PHASE I STUDY OF CONCURRENT HIGH-DOSE THREE-DIMENSIONAL CONFORMAL RADIOTHERAPY WITH CHEMOTHERAPY USING CISPLATIN AND VINORELBINE FOR UNRESECTABLE STAGE III NON-SMALL-CELL LUNG CANCER

被引:31
作者
Sekine, Ikuo [1 ]
Sumi, Minako [2 ]
Ito, Yoshinori [2 ]
Horinouchi, Hidehito
Nokihara, Hiroshi
Yamamoto, Noboru
Kunitoh, Hideo
Ohe, Yuichiro
Kubota, Kaoru
Tamura, Tomohide
机构
[1] Natl Canc Ctr, Div Internal Med & Thorac Oncol, Chuo Ku, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Div Radiat Oncol, Tokyo 1040045, Japan
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2012年 / 82卷 / 02期
关键词
Lung cancer; Chemotherapy; Radiotherapy; High dose; Conformal; THORACIC RADIOTHERAPY; RADIATION-THERAPY; TRIAL;
D O I
10.1016/j.ijrobp.2011.01.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: To determine the maximum tolerated dose in concurrent three-dimensional conformal radiotherapy (3D-CRT) with chemotherapy for unresectable Stage III non small-cell lung cancer (NSCLC). Patients and Methods: Eligible patients with unresectable Stage III NSCLC, age >= 20 years, performance status 0-1, percent of volume of normal lung receiving 20 GY or more (V(20)) <= 30% received three to four cycles of cisplatin (80 mg/m(2) Day 1) and vinorelbine (20 mg/m(2) Days 1 and 8) repeated every 4 weeks. The doses of 3D-CRT were 66 Gy, 72 Gy, and 78 Gy at dose levels 1 to 3, respectively. Results: Of the 17, 16, and 24 patients assessed for eligibility, 13 (76%), 12(75%), and 6(25%) were enrolled at dose levels 1 to 3, respectively. The main reasons for exclusion were V(20) >30% (n = 10) and overdose to the esophagus (n = 8) and brachial plexus (n = 2). There were 26 men and 5 women, with a median age of 60 years (range, 41-75). The full planned dose of radiotherapy could be administered to all the patients. Grade 3-4 neutropenia and febrile neutropenia were noted in 24(77%) and 5(16%) of the 31 patients, respectively. Grade 4 infection, Grade 3 esophagitis, and Grade 3 pulmonary toxicity were noted in 1 patient, 2 patients, and 1 patient, respectively. The dose-limiting toxicity was noted in 17% of the patients at each dose level. The median survival and 3-year and 4-year survival rates were 41.9 months, 72.3%, and 49.2%, respectively. Conclusions: 72 Gy was the maximum dose that could be achieved in most patients, given the predetermined normal tissue constraints. (C) 2012 Elsevier Inc.
引用
收藏
页码:953 / 959
页数:7
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