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临床试验/NCT03458975
NCT03458975已完成2 期

Targeted Delivery of Chemotherapy With Ultrasound and Microbubbles

University Hospital, Tours1 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2019年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
7
试验地点
1
主要终点
Objective response for liver metastases

研究概览

简要总结

The oscillations of ultrasound (US) contrast agent microbubbles under their activation by US waves engender a modulation of the permeability of biological barriers amplifying hence the extravasation of drugs and/or fluorescent markers through a process known as sonoporation. In such a way, the bioavailability of the therapeutic agent is augmented only in the area where US waves are focused. The objective now is to translate this therapeutic approach to the clinic by performing a feasibility study with the development of a therapy regime optimized for hepatic metastases of colorectal cancer.

In order to demonstrate the clinical feasibility of the therapeutic approach based on ultrasound and microbubbles, we will focus on patients with liver metastases of colorectal cancer treated with monoclonal antibodies in combination with chemotherapy.

详细描述

Despite the increasing number of active molecules and the availability of news targeted therapies for cancer, therapeutic achievements remain modest for a number of tumor types. One of the major obstacles is inherent to the absence of specific delivery in the tumor tissue.

We have demonstrated recently that the oscillations of ultrasound (US) contrast agent microbubbles under their activation by US waves engender a modulation of the permeability of biological barriers amplifying hence the extravasation of drugs and/or fluorescent markers through a process known as sonoporation. In such a way, the bioavailability of the therapeutic agent is augmented only in the area where US waves are focused. The objective now is to translate this therapeutic approach to the clinic by performing a feasibility study with the development of a therapy regime optimized for hepatic metastases of colorectal cancer.

In order to demonstrate the clinical feasibility of the therapeutic approach based on ultrasound and microbubbles, we will focus on patients with liver metastases of colorectal cancer treated with monoclonal antibodies in combination with chemotherapy.

The work aims into evaluating the therapeutic efficacy of the proposed approach on a number of selected patients. We will follow the usual treatment schemes and we will apply imaging protocols to visualize tumor progression.

This technique of optimization of the intratumoral availability of anticancer drugs and based on sonoporation will improve the efficacy and safety of systemic chemotherapy by providing increased tumor uptake relative to normal tissue. This technique provides an ideal and easy strategy to optimize intratumoral drug delivery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

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

  • patient with liver metastases from colorectal cancer; patient with minimum two liver metastases which satisfy all the following criteria: diameter between 10 and 35 mm; arterially enhancing liver metastases detected with contrast enhanced ultrasound (CEUS); measurable liver metastases with CT-scan (Acceptability of a patient with more than 4 metastases or a patient with an odd number of metastases ≥ 2).
  • age ≥ 18 years;
  • ECOG/OMS 0-1;
  • life expectancy of at least 12 weeks;
  • adequate bone marrow, liver and kidney function;
  • written informed consent obtained from subject;
  • subjects covered by or having the rights to social security;
  • bi-weekly chemotherapy regimen
  • neo-adjuvant standard chemotherapy or palliative standard chemotherapy (first or second metastatic line) following the recommendations in force (national thesaurus of digestive oncology - colorectal cancer chapter: Phelip JM, Benhaim L, Bouché O, Christou N, Desolneux G, Dupré A, Léonard D, Michel P, Penna C, Rousseaux B, Tougeron D, Tournigand C. "Cancer colorectal métastatique". Thésaurus National de Cancérologie Digestive, Janvier 2019, http://www.tncd.org).

排除标准

  • Previous local treatment of selected liver metastases (radiofrequency, radioembolization, ...);
  • Indication for local ablative therapy of selected liver metastasis (radiofrequency ablation or other validated hepatic-directed modality of treatment);
  • Previous malignancy other than colorectal adenocarcinoma within 3 years prior to the inclusion with the exception for curatively treated basal cell carcinoma of the skin and/or curatively resected in situ cervical or breast cancer;
  • Known contraindication to the injection of Sonovue®, of Gadolinium, of iodated contrast agent;
  • contraindication to MRI or perfusion CT scan;
  • Patient under legal protection;
  • Pregnant or lactating woman, or woman with ability to procreate and without contraception;
  • Inclusion in another therapeutic trial
  • Uracilemia greater than or equal to 150ng/mL (suggestive of a complete DPD deficiency).
  • Presence of any material with potential interaction with ultrasound beam (metal, etc.) or healing tissue, and which cannot be bypassed

研究组 & 干预措施

Selected liver metastases of the patient

Active Comparator

Liver metastases randomized to receive sonoporation (US waves + gaseous microbubbles). The patient continue to receive the usual systemic chemotherapy

干预措施: MRI (Radiation)

Selected liver metastases of the patient

Active Comparator

Liver metastases randomized to receive sonoporation (US waves + gaseous microbubbles). The patient continue to receive the usual systemic chemotherapy

干预措施: Perfusion CT scan (Radiation)

Selected liver metastases of the patient

Active Comparator

Liver metastases randomized to receive sonoporation (US waves + gaseous microbubbles). The patient continue to receive the usual systemic chemotherapy

干预措施: Contrast enhanced ultrasound (Other)

Selected liver metastases of the patient

Active Comparator

Liver metastases randomized to receive sonoporation (US waves + gaseous microbubbles). The patient continue to receive the usual systemic chemotherapy

干预措施: Sonoporation (Drug)

Not-selected liver metastases of the patient

Placebo Comparator

Liver metatstases not randomized to receive sonoporation (US waves + gaseous microbubbles). The patient continue to receive the usual systemic chemotherapy like the active comparator arm

干预措施: MRI (Radiation)

Not-selected liver metastases of the patient

Placebo Comparator

Liver metatstases not randomized to receive sonoporation (US waves + gaseous microbubbles). The patient continue to receive the usual systemic chemotherapy like the active comparator arm

干预措施: Perfusion CT scan (Radiation)

Not-selected liver metastases of the patient

Placebo Comparator

Liver metatstases not randomized to receive sonoporation (US waves + gaseous microbubbles). The patient continue to receive the usual systemic chemotherapy like the active comparator arm

干预措施: Contrast enhanced ultrasound (Other)

结局指标

主要结局

Objective response for liver metastases

时间窗: 2 months

Objective response for liver metastases with spiral CT scan and defined as decrease of at least 30% in the longer diameter of each selected liver metastases

次要结局

  • Safety(Day 3, Day 17, Day 32, Day 47)
  • Tolerance(Day 3, Day 17, Day 32, Day 47)
  • Maximum percent reduction in tumor density on CT scan(2 months)
  • Maximum percent reduction in tumor density on MRI(2 months)
  • Assessment of tumor vascularity by MRI(2 months)
  • Assessment of tumor vascularity by Dynamic Contrast-Enhanced US (DCE-US)(2 months)
  • Dosage of antibody anti-VEGF or anti-EGFR by ELISA test(Day1, Day 3, Day 15, Day 17, Day 32, Day 45)
  • Assessment of tumor vascularity by Perfusion CT scan(2 months)
  • Dosage of antibody anti-VEGF or anti-EGFR(Day1, Day 3, Day 15, Day 17, Day 32, Day 45)
  • Dosage of cytokines(Day1, Day 3, Day 15, Day 17, Day 32, Day 45)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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