Bowman-Birk Inhibitor Concentrate in Preventing Cancer in Patients With Oral Leukoplakia

National Cancer Institute (NCI)

Status and phase: Completed; Phase 2

Conditions: Oropharyngeal Cancer; Lip and Oral Cavity Cancer; Tongue Cancer; Oral Leukoplakia

Treatments: Other: laboratory biomarker analysis; Drug: Bowman-Birk inhibitor concentrate; Other: placebo

Study type: Interventional

Funder types: NIH

Identifiers

NCT00330382

98-34

NCI-2009-00888

U01CA072294 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This randomized phase II trial is studying how well Bowman-Birk inhibitor concentrate works in preventing cancer in patients with oral leukoplakia. Chemoprevention is the use of certain substances to keep cancer from forming, growing, or coming back. The use of Bowman-Birk inhibitor concentrate, a substance made from soy, may keep cancer from forming in patients with oral leukoplakia

Full description

PRIMARY OBJECTIVES:

I. Determine if chemoprevention by the Bowman-Birk inhibitor concentrate (BBIC) can prevent cancer in patients with oral leukoplakia (OL).

II. Determine the clinical and histologic response rate of OL to BBIC.

SECONDARY OBJECTIVES:

I. Measure the effect of BBIC on intermediate marker endpoint levels. II. Correlate the clinical and histologic responses of OL with cellular levels of proteolytic activity, erb-B2 (neu), retinioc acid receptor β, bcl-2, and mutant p53 expression, and serum levels of neu.

III. Determine the individual and group side effects of BBIC.

OUTLINE: This is a multicenter, randomized, double-blind, placebo-controlled, study. Prior to randomization, all patients receive oral placebo for 4 weeks. Patients who show good compliance (> 75% packet count) are randomized to 1 of 2 treatment arms.

ARM I: Patients receive oral Bowman-Birk inhibitor concentrate twice daily for 6 months in the absence of disease progression or unacceptable toxicity.

ARM II: Patients receive oral placebo twice daily for 6 months in the absence of disease progression or unacceptable toxicity.

Patients complete questionnaires about diet, tobacco, and alcohol usage at baseline and at the completion of study treatment. Blood, urine, and biopsy tissue are collected at baseline and at the completion of study treatment. Oral mucosal cells are collected at baseline, during the run-in phase, at randomization, after completion of study treatment, and at 3 months after completion of study treatment. Samples are examined for protease activity, levels of bcl-2 and erbB-2, mutant p53 oncogene expression and epidermal growth factor receptor, and retinoic acid receptor-β expression.

After completion of study treatment, patients are followed at 3 months.

Enrollment: 325 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Histologically and clinically confirmed oral leukoplakia and/or erythroplakia

• Bidimensionally measurable disease (≥ 100 mm^2 for total area of all lesions) after biopsy

• No presence of obvious head and neck aerodigestive tract cancer, carcinoma in situ, or previously treated head and neck cancer within the past 2 years

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No history of allergic reaction to soybeans, sorbitol, sucrose, artificial flavorings, aspartame, saccharin, or lidocaine

• At least 6 months since prior Bowman-Birk inhibitor concentrate

• At least 6 months since prior participation in another randomized clinical trail

• At least 3 months since prior systemic steroids or topical oral steroid preparations

  • Topical nasal steroid sprays or cutaneous preparations with minimal systemic absorption for nasal or dermatologic disorders allowed

• More than 6 months since prior beta carotene capsules

• At least 2 years since prior retinoid or other beta carotene therapy, including > 25,000 IU of vitamin A for any reason

  • Up to 2 multivitamins per day allowed

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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325 participants in 2 patient groups, including a placebo group

Arm I (Bowman-Birk inhibitor concentrate)

Experimental group

Description:

Patients receive oral Bowman-Birk inhibitor concentrate twice daily for 6 months

Treatment:

Other: laboratory biomarker analysis

Drug: Bowman-Birk inhibitor concentrate

Arm II (placebo)

Placebo Comparator group

Description:

Patients receive oral placebo twice daily for 6 months

Treatment:

Other: laboratory biomarker analysis

Other: placebo