跳至主要内容
临床试验/JPRN-UMIN000011154
JPRN-UMIN000011154已完成未知

A PHASE III RANDOMIZED TRIAL OF PULSE ACTINOMYCIN-D VERSUS MULTI-DAY METHOTREXATE FOR THE TREATMENT OF LOW-RISK GESTATIONAL TROPHOBLASTIC NEOPLASIA - GOG-0275

Gynecologic Oncology Group0 个研究点目标入组 6 人开始时间: 2013年7月16日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
6

研究概览

简要总结

Schink JC, et al. Gynecol Oncol 2020; 158(2): 354-360

研究设计

研究类型
Interventional

入排标准

年龄范围
18years-old 至 ot applicable(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1)Patients who do not have GTN as defined in Key inclusion criteria 1). 2)Patients with non-gestational choriocarcinoma. 3)Patients who have previously been treated with cytotoxic chemotherapy. However, patients who received prior low-dose methotrexate for treatment of an ectopic pregnancy will be eligible for this study. 4)Patients who have received prior pelvic radiation. 5)Patients with placental site trophoblastic tumor (PSTT) or epithelioid trophoblastic tumor (ETT). 6)Patients with GOG Performance status of 3 or 4. 7)Patients with a history of other invasive malignancies, with the exception of non-melanoma skin cancer, are excluded if there is any evidence of other malignancy being present within the last five years. Patients are also excluded if their previous cancer treatment contraindicates this protocol therapy. 8)Patients whose circumstances at the time of study entry do not permit completion of the study or required follow-up. 9)Patients who wish to breast-feed during treatment.

研究者

相似试验