Actively Recruiting
Colorectal Metastasis Prevention International Trial 2
Led by Assaf-Harofeh Medical Center · Updated on 2019-04-18
200
Participants Needed
6
Research Sites
417 weeks
Total Duration
On this page
Sponsors
A
Assaf-Harofeh Medical Center
Lead Sponsor
S
Sheba Medical Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
The short perioperative period (days to weeks around surgery) is characterized by stress-inflammatory responses, including catecholamines (CAs, e.g., adrenaline) and prostaglandins (PGs, e.g., prostaglandin-E2) release, and induce deleterious pro-metastatic effects. Animal studies implicated excess perioperative release of CAs and PGs in facilitating cancer progression by affecting the malignant tissue, its local environment, and anti-metastatic immune functions. Congruently, animal studies conducted by the investigators indicate that combined use of the beta-adrenergic blocker, propranolol, and the prostaglandins inhibitor, etodolac - but neither drug separately - efficiently prevented post-operative metastatic development. Two recently conducted clinical trials, conducted by the investigators, in three medical centers in Israel, recruiting breast (n=38) and colorectal (n=34) cancer patients, assessing the safety and short-term efficacy of perioperative propranolol and etodolac treatment. Drugs were well tolerated, without severe adverse events. Importantly, molecular/biological analyses of the excised primary tumor indicated that drug treatment caused promising anti-metastatic transformations, as well as improvements in immune and inflammatory indices. These included (i) decreased tumor cell capacity to migrate, (ii) reduced pro-metastatic capacity of the malignant tissue, and (iii) improvement in immune infiltrating into the tumor (Paper published in Clinical Cancer Research, 2017). Herein, the investigators propose to conduct a double-blind placebo-controlled two-arm Phase II clinical trial in 200 colorectal cancer patients undergoing curative surgery in Israel. A perioperative 20-day drug treatment will be initiated 5 days before surgery. Primary outcomes will include (i) 3-year disease-free-survival (DFS), and 5-year overall survival (OS); and (ii) biological markers in blood samples, and in the excised tumor tissue. Secondary outcomes will include safety indices and psychological measures of depression, anxiety, distress, and fatigue
CONDITIONS
Official Title
Colorectal Metastasis Prevention International Trial 2
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients planned for surgery for primary resection of colon or rectal cancer with curative intent
- Single colonic or rectal carcinoma confirmed by colonoscopy and tumor biopsy
- No evidence of metastatic disease before surgery based on imaging
- ASA score of 1-3 or ECOG Performance Status of 0 to 1
- Signed informed consent form
- Willing and able to comply with study procedures (physically and mentally)
- Men and women aged 20 to 80 years
You will not qualify if you...
- Presence of metastatic disease before surgery
- Planned surgery without curative intent
- Renal failure with creatinine level above 1.5
- Significant heart failure (NYHA class 3 or higher)
- Significant liver failure (cirrhosis or bilirubin level above 2)
- Current asthma or Chronic Obstructive Pulmonary Disease (COPD)
- Pharmacological treatment for diabetes mellitus (type 1 or 2)
- Peripheral vascular disease
- Known allergy to study drugs or related medications
- Chronic treatment with beta-adrenergic blockers or COX inhibitors
- Bradycardia or second/third degree AV block
- History of stroke or transient ischemic attack
- Printzmetal's angina
- Right-sided heart failure due to pulmonary hypertension
- Significant cardiomegaly
- Current pheochromocytoma
- Chronic digoxin treatment
- Active peptic disease
- Pregnancy
- Participation in another interventional study
- History or presence of other malignant diseases except current colorectal cancer
- Chemotherapy in last 10 years except recent neo-adjuvant therapy for rectal cancer
- Use of immunosuppressive medications
- Immunodeficiency or autoimmune diseases treated with immunosuppressives
- Suffering from sick sinus syndrome
AI-Screening
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Trial Site Locations
Total: 6 locations
1
HaEmek Medical Center
Afula, Israel, 1834111
Not Yet Recruiting
2
Rambam Health Care Campus
Haifa, Israel, 3109601
Not Yet Recruiting
3
Rabin Medical Center
Petah Tikva, Israel, 4941492
Not Yet Recruiting
4
Sourasky Medical Center
Tel Aviv, Israel, 6423906
Not Yet Recruiting
5
Sheba Medical Center
Tel Litwinsky, Israel, 45858
Not Yet Recruiting
6
Asaf Harofeh Medical Center
Ẕerifin, Israel, 70300
Actively Recruiting
Research Team
O
Oded Zmora, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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