Endoscopic Treatment of Inoperable Colorectal Cancer With the EndoVe System

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.

Quicker recovery time- This is beneficial for the patient in terms of reduced exposure to the hospital environment through a shorter in-patient stay.

Research: The potential benefits of studying novel medical instruments in general include the development of new alternatives to conventional or existing therapies for certain cancers. In particular, the widespread availability of the novel instrument being tested here may lessen the requirement for more invasive procedures. It will reduce the amount of chemotherapy drug being used, therefore reducing the systemic effects as well as the side effects.

The approach is currently being applied to inoperable cases but in the future it may potentially be applied to both earlier stage cancers and other internal cancers e.g. oesophagus, stomach etc.

Because the treatment procedure is short (outpatient basis), it allows these patients greater time outside of the hospital environment to maximise and allowing for a greater quality of life (this for both individual patient and community at large).

If this treatment approach is proven to be safe and effective, patients with inoperable colorectal cancers will have a minimally invasive option for palliation of symptoms.

Inclusion criteria

• 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:

Exclusion criteria

• 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.