Calcitriol in Preventing Lung Cancer in Smokers and Former Smokers at High Risk of Lung Cancer
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Purpose
RATIONALE: Calcitriol may prevent lung cancer in patients with metaplasia or dysplasia of the lungs.
PURPOSE: This clinical trial is studying the side effects and best dose of calcitriol in preventing lung cancer in current smokers and former smokers at high risk of lung cancer.
| Condition | Intervention | Phase |
|---|---|---|
|
Lung Cancer Precancerous Condition Tobacco Use Disorder |
Drug: calcitriol Other: laboratory biomarker analysis Other: pharmacological study |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | A Pilot Study of Oral Calcitriol in Patients at High Risk for Lung Cancer |
- Grade III-IV toxicities or any grade II toxicities lasting more than 2 weeks [ Time Frame: 3 months ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 40 |
| Study Start Date: | July 2008 |
| Estimated Primary Completion Date: | December 2013 (Final data collection date for primary outcome measure) |
-
Drug: calcitriol
OBJECTIVES:
Primary
- To establish the safety of calcitriol in patients at high risk of lung cancer.
- To determine the dose-limiting toxicities of calcitriol in these patients.
OUTLINE: Patients receive oral calcitriol on day 1. Courses repeat every 2 weeks for 3 months in absence of unacceptable toxicity.
Patients undergo blood collection periodically for pharmacokinetic and molecular analysis.
After completion of study therapy, patients are followed periodically.
Eligibility| Ages Eligible for Study: | 40 Years to 79 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
- Pathologically confirmed squamous metaplasia or squamous dysplasia of the lungs by autofluorescence bronchoscopy within the past 5 years
- Must be a current or former smoker
No evidence of concurrent disease with lung cancer or head and neck cancer
- History of treated lung cancer or head and neck cancer treated with curative intent allowed, provided that there has been no evidence of disease for > 1 year
PATIENT CHARACTERISTICS:
- ECOG performance status 0-1
- Total granulocyte count > 1,500 x 10^9cells/L
- Platelet count > 100,000 x 10^9cells/L
- Calculated Creatinine clearance > 60 mL/min (using the Cockcroft-Gault formula)
- Calcium concentration 50-300 mg/24 hours
- Total bilirubin 0.2-1.3 mg%
- ALT/AST ≤ 2.5 times upper limit of normal (ULN)
- Alkaline phosphatase ≤ 2.5 times ULN
- Albumin ≥ 2.5 g/dL
- Ionized serum calcium normal (1.19-1.29 mmol/L)
- Corrected serum calcium ≤ 10.2 mg/dL
- Willing to attend all scheduled study visits, complete all study questionnaires, and allow biological specimen collection, including a bronchoscopy
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception during and for at least 1 month after completion of study therapy
No life-threatening medical conditions that would preclude bronchoscopy, including but not limited to, any of the following:
- Acute cardiac failure
- Uncontrolled hypertension
- Uncontrolled diabetes mellitus
- Unstable coronary artery disease
- No severe metabolic disorders that would preclude calcitriol administration
- No history of any other malignancy within 3 years except for nonmelanoma skin cancer or cervical carcinoma in situ
- No history or evidence of kidney stones
- No patients who are susceptible to calcium-related dysrhythmias
- No known hypersensitivity to calcitriol
- No known allergies to tree nuts (i.e., almonds)
PRIOR CONCURRENT THERAPY:
- At least 2 months since prior and no concurrent calcium supplements
- Concurrent multivitamin supplement allowed provided the amount of vitamin D in the supplement is not in excess of the recommended daily dose
- No concurrent thiazides, phenobarbital, or digitalis
- No concurrent digoxin
- No concurrent bile acid binding drugs (i.e., cholestyramine, colestipol)
- No concurrent danazol or aluminum-based antacids
- No concurrent ketoconazole or other azole antifungals
Contacts and Locations| United States, New York | |
| Roswell Park Cancer Institute | Recruiting |
| Buffalo, New York, United States, 14263-0001 | |
| Contact: AskRPCI 877-275-7724 AskRPCI@RoswellPark.org | |
| Principal Investigator: | Alex A. Adjei, MD, PhD | Roswell Park Cancer Institute |
More Information
Additional Information:
No publications provided
| Responsible Party: | Roswell Park Cancer Institute |
| ClinicalTrials.gov Identifier: | NCT00690924 History of Changes |
| Other Study ID Numbers: | CDR0000596506, P30CA016056, RPCI-I-90206 |
| Study First Received: | June 4, 2008 |
| Last Updated: | December 17, 2012 |
| Health Authority: | United States: Institutional Review Board United States: Food and Drug Administration |
Keywords provided by Roswell Park Cancer Institute:
|
lung cancer tobacco use disorder squamous lung dysplasia |
Additional relevant MeSH terms:
|
Lung Neoplasms Precancerous Conditions Tobacco Use Disorder Respiratory Tract Neoplasms Thoracic Neoplasms Neoplasms by Site Neoplasms Lung Diseases Respiratory Tract Diseases Substance-Related Disorders Mental Disorders Calcitriol |
Vitamins Micronutrients Growth Substances Physiological Effects of Drugs Pharmacologic Actions Bone Density Conservation Agents Calcium Channel Agonists Membrane Transport Modulators Molecular Mechanisms of Pharmacological Action Vasoconstrictor Agents Cardiovascular Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on June 18, 2013