A German multicenter, randomized phase III trial comparing irinotecan-carboplatin with etoposide-carboplatin as first-line therapy for extensive-disease small-cell lung cancer

被引:79
作者
Schmittel, A. [1 ]
Sebastian, M. [2 ]
von Weikersthal, L. Fischer [3 ]
Martus, P. [4 ]
Gauler, T. C. [5 ]
Kaufmann, C. [1 ]
Hortig, P. [6 ]
Fischer, J. R. [7 ]
Link, H. [8 ]
Binder, D. [9 ]
Fischer, B. [2 ]
Caca, K. [10 ]
Eberhardt, W. E. E. [5 ]
Keilholz, U. [1 ]
机构
[1] Charite, Dept Hematol & Oncol, D-12200 Berlin, Germany
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Med Clin 3, Mainz, Germany
[3] Med Versorgungszentrum Gesundheitszentrum St Mari, Amberg, Germany
[4] Charite, Dept Clin Epidemiol & Biostat, D-12200 Berlin, Germany
[5] Univ Duisburg Essen, W German Tumor Ctr, Dept Med Canc Res, Essen, Germany
[6] Charite, Dept Cardiol & Pneumol, D-12200 Berlin, Germany
[7] Lowenstein Hosp, Clin Internal Med Oncol 2, Lowenstein, Germany
[8] W Pfalz Klinikum, Med Clin 1, Kaiserslautern, Germany
[9] Charite, Campus Virchow Clin, Dept Internal Med Infect & Resp Dis, D-12200 Berlin, Germany
[10] Klinikum Ludwigsburg, Med Clin 1, Ludwigsburg, Germany
关键词
carboplatin; etoposide; extensive disease; irinotecan; SCLC; trial; PLUS CARBOPLATIN; CISPLATIN; ETOPOSIDE/CISPLATIN; COMBINATION; UGT1A1;
D O I
10.1093/annonc/mdq652
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: This trial was designed to prove superiority of irinotecan over etoposide combined with carboplatin in extensive-disease small-cell lung cancer. Patients and methods: Patients were randomly assigned to receive carboplatin area under the curve 5 mg.min/ml either in combination with irinotecan 50 mg/m(2) on days 1, 8, and 15 (IP) or etoposide 140 mg/m(2) on days 1-3 (EP). Primary end point was progression-free survival (PFS) at 6 months. Secondary end points were overall survival (OS), response rate, and toxicity. Results: Of 226 patients, 216 were eligible. Median PFS was 6.0 months [95% confidence interval (CI) 5.0-7.0] in the IP arm and 6.0 months (95% CI 5.2-6.8) in EP arm (P = 0.07). Median survival was 10.0 months (95% CI 8.4-11.6) and 9.0 months (95% CI 7.6-10.4) in the IP and EP arm (P = 0.06), respectively. Hazard ratios for disease progression and OS were 1.29 (95% CI 0.96-1.73, P = 0.095) and 1.34 (95% CI 0.97-1.85, P = 0.072), respectively. No difference in response rates was observed. Grade 3 and 4 hematologic toxicity favored the IP arm, whereas diarrhea was significantly more frequent in the IP arm. Conclusion: This trial failed to show superiority of irinotecan over etoposide in combination with carboplatin.
引用
收藏
页码:1798 / 1804
页数:7
相关论文
共 13 条
[1]   Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter:: A balanced polymorphism for regulation of bilirubin metabolism? [J].
Beutler, E ;
Gelbart, T ;
Demina, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) :8170-8174
[2]   Predictive Role of the UGT1A1, UGT1A7, and UGT1A9 Genetic Variants and Their Haplotypes on the Outcome of Metastatic Colorectal Cancer Patients Treated With Fluorouracil, Leucovorin, and Irinotecan [J].
Cecchin, Erika ;
Innocenti, Federico ;
D'Andrea, Mario ;
Corona, Giuseppe ;
De Mattia, Elena ;
Biason, Paola ;
Buonadonna, Angela ;
Toffoli, Giuseppe .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (15) :2457-2465
[3]   Randomized phase III trial comparing irinotecan/cisplatin with etoposide/cisplatin in patients with previously untreated extensive-stage disease small-cell lung cancer [J].
Hanna, N ;
Bunn, PA ;
Langer, C ;
Einhorn, L ;
Guthrie, T ;
Beck, T ;
Ansar, R ;
Ellis, P ;
Byrne, M ;
Morrison, M ;
Hariharan, S ;
Wang, B ;
Sandler, A .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (13) :2038-2043
[4]   Irinotecan plus carboplatin versus oral etoposide plus carboplatin in extensive small-cell lung cancer:: A Randomized phase III trial [J].
Hermes, Andreas ;
Bergman, Bengt ;
Bremnes, Roy ;
Ek, Lars ;
Fluge, Sverre ;
Sederholm, Christer ;
Sundstrom, Stein ;
Thaning, Lars ;
Vilsvik, Jan ;
Aasebo, Ulf ;
Soerenson, Sverre .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (26) :4261-4267
[5]   CREATININE CLEARANCE - BEDSIDE ESTIMATE [J].
JELLIFFE, RW .
ANNALS OF INTERNAL MEDICINE, 1973, 79 (04) :604-605
[6]   Phase III Trial of Irinotecan/Cisplatin Compared With Etoposide/Cisplatin in Extensive-Stage Small-Cell Lung Cancer: Clinical and Pharmacogenomic Results From SWOG S0124 [J].
Lara, Primo N., Jr. ;
Natale, Ronald ;
Crowley, John ;
Lenz, Heinz Josef ;
Redman, Mary W. ;
Carleton, Jane E. ;
Jett, James ;
Langer, Corey J. ;
Kuebler, J. Philip ;
Dakhil, Shaker R. ;
Chansky, Kari ;
Gandara, David R. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (15) :2530-2535
[7]  
Lassen U, 1996, ANN ONCOL, V7, P365
[8]   Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer [J].
Noda, W ;
Nishiwaki, Y ;
Kawahara, M ;
Negoro, S ;
Sugiura, T ;
Yokoyama, A ;
Fukuoka, M ;
Mori, K ;
Watanabe, K ;
Tamura, T ;
Yamamoto, S ;
Saijo, N .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (02) :85-91
[9]   Phase I dose escalation study of carboplatin to a fixed dose of irinotecan as first-line treatment of small cell lung cancer [J].
Schmittel, A ;
Schulze, K ;
Hütter, G ;
Krebs, P ;
Thiel, E ;
Keilholz, U .
ONKOLOGIE, 2004, 27 (03) :280-284
[10]   A randomized phase II trial of irinotecan plus carboplatin versus etoposide plus carboplatin treatment in patients with extended disease small-cell lung cancer [J].
Schmittel, A ;
von Weikersthal, LF ;
Sebastian, M ;
Martus, P ;
Schulze, K ;
Hortig, P ;
Reeb, M ;
Thiel, E ;
Keilholz, U .
ANNALS OF ONCOLOGY, 2006, 17 (04) :663-667