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临床试验/NCT01904916
NCT01904916终止不适用

Protocol to Obtain Tumor Biopsies From Patients With Locally Advanced (Incurable) or Metastatic Cancer to Improve Selection for Clinical Trials. (CPCT - 05 Biopsy Protocol Patient Selection)

P.O. Witteveen4 个研究点 分布在 1 个国家目标入组 195 人开始时间: 2014年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
195
试验地点
4
主要终点
Percentage of screened patients allocated to trials based upon outcome of genetic screening effort.

研究概览

简要总结

Our knowledge on the genetic mutations in cancer is rapidly expanding and we are increasingly testing drugs in mainly metastatic cancer patient populations with rare mutations. Successful examples of this new strategy are ALK inhibitors in ALK translocated NSCLC (less than 5% frequency) and EGFR inhibitors in EGFR mutant NSCLC (approximately 5% frequency). Selecting molecularly stratified patient populations for studies benefits the patient as it increases the odds of obtaining benefit from experimental treatment, especially in early clinical trials. Moreover it increases the speed and efficacy of drug development as signs of efficacy are picked up in earlier phases. Therefore, broad screening of molecular lesions in the tumors of patients that are being considered for participation in trials is crucial. This pre-selection increases our ability to perform several trials in parallel and thus include more patients in more meaningful trials. With the still dismal prognosis of patients with metastatic cancer, increasing the accrual rate to pivotal trials in selected patient populations is a key factor in improving prognosis.

The advent of Next Generation Sequencing (NGS) platforms enables us to probe a limited number of cancer related genes within 2-4 weeks. We have extensively piloted this approach and are now able to deliver clinically meaningful turn-around-times. This development enables us to use this technology to enrich clinical trials using targeted therapies for patients with specific mutations.

We will obtain tumor biopsies of a metastatic or locally advanced lesion and a peripheral blood sample from all patients included in the trial; the biopsies to obtain information on the tumor related genetic mutations (mutational profile) and the blood samples to assess each patient's germline DNA background variation. As patients will be asked to undergo an invasive procedure it is important to address the potential safety issues. Review of the literature and our own experience show that tumor biopsies can be performed with only minor complications and acceptable risks. We will recruit patients with metastatic or locally advanced solid tumors from patients that can potentially be included in clinical trials.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

  • Locally advanced (incurable) or metastatic cancer from a histological or cytological proven solid tumor
  • Indication for systemic treatment with anti-cancer agents (with no treatment options with curative intent)
  • Measurable locally advanced (incurable) or metastatic lesion(s), according to RECIST 1.1 criteria.
  • Safe biopsy of a metastatic or locally advanced lesion possible
  • No contraindications for lidocaine (or its derivatives) and/or midazolam and/or phentanyl
  • Adequate organ function
  • WHO performance status 0-2
  • Age > 18 yr
  • Expected adequacy to follow up
  • Written informed consent

排除标准

  • If one or more of the above mentioned inclusion criteria is not met

研究组 & 干预措施

Histological biopsy procedure

Other

This is a diagnostic multicenter study combining histological biopsy of tumor material with DNA sequencing using Ion Torrent®, Next Generation Sequencing (NGS) platform. The study aims improve stratification of cancer patients by obtaining fresh tumor biopsies for next-generation sequencing for participation in clinical trials.

干预措施: Histological biopsy procedure (Procedure)

结局指标

主要结局

Percentage of screened patients allocated to trials based upon outcome of genetic screening effort.

时间窗: 1 year

次要结局

  • Number and nature of (serious) adverse events of the performed histological biopsies.(2 days after each biopsy procedure)
  • Number of samples stored for future related research.(1 year)
  • Number of samples with an adequate microRNA, (phospho)proteomic profiles and organoid cultures that allows biomarker discovery efforts. These profiles will be deposited in the CPCT database.(1 year)

研究者

发起方
P.O. Witteveen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

P.O. Witteveen

Investigator

UMC Utrecht

研究点 (4)

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