首页> 外文期刊>Japanese Journal of Clinical Oncology >Treatment with Medroxyprogesterone Acetate Plus Levonorgestrel-releasing Intrauterine System for Early-stage Endometrial Cancer in Young Women: Single-arm, Prospective Multicenter Study: Korean Gynecologic Oncology Group Study (KGOG2009)
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Treatment with Medroxyprogesterone Acetate Plus Levonorgestrel-releasing Intrauterine System for Early-stage Endometrial Cancer in Young Women: Single-arm, Prospective Multicenter Study: Korean Gynecologic Oncology Group Study (KGOG2009)

机译:醋酸甲羟孕酮联合左炔诺孕酮释放子宫内系统治疗年轻女性早期子宫内膜癌:单臂,前瞻性多中心研究:韩国妇科肿瘤小组研究(KGOG2009)

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摘要

A prospective multicenter trial has been started in Korea to investigate the treatment efficacy of a levonorgestrel-releasing intrauterine system plus medroxyprogesterone acetate in young women with early-stage endometrial cancer. A number of studies have reported the effectiveness of hormonal therapy using systemic progestin in women clinically diagnosed with early endometrial adenocarcinoma at Stage IA, Grade 1, who want to maintain reproductive potential. In addition, several recent studies reported the use of a levonorgestrel-releasing intrauterine system to treat patients at a high risk of perioperative complications who cannot tolerate systemic progesterone because of its adverse effects. However, there has been no prospective multicenter trial that investigated the effectiveness of treatment with systemic progesterone in combination with intrauterine progesterone in young women with endometrial cancer. Young patients with histologically confirmed Grade 1 endometrioid adenocarcinoma that is presumably confined to the endometrium, who desired to preserve their fertility potential, undergo levonorgestrel-releasing intrauterine system insertion and are administered medroxyprogesterone acetate at a dosage of 500 mg/day concurrently. The follow-up and treatment response assessment were implemented at a 3-month interval with office endometrial aspiration biopsy with the levonorgestrel-releasing intrauterine system in place, and dilatation and curettage after removal of the levonorgestrel-releasing intrauterine system. The primary endpoint is the complete response rate. The secondary endpoint is to estimate the consistency of the results of the office endometrial aspiration biopsy with the levonorgestrel-releasing intrauterine system in the uterus and a dilatation and curettage after removal of the levonorgestrel-releasing intrauterine system.
机译:韩国已开始一项前瞻性多中心试验,以研究左炔诺孕酮释放子宫内系统联合醋酸甲羟孕酮在患有早期子宫内膜癌的年轻妇女中的治疗效果。许多研究报告了使用全身性孕激素进行激素治疗在临床上被诊断为IA期1级,希望保持生殖潜能的早期子宫内膜腺癌的妇女的有效性。此外,最近的一些研究报道了使用左炔诺孕酮宫内释放系统治疗因围手术期并发症而由于其不良反应而不能耐受全身性黄体酮的高风险患者。但是,尚无一项前瞻性的多中心试验来研究全身性孕酮联合宫内孕酮治疗子宫内膜癌年轻女性的有效性。经组织学确认为子宫内膜样1样腺癌的年轻患者可能局限于子宫内膜,希望保留其生育力,接受左炔诺孕酮释放子宫内系统插入,并同时服用醋酸甲羟孕酮,剂量为500 mg /天。随访和治疗反应评估每隔三个月进行一次,进行子宫内膜抽吸活检,并使用左炔诺孕酮释放子宫系统,并在切除左炔诺孕酮释放子宫系统后进行扩张和刮除术。主要终点是完整的响应率。次要终点是评估办公室子宫内膜穿刺活检与子宫内释放左炔诺孕酮的子宫系统以及切除左炔诺孕酮的释放子宫内系统后的刮宫术的一致性。

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  • 来源
    《Japanese Journal of Clinical Oncology》 |2012年第12期|p.1215-1218|共4页
  • 作者单位

    1Department of Obstetrics and Gynecology, Gangnam CHA Medical Center, CHA University 2Department of Obstetrics and Gynecology, Seoul Metropolitan Boramae Hospital 3Department of Obstetrics and Gynecology, Seoul National University Hospital, Seoul, Republic of Korea 4Department of Obstetrics and Gynecology, Cancer Biostatistics Branch National Cancer Center, Goyang, Republic of Korea 5Department of Pathology, Cheil General Hospital and Women's Health care Center, Kwandong University College of Medicine, Seoul, Republic of Korea 6Department of Pathology, Chungnam National University College of Medicine, Daejeon, Republic of Korea;

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