A Phase I Study of CCI-779 (Temsirolimus) in Combination With Topotecan in Patients With Gynecologic Malignancies
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- Tolerability of regimen
研究概览
简要总结
The aim of the trial is to determine the recommended phase II dose of weekly intravenous topotecan in combination with a fixed dose (25 mg or 15 mg) of weekly intravenous temsirolimus in patients with and without prior pelvic radiation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Factorial
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Histologically confirmed recurrent or metastatic ovarian carcinoma, fallopian tube carcinoma, primary peritoneal carcinoma, cervical carcinoma, endometrial carcinoma, vulvar carcinoma, vaginal carcinoma, or carcinosarcoma of the ovary, endometrium or cervix.
- •Prior Therapy: at least one and may have up to three prior cytotoxic chemotherapeutic regimens for the management of primary disease.
- •Must be at least 18 years of age.
- •GOG performance status must be 0 or
- •Patients must have adequate organ and marrow function as defined below:
- •hemoglobin ≥10g/dL
- •absolute neutrophil count ≥1,500/uL
- •platelets ≥100,000/uL
- •total bilirubin below the institutional upper limit of normal
- •AST(SGOT)/ALT(SGPT) below the institutional upper limit of normal
- •creatinine below the institutional upper limit of normal
- •cholesterol ≤ 350 mg/dL (fasting)
- •triglycerides ≤ 400 mg/dL (fasting)
- •albumin ≥ 3.0 mg/dL
- •negative pregnancy test for women able to have children
- •Ability to understand and the willingness to sign a written informed consent document.
排除标准
- •Prior therapy with topotecan
- •More than 3 prior cytotoxic chemotherapeutic regimens or treatment with temsirolimus or any other mTOR inhibitor
- •Concomitant hormonal therapy or radiation therapy
- •Clinically significant infections or other medical problems of significant severity
- •History of unstable angina or myocardial infarction within the past six months
- •Known brain metastases unless the metastases have been controlled by prior surgery or radiotherapy, and the patient has been neurologically stable and off of steroids for at least 4 weeks.
- •Any requirement for oxygen
- •Cannot be receiving potent enzyme-inducing antiepileptic drugs (EIAEDs; e.g., phenytoin, carbamazepine, phenobarbital) nor any other potent CYP3A4 inducer such as rifampin or St. John's wort, as these may decrease temsirolimus levels. Use of agents that potently inhibit CYP3A4 (and hence may raise temsirolimus levels), such as ketoconazole, is discouraged, but not specifically prohibited.
研究组 & 干预措施
A
Arm A will consist of subjects without prior pelvic radiation or with radiation to a field smaller than the whole pelvis. Subjects will receive weekly CCI-779 and topotecan at the assigned dose.
干预措施: Topotecan (Drug)
A
Arm A will consist of subjects without prior pelvic radiation or with radiation to a field smaller than the whole pelvis. Subjects will receive weekly CCI-779 and topotecan at the assigned dose.
干预措施: CCI-779 (temsirolimus) (Drug)
B
Arm A will consist of subjects with prior whole pelvic radiation. Subjects will receive weekly CCI-779 and topotecan at the assigned dose.
干预措施: Topotecan (Drug)
B
Arm A will consist of subjects with prior whole pelvic radiation. Subjects will receive weekly CCI-779 and topotecan at the assigned dose.
干预措施: CCI-779 (temsirolimus) (Drug)
结局指标
主要结局
Tolerability of regimen
时间窗: 4 weeks
次要结局
未报告次要终点