Sequential chemotherapy with paclitaxel plus cisplatin, followed by vinorelbine, followed by gemcitabine in advanced non-small cell lung cancer: an Alpe-Adria Thoracic Oncology Multidisciplinary group study (ATOM 001)

被引:11
作者
Grossi, F
Belvedere, O
Fasola, G
Barbone, F
Rizzato, S
Sibau, A
Recchia, L
Vigevani, E
Ceschia, T
Morelli, A
Guglielmi, A
Puglisi, F
Follador, A
Talmassons, G
Sobrero, AF
机构
[1] Natl Inst Canc Res, Dis Management Team Lung Canc Med Oncol A, I-16132 Genoa, Italy
[2] Univ Udine, Dept Med Oncol, I-33100 Udine, Italy
[3] Osped S Maria Misericordia, I-33100 Udine, Italy
[4] Univ Udine, Epidemiol Unit, DPMSC, I-33100 Udine, Italy
[5] San Polo Hosp, Med Oncol Unit, I-34074 Monfalcone, Italy
[6] Tolmezzo Hosp, Med Oncol Unit, I-33028 Tolmezzo, Italy
[7] Osped S Maria Misericordia, Unit Radiat Therapy, I-33100 Udine, Italy
[8] Osped S Maria Misericordia, Unit Cardiothorac Surg, I-33100 Udine, Italy
[9] San Martino Hosp, Med Oncol Unit, I-16132 Genoa, Italy
[10] Osped S Maria Misericordia, Unit Pulmonol, I-33100 Udine, Italy
关键词
non-small cell lung cancer; advanced chemotherapy; sequential chemotherapy; phase II;
D O I
10.1016/j.lungcan.2004.03.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim of this study was to determine the activity and toxicity of a sequential chemotherapy regimen in advanced non-small cell lung cancer (NSCLC). Fifty-one previously untreated stage IIIB/IV NSCLC patients were enrolled to receive two cycles of cisplatin plus paclitaxel (80/175 mg/m(2) every 21 days), followed by two cycles of vinorelbine (30 mg/m(2) on days 1 and 8 every 21 days), followed by two cycles of gemcitabine (1000 mg/m(2) on days 1, 8, and 15 every 28 days). Forty-one patients (82%) completed the planned six cycles. Grade 3-4 neutropenia was the major toxicity (41% of patients) and it was mainly associated with vinorelbine administration. Response rate after cisplatin plus paclitaxel was 18%; this percentage increased to 41% after vinorelbine, and it reached 43% upon completion of the entire six cycle treatment program. Median survival time was 14.4 months, 1-year survival rate was 53%, and 2-year survival rate was 18%. Median time to disease progression was 6.8 months. This sequential chemotherapy regimen is feasible and active in patients with advanced NSCLC. This pilot experience provides the basis for an ongoing randomized phase III trial comparing our sequential regimen versus cisplatin plus gemcitabine. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:99 / 106
页数:8
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