A Clinical Trial of COX and EGFR Inhibition in Familial Polyposis Patients (FAPEST)

Utah System of Higher Education (USHE)

Status and phase: Completed; Phase 2

Conditions: Adenomatous Polyposis Coli

Treatments: Drug: Sulindac; Drug: Placebo A; Drug: Placebo B; Drug: Erlotinib

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT01187901

00039278

P01CA073992 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to determine in a randomized, placebo-controlled, phase II trial if the combination of sulindac and erlotinib causes a significant regression of duodenal and colorectal adenomas in familial adenomatous polyposis (FAP) and attenuated FAP (AFAP) patients.

Full description

This will be a single-center, phase-II, six-month-long, placebo-controlled, double blinded, randomized trial of the epidermal growth factor receptor (EGFR) inhibitor, erlotinib (Tarceva) and the cyclooxygenase (COX-2) inhibitor, sulindac in patients with familial adenomatous polyposis (FAP) or attenuated FAP. FAP is an autosomal dominant inherited colon cancer predisposition with a 100% risk of colon cancer in the absence of preventive care (endoscopy and surgery). Efficacious chemoprevention for duodenal adenomas is an unmet clinical need in FAP patients that would reduce the morbidity from duodenectomy and risk of duodenal adenocarcinoma. Currently the only Food and Drug Administration (FDA)-approved chemopreventive agent is celecoxib which results in a modest reduction of duodenal and colorectal polyps and is associated with cardiac toxicity at effective doses. If it can be shown that combinatorial inhibition of COX-2 and EGFR activity leads to successful regression in duodenal adenomatous polyps in FAP, it could be used as an effective chemopreventive regimen in FAP patients with duodenal adenomas or who have undergone surgical resection of duodenal adenomas or have many rectal adenomas. FAP and AFAP patients will be screened by endoscopy for presence of 5 or more duodenal polyps, then randomized to either A) erlotinib at 75 mg/day and sulindac at 150 mg/day or B) placebo for 6 months. The endpoint will be endoscopy at 6 months.

Primary Aim : To determine if the combination of sulindac and erlotinib causes a significant regression of duodenal polyp burden at 6 mohths in FAP and attenuated FAP patients.

Secondary Aim: To measure if combination of sulindac and erlotinib cause a reduction in total duodenal polyp count, and change in duodenal polyp burden or count stratified by genotype and initial polyp burden.

Enrollment: 92 patients

Sex: All

Ages: 18 to 69 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients who are 18 years or older with a clinical or genetic diagnosis of FAP or attenuated FAP.
• Presence of duodenal polyps with a sum of diameters ≥ 5mm.
• Minimum of two weeks since any major surgery
• WHO performance status ≤1
• Adequate bone marrow function as show by: normal leukocyte count, platelet count ≥ 120 x 109/L, Hgb > 12 g/dL
• Adequate liver function as shown by: normal serum bilirubin(≤ 1.5 Upper Limit Normal {ULN}) and serum transaminases (≤ 2.0 ULN)
• Patient must discontinue taking any Nonsteroidal anti-inflammatory drugs (NSAIDS) within one month of treatment initiation.
• Patients must be able to provide written informed consent.

Exclusion criteria

• Prior treatment with any investigational drug within the preceding 4 weeks.

• Malignancies within the past 3 years except for adequately treated carcinoma of the cervix or basal or squamous cell carcinomas of the skins.

• Patients who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study as determined by the Principal Investigator such as:

  1. Unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction ≤ 6 months prior to first study treatment, serious uncontrolled cardiac arrhythmia
  2. Severely impaired lung function
  3. Any active (acute or chronic) or uncontrolled infection/ disorders.
  4. Nonmalignant medical illnesses that are uncontrolled or whose control may be jeopardized by the treatment with the study therapy
  5. Liver disease such as cirrhosis, chronic active hepatitis or chronic persistent hepatitis

• Screening clinical laboratory values that indicate any of the following:

  1. anemia
  2. thrombocytopenia
  3. leucopenia
  4. elevations of transaminases greater than 2X ULN
  5. elevation of bilirubin > 1.5 X ULN
  6. alkaline phosphatase elevation > 1.5 X ULN
  7. increased creatinine, urinary protein, or urinary casts outside the clinically normal range.

• Gastrointestinal bleeding (symptoms including dyspnea, fatigue, angina, weakness, malaise, melena, hematochezia, hematemesis, anemia or abdominal pain will require clinical assessment to rule out gastrointestinal bleeding).

• Patient who is currently taking any anti-coagulation medication.

• Women who are pregnant or breast feeding.

• Patients with a known hypersensitivity to sulindac or erlotinib or to their excipients

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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92 participants in 2 patient groups, including a placebo group

Erlotinib and Sulindac

Active Comparator group

Description:

Erlotinib 75 mg per day in combination with sulindac 150 mg twice daily for 6 months.

Treatment:

Drug: Erlotinib

Drug: Sulindac

Placebo A and Placebo B

Placebo Comparator group

Description:

Placebo capsules matching erlotinib active comparator (Placebo A) once daily and placebo capsules matching sulindac active comparator (Placebo B) twice daily for 6 months

Treatment:

Drug: Placebo B

Drug: Placebo A