Manni A, Boucher A E, Demers L M, Harvey H A, Lipton A, Simmonds M A, Bartholomew M
Department of Medicine, Milton S. Hershey Medical Center, Pennsylvania State University, Hershey 17033.
J Steroid Biochem Mol Biol. 1990 Dec 20;37(6):1083-7. doi: 10.1016/0960-0760(90)90470-6.
Newly developed somatostatin analogues may be useful agents in the treatment of breast and prostate cancer. Potential mechanisms of antitumor action include suppression of circulating levels of trophic hormones and growth factors as well as direct effects at the tumor level, potentially involving autocrine/paracrine mechanisms. Pilot clinical trials conducted in heavily pretreated women with advanced breast cancer indicate that SMS 201-995 (Sandostatin R) has minimal toxicity and moderately suppresses stimulated growth hormone secretion and basal somatomedin-C level. Somatostatin analogues have also been found to retard the growth of experimental prostate cancer, particularly when used in combination with LHRH analogues. The therapeutic efficacy of these compounds used alone or in combination with other agents in the treatment of breast and prostate cancer remains to be established in larger clinical trials involving less heavily pretreated patients.
新开发的生长抑素类似物可能是治疗乳腺癌和前列腺癌的有效药物。抗肿瘤作用的潜在机制包括抑制营养激素和生长因子的循环水平,以及在肿瘤水平的直接作用,这可能涉及自分泌/旁分泌机制。在接受过大量治疗的晚期乳腺癌女性中进行的初步临床试验表明,SMS 201-995(善得定R)毒性极小,并能适度抑制刺激后的生长激素分泌和基础生长调节素C水平。生长抑素类似物还被发现可延缓实验性前列腺癌的生长,特别是与促性腺激素释放激素类似物联合使用时。这些化合物单独使用或与其他药物联合用于治疗乳腺癌和前列腺癌的疗效,仍有待在涉及预处理程度较低的患者的更大规模临床试验中确定。