Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Purdue University, West Lafayette, IN, USA.
J Vet Intern Med. 2010 Sep-Oct;24(5):1124-30. doi: 10.1111/j.1939-1676.2010.0569.x. Epub 2010 Jul 28.
Transitional cell carcinoma (TCC) is the most common cancer of the urinary tract in dogs. The most frequent cause of death is urinary obstruction from the primary tumor. Standard medical therapy for TCC is only partially effective.
HYPOTHESIS/OBJECTIVES: Intravesical administration of mitomycin C (MMC) in dogs with invasive TCC will result in antitumor activity against the primary tumor and minimal systemic drug absorption.
Thirteen privately owned dogs with naturally occurring, histopathologically diagnosed TCC of the urinary bladder.
A prospective phase I trial was performed. MMC was given intravesically (600 μg/mL initial concentration) for 1 h/d for 2 consecutive days each month. The MMC concentration was escalated to a maximum of 800 μg/mL in groups of 3 dogs until the maximum tolerated dose (MTD) was determined. Serum assays for MMC were performed to determine the extent of systemic absorption of the MMC.
The MTD of MMC based on local toxicoses was 700 μg/mL (1-h dwell time, 2 consecutive days). In addition, 2 dogs had severe myelosuppression and appeared to have systemic absorption of MMC. Five dogs had partial remission, and 7 dogs had stable disease.
Intravesical MMC has antitumor activity in dogs with invasive TCC. Further study is needed to determine the cause of the myelosuppression associated with MMC administration, and to develop strategies to minimize this risk.
膀胱癌(TCC)是犬最常见的泌尿道肿瘤。导致犬类死亡的最常见原因是原发性肿瘤导致的尿路阻塞。TCC 的标准医学疗法仅部分有效。
假设/目的:对于患有侵袭性 TCC 的犬,膀胱内给予丝裂霉素 C(MMC)将对原发性肿瘤产生抗肿瘤活性,并且全身药物吸收最小。
13 只患有自发性、组织病理学诊断为膀胱 TCC 的私人拥有犬。
进行了一项前瞻性 I 期试验。MMC 以 600 μg/mL 的初始浓度经膀胱内给药(1 小时/天,连续 2 天/月)。MMC 浓度增加到 800 μg/mL,每组 3 只犬,直到确定最大耐受剂量(MTD)。进行 MMC 的血清检测以确定 MMC 的全身吸收程度。
基于局部毒性的 MMC 的 MTD 为 700 μg/mL(1 小时驻留时间,连续 2 天)。此外,有 2 只犬出现严重的骨髓抑制,似乎有 MMC 的全身吸收。5 只犬有部分缓解,7 只犬有稳定的疾病。
膀胱内 MMC 对患有侵袭性 TCC 的犬具有抗肿瘤活性。需要进一步研究以确定与 MMC 给药相关的骨髓抑制的原因,并制定策略将这种风险降至最低。