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N/A N=16 Prevention

Calcitriol in Preventing Lung Cancer in Smokers and Former Smokers at High Risk of Lung Cancer

Lung Cancer · Precancerous Condition · Tobacco Use Disorder

Enrolled (actual)
16
Serious AEs
0.0%
Results posted
Oct 2017
Primary outcome: Primary: Grade III-IV Toxicities or Any Grade II Toxicities Lasting More Than 2 Weeks — 1; 0; 0; 0 participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
calcitriol (Drug); laboratory biomarker analysis (Other); pharmacological study (Other)
Age
Adult, Older Adult · 40+ yrs
Sex
All
Sponsor
Roswell Park Cancer Institute
Primary completion
Mar 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Grade III-IV Toxicities or Any Grade II Toxicities Lasting More Than 2 Weeks
1; 0; 0; 0

Summary

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.

Eligibility Criteria

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00690924). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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