A Phase I Trial of Sirolimus or Everolimus or Temsirolimus (mTOR Inhibitor) and Vorinostat (Histone Deacetylase Inhibitor) in Patients With Advanced Cancer
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 249
- 试验地点
- 1
- 主要终点
- Maximum Tolerated Dose (MTD)
研究概览
简要总结
The goal of this clinical research study is to find the highest tolerable dose of the combination vorinostat given in combination with either sirolimus, everolimus or temsirolimus that can be given to patients with advanced cancer. The safety of this drug combination will also be studied.
The Study Drugs:
Vorinostat is designed to prevent or slow down the growth of cancer cells by blocking proteins.
Everolimus is designed to stop cells from dividing. This may stop or slow the growth or spread of cancer cells.
Temsirolimus is designed to block a protein called mTOR (a protein that is thought to cause cancer cells to grow) inside the cancer cell. This may interfere with the growth or spread of cancer cells or possibly kill them.
Sirolimus is designed to block a protein called mTOR inside the cancer cell. This may interfere with the growth or spread of cancer cells or possibly kill the cancer cells.
This is an investigational study. Sirolimus is FDA approved and commercially available as an anti-rejection drug for kidney transplant recipients. Everolimus is FDA-approved and commercially available for the treatment of pancreatic neuroendocrine tumor, subependymal giant cell astrocytoma, and renal cell carcinoma. Temsirolimus is FDA approved and commercially available for the treatment of renal cell carcinoma. Vorinostat is FDA approved and commercially available for the treatment of cutaneous T-cell lymphoma. The combination of these drugs is investigational.
Up to 249 patients will take part in this study. All will be enrolled at MD Anderson.
详细描述
Study Drug Groups:
If you are found to be eligible to take part in this study, you will be assigned to a dose level of vorinostat and either sirolimus, everolimus, or temsirolimus based on when you joined this study. Up to 9 dose levels of sirolimus and vorinostat will be tested. Up to 3 dose levels of everolimus and vorinostat will be tested. Up to 3 dose levels of temsirolimus and vorinostat will be tested. Three (3) to 9 participants will be enrolled at each dose level. The first group of participants will receive the lowest dose level of the study drug combination. Each new group will receive a higher dose than the group before it, if no intolerable side effects were seen. This will continue until the highest tolerable dose of the combination vorinostat and sirolimus, everolimus, or temsirolimus is found.
Once the highest tolerated dose of the combinations are found, up to 14 participants with the tumor type that is most likely to respond to the study drug combinations will receive the study drugs at that dose level.
Study Drug Administration:
Each study "cycle" is 28 days.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients must have a histologically-confirmed metastatic or locally advanced cancer that has failed to respond to standard therapy, progressed despite standard therapy, or for which standard therapy that increases survival by at least three months does not exist
- •There is no limit on the number of prior treatment regimens
- •Patients must be off prior cytotoxic chemotherapy for at least three weeks. For biologic or targeted therapy, there should be five half lives or three weeks, whichever is shorter, between their last treatment and the first dose on this trial.
- •Patients may receive palliative radiation therapy before or during treatment on protocol, provided that there is measurable or evaluable disease out of the radiation field. Patients may receive palliative radiation therapy, if needed, 48 hours after last dose of investigational drug. In addition patients may be enrolled on trial seven days following palliative radiation. We will closely monitor for the appearance of radiation recall reactions. Hormonal therapy may continue in patients who have been on such treatment for three months or longer.
- •ECOG performance status 0-3
- •Patients must have adequate organ and marrow function as defined by: absolute neutrophil count >/= 1000uL, platelets >/= 50,000uL, bilirubin </=2mg/dL (exceptions may apply to benign non-malignant indirect hyperbilirubinemia such as Gilbert syndrome), ALT </= 2 x ULN or </=5x ULN if liver metastases present, creatinine </= 2mg/dL
- •As the effect of sirolimus or everolimus or temsirolimus and vorinostat in combination on the developing human fetus is not known, women of child-bearing potential and men must agree to use adequate contraception (abstinence; hormonal or barrier method of birth control) for the study and at least 3 months after completion
- •Female patients with child-bearing potential must have a negative serum or urine pregnancy test within 7 days of study enrollment. Nursing mothers should discontinue nursing
- •Ability to understand and the willingness to sign a written informed consent document
- •Measurable or evaluable disease
- •Patient must be able to swallow pills
排除标准
- •Myocardial infarction within 3 months prior to starting treatment
- •Concomitant use of phenytoin, carbamazepine, barbiturates, rifampin, phenobarbital or St. Johns wort, cyclosporine, diltiazem, ketoconazole should be discontinued if possible. The list of CYP3A4 inhibitors: http://medicine.iupui.edu/clinpharm/ddis/clinical-table/
- •Patient has a known hypersensitivity to the components of study drugs, its analogues, or drugs of similar chemical or biologic composition
- •Patient is pregnant or breastfeeding
- •Major surgical procedure within 28 days of day 1 of therapy
- •Use of any other concurrent investigational agents or anticancer agents except for hormonal therapy as outlined in inclusion criteria
研究组 & 干预措施
Arm B: Vorinostat + Everolimus
Escalation and Expansion Phase: Vorinostat dose 300 mg by mouth on Days 7 - 28. Rest of cycles: 300 mg by mouth on Days 1 - 28.
Escalation Phase: Everolimus starting dose 5 mg by mouth on Days 1 - 28.
Expansion Phase: MTD from Escalation Phase.
干预措施: Everolimus (Drug)
Arm A: Vorinostat + Sirolimus
Escalation Phase: Vorinostat starting dose 100 mg by mouth on Days 7 - 28 of Cycle 1; For all other cycles, dose of 100 mg Days 1-28.
Expansion Phase starting dose: MTD from Escalation Phase.
Escalation Phase: Sirolimus starting dose1 mg by mouth on Days 1 - 28.
Expansion Phase starting dose: MTD from Escalation Phase.
干预措施: Sirolimus (Drug)
Arm C: Vorinostat + Temsirolimus
Escalation and Expansion Phase: Vorinostat dose 300 mg by mouth on Days 7 - 28. Rest of cycles: 300 mg by mouth on Days 1 - 28.
Escalation Phase: Temsirolimus starting dose 12.5 mg by vein on Days 1, 8, 15, 22.
Expansion Phase: MTD from Escalation Phase.
干预措施: Temsirolimus (Drug)
Arm A: Vorinostat + Sirolimus
Escalation Phase: Vorinostat starting dose 100 mg by mouth on Days 7 - 28 of Cycle 1; For all other cycles, dose of 100 mg Days 1-28.
Expansion Phase starting dose: MTD from Escalation Phase.
Escalation Phase: Sirolimus starting dose1 mg by mouth on Days 1 - 28.
Expansion Phase starting dose: MTD from Escalation Phase.
干预措施: Vorinostat (Drug)
Arm B: Vorinostat + Everolimus
Escalation and Expansion Phase: Vorinostat dose 300 mg by mouth on Days 7 - 28. Rest of cycles: 300 mg by mouth on Days 1 - 28.
Escalation Phase: Everolimus starting dose 5 mg by mouth on Days 1 - 28.
Expansion Phase: MTD from Escalation Phase.
干预措施: Vorinostat (Drug)
Arm C: Vorinostat + Temsirolimus
Escalation and Expansion Phase: Vorinostat dose 300 mg by mouth on Days 7 - 28. Rest of cycles: 300 mg by mouth on Days 1 - 28.
Escalation Phase: Temsirolimus starting dose 12.5 mg by vein on Days 1, 8, 15, 22.
Expansion Phase: MTD from Escalation Phase.
干预措施: Vorinostat (Drug)
结局指标
主要结局
Maximum Tolerated Dose (MTD)
时间窗: 28 days
Maximum tolerated dose (MTD) defined by dose-limiting toxicities (DLTs) that 1) occur during the first four weeks of therapy, 2) are related to the study medications (attributions: possible, probable, and likely) and 3) fulfill one of the following criteria (as graded by the NCI Common Terminology Criteria for Adverse Events). MTD is defined as highest dose level in which 6 patients have been treated with less than 2 DLTs.
次要结局
- Tumor Response(After 4, 28 day cycles)