CYTOSINE-ARABINOSIDE AND CISPLATIN FOR ADVANCED BREAST-CANCER - A PHASE-II STUDY OF THE CANCER AND LEUKEMIA GROUP-B

被引:0
|
作者
OSTER, MW
SCHILSKY, RL
FARAGGI, D
KORZUN, AH
PERRY, M
MOORE, A
KALRA, J
WOOD, WC
HENDERSON, IC
机构
[1] LONG ISL JEWISH MED CTR,NEW HYDE PK,NY
[2] COLUMBIA UNIV COLL PHYS & SURG,NEW YORK,NY 10032
[3] CORNELL UNIV,MED CTR,COLL MED,NEW YORK,NY 10021
[4] UNIV CHICAGO,PRITZKER SCH MED,CHICAGO,IL 60637
[5] HARVARD UNIV,SCH PUBL HLTH,BOSTON,MA 02115
[6] HARVARD UNIV,SCH MED,BOSTON,MA 02115
[7] UNIV MISSOURI,MED CTR,SCH MED,COLUMBIA,MO 65201
关键词
D O I
10.1002/1097-0142(19911015)68:8<1696::AID-CNCR2820680807>3.0.CO;2-B
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Forty-four women with advanced breast cancer participated in a prospective clinical trial to evaluate the efficacy and toxicity of a regimen consisting of cytosine arabinoside and cisplatin. All patients had previously received chemotherapy. Three patients (7%) responded to therapy with response durations of 153, 160, and 441 days. The median time to disease progression and median survival time in all 44 patients were 2.3 and 5 months, respectively. This regimen had significant toxicity, with most patients experiencing severe or life-threatening hematologic, renal, or infectious complications. This regimen cannot be recommended for previously treated patients with advanced breast cancer.
引用
收藏
页码:1696 / 1698
页数:3
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