Actively Recruiting

Phase 2
Age: 20Years - 80Years
All Genders
NCT03919461

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

Age: 20Years - 80Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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Colorectal Metastasis Prevention International Trial 2 | DecenTrialz