共 2 条
Comparison of outcomes in patients treated with multi-agent regiments of cisplatin, adriamycin, and VP-16 versus carboplatin and paclitaxel for advanced and recurrent endometrial cancer
被引:0
作者:
Olawaiye, A. B.
[2
]
Godoy, H. E.
[1
]
Shahzad, M. M. K.
[3
]
Rauh-Hain, J. A.
[4
]
Lele, S. B.
[1
]
Odunsi, K.
[1
,5
]
机构:
[1] Roswell Pk Canc Inst, Dept Gynecol Oncol, Buffalo, NY 14263 USA
[2] Univ Pittsburgh, Magee Womens Hosp, UPMC, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA 15213 USA
[3] Univ Wisconsin, Dept Obstet & Gynecol, Madison, WI 53706 USA
[4] Massachusetts Gen Hosp, Dept Obstet & Gynecol, Boston, MA 02114 USA
[5] Roswell Pk Canc Inst, Dept Immunol, Buffalo, NY 14263 USA
关键词:
Advanced endometrial carcinoma;
Multi-agent chemotherapies;
Adriamycin;
Cisplatin;
Etoposide;
PHASE-III TRIAL;
MEDROXYPROGESTERONE ACETATE;
MEGESTROL-ACETATE;
OVARIAN-CANCER;
CARCINOMA;
TAMOXIFEN;
ETOPOSIDE;
D O I:
暂无
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Objective: The objective of this study was to compare the efficacy of two multi-agent chemotherapeutic regiments that were previously used at the Institution for treatment of advanced and recurrent endometrial cancer. Methods: A retrospective review of patients with Stage III, IV, and recurrent endometrial cancer who received adjuvant chemotherapy at Roswell Park Cancer Institute over a period of 21 years. Two patient groups were defined based on treatment received: cisplatin, adriamycin, and VP-16 with or without megace (PAV-M), or carboplatin and paclitaxel (CT). Results: Forty-two patients with advanced or recurrent endometrial cancer were included in this review based on regimen received. Median duration of follow up was 55 months. Treatment with PAV-M resulted in more dose modifications compared to CT group (42% vs 11%, respectively). There were no significant differences in disease-free survival or overall survival. Conclusions: PAV/PAV-M is active in patients with advanced or recurrent endometrial cancer. However, toxicity associated with this triplet regimen may limit clinical use.
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页码:477 / 479
页数:3
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