Randomized Phase II Study of Weekly Paclitaxel plus Carboplatin Versus Biweekly Paclitaxel plus Carboplatin for Patients with Previously Untreated Advanced Non-Small Cell Lung Cancer

被引:2
作者
Takayama, Koichi [1 ,2 ]
Ichiki, Masao [3 ]
Tokunaga, Shoji [4 ]
Inoue, Koji [5 ]
Kawasaki, Masayuki [6 ]
Uchino, Junji [1 ]
Nakanishi, Yoichi [2 ]
机构
[1] Kyoto Prefectural Univ Med, Kyoto, Japan
[2] Kyushu Univ, Fukuoka, Fukuoka, Japan
[3] Kyushu Med Ctr, Fukuoka, Fukuoka, Japan
[4] Kyushu Univ Hosp, Med Informat Ctr, Fukuoka, Fukuoka, Japan
[5] Kitakyushu Municipal Med Ctr, Kitakyushu, Fukuoka, Japan
[6] Fukuoka Higashi Med Ctr, Koga, Japan
关键词
CHEMOTHERAPY-INDUCED NEUTROPENIA; TRIAL; BEVACIZUMAB; MULTICENTER; MORTALITY; CISPLATIN; VINORELBINE; COMBINATION; GEFITINIB; SCHEDULE;
D O I
10.1634/theoncologist.2019-0513
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lessons Learned This clinical trial, evaluating the efficacy and safety of a carboplatin plus paclitaxel regimen in a biweekly or weekly schedule instead of the more toxic 3-weekly administration, showed that the weekly regimen was better in efficacy than the biweekly regimen, with mild toxicities, for patients with non-small cell lung cancer (NSCLC). The weekly carboplatin plus paclitaxel regimen could be considered as an alternative to the 3-weekly regimen in Japanese patients with NSCLC. Background Combination therapy comprising carboplatin (C) and paclitaxel (P) is the most commonly used regimen for the treatment of advanced non-small cell lung cancer (NSCLC). Common toxicities associated with the regimen, such as neuropathy and myelosuppression, cause its discontinuation. In the present study, we conducted a clinical trial evaluating the efficacy of biweekly (B) and weekly (W) PC therapy to identify the appropriate chemotherapy schedule for Asian patients. Methods Chemonaive patients with IIIB/IV NSCLC and a performance status of 0-1 were randomly assigned to a biweekly regimen (paclitaxel 135 mg/m(2) with carboplatin area under the curve [AUC] 3 on days 1 and 15 of every 4 weeks) or to a weekly regimen (paclitaxel 90 mg/m(2) on days 1, 8, and 15 with carboplatin AUC 6 on day 1 of every 4 weeks). Results A total of 140 patients were enrolled in the study. The objective response rates (ORRs) were 28.1% (B) and 38.0% (W). The most common toxicity was neutropenia, with incidence rates of 62.0% (B) and 57.8% (W). Progression-free survivals (PFSs) were 4.3 months (B) and 5.1 months (W), and overall survival durations were 14.2 months (B) and 13.3 months (W). Conclusion The ORR and PFS in the weekly regimen were better than those in the biweekly schedule, although a statistical difference was not observed. The toxicity profile was generally mild for both regimens. The weekly CP regimen was suitable to be considered as an alternative to the current 3-weekly regimen in NSCLC treatment.
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页码:1420 / +
页数:7
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共 22 条
  • [1] Randomized, phase III study of weekly paclitaxel in combination with carboplatin versus standard every-3-weeks administration of carboplatin and paclitaxel for patients with previously untreated advanced non-small-cell lung cancer
    Belani, Chandra P.
    Ramalingam, Suresh
    Perry, Michael C.
    LaRocca, Renato V.
    Rinaldi, David
    Gable, Preston S.
    Tester, William J.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (03) : 468 - 473
  • [2] Multicenter, randomized trial for stage IIIB or IV non-small-cell lung cancer using weekly paclitaxel and carboplatin followed by maintenance weekly paclitaxel or observation
    Belani, CP
    Barstis, J
    Perry, MC
    La Rocca, RV
    Nattam, SR
    Rinaldi, D
    Clark, R
    Mills, GM
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (15) : 2933 - 2939
  • [3] Randomized phase III trial comparing cisplatin-etoposide to carhoplatin-paclitaxel in advanced or metastatic non-small cell lung cancer
    Belani, CP
    Lee, JS
    Socinski, MA
    Robert, F
    Waterhouse, D
    Rowland, K
    Ansari, R
    Lilenbaum, R
    Natale, RB
    [J]. ANNALS OF ONCOLOGY, 2005, 16 (07) : 1069 - 1075
  • [4] Chemotherapy-induced neutropenia and treatment efficacy in advanced non-small-cell lung cancer: a pooled analysis of three randomised trials
    Di Maio, M
    Gridelli, C
    Gallo, C
    Shepherd, F
    Piantedosi, FV
    Cigolari, S
    Manzione, L
    Illiano, A
    Barbera, S
    Robbiati, SF
    Frontini, L
    Piazza, E
    Ianniello, GP
    Veltri, E
    Castiglione, F
    Rosetti, F
    Gebbia, V
    Seymour, L
    Chiodini, P
    Perrone, F
    [J]. LANCET ONCOLOGY, 2005, 6 (09) : 669 - 677
  • [5] Japanese-US Common-Arm Analysis of Paclitaxel Plus Carboplatin in Advanced Non-Small-Cell Lung Cancer: A Model for Assessing Population-Related Pharmacogenomics
    Gandara, David R.
    Kawaguchi, Tomoya
    Crowley, John
    Moon, James
    Furuse, Kiyoyuki
    Kawahara, Masaaki
    Teramukai, Satoshi
    Ohe, Yuichiro
    Kubota, Kaoru
    Williamson, Stephen K.
    Gautschi, Oliver
    Lenz, Heinz Josef
    McLeod, Howard L.
    Lara, Primo N., Jr.
    Coltman, Charles Arthur, Jr.
    Fukuoka, Masahiro
    Saijo, Nagahiro
    Fukushima, Masanori
    Mack, Philip C.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (21) : 3540 - 3546
  • [6] Impact of smoking and smoking cessation on lung cancer mortality in the Asia-Pacific region
    Huxley, R.
    Jamrozik, K.
    Lam, T. H.
    Barzi, F.
    Ansary-Moghaddam, A.
    Jiang, C. Q.
    Suh, I.
    Woodward, M.
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 2007, 165 (11) : 1280 - 1286
  • [7] Phase I and pharmacokinetic study of carboplatin and paclitaxel with a biweekly schedule in patients with advanced non-small-cell lung cancer
    Ichiki, M
    Gohara, R
    Fujiki, R
    Hoashi, S
    Rikimaru, T
    Aizawa, H
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2003, 52 (01) : 67 - 72
  • [8] A multicenter phase II study of carboplatin and paclitaxel with a biweekly schedule in patients with advanced non-small-cell lung cancer: Kyushu thoracic oncology group trial
    Ichiki, Masao
    Kawasaki, Masayuki
    Takayama, Koichi
    Ninomiya, Kiyoshi
    Kuba, Mutsuo
    Iwami, Fumiyuki
    Miyazaki, Naoki
    Oishi, Kazunori
    Takeo, Sadanori
    Aizawa, Hisamichi
    Nakanishi, Yoichi
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2006, 58 (03) : 368 - 373
  • [9] An Updated Report of the Trends in Cancer Incidence and Mortality in Japan
    Katanoda, Kota
    Matsuda, Tomohiro
    Matsuda, Ayako
    Shibata, Akiko
    Nishino, Yoshikazu
    Fujita, Manabu
    Soda, Midori
    Ioka, Akiko
    Sobue, Tomotaka
    Nishimoto, Hiroshi
    [J]. JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2013, 43 (05) : 492 - 507
  • [10] Trends in Lung Cancer Mortality Rates in Japan, USA, UK, France and Korea Based on the WHO Mortality Database
    Katanoda, Kota
    Yako-Suketomo, Hiroko
    [J]. JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2012, 42 (03) : 239 - 240