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临床试验/NCT00544648
NCT00544648终止1 期

A Phase I/II Study of Nab-Paclitaxel and Carboplatin With Concurrent Radiation Therapy for Unresectable Stage III Non-Small-Cell Lung Cancer (NSCLC)

Vanderbilt-Ingram Cancer Center6 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2007年11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
终止
入组人数
13
试验地点
6
主要终点
Maximum Tolerated Dose of Nab-paclitaxel When Combined Concurrently With Carboplatin and Radiation (Phase I)

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Nab-paclitaxel (paclitaxel albumin-stabilized nanoparticle formulation) may make tumor cells more sensitive to radiation therapy. Giving nab-paclitaxel together with radiation therapy and carboplatin may kill more tumor cells.

PURPOSE: This phase I/II trial is studying the side effects and best dose of giving nab-paclitaxel together with carboplatin and radiation therapy and to see how well it works in treating patients with stage III non-small-cell lung cancer that cannot be removed by surgery.

详细描述

OBJECTIVES:

Primary

  • To determine the maximum tolerated dose of nab-paclitaxel when combined concurrently with carboplatin and radiation followed by two courses of nab-paclitaxel carboplatin as consolidation. (Phase I)
  • To evaluate the progression-free survival in patients with stage III unresectable non-small cell lung cancer treated with nab-paclitaxel, carboplatin, and radiotherapy followed by two courses of nab-paclitaxel with carboplatin as consolidation. (Phase II)

Secondary

  • To assess safety and tolerability and identify dose-limiting toxicities in patients receiving nab-paclitaxel combined concurrently with carboplatin and radiotherapy. (Phase I)
  • To assess progression-free survival, response rates, and survival. (Phase I)
  • To assess overall survival and response rates in all patients treated on this study. (Phase II)
  • To assess the safety and tolerability of patients receiving nab-paclitaxel combined concurrently with carboplatin and radiotherapy followed by two courses of nab-paclitaxel/carboplatin as consolidation. (Phase II) OUTLINE: This is a multicenter study.
  • Phase I:

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

Treatment

Experimental

nab-paclitaxel+ carboplatin + radiation

干预措施: carboplatin (Drug)

Treatment

Experimental

nab-paclitaxel+ carboplatin + radiation

干预措施: nab-paclitaxel (Drug)

Treatment

Experimental

nab-paclitaxel+ carboplatin + radiation

干预措施: Radiation therapy (Radiation)

结局指标

主要结局

Maximum Tolerated Dose of Nab-paclitaxel When Combined Concurrently With Carboplatin and Radiation (Phase I)

时间窗: 7 weeks

The highest dose in milligrams per meter of body surface squared (mg/m2) of nab-paclitaxel in combination with carboplatin while maintaining tolerability. Cohorts of 3-6 patients received escalating doses of nab-paclitaxel in combination with carboplatin until the maximum tolerated dose (MTD) was achieved. The MTD is defined as the dose preceding that at which 2 or more of 6 patients experience dose-limiting toxicity (DLT) during the initial cycle of therapy. DLTs per Common Toxicity Criteria v 3.0: recurring non-hematological (except esophagitis) \> Grade 2, non-hematological or esophagitis \> Grade 3 toxicities that are symptomatically unacceptable to patient and result in treatment delay for \> 2 weeks, persistent toxicity resulting in treatment delay for \> 2 weeks.

Progression-free Survival (Phase II)

时间窗: On-study to lesser of date of progression or date of death from any cause (assessed up to 2 years)

Estimated probable duration of life without disease progression, from on-study date to earlier of progression date, or date of death from any cause, using the Kaplan-Meier method with censoring (see Analysis Population Description for additional details). Disease progression is defined by Response Evaluation in Solid Tumors (RECIST) v.1.1: \>= 20% increase in sum of the longest diameter of target lesions, unequivocal progression of non-target lesions, or appearance of new lesions

次要结局

  • Progression-free Survival (Phase I)(On-study to lesser of date of progression or date of death from any cause (assessed up to 2 years))
  • Overall Survival (Phase I)(On-study date to date of death from any cause (assessed up to 2 years))
  • Response (Phase I)(On-treatment date to date of progressive disease (assessed up to 2 years))
  • Number of Patients With Each Worst Grade Toxicity (Phase I)(On-study date to 30 days following final dose of study drug)
  • Overall Survival (Phase II)(Time Frame: date on study to date of death from any cause or last known date alive)
  • Number of Patients With Each Worst Grade Toxicity (Phase II)(at 16 weeks)
  • Response (Phase II)(On-treatment date to date of progressive disease (assessed up to 2 years))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Vicki Keedy, MD

Assistant Professor of Medicine; Clinical Director, Sarcoma Program; Medical Director, Clinical Trials Shared Resource; Medical Oncologist

Vanderbilt-Ingram Cancer Center

研究点 (6)

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