Surgery Plus Sulindac or Surgery Alone for Advanced Colorectal Cancer

National Cancer Institute (NCI)

Status and phase: Terminated; Phase 2

Conditions: Colorectal Adenocarcinoma; Liver Metastasis; Colorectal Cancer

Treatments: Drug: Sulindac; Drug: Placebo; Other: Validate assays and shipping methods

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT01856322

13-C-0126

130126

Details and patient eligibility

About

Background:

• Some types of inflammation may increase the risk of cancers in the intestinal track. Because of this possibility, anti-inflammatory drugs may be able to prevent tumor growth and spread. One such drug, sulindac, may be helpful to study. Researchers want to see if people who are having surgery to remove intestinal tumors from advanced colorectal cancer will benefit from sulindac. It will be tested against a placebo.

Objectives:

• To see if sulindac can improve treatment outcomes in people who are having surgery for advanced colorectal cancer.

Eligibility:

• Individuals at least 18 years of age who are having surgery for advanced colorectal cancer.

Design:

• Participants will be screened with a physical exam and medical history. Blood samples will be collected. Imaging studies and heart and lung function tests may also be given.
• Participants will be separated into two groups. One group will take sulindac. The other will take a placebo.
• Participants will take sulindac or placebo twice daily from about 2 to 3 weeks before the scheduled surgery. Seven days before the surgery, they will stop taking the pills.
• Participants will have surgery to remove their tumors. The surgery will also remove affected organ tissue.
• Participants will start to take the pills again once they have recovered from surgery. They will continue taking the sulindac or placebo twice a day for 3 years, or for as long as the tumors do not return.

Full description

• Despite strong evidence for a causative role of inflammatory mediators in intestinal cancer, the underlying mechanisms remain obscure. Established evidence indicates activation of the Wnt/beta-catenin pathway is an early step in the malignant transformation of colorectal adenomas with persistent activation in 90% of colorectal cancers. Activation of this pathway ultimately effects transcription of the S100A4 gene.
• S100A4 transcript serum levels have been shown to correlate with risk of recurrence in colorectal cancer and patients with systemic metastases are found to have increased S100A4 transcript expression.
• S100A4 may be a novel prognostic biomarker in colorectal cancer.
• Cyclooxygenase-2 is a key enzyme involved in the inflammatory response and is a key target of molecular chemoprevention in colorectal adenoma prevention trials.
• Recent studies demonstrate mitigation of Wnt/beta-catenin signaling by COX-2 inhibition via administration of the non-steroidal anti-inflammatory drug (NSAID) sulindac using in vitro and in vivo animal models.
• We hypothesize that sulindac administration will abrogate Wnt/beta-catenin mediated signaling and thus decrease S100A4 activity in patients with colorectal metastases.
• We propose to define the benefit of sulindac administration to patients with colorectal metastases following resection and validate the use of circulating S100A4 transcripts as a novel biomarker for disease recurrence.

Enrollment: 3 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

-INCLUSION CRITERIA

1. Histologically confirmed colorectal adenocarcinoma with metastatic disease confined to the liver, or limited extrahepatic intra-abdominal disease Note: limited sites of disease include:

   • porta hepatis lymph node metastases
   • pelvic lymph node metastases (internal iliac, external iliac or obturator)

2. Hepatic and intra-abdominal metastases must be measurable by computed tomography (CT), magnetic resonance imaging (MRI) and/or positron emission tomography (PET) scan

3. Liver disease must be amenable to gross total resection (R0/R1) with adequate functional liver remnant which requires preservation of at least 2 contiguous hepatic segments with adequate inflow, outflow, and biliary drainage with a functional liver remnant (FLR) volume of more than 20% (for healthy liver)

4. Greater than or equal to 18 years of age.

5. Must be able to understand and sign the Informed Consent Documentation.

6. Clinical performance status of Eastern Cooperative Oncology Group (ECOG) less than or equal to 2.

7. Life expectancy of greater than six months.

8. Patients of both genders must be willing to practice birth control during and for one week after taking sulindac/placebo.

9. Hematology:

   • Absolute neutrophil count greater than 1500/mm^3 without the support of Filgrastim.
   • Platelet count greater than 75,000/mm^3.
   • Hemoglobin greater than 8.0 g/dl.

10. Chemistry:

    • Serum creatinine less than or equal to 1.5 mg/dl unless the measured creatinine clearance is greater than 60mL/min/1.73m^2.
    • Total bilirubin less than or equal to 2 mg/dl, except for patients with diagnosis of Gilberts disease or hepatic pedicle obstruction then total bilirubin must be less than or equal to 5 mg/dl.

11. International normalized ratio (INR) less than or equal to 1.8.

INCLUSION CRITERIA for NORMAL VOLUNTEERS

• Age greater than 18
• Able to read and understand the informed consent
• No self-reported co morbidities of history of cancer

EXCLUSION CRITERIA

1. Women of child-bearing potential who are pregnant or breast feeding because of the potentially dangerous effects of the chemotherapy on the fetus or infant.

2. Active systemic infections, coagulation disorders or other major medical illnesses precluding major surgery.

3. Patients receiving warfarin anticoagulation, who cannot be transferred to other agents, such as low molecular weight heparins, anti-factor Xa (anti-Xa) agents, etc.

4. Active bleeding disorders

5. Patients with uncontrolled hypertension (would suggest: systolic blood pressure (SBP)> 155, diastolic blood pressure (DBP)> 90), unstable coronary disease (unstable angina, evidence of congestive heart failure (CHF), or myocardial infarction (MI) within 6-12 months of study)

6. Childs B or C cirrhosis or with evidence of severe portal hypertension by history, endoscopy, or radiologic studies or with evidence of moderate to severe ascites.

7. Prior history of gastrointestinal (GI) bleeding unrelated to a cancer diagnosis

   Note: Patients who have a normal upper and lower endoscopy may be enrolled at the discretion of the principal investigator (PI).

8. Renal insufficiency Discretion of principle investigator.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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3 participants in 3 patient groups, including a placebo group

Sulindac

Active Comparator group

Description:

one tablet twice daily

Treatment:

Drug: Sulindac

Placebo

Placebo Comparator group

Description:

one tablet twice daily

Treatment:

Drug: Placebo

Normal Volunteers (or control group)

Other group

Description:

Normal volunteers (or control group) enrolled with the only purpose to validate assays and the shipping method.

Treatment:

Other: Validate assays and shipping methods