Docetaxel and granulocyte colony-stimulating factor in patients with advanced non-small-cell lung cancer previously treated with platinum-based chemotherapy: a multicenter phase II trial

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作者
K. Alexopoulos
C. Kouroussis
N. Androulakis
E. Papadakis
M. Vaslamatzis
S. Kakolyris
G. Samelis
E. Patila
A. Vossos
E. Samantas
V. Georgoulias
机构
[1] Department of Medical Oncology,
[2] Evagelismos General Hospital,undefined
[3] Athens,undefined
[4] Greece,undefined
[5] Department of Medical Oncology,undefined
[6] University General Hospital of Heraklion,undefined
[7] P.O. Box 1352,undefined
[8] 71110 Heraklion,undefined
[9] Crete,undefined
[10] Greece e-mail: georgoul@med.uch.gr,undefined
[11] Tel.: (30-81) 392747,undefined
[12] Fax: (30-81) 392802,undefined
[13] First Department of Respiratory Medicine,undefined
[14] Sotiria Hospital of Chest Diseases,undefined
[15] Athens,undefined
[16] Greece,undefined
[17] Department of Medical Oncology,undefined
[18] Ippokration General Hospital,undefined
[19] Athens,undefined
[20] Greece,undefined
[21] Third Department of Medical Oncology,undefined
[22] Agii Anargyri Anticancer Hospital,undefined
[23] Kifissia,undefined
[24] Greece,undefined
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Key words Docetaxel; Non-small-cell lung cancer; Chemotherapy; Second-line treatment;
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摘要
Purpose: To investigate the activity of docetaxel and granulocyte colony-stimulating factor support (G-CSF) in patients with advanced non-small-cell lung cancer (NSCLC) previously treated with cisplatin. Patients and methods: A total of 60 patients with locoregional and metastatic NSCLC who had relapsed or progressed after first-line treatment with cisplatin-based regimens were enrolled into the trial. Docetaxel at 100 mg/m2 was given as a 1-h infusion with G-CSF (rhG-CSF given s.c. at 150 μg/m2) support from day 2 to day 8 every 3 weeks; all patients received premedication with corticosteroids. Results: In all, 1 (1.6%) and 14 (23.3%) patients achieved a complete response (CR) and a partial response (PR), respectively, for an overall response rate of 25% (95% CI 14.0–35.9%); stable disease (SD) and progressive disease (PD) were documented in 18 (30%) and 27 (45%) patients, respectively. The median duration of response was 20 weeks and the median time to tumor progression was 28 weeks. The median overall survival was 32 weeks and the 1-year survival rate was 23%. A total of 263 courses were given at a median of 3 cycles/patient. Grade 3 and 4 neutropenia occurred in 11 (18%) and 14 (23%) patients, respectively, with 18 (30%) patients requiring hospitalization for neutropenic fever; 1 patient died of sepsis. Grade 2 peripheral neuropathy occurred in 9 patients (15%) and grade 3 asthenia, in 4 (7%). Other toxicities were mild. Conclusions: Docetaxel has considerable single-agent activity in patients with NSCLC who have relapsed or progressed after first-line chemotherapy with cisplatin-based regimens.
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页码:257 / 262
页数:5
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