Zacharski L R, Moritz T E, Baczek L A, Rickles F R, Edwards R L, Forman W B, Forcier R J, Cornell C J, Haakenson C M, Ballard H S
Veterans Administration (VA) Medical Center, White River Junction, VT 05001.
J Natl Cancer Inst. 1988 Mar 16;80(2):90-7. doi: 10.1093/jnci/80.2.90.
Mopidamol (RA-233), a derivative of dipyridamole, is a phosphodiesterase inhibitor that has been shown previously to limit progression of malignancy in certain experimental animal models and in a pilot study in humans. RA-233 plus chemotherapy was compared with chemotherapy alone in a 5-year double-blind trial involving 719 patients with advanced carcinomas of the lung and of the colon. RA-233 treatment was associated with a statistically significant prolongation of survival in patients with non-small cell lung cancer (N-SCLC) limited to one hemithorax and with reduction in mean plasma fibrogen concentration. RA-233 was not toxic. The favorable effects on survival could not be explained by any factor other than the RA-233 treatment. In other tumor categories tested, no differences in survival were observed. These results suggest that RA-233 is useful in the treatment of N-SCLC of limited extent. They also suggest that therapeutic intervention aimed at modified intracellular pathways might constitute a novel investigative approach to the treatment of cancer.
莫匹达莫(RA - 233)是双嘧达莫的衍生物,是一种磷酸二酯酶抑制剂,此前已证实在某些实验动物模型和一项人体初步研究中,它可限制恶性肿瘤的进展。在一项涉及719例晚期肺癌和结肠癌患者的5年双盲试验中,对RA - 233加化疗与单纯化疗进行了比较。RA - 233治疗与局限于一侧胸腔的非小细胞肺癌(N - SCLC)患者的生存期在统计学上有显著延长以及平均血浆纤维蛋白原浓度降低相关。RA - 233无毒。除RA - 233治疗外,其他任何因素都无法解释对生存期的有利影响。在测试的其他肿瘤类别中,未观察到生存期的差异。这些结果表明,RA - 233可用于治疗局限性非小细胞肺癌。它们还表明,针对细胞内途径改变的治疗干预可能构成一种新型的癌症治疗研究方法。