Nivolumab in routine practice for older patients with advanced or metastatic non-small cell lung cancer

被引:18
|
作者
Sabatier, Renaud [1 ,2 ]
Nicolas, Emanuel [1 ,2 ]
Paciencia, Maria [3 ]
Jonville-Bera, Annie-Pierre [4 ]
Madroszyk, Anne [1 ]
Cecile, Maud [1 ]
Braticevic, Cecile [1 ]
Duran, Segolene [5 ]
Tassy, Louis [1 ]
Rouby, Franck [6 ,7 ]
Micallef, Joelle [6 ,7 ]
Rousseau, Frederique [1 ]
机构
[1] Inst Paoli Calmettes, Dept Med Oncol, 232 Bd St Marguerite, F-13009 Marseille, France
[2] Aix Marseille Univ, Inst Paoli Calmettes, INSERM, CNRS,U7258,U1068,CRCM, F-13009 Marseille, France
[3] Inst Paoli Calmettes, Dept Biopathol, F-13009 Marseille, France
[4] CHRU, Dept Clin Pharmacol, Reg Ctr Pharmacovigilance, Tours, France
[5] Inst Paoli Calmettes, Dept Pharm, Pharmacovigilance Unit, F-13009 Marseille, France
[6] Assistance Publ Hop Marseille, Dept Clin Pharmacol, Reg Ctr Pharmacovigilance Marseille Provence Cors, Marseille, France
[7] Aix Marseille Univ, Neurosci Inst, CNRS, UMR 7289, Marseille, France
关键词
Metastatic non-small cell lung cancer; Nivolumab; Older patients; Safety; Pharmacovigilance; QUALITY-OF-LIFE; ELDERLY-PATIENTS; COST-EFFECTIVENESS; OPEN-LABEL; DOCETAXEL; CHEMOTHERAPY; PEMBROLIZUMAB; NSCLC; IMMUNOTHERAPY; EPIDEMIOLOGY;
D O I
10.1016/j.jgo.2018.02.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Nivolumab is approved worldwide as second-line treatment for metastatic non-small cell lung cancer (NSCLC). Despite the fact that most of these cancers are being diagnosed in the older patients, few of the patients were included in pivotal trials. We aimed to describe efficacy and safety in a "real-world" older population. Patients and Methods: We retrospectively collected data from older patients (>= 70 years old) with advanced or metastatic NSCLC treated with Nivolumab in our institution. We analyzed safety (CTCAE v4.0 criteria), efficacy (clinical benefit rate, progression-free survival, and overall survival), and correlated these features to geriatric parameters and PD-L1 expression. Along with this cohort, we assessed safety at a national level by retrieving all cases of Nivolumab (prescribed for NSCLC) induced adverse events analyzed by the French pharmacovigilance network during the inclusion period. Results: From July 2015 to September 2016, 30 patients were enrolled with a median age of 752. Clinical benefit rate was 30.6%. Median progression-free survival and overall survival were 33 and 7.1 months, respectively. Fifteen patients (50%) presented an immune-related adverse event (IrAE) of any grade, including four high grade IrAEs. Two hundred and eighty IrAEs had been notified to the French pharmacovigilance network including 91 (35.2%) concerning older patients. Frequency and pattern of IrAEs were similar for older patients and younger subjects. Conclusions: Even though frequency and patterns of IrAEs are different from pivotal studies, these results don't seem specific to older patients. Further prospective investigations are needed to better characterize and predict the impact of Nivolumab on older patients with NSCLC. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:494 / 500
页数:7
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