Cisplatin treatment of transitional cell carcinoma of the urinary bladder in dogs: 18 cases (1983-1993)

被引:0
作者
Chun, R
Knapp, DW
Widmer, WR
Glickman, NW
DeNicola, DB
Bonney, PL
机构
[1] PURDUE UNIV,SCH VET MED,DEPT VET CLIN SCI,W LAFAYETTE,IN 47907
[2] PURDUE UNIV,SCH VET MED,CTR APPL ETHOL & HUMAN ANIM INTERACT,W LAFAYETTE,IN 47907
[3] PURDUE UNIV,SCH VET MED,DEPT VET PATHOBIOL,W LAFAYETTE,IN 47907
关键词
canine species; carcinoma; transitional cell; cisplatin; oncology;
D O I
暂无
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Objective-To determine whether cisplatin administered at a dosage of 60 mg/m(2) of body surface area, IV, every 21 days, would induce remission of transitional cell carcinoma of the urinary bladder in dogs. Design-Retrospective analysis of medical records. Animals-18 dogs with histologically confirmed transitional cell carcinoma of the urinary bladder. Procedure-Clinical staging was performed by means of physical examination, contrast cystography or ultrasonography, and thoracic radiography prior to and 42 days after the initiation of cisplatin treatment. Dogs with clinical signs of tumor progression were reevaluated earlier than 42 days in some instances. Complete remission (CR) was defined as complete resolution of measurable tumor. Partial remission (PR) was defined as a greater than or equal to 50% reduction in tumor volume without development of new tumors. Stable disease was defined as < 50% change in tumor volume at 42 days without development oi new lesions. Progressive disease (PD) was defined as greater than or equal to 50% increase in tumor volume or development of new tumors at any lime. Dogs were reevaluated at 42-day intervals until they had a CR, developed PD, or developed unacceptable adverse effects. Results-Three dogs had a PR, 4 had stable disease, and 9 had PD. Tumor response could not be assessed in 2 dogs: 1 dog developed grand mal seizures 3 hours after the first dose of cisplatin was given and was euthanatized; the other dog continued to have clinical signs of urinary tract obstruction and was euthanatized 8 days after the first dose of cisplatin. Four dogs developed renal azotemia that was suspected to be secondary to cisplatin nephrotoxicity. Clinical implications-The cisplatin dosage was higher than that reported in studies of dogs with transitional cell carcinoma of the bladder. Even with this higher dosage, none of the dogs had a CR, and only 3 of 18 had a PR. A more effective, less toxic treatment for transitional cell carcinoma in dogs is needed.
引用
收藏
页码:1588 / &
页数:5
相关论文
共 17 条
[1]  
ANDERSON WI, 1989, CORNELL VET, V79, P263
[2]  
*BMDP STAT SOFTW, 1994, US GUID BMDP NEW SYS, P131
[3]   URINARY-BLADDER NEOPLASIA IN THE DOG - A REVIEW OF 70 CASES [J].
BURNIE, AG ;
WEAVER, AD .
JOURNAL OF SMALL ANIMAL PRACTICE, 1983, 24 (03) :129-143
[4]  
*DIV SURV EP EP PR, 1994, EP INF VERS 6 02 US, P73
[5]  
FAIR WR, 1993, CANCER PRINCIPLES PR, P1052
[6]  
GILSON SD, 1990, J AM VET MED ASSOC, V196, P1811
[7]   CISPLATIN THERAPY IN 41 DOGS WITH MALIGNANT-TUMORS [J].
KNAPP, DW ;
RICHARDSON, RC ;
BONNEY, PL ;
HAHN, K .
JOURNAL OF VETERINARY INTERNAL MEDICINE, 1988, 2 (01) :41-46
[8]   PIROXICAM THERAPY IN 34 DOGS WITH TRANSITIONAL-CELL CARCINOMA OF THE URINARY-BLADDER [J].
KNAPP, DW ;
RICHARDSON, RC ;
CHAN, TCK ;
BOTTOMS, GD ;
WIDMER, WR ;
DENICOLA, DB ;
TECLAW, R ;
BONNEY, PL .
JOURNAL OF VETERINARY INTERNAL MEDICINE, 1994, 8 (04) :273-278
[9]   CISPLATIN (CISDIAMMINEDICHLOROPLATINUM) FOR TREATMENT OF TRANSITIONAL CELL-CARCINOMA OF THE URINARY-BLADDER OR URETHRA - A RETROSPECTIVE STUDY OF 15 DOGS [J].
MOORE, AS ;
CARDONA, A ;
SHAPIRO, W ;
MADEWELL, BR .
JOURNAL OF VETERINARY INTERNAL MEDICINE, 1990, 4 (03) :148-152
[10]   CANINE BLADDER AND URETHRAL TUMORS - A RETROSPECTIVE STUDY OF 115 CASES (1980-1985) [J].
NORRIS, AM ;
LAING, EJ ;
VALLI, VEO ;
WITHROW, SJ ;
MACY, DW ;
OGILVIE, GK ;
TOMLINSON, J ;
MCCAW, D ;
PIDGEON, G ;
JACOBS, RM .
JOURNAL OF VETERINARY INTERNAL MEDICINE, 1992, 6 (03) :145-153