Philip P A, Carmichael J, Tonkin K, Buamah P K, Britton J, Dowsett M, Harris A L
ICRF Clinical Oncology Unit, Churchill Hospital, Headington, Oxford, UK.
Br J Cancer. 1993 Feb;67(2):379-82. doi: 10.1038/bjc.1993.69.
Eighteen consecutive patients with measurable locally advanced or metastatic pancreatic adenocarcinoma were treated with goserelin (Zoladex) 3.6 mg subcutaneously every 4 weeks. Hydrocortisone 20 milligrams twice daily was commenced with the second injection of goserelin. Objective tumour response was monitored by computerised tomography of the abdomen. There was no objective remission in disease sites. Serial measurements of serum tumour markers showed no reduction in serum CA 19-9 and CA 195 concentrations. The median duration of survival of all cases was 5 months. Administration of goserelin resulted in significant reductions in oestradiol, testosterone, androstenedione in males and reductions in FSH and LH in both males and females. The addition of hydrocortisone resulted in further reductions of androstenedione and testosterone levels in males. Thus goserelin showed no anti-tumour effect, but concentrations required for direct inhibitory effects may be higher than those required to produce effects on hormone suppression.
18例可测量的局部晚期或转移性胰腺腺癌患者接受了戈舍瑞林(诺雷德)治疗,每4周皮下注射3.6毫克。在第二次注射戈舍瑞林时开始每日两次口服20毫克氢化可的松。通过腹部计算机断层扫描监测客观肿瘤反应。疾病部位无客观缓解。血清肿瘤标志物的系列测量显示血清CA 19-9和CA 195浓度没有降低。所有病例的中位生存期为5个月。戈舍瑞林治疗导致男性雌二醇、睾酮、雄烯二酮显著降低,男性和女性的促卵泡激素和促黄体生成素降低。添加氢化可的松导致男性雄烯二酮和睾酮水平进一步降低。因此,戈舍瑞林没有显示出抗肿瘤作用,但产生直接抑制作用所需的浓度可能高于产生激素抑制作用所需的浓度。