A Phase I/II Study of Weekly Topotecan and Gefitinib (Iressa) in Patients With Platinum-Resistant Ovarian, Peritoneal, of Fallopian Tube Cancer
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 19
- 试验地点
- 1
- 主要终点
- Dose Limiting Toxicity (DLT)
研究概览
简要总结
The purposes of this study are:
- To determine the dose limiting toxicity (DLT) and the maximum tolerated dose (MTD) weekly of topotecan in combination with standard dose gefitinib in patients with relapsed, platinum-resistant, ovarian, peritoneal or fallopian tube cancers that are epidermal growth factor receptor (EGF-R) positive (>/= 1+).
- To determine the response rate and response duration in this patient population treated with the maximum tolerated dose (MTD) of topotecan administered on a weekly schedule in combination with standard dose gefitinib, given by way of the mouth (PO) daily.
详细描述
Gefitinib inhibits the activity of a molecule present on the cancer cell that plays a role in cancer cell growth. Topotecan is an FDA approved drug used to treat ovarian cancer that is still present after treatment with chemotherapy. It is also used to treat recurrent ovarian cancer (patients whose cancer returns after they have been cancer-free for a period of time).
Before treatment starts, you will have a complete physical exam, routine blood tests (about 2-3 teaspoons), a chest x-ray, and a CT scan or MRI. Women who are able to have children must have a negative blood pregnancy test.
There are 2 phases to this study. In the first phase, 3 different dose levels of topotecan are being studied. The dose of topotecan that you receive will depend on when you are enrolled. It will also depend on whether or not other participants had side effects from their treatment. Although the dose of topotecan will vary, the dose of gefitinib is the same for all participants. Up to 6 participants may be treated at each dose. The goal of this portion of the study is to find the highest safe dose of this drug combination. Up to 18 patients will be treated on this part of the study.
Once the highest safe dose of topotecan has been found, the second phase of the study will begin. In this phase, all participants will receive the same dose of topotecan and gefitinib. Up to 40 patients will be enrolled in this part of the study (but 6 will be from the 1st portion of the study.
Each treatment cycle is 28 days long. You will take one gefitinib tablet by mouth every day beginning on Day 1. In addition, you will be given topotecan through a catheter (tube) placed in a vein over 30 minutes on Days 1, 8, and 15.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Women with platinum-resistant, histologically confirmed epithelial ovarian, fallopian tube or peritoneal cancer. Resistance is defined as: Progression of disease during platinum chemotherapy, or progression of disease within 6 months of completing platinum chemotherapy, or failure to achieve a complete response, with persistent macroscopic disease, after an adequate trial of primary therapy.
- •EGF-R expression must be positive (e.g., 1+ or greater) See appendix G.
- •Patients with a known hypersensitivity to platinum compounds, who have failed a desensitization regimen, or in the opinion of the investigator, are not good candidates for desensitization, are eligible.
- •Patients must have measurable disease.
- •Unlimited number of prior chemotherapy regimens are allowed.
- •Zubrod performance status </=
- •Patients must have adequate hepatic, renal, and bone marrow function, defined as serum creatinine </= 2 mg/dl (estimated creatinine clearance 50 ml/min); total bilirubin < /=2.0 X the upper limit of normal (ULN); alanine aminotransferase (ALT) </= 2X ULN; white blood count (WBC) >/= 3,000/mm3; absolute neutrophil count (ANC) >/= 1,500/mm3; platelets >/= 100,000/mm
- •At least three weeks must have elapsed from completion of chemotherapy or radiation therapy.
- •At least 30 days must have elapsed from completion of treatment with a non-approved or investigational drug.
- •Patients must sign an informed consent indicating that they are aware of the investigational nature of the study, in keeping with the policies of the hospital. The only approved consent is appended to this protocol.
- •Women of childbearing potential must be willing to practice acceptable methods of birth control to prevent pregnancy.
排除标准
- •Patients with borderline or low malignant potential tumors are not eligible.
- •Patients who have had prior therapy with topoisomerase I inhibitors.
- •Patients who are pregnant or lactating.
- •Concurrent chemotherapy, radiation therapy, or surgery (excluding palliative radiation).
- •Concurrent, uncontrolled, medical or psychiatric disorders.
- •Patients with an active infection.
- •Patients with a known hypersensitivity to topotecan or iressa.
- •Patients with severe cardiovascular disease (i.e. arrhythmias requiring chronic treatment or congestive heart failure) (NYHA classification III or IV).
- •History of other malignancy (except nonmelanoma skin cancer or carcinoma in situ of the cervix), unless in complete remission and off all therapy for that disease for a minimum of 5 years.
- •Patients with overt psychosis or mental disability or otherwise incompetent to give informed consent.
- •Patients who have had prior anti-EGFR therapy (i.e. Tarceva, Cetuximab).
- •Evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the subject to participate in the trial.
- •Concomitant use of phenytoin, carbamazepine, rifampicin, barbiturates, or St. John's Wort.
- •Any evidence of clinically active interstitial lung disease (patient with chronic stable radiographic changes who are asymptomatic are eligible).
研究组 & 干预措施
Topotecan + Gefitinib
Phase I: Topotecan: 2.0, 3.0, or 4.0 mg/m^2 by vein Days 1, 8 and 15 of 28 day cycle.
Gefitinib: 250 mg by mouth daily.
Phase II: Topotecan starting dose: MTD from Phase I by vein Days 1, 8, and 15 of 28 day cycle.
Gefitinib: 250 by mouth daily for 28 Days.
干预措施: Topotecan (Drug)
Topotecan + Gefitinib
Phase I: Topotecan: 2.0, 3.0, or 4.0 mg/m^2 by vein Days 1, 8 and 15 of 28 day cycle.
Gefitinib: 250 mg by mouth daily.
Phase II: Topotecan starting dose: MTD from Phase I by vein Days 1, 8, and 15 of 28 day cycle.
Gefitinib: 250 by mouth daily for 28 Days.
干预措施: Gefitinib (Drug)
结局指标
主要结局
Dose Limiting Toxicity (DLT)
时间窗: Continual reassessment method, prior to each 28 day cycle, an average of 60 days
Dose-limiting toxicity defined as any Grade 4 hematological toxicity and any \> Grade 3 non-hematologic toxicity. The DLT (dose-limiting toxicity) is defined as any Grade 4 hematological toxicity and any \> Grade 3 non-hematologic toxicity.
Maximum Tolerated Dose (MTD) of Topotecan
时间窗: At end of first course, prior to each new course (28 day cycle). Continual reassessment method (CRM) during each course for toxicity, an average of 60 days
Maximum tolerated dose is highest dose level in which 6 patients treated with at most 1 experiencing DLT.
次要结局
- Response Rate(61 weeks)