Treatment of Inoperable Colorectal Cancer With Electrochemotherapy Through an Endoscopic System
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 10
- 试验地点
- 2
- 主要终点
- treatment safety
研究概览
简要总结
A new approach to treating solid tumours (both operable and inoperable) has been carried out by the Cork Cancer Research Centre (CCRC) at the Mercy University Hospital, Cork, Ireland since 2002.
The approach simply allows a greater concentration of chemotherapy drugs to enter the tumour cells rather than healthy cells. The uptake of the chemotherapeutic drug directly by the tumour is aided through applying short electric pulses to the tumor mass (referred to as - Electrochemotherapy or ECT). The pulses make the tumour more porous which allows the drug easier access into the cancer cells, whereas other tissues and organs in the body remain relatively poor at absorbing the drug, thereby reducing the potential side effects on healthy tissues. This approach to date has been limited to skin based tumours due to the requirement for the electrodes to be placed directly in contact with the tumour. Procedures with electrochemotherapy have been applied to human patients in other countries of the EU, the US and Japan.
The drug concentration used is significantly reduced due to the more targeted absorption by the tumor and this significantly reduces side effects normally associated with chemotherapy.
A large number of preclinical and clinical Phase I and I/II studies have demonstrated the efficiency and safety of ECT. These studies have included patients with melanoma, head and neck squamous cell carcinoma, merkel cell carcinomas, basal cell carcinoma and adenocarcinoma nodules. Case reports concerning other primary tumours have also been reported.
The investigators have developed an endoscopic approach (EndoVe system) for delivering the electric pulses to internal cancers and are currently seeking to evaluate its efficacy in the treatment of inoperable colorectal cancer. The treatment procedure is similar to standard endoscopic colorectal examination (colonoscopy) with the added element of an intravenous injection of bleomycin followed after eight minutes by the delivery of electric pulses (each one less than 1msec in duration). The pulses are endoscopically delivered directly to the tumour mass. The entire procedure is minimally invasive and does not require intensive care follow up or stitches. If the treatment is successful the tumour will shrink in size in the weeks following the procedure.
The objective of this study is to investigate the efficacy and safety of this approach in reducing the size of the tumour.
详细描述
The objective is to conduct treatment in a minimally invasive manner (using the endoscope) and without the requirement for repeated doses of chemotherapy. The single dose of the drug used (15,000 IU/m2 x Body Surface Area of bleomycin) has been well tolerated in all patients treated previously with this approach to skin based cancers (in excess of 300 treatments since 2003 in our hospital). Therefore, it is anticipated that patients are unlikely to suffer side effects from the low concentration of drug used.
There are no known side effects of the instrument being tested. The pulse generator used has been certified by European electrical safety bodies charged with assessing compliance of new equipment with the present security rules for electrical devices. The electrical pulse generator has the CE mark and is approved for use clinically; the endoscopic electrodes used are a prototype system and are not currently CE approved.
The treatment is provided on an outpatient basis and does not involve an overnight stay. The procedure is very similar to a colonoscopy examination with the added element of a low dose chemotherapy drug being injected intravenously.
It reduces operative time; therefore there are fewer anaesthetic risks
At this time, the only option for patients with inoperable colorectal cancers is symptom relief e.g. a defunctioning colostomy or stent placement. Both carry a risk profile greater than the treatment with the EndoVe system.
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
- 否
入选标准
- •Histologically verified colorectal tumour.
- •Case reviewed by a multidisciplinary team (MDT) (surgery, radiology, oncology, gastroenterology) and there are no curable options with the standard of care. The MDT considers all available treatment options and enrolment to this study is agreed as being appropriate; Or the case is curable but patient refuses to undergo the standard of care. The MDT considers all possible alternatives, which are also discussed with the patient, and the MDT considers enrolment to this study as being the most appropriate option; Or patients with advanced local disease with impending obstruction on endoscopic evaluation who are otherwise not suitable for surgical intervention or stenting, the MDT would also consider these patients for enrolment into this study.
- •Men or women aged at least 18 years.
- •Performance status (Karnofsky > 60% or ECOG/WHO < 2).
- •Treatment free interval of at least 2 weeks after previously applied therapy.
- •Patients must be mentally capable of understanding the information given.
- •Patients must give written informed consent.
- •a) A female of Non-Childbearing potential (i.e. physiologically incapable of becoming pregnant) is eligible to participate in the study if she:
- •has had a hysterectomy
- •has had a bilateral oophorectomy (ovariectomy) - has had a bilateral tubal ligation
- •Is post-menopausal:
排除标准
- •Coagulation disorder
- •Patients with pre-existing renal dysfunction are excluded. [Note: Creatinine clearance will be measured for all patients. For Bleomycin treatment: creatinine clearance must be greater than 40ml/min.]
- •Patients with a clinically manifested arrhythmia or with a pacemaker
- •Patients with epilepsy.
- •Pregnancy or lactation/breastfeeding.
- •Patient known to be Hepatitis B/C or HIV positive.
- •Concurrent treatment with an investigational medicinal product or participation in another clinical study.
- •Patients who have undergone a regime of Bevacizumab in the previous 4 weeks.
- •Patients with any other clinical condition or prior therapy that, in the opinion of the investigator, would make the patient unsuitable for the study or unable to comply with the study requirements.
- •Highly inflamed colon tissue which is ulcerated and bleeding.
- •Additional exclusion criteria specifically regarding patients where Bleomycin is study drug:
- •Contraindications for bleomycin use including acute pulmonary infection and severe pulmonary disease.
- •Contraindication for bleomycin use: allergic reactions to bleomycin observed in previous treatment.
- •Contraindication for bleomycin use: if cumulative dose of 250mg BLM/m2 was previously exceeded.
- •Additional exclusion criteria specifically regarding patients where Cisplatin is study drug:
- •Patients with hypersensitivity to Cisplatin or other platinum compounds or to any of the excipients are to be excluded from receiving Cisplatin for the study.
- •Cisplatin is contraindicated in combination with live vaccines, including yellow fever vaccine.
- •Cisplatin is contraindicated in combination with phenytoin in prophylactic use.
- •Cisplatin is contraindicated in patients with myelosuppression.
- •Cisplatin is contraindicated in patients in a dehydrated condition (pre- and post-hydration is required to prevent serious renal dysfunction).
- •Cisplatin is contraindicated in patients with a pre-existing hearing impairment.
- •Cisplatin is contraindicated in patients with neuropathy caused by cisplatin.
- •Contraindication for Cisplatin use: Allergic reactions to Cisplatin observed in previous treatment.
研究组 & 干预措施
EndoVe treatment
Use of the EndoVe device to safely and effectively ablate rectal tumor tissue
干预措施: EndoVe endoscopic electroporation (Device)
结局指标
主要结局
treatment safety
时间窗: 3 months
Evaluate safety of treatment approach at regular checkup intervals following treatment
Tumor regression
时间窗: 3 months
Follow up examination of tumor volume following treatment via endoscopy and transrectal ultrasound.
次要结局
未报告次要终点
研究者
Dr Declan Soden
Principal Investigator
Mercy University Hospital, Cork, Ireland