Bonfil R D, Russo D M, Schmilovich A J, Garcia-Palazzo I B
Laboratory of Fundación de Investigación del Cáncer, CEFYBO, Buenos Aires, Argentina.
J Urol. 1997 Sep;158(3 Pt 1):912-5.
To ascertain intravesical vinorelbine tartrate (VNR) antitumor activity against MB-49, a murine transitional cell carcinoma of the bladder (TCC), in an in vivo setting.
C57B1/6J female mice were intravesically implanted with 5 x 10(4) MB-49 cells and treated locally with VNR. Tumor incidence and volume analyses, as well as survival studies were carried out.
Tumor incidence was significantly lower in VNR-treated mice (48%, n = 23) than in controls (84%, n = 19), as evaluated sixteen days after MB-49 orthotopic inoculation. Intravesical tumor volume was also significantly smaller in treated mice respect to controls (median [range]: 0.5 [0.4 to 61.8] mm.3 versus 47.7 [4.2 to 179.7] mm.3 respectively, p < 0.001 Kruskal-Wallis test). Median survival duration of the animals treated with VNR was 68 [21 to 68] days, and was significantly greater (p = 0.01, Kruskal-Wallis test) than that of untreated controls (18 [16 to 20] days).
Intravesical VNR treatment demonstrated an evident antitumor effect against the TCC model assayed. The results obtained suggest a potential use of VNR as intravesical treatment for superficial TCC following transurethral bladder tumor resection to prevent recurrence or retard tumor growth.
在体内环境中确定酒石酸长春瑞滨(VNR)对MB - 49(一种小鼠膀胱移行细胞癌(TCC))的膀胱内抗肿瘤活性。
将5×10⁴个MB - 49细胞膀胱内植入C57B1/6J雌性小鼠,并对其进行VNR局部治疗。进行肿瘤发生率和体积分析以及生存研究。
在MB - 49原位接种16天后评估,VNR治疗组小鼠的肿瘤发生率(48%,n = 23)显著低于对照组(84%,n = 19)。治疗组小鼠的膀胱内肿瘤体积相对于对照组也显著更小(中位数[范围]:分别为0.5[0.4至61.8]mm³ 与47.7[4.2至179.7]mm³,p < 0.001,Kruskal - Wallis检验)。接受VNR治疗的动物的中位生存持续时间为68[21至68]天,且显著长于未治疗的对照组(18[16至20]天,p = 0.01,Kruskal - Wallis检验)。
膀胱内VNR治疗对所检测的TCC模型显示出明显的抗肿瘤作用。所获得的结果表明VNR在经尿道膀胱肿瘤切除术后作为浅表TCC的膀胱内治疗以预防复发或延缓肿瘤生长具有潜在用途。