Phase II study of concurrent thoracic radiotherapy in combination with weekly paclitaxel plus carboplatin in locally advanced non-small cell lung cancer: LOGIK0401

被引:14
作者
Takayama, Koichi [1 ]
Inoue, Koji [2 ]
Tokunaga, Shoji [3 ]
Matsumoto, Takemasa [4 ]
Oshima, Tsukasa [5 ]
Kawasaki, Masayuki [6 ]
Imanaga, Tomotoshi [7 ]
Kuba, Mutsuo [8 ]
Takeshita, Masafumi [2 ]
Harada, Taishi [1 ]
Shioyama, Yoshiyuki [9 ]
Nakanishi, Yoichi [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Chest Dis Res Inst, Higashi Ku, Fukuoka 8128582, Japan
[2] Kitakyushu Municipal Med Ctr, Kitakyushu, Fukuoka, Japan
[3] Kyushu Univ Hosp, Med Informat Ctr, Fukuoka 812, Japan
[4] Fukuoka Univ, Dept Resp Med, Fukuoka 81401, Japan
[5] Kyushu Kosei Nenkin Hosp, Kitakyushu, Fukuoka, Japan
[6] Fukuoka Higashi Med Ctr, Koga, Japan
[7] Steel Mem Yawata Hosp, Kitakyushu, Fukuoka, Japan
[8] Natl Hosp Org Okinawa Natl Hosp, Ginowan, Japan
[9] Kyushu Univ, Grad Sch Med Sci, Dept Clin Radiol, Higashi Ku, Fukuoka 8128582, Japan
关键词
Locally advanced NSCLC; Chemoradiotherapy; Consolidation chemotherapy; Carboplatin; Paclitaxel; Vinorelbine; LEUKEMIA GROUP-B; CONSOLIDATION DOCETAXEL; HOOSIER ONCOLOGY; CHEST RADIATION; US ONCOLOGY; CISPLATIN; CHEMORADIOTHERAPY; TRIAL; VINORELBINE; CHEMOTHERAPY;
D O I
10.1007/s00280-013-2335-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Concurrent chemoradiotherapy for regionally advanced stage III non-small cell lung cancer is the standard treatment method. However, the clinical implications of consolidation chemotherapy following chemoradiation have been unclear. Therefore, we conducted a phase II study of concurrent weekly carboplatin plus paclitaxel treatment in combination with radiotherapy followed by vinorelbine monotherapy. The primary endpoint was the 1-year survival rate. Chemonaive PS 0-1 patients with stage IIIA/B NSCLC were enrolled. During the concurrent chemoradiation phase, patients were treated with weekly paclitaxel 40 mg/m(2) plus carboplatin AUC 2. The primary tumor and involved nodes received 60 Gy in 2-Gy fractions over 6 weeks. During the consolidation phase, vinorelbine 25 mg/m(2) on days 1 and 8 was repeated for three cycles. A total of 40 eligible patients (72.5 % male; median age, 63 years; range 29-74 years) were analyzed for efficacy. Squamous cell carcinoma was the most common histology (47.5 %), and more patients had clinical stage IIIB (55 %) cancer. The average radiation dose was 56.5 Gy, and the average number of carboplatin plus paclitaxel cycles was 4.93. Seventeen patients proceeded to the consolidation chemotherapy phase, and 14 completed three cycles of vinorelbine monotherapy. The objective response rate was 75.0 %, including 1 patient who achieved a complete response. Progression-free survival and overall survival (OS) were 46 weeks [95 % confidence interval (CI) 31-64 weeks] and 110 weeks (95 % CI 90-184 weeks), respectively. The OS rate at 1 and 2 years was 85.0 % (95 % CI 69.6-93.0 %) and 53.9 % (95 % CI 37.1-68.0 %), respectively. Concurrent chemoradiation with weekly carboplatin and paclitaxel followed by vinorelbine consolidation is effective for stage III non-small cell lung cancer and shows a generally mild toxicity profile.
引用
收藏
页码:1353 / 1359
页数:7
相关论文
共 19 条
[1]
Meta-Analysis of Concomitant Versus Sequential Radiochemotherapy in Locally Advanced Non-Small-Cell Lung Cancer [J].
Auperin, Anne ;
Le Pechoux, Cecile ;
Rolland, Estelle ;
Curran, Walter J. ;
Furuse, Kiyoyuki ;
Fournel, Pierre ;
Belderbos, Jose ;
Clamon, Gerald ;
Ulutin, Hakki Cuneyt ;
Paulus, Rebecca ;
Yamanaka, Takeharu ;
Bozonnat, Marie-Cecile ;
Uitterhoeve, Apollonia ;
Wang, Xiaofei ;
Stewart, Lesley ;
Arriagada, Rodrigo ;
Burdett, Sarah ;
Pignon, Jean-Pierre .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (13) :2181-2190
[2]
Combined chemoradiotherapy regimens of paclitaxel and carboplatin for locally advanced non-small-cell lung cancer: A randomized phase II locally advanced multi-modality protocol [J].
Belani, CP ;
Choy, H ;
Bonomi, P ;
Scott, C ;
Travis, P ;
Haluschak, J ;
Curran, WJ .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :5883-5891
[3]
Multiinstitutional phase II trial of paclitaxel, carboplatin, and concurrent radiation therapy for locally advanced non-small-cell lung cancer [J].
Choy, H ;
Akerley, W ;
Safran, H ;
Graziano, S ;
Chung, C ;
Williams, T ;
Cole, B ;
Kennedy, T .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (10) :3316-3322
[4]
Sequential vs Concurrent Chemoradiation for Stage III Non-Small Cell Lung Cancer: Randomized Phase III Trial RTOG 9410 [J].
Curran, Walter J., Jr. ;
Paulus, Rebecca ;
Langer, Corey J. ;
Komaki, Ritsuko ;
Lee, Jin S. ;
Hauser, Stephen ;
Movsas, Benjamin ;
Wasserman, Todd ;
Rosenthal, Seth A. ;
Gore, Elizabeth ;
Machtay, Mitchell ;
Sause, William ;
Cox, James D. .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2011, 103 (19) :1452-1460
[5]
Oral Vinorelbine and Cisplatin with Concurrent Radiotherapy After Induction Chemotherapy with Cisplatin and Docetaxel for Patients with Locally Advanced Non-small Cell Lung Cancer The GFPC 05-03 Study [J].
Descourt, Renaud ;
Vergnenegre, Alain ;
Barlesi, Fabrice ;
Lena, Herve ;
Fournel, Pierre ;
Falchero, Lionel ;
Berard, Henri ;
Hureaux, Jose ;
Le Caer, Herve ;
Chavaillon, Jean Michel ;
Geriniere, Laurence ;
Monnet, Isabelle ;
Chouabe, Stephane ;
Robinet, Gilles .
JOURNAL OF THORACIC ONCOLOGY, 2011, 6 (02) :351-357
[6]
Improved survival in stage III non-small-cell lung cancer: Seven-year follow-up of cancer and leukemia group B (CALGB) 8433 trial [J].
Dillman, RO ;
Herndon, J ;
Seagren, SL ;
Eaton, WL ;
Green, MR .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (17) :1210-1215
[7]
Phase III study of concurrent versus sequential thoracic radiotherapy in combination with mitomycin, vindesine, and cisplatin in unresectable stage III non-small-cell lung cancer [J].
Furuse, K ;
Fukuoka, M ;
Kawahara, M ;
Nishikawa, H ;
Takada, Y ;
Kudoh, S ;
Katagami, N ;
Ariyoshi, Y .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) :2692-2699
[8]
Furuse K, 1996, ANN ONCOL, V7, P815
[9]
Furuse K, 1996, ONCOLOGY, V53, P169
[10]
Gandara David R, 2003, J Clin Oncol, V21, P2004, DOI 10.1200/JCO.2003.04.197