A randomized phase III trial in advanced endometrial carcinoma of surgery and volume directed radiation followed by cisplatin and doxorubicin with or without paclitaxel: A Gynecologic Oncology Group study

被引:161
作者
Homesley, Howard D. [1 ]
Filiaci, Virginia [2 ]
Gibbons, Susan K. [3 ]
Long, Harry J. [4 ]
Cella, David [5 ]
Spirtos, Nick M. [6 ,7 ]
Morris, Robert T. [8 ]
DeGeest, Koen [9 ]
Lee, Roger [10 ]
Montag, Anthony [11 ]
机构
[1] Leo Jenkins Canc Ctr, Brody Sch Med, Div Gynecol Oncol, Greenville, NC 27834 USA
[2] Roswell Pk Canc Inst, Gynecol Oncol Grp, Stat & Data Ctr, Buffalo, NY 14263 USA
[3] Albany Med Ctr, Albany, NY USA
[4] Mayo Clin, Rochester, MN USA
[5] Evanston NW Healthcare & NW Univ, Ctr Outcomes Res & Educ, Evanston, IL USA
[6] Univ Nevada, Sch Med, Las Vegas, NV 89154 USA
[7] Womens Canc Ctr, Las Vegas, NV USA
[8] Wayne State Univ, Detroit, MI USA
[9] Univ Iowa Hosp & Clin, Iowa City, IA 52242 USA
[10] Tacoma Gen Hosp, Tacoma, WA USA
[11] Univ Chicago, Chicago, IL 60637 USA
关键词
Advanced endometrial carcinoma; Surgery; Radiation and chemotherapy; WHOLE ABDOMINOPELVIC IRRADIATION; PAPILLARY SEROUS CARCINOMA; ABDOMINAL IRRADIATION; PERITONEAL CYTOLOGY; ADJUVANT THERAPY; STAGE-III; CANCER; CHEMOTHERAPY; RADIOTHERAPY; NEUROTOXICITY;
D O I
10.1016/j.ygyno.2008.11.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objectives. After surgical debulking and volume-directed irradiation of the pelvis/para-aortic lymph nodes, treatment was randomized to compare recurrence-free survival (RFS) and toxicity between two chemotherapy regimens for the treatment of women with advanced stage endometrial carcinoma, Methods. Treatment was randomized between 6 cycles of cisplatin [C] (50 mg/m(2)) and doxorubicin [D] (45 mg/m(2)) with or without paclitaxel [P] (160 mg/m(2)). Initially in paclitaxel treated patients and, after May 2002, all patients received granulocyte growth factor with each cycle. Results. Of 659 patients enrolled following Surgery, 552 eligible patients were randomized to chemotherapy after irradiation. Accrual closed to Stage IV patients in June, 2003. Approximately 80% completed six cycles of chemotherapy, Three deaths resulted from bowel complications and one death was due to renal failure. Hematologic adverse events, sensory neuropathy and myalgia, were more frequent and severe in the paclitaxel arm (p<0.01) which was confirmed by Quality of Life assessments. Percentage of patients alive and recurrence-free at 36 months was 62% for CD vs. 64% for CDP. The hazard of recurrence or death relative to the CD arm stratified by stage is 0.90 (95% CI is 0.69 to 1.17, p=0.21, one-tail). However, in Subgroup analysis, CDP was associated with a 50% reduction in the risk of recurrence or death among patients with gross residual disease (95% CI: 0.26 to 0.92). Stage, residual disease, histology/grade, positive para-aortic node and cytology, pelvic metastases and age were significantly associated with RFS. Conclusion. The addition of paclitaxel to cisplatin and doxorubicin following surgery and radiation was not associated with a significant improvement in RFS but was associated with increased toxicity. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:543 / 552
页数:10
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