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临床试验/NCT00625092
NCT00625092已完成1 期

Phase I Hyperthermic Intraperitoneal Oxaliplatin for Peritoneal Malignancies

Masonic Cancer Center, University of Minnesota1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2007年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
17
试验地点
1
主要终点
Maximum tolerated dose of hyperthermic intraperitoneal oxaliplatin

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as oxaliplatin, leucovorin, and fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Hyperthermia therapy kills tumor cells by heating them to several degrees above normal body temperature. Peritoneal infusion of heated and nonheated chemotherapy drugs after surgery may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of hyperthermic intraperitoneal oxaliplatin followed by intraperitoneal leucovorin and fluorouracil in treating patients with peritoneal cancer.

详细描述

OBJECTIVES:

Primary

  • To determine the safety and optimal dose of hyperthermic intraperitoneal oxaliplatin when administered during cytoreductive surgery and followed by intraperitoneal leucovorin calcium and fluorouracil in patients with peritoneal malignancies.

Secondary

  • To determine the outcome of cytoreductive surgery in these patients.
  • To determine the time to disease progression and pattern of failure in patients treated with this regimen.
  • To determine the 1 and 5 year survival in patients treated with this regimen.
  • To compare quality-of-life pre- and post-surgery in these patients.
  • To characterize total- and free-platinum pharmacokinetics in the plasma and total platinum in the intraperitoneal space at baseline, during, and after hyperthermic intraperitoneal chemotherapy (HIPC).
  • To assess for the presence of genetic polymorphisms in the XDP and XRCC1 DNA repair genes.
  • To assess tumor and normal tissue concentrations for total platinum obtained at baseline and immediately after HIPC.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Hyperthermic Treatment

Experimental

Patients receiving combination of hyperthermic intraperitoneal chemotherapy (HIPC) with oxaliplatin plus intraperitoneal 5-Fu and intraperitoneal leucovorin with peritoneal metastases.

干预措施: fluorouracil (Drug)

Hyperthermic Treatment

Experimental

Patients receiving combination of hyperthermic intraperitoneal chemotherapy (HIPC) with oxaliplatin plus intraperitoneal 5-Fu and intraperitoneal leucovorin with peritoneal metastases.

干预措施: leucovorin calcium (Drug)

Hyperthermic Treatment

Experimental

Patients receiving combination of hyperthermic intraperitoneal chemotherapy (HIPC) with oxaliplatin plus intraperitoneal 5-Fu and intraperitoneal leucovorin with peritoneal metastases.

干预措施: oxaliplatin (Drug)

Hyperthermic Treatment

Experimental

Patients receiving combination of hyperthermic intraperitoneal chemotherapy (HIPC) with oxaliplatin plus intraperitoneal 5-Fu and intraperitoneal leucovorin with peritoneal metastases.

干预措施: cytoreductive surgery (Procedure)

结局指标

主要结局

Maximum tolerated dose of hyperthermic intraperitoneal oxaliplatin

时间窗: 30 Days Post Treatment

次要结局

  • Overall survival(1 Year and 5 Years)
  • Changes in quality-of-life(Baseline and at 4, 8, and 12 months)
  • Time to Disease Progression(Monthly)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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