Piver M S, Barlow J J, Lurain J R, Blumenson L E
Cancer. 1980 Jan 15;45(2):268-72. doi: 10.1002/1097-0142(19800115)45:2<268::aid-cncr2820450211>3.0.co;2-8.
A prospective trial was initiated in 1972 utilizing Depo-Provera in women with metastatic or recurrent endometrial adenocarcinoma to evaluate if the objective response and survival would be significantly improved in comparison to patients previously treated with Delalutin at a similar dose. One hundred fourteen patients were included in the study: 70 received Delalutin and 44 Depo-Provera. There was no significant increase in the objective response or survival between the Delalutin or Depo-Provera patients. Of the 114 patients, 15.8% achieved an objective response, with 7.0% being complete responders. There was no significant increase in objective response to Delalutin or Depo-Provera in relationship to the size of the tumor masses, the number of metastases, site of metastases, histologic grade of the primary, histologic grade of recurrence or metastases, or prior radiation therapy. The only significant correlate was that patients whose disease recurred 3 or more years after the initial therapy had a significant (P = 0.01) increase in response (33.3%) compared to those with recurrence less than 3 years after their original treatment (8.3%).
1972年开展了一项前瞻性试验,对患有转移性或复发性子宫内膜腺癌的女性使用醋酸甲羟孕酮,以评估与先前接受类似剂量己酸孕酮治疗的患者相比,客观缓解率和生存率是否会显著提高。该研究纳入了114名患者:70名接受己酸孕酮治疗,44名接受醋酸甲羟孕酮治疗。己酸孕酮组和醋酸甲羟孕酮组患者的客观缓解率或生存率均未显著提高。114名患者中,15.8%达到客观缓解,其中7.0%为完全缓解者。己酸孕酮或醋酸甲羟孕酮的客观缓解率与肿瘤肿块大小、转移灶数量、转移部位、原发灶组织学分级、复发或转移灶组织学分级或既往放疗情况均无显著增加。唯一显著的相关因素是,初始治疗后3年或更长时间疾病复发的患者,其缓解率(33.3%)相比初始治疗后不到3年复发的患者(8.3%)有显著(P = 0.01)提高。