3 ]
Conkling, Paul [4 ]
Park, Keunchil [5 ]
Cortinovis, Diego [6 ]
de Marinis, Filippo [7 ]
Rittmeyer, Achim [8 ]
Patel, Jyoti D. [9 ]
von Pawel, Joachim [10 ]
O'Hear, Carol [11 ]
Lai, Catherine [11 ]
Hu, Sylvia [11 ]
Ballinger, Marcus [11 ]
Sandler, Alan [11 ]
Gandhi, Mayank [11 ]
Fehrenbacher, Lou [12 ]
机构
[1] Univ Michigan, 1500 E Med Ctr Dr,7217CC, Ann Arbor, MI 48109 USA
[2] Northwestern Univ, Dept Neurol, 710 N Lake Shore Dr,Abbott Hall 1114, Chicago, IL 60611 USA
[3] Blue Ridge Canc Care, 2600 Res Ctr Dr,Suite A, Blacksburg, VA 24060 USA
[4] Virginia Oncol Associates, 5900 Lake Wright Dr, Norfolk, VA 23502 USA
[5] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med, 81 Invon Ro, Seoul 135710, South Korea
[6] AOU San Gerardo, Med Oncol Unit, Via Pergolesi 33 Monza, I-20141 Lombardia, Italy
[7] IRCCS, IEO, European Inst Oncol, Via Ripamonti 435, I-20141 Milan, Italy
[8] Pneumol Lehrklin Univ Gottingen, Lungenfachklin Immenhausen, Robert Koch Str 3, D-34376 Immenhausen, Germany
[9] Univ Chicago, 5841 S Maryland Ave,MC 2115, Chicago, IL 60637 USA
[10] Asklepios Fachkliniken Munchen Gauting, Gauting, Germany
[11] Genentech Inc, 1 DNA Way, San Francisco, CA 94080 USA
[12] Kaiser Permanente Med Ctr, 975 Sereno Dr, Vallejo, CA 94589 USA
关键词
Atezolizumab; Brain; Central nervous system; Metastasis; Non-small cell lung cancer (5/6); OPEN-LABEL; MULTICENTER; DOCETAXEL; MELANOMA; THERAPY;
D O I
10.1016/j.lungcan.2018.12.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: To assess the safety and efficacy of atezolizumab and docetaxel in patients with and without a history of asymptomatic, treated brain metastases in the phase III OAK trial. Materials and methods: Patients received 1200 mg atezolizumab or 75 mg/m(2) docetaxel every 3 weeks until unacceptable toxicity, disease progression, or loss of clinical atezolizumab benefit. Patients with asymptomatic, treated supratentorial metastases were eligible. Patients had brain scans before enrollment; follow-up brain scans and treatment were required when clinically indicated. Results: Approximately 14% of patients in each arm had a history of asymptomatic, treated brain metastases (61/425 in the atezolizumab arm and 62/425 in the docetaxel arm). Fewer treatment-related adverse events (AEs), serious AEs, and treatment-related neurologic AEs were reported with atezolizumab than with docetaxel, regardless of history of asymptomatic, treated brain metastases. In patients with a history of asymptomatic, treated brain metastases, median overall survival (OS) was longer with atezolizumab than with docetaxel (16.0 vs 11.9 months; hazard ratio = 0.74; 95% CI: 0.49-1.13). Median OS was also longer with atezolizumab in patients without a history of asymptomatic, treated brain metastases (13.2 vs 9.3 months; hazard ratio = 0.74; 95% CI: 0.63-0.88). Landmark analyses showed that patients with a history of asymptomatic, treated brain metastases had a lower probability of developing new symptomatic brain lesions with atezolizumab vs docetaxel at 6-24 months. Patients without a history had a lower probability with atezolizumab at 18-24 + months. Conclusion: Atezolizumab had an acceptable neurologic safety profile, showed a trend toward an OS benefit, and led to a prolonged time to radiographic identification of new symptomatic brain lesions compared with docetaxel in patients who had a history of asymptomatic, treated brain metastases. Clinicaltrials.gov registration number: NCT02008227.
引用
收藏
页码:105 / 112
页数:8
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