INTRAPERITONEAL CHEMOTHERAPY IN THE MANAGEMENT OF OVARIAN-CANCER

被引:50
作者
MARKMAN, M
REICHMAN, B
HAKES, T
CURTIN, J
JONES, W
LEWIS, JL
BARAKAT, R
RUBIN, S
MYCHALCZAK, B
SAIGO, P
ALMADRONES, L
HOSKINS, W
机构
[1] MEM SLOAN KETTERING CANC CTR,BREAST GYNECOL SERV,NEW YORK,NY 10021
[2] MEM SLOAN KETTERING CANC CTR,DEPT MED,DIV SOLID TUMOR ONCOL,NEW YORK,NY 10021
[3] MEM SLOAN KETTERING CANC CTR,DEPT SURG,GYNECOL SERV,NEW YORK,NY 10021
[4] MEM SLOAN KETTERING CANC CTR,DEPT RADIAT ONCOL,NEW YORK,NY 10021
[5] MEM SLOAN KETTERING CANC CTR,DEPT PATHOL,NEW YORK,NY 10021
关键词
INTRAPERITONEAL CHEMOTHERAPY; CANCER CHEMOTHERAPY; OVARIAN CANCER; CISPLATIN;
D O I
10.1002/cncr.2820710423
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
During the past decade, intraperitoneal therapy of ovarian cancer has evolved from a pharmacologic model into an established treatment technique for women with this malignancy. Approximately 40% of patients with small-volume residual ovarian cancer (microscopic disease or macroscopic tumor, less-than-or-equal-to 0.5 cm in maximum tumor diameter), after an objective response to initial organoplatinum-based systemic chemotherapy, may have a surgically documented complete response to platinum-based intraperitoneal chemotherapy. Patients who have not responded to systemic platinum administration rarely will respond to the drug given intraperitoneally, despite the presence of only small-volume residual disease when this regional treatment strategy is used. Other agents with antineoplastic activity after intraperitoneal administration in women with ovarian cancer include mitoxantrone, taxol, alpha-interferon and gamma-interferon, and interleukin-2. Although intraperitoneal therapy currently is being examined as a component of the initial chemotherapeutic program for patients with ovarian cancer, a precise role for regional drug delivery in this clinical setting remains to be defined.
引用
收藏
页码:1565 / 1570
页数:6
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