Klijn J G
Med Oncol Tumor Pharmacother. 1984;1(2):123-8. doi: 10.1007/BF02934984.
Twenty-one premenopausal patients with metastatic breast cancer (unselected for receptor status) were treated during 3-14 months with the potent LHRH-agonist Buserelin (Hoe 766) as a first-line therapy. In one-third of 12 patients treated with Buserelin alone an objective tumour response was observed in the absence of side effects. The longest duration of response occurred in 2 patients with complete remissions (14+ and 13+ months). After addition and in combination with tamoxifen this LHRH-agonist treatment caused an objective response in about half (8/17) of the patients. A problem appears to be the great variation in hormonal response especially during the combination treatment with tamoxifen, which was not found during combination treatment with megestrol acetate in 4 patients. Ultimately, of the whole group of 21 patients, 9 patients (43%) showed an objective remission, 6 stable disease and 6 progression of tumour growth.
21例绝经前转移性乳腺癌患者(未选择受体状态)接受强效促性腺激素释放激素(LHRH)激动剂布舍瑞林(Hoe 766)治疗3至14个月,作为一线治疗。在仅接受布舍瑞林治疗的12例患者中,三分之一的患者在无副作用的情况下出现了客观肿瘤反应。反应持续时间最长的是2例完全缓解的患者(分别为14 +和13 +个月)。在添加他莫昔芬并与之联合使用后,这种LHRH激动剂治疗使约一半(8/17)的患者出现客观反应。一个问题似乎是激素反应差异很大,尤其是在与他莫昔芬联合治疗期间,而在4例与醋酸甲地孕酮联合治疗的患者中未发现这种情况。最终,在整个21例患者组中,9例患者(43%)出现客观缓解,6例病情稳定,6例肿瘤进展。