Anderson I C, Shipp M A, Docherty A J, Teicher B A
Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Cancer Res. 1996 Feb 15;56(4):715-8.
The efficacy of combination therapy including an oral gelatinase inhibitor (CT1746) and cytotoxic agent was analyzed using the murine Lewis lung carcinoma model. Primary tumors, pulmonary metastases, and sera from tumor-bearing animals had increased gelatinase B activity that was inhibited by CT1746 levels achievable in vivo. The combination of CT1746 and cyclophosphamide (CTX) was significantly more effective than either single agent in delaying local tumor growth (CT1746/CTX, 30.9 +/- 1.7 days; CT1746, 2.6 +/- 0.3 days; CTX, 19.5 +/- 1.1 days; P < .001) and reducing the number and size of pulmonary metastases [CT1746/CTX, 5 +/- 2 (15% metastases > 3 mm); CT1746, 15 +/- 4 (55% > 3 mm); CTX, 11 +/- 3 (63% > 3 mm); no treatment, 24 +/- 5 (62% > 3 mm); P < .001]. These data support the notion of combining matrix metalloproteinase inhibitors and cytotoxic agents to treat certain epithelial malignancies.
使用小鼠Lewis肺癌模型分析了包括口服明胶酶抑制剂(CT1746)和细胞毒性药物在内的联合治疗的疗效。原发性肿瘤、肺转移灶以及荷瘤动物的血清中明胶酶B活性升高,而体内可达到的CT1746水平可抑制该活性。CT1746与环磷酰胺(CTX)联合使用在延迟局部肿瘤生长方面(CT1746/CTX,30.9±1.7天;CT1746,2.6±0.3天;CTX,19.5±1.1天;P<.001)以及减少肺转移灶的数量和大小方面(CT1746/CTX,5±2(15%转移灶>3mm);CT1746,15±4(55%>3mm);CTX,11±3(63%>3mm);未治疗,24±5(62%>3mm);P<.001)均明显比单一药物更有效。这些数据支持将基质金属蛋白酶抑制剂和细胞毒性药物联合用于治疗某些上皮性恶性肿瘤的观点。