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临床试验/NCT00222443
NCT00222443已完成1 期

Pilot Study Combining Temozolomide, Oncovin, Camptosar and Oral Antibiotic in Children and Adolescents With Recurrent Malignancy

University of Oklahoma2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2004年9月最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
40
试验地点
2
主要终点
Determine toxicity and maximum tolerated dose of escalating daily protracted irinotecan.

研究概览

简要总结

Determine toxicity and maximum tolerated dose of escalating daily protracted irinotecan, with weekly vincristine, temozolomide and vantin; to evaluate the feasibility of repetitive cycles of this chemotherapy and to estimate the response rate to this combination in children and adolescents with recurrent solid tumors and lymphomas.

详细描述

Determine toxicity and maximum tolerated dose of escalating daily protracted irinotecan, with weekly vincristine, temozolomide and vantin; to evaluate the feasibility of repetitive cycles of this chemotherapy and to estimate the response rate to this combination in children and adolescents with recurrent solid tumors and lymphomas.

Temozolomide is given by mouth one hour prior to each daily irinotecan dose days 1-5 of each cycle. 100 mg/m2/day. Irinotecan is given IV in dose escalation (minimum of 3 and up to 6 patients per cohort) starting at 15 mg/m2/day daily for 5 days for 2 weeks. Vincristin is given IV 1.5 mg/m2/dose (max dose 2mg) days 1 and 8 of each cycle. Vantin is given 10 mg/kg/day divided in 2 oral doses (max dose 400 mg/day) started 48 hours prior to the start of each treatment cycle and continued for 48 hours after last irinotecan dose. Cycle repeated every 28 days.

Therapy will continue for a minimum of two cycles unless there is progression of disease or unacceptable toxicity and may be continued as long as patient tolerates therapy and there is continued disease control up to one year of therapy.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
1 Year 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Under age 21 years at time of study entry
  • Malignant solid tumor, including CNS tumors and lymphomas
  • Recurrent or refractory disease not amenable to other potentially curative therapies
  • At least three weeks since last myelosuppressive chemotherapy > 6 months from allogeneic stem cell transplant
  • Adequate renal and hepatic function
  • Adequate peripheral blood counts unless bone marrow is involved

排除标准

  • Patients with leukemia not eligible
  • Patients with uncontrolled infection excluded
  • Patients who have received more than 4 prior chemotherapies
  • Patients who are receiving P450 enzyme-inducing anticonvulsants
  • Patients who are receiving any other cancer chemotherapy or any other investigational agent
  • Possible pregnancy will be excluded

结局指标

主要结局

Determine toxicity and maximum tolerated dose of escalating daily protracted irinotecan.

Evaluate feasibility of repetitive cycles of this combination .

次要结局

  • Estimate response rate in children and adolescents with recurrent solid tumors and lymphomas.

研究者

申办方类型
Other

研究点 (2)

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