Phase III randomized trial of 12 versus 3 months of maintenance paclitaxel in patients with advanced ovarian cancer after complete response to platinum and paclitaxel-based chemotherapy: A Southwest Oncology Group and Gynecologic Oncology Group trial

被引:333
作者
Markman, M
Liu, PY
Wilczynski, S
Monk, B
Copeland, LJ
Alvarez, RD
Jiang, C
Alberts, D
机构
[1] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[2] Ohio State Univ, Ctr Hlth, Columbus, OH 43210 USA
[3] SW Oncol Grp, Ctr Stat, Seattle, WA USA
[4] Univ Calif Irvine, Med Ctr, Orange, CA USA
[5] City Hope Natl Med Ctr, Duarte, CA 91010 USA
[6] Univ Alabama, Med Ctr, Birmingham, AL 35294 USA
[7] Univ Arizona, Ctr Canc, Tucson, AZ USA
关键词
D O I
10.1200/JCO.2003.07.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine whether continuing paclitaxel for an extended time period in women with advanced ovarian cancer who had achieved a clinically defined complete response to a platinum/paclitaxel-based chemotherapy could prolong subsequent progression-free survival (PFS) and affect ultimate survival. Patients and Methods: Patients were randomly assigned to either three or 12 cycles of single-agent paclitaxel administered every 28 days and were then followed up for progression-free and overall survival. Results: As of September 6, 2001, 277 patients (262 assessable) had entered the trial, with a total of 54 PFS events having developed among 222 patients with follow-up data. With the exception of peripheral neuropathy, there were no major differences in toxicity between the regimens. The median PFS was 21 and 28 months in the three-cycle and 12-cycle paclitaxel arms, respectively. One-sided P values from an unadjusted log-rank test and an adjusted Cox model analysis (for stratification factors) were .0035 and .0023, respectively, both in favor of the 12-cycle arm. The Cox model-adjusted three-cycle versus the 12-cycle progression hazard ratio was estimated to be 2.31 (99% confidence interval, 1.08 to 4.94). With a protocol-specified early termination boundary of P = .005, these findings led the Southwest Oncology Group Data Safety Monitoring Committee to discontinue the trial. As of the date of study closure, there was no difference in overall survival between the treatment arms. Conclusion: Twelve cycles of single-agent paclitaxel administered to women with advanced ovarian cancer who attain a clinically defined complete response to initial platinum/paclitaxel-based chemotherapy significantly prolongs the duration of PFS. (C) 2003 by American Society of Clinical Oncology.
引用
收藏
页码:2460 / 2465
页数:6
相关论文
共 19 条
[1]  
Abe O, 1998, LANCET, V352, P930
[2]   Intraperitoneal cisplatin plus intravenous cyclophosphamide versus intravenous cisplatin plus intravenous cyclophosphamide for stage III ovarian cancer [J].
Alberts, DS ;
Liu, PY ;
Hannigan, EV ;
OToole, R ;
Williams, SD ;
Young, JA ;
Franklin, EW ;
ClarkePearson, DL ;
Malviya, VK ;
DuBeshter, B ;
Adelson, MD ;
Hoskins, WJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (26) :1950-1955
[3]   A PROSPECTIVE RANDOMIZED COMPARISON OF 6 AND 12 CYCLES OF CYCLOPHOSPHAMIDE, ADRIAMYCIN, AND CISPLATIN IN ADVANCED EPITHELIAL OVARIAN-CANCER - A DANISH OVARIAN STUDY-GROUP TRIAL (DACOVA) [J].
BERTELSEN, K ;
JAKOBSEN, A ;
STROYER, I ;
NIELSEN, K ;
SANDBERG, E ;
ANDERSEN, JE ;
AHRONS, S ;
NYLAND, M ;
PEDERSEN, PH ;
LARSEN, G ;
RASMUSSEN, P ;
KIAER, H ;
BICHEL, P ;
JACOBSEN, M ;
HOLUND, B .
GYNECOLOGIC ONCOLOGY, 1993, 49 (01) :30-36
[4]  
Browder T, 2000, CANCER RES, V60, P1878
[5]   EVALUATION OF OPTIMAL DURATION OF CHEMOTHERAPY IN FAVORABLE-PROGNOSIS DISSEMINATED GERM-CELL TUMORS - A SOUTHEASTERN-CANCER-STUDY-GROUP PROTOCOL [J].
EINHORN, LH ;
WILLIAMS, SD ;
LOEHRER, PJ ;
BIRCH, R ;
DRASGA, R ;
OMURA, G ;
GRECO, FA .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (03) :387-391
[6]   PHASE-II STUDY AND LONG-TERM FOLLOW-UP OF PATIENTS TREATED WITH TAXOL FOR ADVANCED OVARIAN ADENOCARCINOMA [J].
EINZIG, AI ;
WIERNIK, PH ;
SASLOFF, J ;
RUNOWICZ, CD ;
GOLDBERG, GL .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (11) :1748-1753
[7]   Recurrent epithelial ovarian carcinoma: A randomized phase III study of pegylated liposomal doxorubicin versus topotecan [J].
Gordon, AN ;
Fleagle, JT ;
Guthrie, D ;
Parkin, DE ;
Gore, ME ;
Lacave, AJ .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (14) :3312-3322
[8]   ACUTE NONLYMPHOCYTIC LEUKEMIA AFTER THERAPY WITH ALKYLATING-AGENTS FOR OVARIAN-CANCER - A STUDY OF 5 RANDOMIZED CLINICAL-TRIALS [J].
GREENE, MH ;
BOICE, JD ;
GREER, BE ;
BLESSING, JA ;
DEMBO, AJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1982, 307 (23) :1416-1421
[9]   RANDOMIZED PROSPECTIVE TRIAL OF 5 VERSUS 10 CYCLES OF CYCLOPHOSPHAMIDE, DOXORUBICIN, AND CISPLATIN IN ADVANCED OVARIAN-CARCINOMA [J].
HAKES, TB ;
CHALAS, E ;
HOSKINS, WJ ;
JONES, WB ;
MARKMAN, M ;
RUBIN, SC ;
CHAPMAN, D ;
ALMADRONES, L ;
LEWIS, JL .
GYNECOLOGIC ONCOLOGY, 1992, 45 (03) :284-289
[10]   A randomized trial of five versus eight courses of cisplatin or carboplatin in advanced epithelial ovarian carcinoma - A North Thames Ovary Group Study [J].
Lambert, HE ;
Rustin, GJS ;
Gregory, WM ;
Nelstrop, AE .
ANNALS OF ONCOLOGY, 1997, 8 (04) :327-333