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Phase II Trial of Carboplatin and Pemetrexed Plus Bevacizumab with Maintenance Bevacizumab as a First-line Treatment for Advanced Non-squamous Non-small Cell Lung Cancer in Elderly Patients
被引:8
|作者:
Takeoka, Hiroaki
[1
]
Yamada, Kazuhiko
[2
]
Naito, Yoshiko
[2
]
Matsuo, Norikazu
[2
]
Ishii, Hidenobu
[2
]
Tokito, Takaaki
[2
]
Azuma, Koichi
[2
]
Ichiki, Masao
[1
]
Hoshino, Tomoaki
[2
]
机构:
[1] Natl Hosp Org, Kyushu Med Ctr, Clin Res Inst, Dept Resp Med, Fukuoka, Fukuoka, Japan
[2] Kurume Univ, Dept Internal Med, Sch Med, Div Respirol Neurol & Rheumatol, 67 Asahi Machi, Kurume, Fukuoka 8300011, Japan
关键词:
Carboplatin;
pemetrexed;
bevacizumab;
elderly;
NSCLC;
THERAPY;
PACLITAXEL;
CISPLATIN;
VINORELBINE;
PARAMOUNT;
EFFICACY;
PLACEBO;
SAFETY;
AVAIL;
D O I:
10.21873/anticanres.12661
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background/Aim: The combination of platinumdoublet chemotherapy with bevacizumab has been established as a first-line treatment option in non-elderly patients with non-squamous (non-sq) non-small cell lung cancer (NSCLC). However, the safety and efficacy of this regimen have not yet been fully established in elderly patients. Patients and Methods: Chemo-naive patients with non-sq NSCLC, aged >= 75 years, having a good performance status (Eastern Cooperative Oncology Group performance status 0-1) and adequate organ function were considered eligible. Patients received carboplatin (area under the curve=5 mg/ml/min), pemetrexed (500 mg/m(2)), and bevacizumab (15 mg/kg) every 3 weeks for up to 4 cycles, followed by maintenance bevacizumab. The primary endpoint was the objective response rate (ORR; target=50%, threshold=30%; Simon's two-stage design), and the secondary endpoints were safety, progression free survival (PFS), and overall survival (OS). Results: Twelve patients were enrolled from June 2013 to July 2017. The study was closed because of slow patient accrual. The median patient age was 80 years. Eleven patients (92%) completed 4 cycles of induction chemotherapy. Seven patients achieved a partial response (PR), yielding an ORR of 58%. The median PFS was 8.4 [95% confidence interval (CI)=4.4-10.5] months, and the median OS was 33.9 (95%CI=13.2-43.3) months. Toxicities were generally mild and consistent with previous reports. There were no treatment-related deaths. Conclusion: A regimen comprising carboplatin and pemetrexed plus bevacizumab followed by maintenance bevacizumab is feasible and potentially efficacious in elderly patients with non-sq NSCLC.
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页码:3779 / 3784
页数:6
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