A PHASE II STUDY OF SYNCHRONOUS THREE-DIMENSIONAL CONFORMAL BOOST TO THE GROSS TUMOR VOLUME FOR PATIENTS WITH UNRESECTABLE STAGE III NON-SMALL-CELL LUNG CANCER: RESULTS OF KOREAN RADIATION ONCOLOGY GROUP 0301 STUDY

被引:33
作者
Cho, Kwan Ho [1 ]
Ahn, Sung Ja [2 ]
Pyo, Hong Ryull
Kim, Kyu-Sik [2 ]
Kim, Young-Chul [2 ]
Moon, Sung Ho
Han, Ji-Youn
Kim, Heung Tae
Koom, Woong Sub [3 ]
Lee, Jin Soo
机构
[1] Natl Canc Ctr, Res Inst Hosp, Proton Therapy Ctr, Goyang 411769, Gyeonggi, South Korea
[2] Chonnam Natl Univ, Hwasun Hosp, Hwasun, Chonnam, South Korea
[3] Yonsei Univ, Med Ctr, Seoul 120749, South Korea
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2009年 / 74卷 / 05期
关键词
Non-small-cell lung cancer; Chemoradiation; Three-dimensional conformal radiotherapy; Synchronous boost; Accelerated radiotherapy; INDUCTION CHEMOTHERAPY; RANDOMIZED TRIAL; SEQUENTIAL CHEMORADIOTHERAPY; CONCURRENT CHEMORADIOTHERAPY; ACCELERATED RADIOTHERAPY; CONCOMITANT BOOST; DOSE-ESCALATION; GROUP RTOG; THERAPY; CISPLATIN;
D O I
10.1016/j.ijrobp.2008.10.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We evaluated the efficacy of synchronous three-dimensional (31)) conformal boost to the gross tumor volume(GTV) in concurrent chemoradiotherapy for patients with locally advanced non-small-cell lung cancer (NSCLC). Methods and Materials: Eligibility included unresectable Stage III NSCLC with no pleural effusion, no supraclavicular nodal metastases, and Eastern Cooperative Oncology Group performance score of 0-1. Forty-nine patients with pathologically proven NSCLC were enrolled. Eighteen patients had Stage IIIA and 31 had Stage IIIB. By using 3D conformal radiotherapy (RT) techniques, a dose of 1.8 Gy was delivered to the planning target volume with a synchronous boost of 0.6 Gy to the GTV, with a total dose of 60 Gy to the GTV and 45 Gy to the planning target volume in 25 fractions during 5 weeks. All patients received weekly chemotherapy consisting of paclitaxel and carboplatin during RT. Results: With a median follow-up of 36.8 months (range, 29.0-45.5 months) for surviving patients, median survival was 28.1 months. One-, 2- and 3-year overall survival rates were 77%, 56.4%, and 43.8%, respectively. Corresponding local progression-free survival rates were 71.2%, 53.7%, and 53.7%. Compliance was 90% for RT and 88% for chemotherapy. Acute esophagitis of Grade 2 or higher occurred in 29 patients. Two patients with T4 lesions died of massive bleeding and hemoptysis during treatment (Grade 5). Overall late toxicity was acceptable. Conclusions: Based on the favorable outcome with acceptable toxicity, the acceleration scheme using 3D conformal GTV boost in this trial is warranted to compare with conventional fractionation in a Phase III trial. (C) 2009 Elsevier Inc.
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收藏
页码:1397 / 1404
页数:8
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