Evaluation of Erlotinib Pharmacokinetics During Doxycycline Treatment for Erlotinib-induced Rash
Data Collection
Bronchial Neoplasms+10
+ Carcinoma, Bronchogenic
+ Carcinoma, Non-Small-Cell Lung
Supportive Care Study
Summary
Study start date: October 1, 2008
Actual date on which the first participant was enrolled.A side effect occurring in a majority of patients taking erlotinib (Tarceva®) consists of a skin rash. Sometimes, symptoms associated with the rash necessitate erlotinib dose reduction or discontinuation. Some physicians have successfully treated the erlotinib-induced rash with doxycycline. At the same time, it has been observed that in patients who develop the erlotinib rash, the cancers respond better to erlotinib treatment. This research study is designed to determine how well doxycycline treats the erlotinib rash and whether doxycycline affects the blood levels of erlotinib.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * Males and females 18 years of age or older. * Subjects must have started Tarceva® therapy within three (3) days of trial enrollment. * Patients must have signed informed consent prior to registration on study. * Currently receiving erlotinib therapy at 150 mg per day for locally advanced or metastatic NSCLC. * Patients - both males and females - with reproductive potential (ie, menopausal for less than 1 year and not surgically sterilized) must utilize barrier methods in combination with spermicidal agents for contraception when engaging in sexual intercourse. Women of childbearing potential must provide a negative pregnancy test (serum or urine) within 14 days prior to registration. Exclusion Criteria: * Allergy to tetracyclines. * Use of concurrent agents for papulopustular rash. * Currently receiving anticancer agents other than erlotinib. * Inability to interrupt other antibiotic therapy. * Current use of topical steroids * Current use of systemic immunosuppressants (e.g., methotrexate, cyclosporine, azathioprine, mycophenolate mofetil) * Photosensitivity or lupus erythematosus. * Active gastroesophageal reflux disease. * Women who have a positive pregnancy test or are lactating by history. * ECOG performance status ≤3. * Self report of current smoking or history of smoking within 60 days of screening, or positive urine cotinine test. * Current use of agents that are known to be strong inducers or inhibitors of CYTP3A4: * inhibitors: atazanavir, clarithromycin, indinavir, itraconazole, ketoconazole, nefazodone, nelfi navir, ritonavir, saquinavir, telithromycin, troleandomycin (TAO), voriconazole, grapefruit or grapefruit juice * inducers: rifampicin, rifabutin, rifapentine, phenytoin, carbamazepine, phenobarbital, and St. John's Wort * Impaired hepatic function (≤ 30 days before randomization): * Alkaline phosphatase \> 3x ULN * Aspartate aminotransferase (AST) \> x ULN * Alanine aminotransferase (ALT) \> 3 x ULN * Total Bilirubin \> 1.5 x ULN
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives