Paclitaxel, cisplatin, and gemcitabine combination chemotherapy within a multidisciplinary therapeutic approach in metastatic nonsmall cell lung carcinoma - A Phase II study

被引:0
|
作者
Rodriguez, J
Cortes, J
Calvo, E
Azinovic, I
Fernandez-Hildago, O
Martinez-Monge, R
Garzon, C
de Irala, J
Martinez-Aguillo, M
Cajal, TRY
Brugarolas, A
机构
[1] Univ Navarra Clin, Dept Oncol, Pamplona 31008, Spain
[2] Univ Navarra Clin, Dept Radiotherapy, Pamplona 31008, Spain
[3] Univ Navarra, Sch Med, Dept Epidemiol & Publ Hlth, E-31080 Pamplona, Spain
关键词
nonsmall cell lung carcinoma; paclitaxel; cisplatin; gemcitabine; phase II study;
D O I
10.1002/1097-0142(20001215)89:12<2622::AID-CNCR15>3.0.CO;2-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Cisplatin-based chemotherapy combinations improve quality of life and survival in advanced nonsmall cell lung carcinoma (NSCLC). The emergence of new active drugs might translate into more effective regimens for the treatment of this disease. METHODS. The objective of this study was to determine the feasibility, response rate, and toxicity of a paclitaxel, cisplatin, and gemcitabine combination to treat metastatic NSCLC. Thirty-five consecutive chemotherapy-naive patients with Stage IV NSCLC and an Eastern Cooperative Oncology Group performance status of 0-2 were treated with a combination of paclitaxel (135 mg/m(2) given intravenously in 3 hours) on Day 1, cisplatin (120 mg/m(2) given intravenously in 6 hours) on Day I, and gemcitabine (800 mg/m(2) given intravenously in 30 minutes) on Days 1 and 8, every 4 weeks. Although responding patients were scheduled to receive consolidation radiotherapy and 24 patients received preplanned second-line chemotherapy after disease progression, the response and toxicity rates reported refer only to the chemotherapy regimen given. RESULTS, All the patients were examined for toxicity; 34 were examinable for response. An objective response was observed in 73.5% of the patients (95% confidence interval [CI], 55.6-87.1%), including 4 complete responses (11.7%). According to intention-to-treat, the overall response rate was 71.4% (95% CI, 53.7-85.4%). After 154 courses of therapy, the median dose intensity was 131 mg/m(2) for paclitaxel (97.3%), 117 mg/m(2) for cisplatin (97.3%), and 1378 mg/m(2) for gemcitabine (86.2%). World Health Organization Grade 3-4 neutropenia and thrombocytopenia occurred in 39.9% and 11.4% of patients, respectively. There was one treatment-related death. Nonhematologic toxicities were mild. After a median follow-up of 22 months, the median progression free survival rate was 7 months, and the median survival time was 16 months. CONCLUSIONS. The combination of paclitaxel, cisplatin, and gemcitabine is well tolerated and shows high activity in metastatic NSCLC. This treatment merits further comparison with other cisplatin-based regimens. Cancer 2000;89:2622-9. (C) 2000 American Cancer Society.
引用
收藏
页码:2622 / 2629
页数:8
相关论文
共 50 条
  • [21] Sequential chemotherapy of cisplatin and vinorelbine followed by paclitaxel and gemcitabine in advanced non-small-cell lung cancer - A single institution phase II study
    Dongiovanni, D
    Fissore, C
    Berruti, A
    Buffoni, L
    Addeo, A
    Barone, C
    Polimeni, MA
    Ottaviani, D
    Bertetto, O
    Dongiovanni, V
    LUNG CANCER, 2005, 47 (02) : 269 - 275
  • [22] Platinum-free combination chemotherapy in patients with advanced or metastatic transitional cell carcinoma - A phase I/II trial of gemcitabine, paclitaxel, and methotrexate
    Lara, PN
    Meyers, FJ
    Law, LY
    Dawson, NA
    Houston, J
    Lauder, I
    Edelman, MJ
    CANCER, 2004, 100 (01) : 82 - 88
  • [23] Gemcitabine and Paclitaxel Combination as Second-Line Chemotherapy in Patients With Small-Cell Lung Cancer: A Phase II Study
    Dazzi, Claudio
    Cariello, Anna
    Casanova, Claudia
    Verlicchi, Alberto
    Montanari, Marco
    Papiani, Giorgio
    Freier, Eva
    Mazza, Valentina
    Milandri, Carlo
    Gamboni, Alessandro
    Papi, Maximilian
    Leoni, Maurizio
    Cruciani, Giorgio
    Vertogen, Bernadette
    CLINICAL LUNG CANCER, 2013, 14 (01) : 28 - 33
  • [24] Phase II study of patients with metastatic nonsmall cell carcinoma of the lung treated with paclitaxel by 3-hour infusion
    Tester, WJ
    Jin, PY
    Reardon, DH
    Cohn, JB
    Cohen, MH
    CANCER, 1997, 79 (04) : 724 - 729
  • [25] A Case of Metastatic Urachal Cancer Including a Neuroendocrine Component Treated with Gemcitabine, Cisplatin and Paclitaxel Combination Chemotherapy
    Ebara, Shin
    Kobayashi, Yasuyuki
    Sasaki, Katsumi
    Araki, Motoo
    Sugimoto, Morito
    Wada, Koichirou
    Fujio, Kei
    Takamoto, Atsushi
    Watanabe, Toyohiko
    Yanai, Hiroyuki
    Nasu, Yasutomo
    ACTA MEDICA OKAYAMA, 2016, 70 (03) : 223 - 227
  • [26] Evaluation of cisplatin, carboplatin, and etoposide in metastatic nonsmall cell lung carcinoma - A phase II study of the southwest oncology group
    Figlin, RA
    Crowley, JJ
    Jacobs, EL
    Muirhead, M
    Goodwin, JW
    Rinehart, JJ
    Livingston, RB
    CANCER, 1996, 78 (05) : 998 - 1003
  • [27] Clinical phase II evaluation of paclitaxel in combination with cisplatin in metastatic or recurrent squamous cell carcinoma of the head and neck
    Thodtmann, R
    Theiss, F
    Kemmerich, M
    Heinrich, B
    Laubenbacher, C
    Quasthoff, S
    Kau, R
    Herzog, M
    Diergarten, K
    Hanauske, AR
    ANNALS OF ONCOLOGY, 1998, 9 (03) : 335 - 337
  • [28] Phase II study of paclitaxel and irinotecan chemotherapy in patients with advanced nonsmall cell lung cancer
    Oshita, Fumihiro
    Saito, Haruhiro
    Yamada, Kouzo
    Noda, Kazumasa
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2007, 30 (04): : 358 - 360
  • [29] Paclitaxel, carboplatin, and gemcitabine in metastatic nasopharyngeal carcinoma - A phase II trial using a triplet combination
    Leong, SS
    Wee, J
    Tay, MH
    Toh, CK
    Tan, SB
    Thng, CH
    Foo, KF
    Lim, WT
    Tan, T
    Tan, EH
    CANCER, 2005, 103 (03) : 569 - 575
  • [30] Chemotherapy with gemcitabine, paclitaxel, and cisplatin in the treatment of patients with advanced transitional cell carcinoma of the urothelium
    Ecke, Thorsten H.
    Bartel, Peter
    Koch, Stefan
    Ruttloff, Juergen
    Theissig, Franz
    ONCOLOGY REPORTS, 2006, 16 (06) : 1381 - 1388