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吉西他滨联合吡罗昔康治疗犬膀胱移行细胞癌的毒性作用及抗肿瘤反应

Toxic effects and antitumor response of gemcitabine in combination with piroxicam treatment in dogs with transitional cell carcinoma of the urinary bladder.

作者信息

Marconato Laura, Zini Eric, Lindner Donna, Suslak-Brown Lisa, Nelson Victoria, Jeglum Ann K

机构信息

Veterinary Oncology Service and Research Center, West Chester, PA 19382, USA.

出版信息

J Am Vet Med Assoc. 2011 Apr 15;238(8):1004-10. doi: 10.2460/javma.238.8.1004.

DOI:10.2460/javma.238.8.1004
PMID:21492043
Abstract

OBJECTIVE

To investigate whether combined treatment with gemcitabine and piroxicam in dogs with transitional cell carcinoma (TCC) of the urinary bladder is tolerated and provides an advantage in terms of survival time over previously reported treatments.

DESIGN

Clinical trial. Animals-38 dogs with TCC of the urinary bladder.

PROCEDURES

Dogs were treated with gemcitabine (800 mg/m(2), IV over 30 to 60 minutes, q 7 d) and piroxicam (0.3 mg/kg [0.14 mg/lb], PO, q 24 h). Complete blood cell counts were monitored prior to each gemcitabine treatment. All toxic effects of gemcitabine in dogs were recorded. Primary tumors were ultrasonographically reevaluated after 4 gemcitabine treatments.

RESULTS

Dogs received a median of 8 gemcitabine treatments (range, 1 to 38 treatments/dog). In response to treatment, 10 of 38 (26.3%) dogs had grade 1 gastrointestinal tract signs, 11 (28.9%) had grade 2, and 5 (13.2%) had grade 3. Grade 1 neutropenia developed in 6 (15.8%) dogs and grade 2 and 3 neutropenia in 2 (5.3%) dogs each. Thrombocytopenia was rare. All dogs had improvement of clinical signs of disease. Two dogs had a complete tumor response, 8 had a partial response, 19 had stable disease, and 8 had progressive disease. Median survival time with treatment was 230 days.

CONCLUSIONS AND CLINICAL RELEVANCE

Administration of gemcitabine in combination with piroxicam treatment failed to provide a longer overall survival time in dogs with TCC of the urinary bladder, compared with previously reported treatment strategies. However, this combination of chemotherapy did provide a new treatment alternative with fewer adverse effects.

摘要

目的

研究吉西他滨与吡罗昔康联合治疗犬膀胱移行细胞癌(TCC)是否可耐受,以及在生存时间方面是否比先前报道的治疗方法更具优势。

设计

临床试验。动物——38只患有膀胱TCC的犬。

步骤

犬接受吉西他滨(800mg/m²,静脉注射30至60分钟,每7天一次)和吡罗昔康(0.3mg/kg[0.14mg/磅],口服,每24小时一次)治疗。在每次吉西他滨治疗前监测全血细胞计数。记录吉西他滨对犬的所有毒性作用。在4次吉西他滨治疗后,对原发性肿瘤进行超声重新评估。

结果

犬接受吉西他滨治疗的中位数为8次(范围为1至38次/犬)。作为对治疗的反应,38只犬中有10只(26.3%)出现1级胃肠道症状,11只(28.9%)出现2级,5只(13.2%)出现3级。6只(15.8%)犬出现1级中性粒细胞减少,2只(5.3%)犬分别出现2级和3级中性粒细胞减少。血小板减少很少见。所有犬的疾病临床症状均有改善。2只犬肿瘤完全缓解,8只部分缓解,19只病情稳定,8只病情进展。治疗后的中位生存时间为230天。

结论及临床意义

与先前报道的治疗策略相比,吉西他滨与吡罗昔康联合给药未能使患有膀胱TCC的犬获得更长的总生存时间。然而,这种化疗联合方案确实提供了一种不良反应较少的新治疗选择。

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