Phase II study of cisplatin/pemetrexed combined with bevacizumab followed by pemetrexed/bevacizumab maintenance therapy in patients with EGFR-wild advanced non-squamous non-small cell lung cancer

被引:8
|
作者
Fukushima, Toshirou [1 ]
Wakatsuki, Yuuki [1 ]
Kobayashi, Takashi [1 ]
Sonehara, Kei [2 ]
Tateishi, Kazunari [2 ]
Yamamoto, Manabu [3 ]
Masubuchi, Takeshi [3 ]
Yoshiike, Fumiaki [4 ]
Hirai, Kazuya [4 ]
Hachiya, Tsutomu [5 ]
Koizumi, Tomonobu [1 ]
机构
[1] Shinshu Univ, Sch Med, Dept Comprehens Canc Therapy, 3-1-1 Asahi Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Sch Med, Dept Internal Med 1, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan
[3] Nagano Red Cross Hosp, Dept Pulm Dis, Nagano, Japan
[4] Nagano Municipal Hosp, Dept Pulm Dis, Nagano, Japan
[5] Suwa Red Cross Hosp, Dept Pulm Dis, Suwa, Japan
关键词
Anti-VEGF agent; EGFR-wild type; Non-small cell lung cancer; Continuation maintenance; CISPLATIN PLUS GEMCITABINE; THYMIDYLATE SYNTHASE EXPRESSION; CARBOPLATIN-PACLITAXEL; CHEMOTHERAPY; PLACEBO; BRAIN; TRIAL; INDUCTION; JAPAN;
D O I
10.1007/s00280-018-3573-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This phase II study was performed to evaluate the efficacy and safety of cisplatin/pemetrexed combined with 15 mg/kg of bevacizumab followed by pemetrexed/bevacizumab maintenance therapy as first-line chemotherapy in advanced non-squamous non-small cell lung cancer (NSCLC) limited to epidermal growth factor receptor (EGFR)-wild type. Fifty patients with advanced or metastatic EGFR-wild type NSCLC aged < 75 years old were enrolled in the study. The patients were treated with four cycles of cisplatin (75 mg/m(2), day 1), pemetrexed (500 mg/m(2), days 1), and bevacizumab (15 mg/kg, day 1), every 3 weeks, followed by pemetrexed plus bevacizumab maintenance until progression for achieving a response over stable disease after induction chemotherapy. Partial response and stable disease were observed in 35 (objective response rate: 70, 95% CI: 55.4-82.1%) and 9 patients, respectively, and 39 (78%) patients received pemetrexed plus bevacizumab maintenance therapy. Median progression-free survival and overall survival periods were 12.0 months (95% CI: 7.5-16.5 months) and 31.0 months (95% CI: 22.2-39.8 months), respectively. Grade 3 adverse events included neutropenia (14%), nausea (10%), anorexia (18%), and hypertension (8%). Coagulation disorder was observed in one patient, but all of these events were reversible and resulted in no treatment-related deaths. The combination of cisplatin/pemetrexed/bevacizumab followed by pemetrexed/bevacizumab maintenance therapy exhibited favorable efficacy and manageable toxicity profiles in patients with EGFR-wild type non-squamous NSCLC (UMIN-CTR number: UMIN000003645).
引用
收藏
页码:1043 / 1050
页数:8
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