Non Small Cell Lung Cancer
Conditions
Keywords
surgically resectable
Brief summary
The purpose of this study is to find out what effects (both good and bad) two medications (VELCADE and Vorinostat) have on patients who have certain types of lung cancer. The study is dose escalating meaning that patients will receive different doses of medication depending on when they enter the study. Participation in the study will last approximately 3 months and will include an initial screening visit, a visit once each week for 3 weeks to receive the study medications, and then 2 additional visits around the time of your surgery to remove your lung cancer tumor.
Interventions
DRUGVelcade and Vorinostat
Subjects will receive one of 3 doses of Velcade (at a dose of 1.0 - 1.6 mg/m2 once weekly for 3 weeks) and one of 4 doses of Vorinostat (at a dose of 100mg every day 3 times a week for 3 weeks to 300mg twice per day, 3 times per week for 3 weeks). Doses determined by a predetermined escalation schedule.
Sponsors
University of Virginia
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histologically confirmed NSCLC (clinical stage IB, IIA, IIB, IIIA, or selected IIIB (T4N0-1M0)), exclusive of patients with MPE * Planned surgical resection * Age \> 18 years * ECOG performance status 0-1 * Patient has adequate organ and marrow function, as defined below: * Patient has a platelet count of \> 100 x 109/L * Patient has a WBC count of \> 3.5 x 109/L * Patient has an absolute neutrophil count of \> 1.5 x 109/L * Patient has hemoglobin of \> 8 gm/dl. Patients may receive transfusions, erythropoietin or darbepoetin to achieve this hemoglobin level. * Patient has a serum creatinine of \< 2.0 mg/dL * Patient has AST \< 1.5 x ULN * Patient has bilirubin \< 1.5 x ULN * Patient has INR \< 1.5 x ULN * Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care. * Female subject is either post-menopausal or surgically sterilized or willing to use an acceptable method of birth control (ie, a hormonal contraceptive, intra-uterine device, diaphragm with spermicide, condom with spermicide, or abstinence) for the duration of the study. * Male subject agrees to use an acceptable method for contraception for the duration of the study
Exclusion criteria
* Previous chemotherapy or radiation therapy within 5 years before enrollment. * Prior history of treatment for a known NSCLC within the last 5 years of if \> 5 years but still thought by the investigator to represent recurrent disease. * Prior exposure to either Velcade or Vorinostat * Prior exposure to any HDAC inhibitors within the previous 30 days. Patients who have received such agents for other indications may enroll after 30-day wash-out period. Subject may not take any other HDAC inhibitor during this trial. * Patient has \>/= Grade 2 peripheral neuropathy within 14 days before enrollment. * Myocardial infarction within 6 months prior to enrollment or has NYHA Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or ECG evidence of acute ischemia or active conduction system abnormalities. Prior to study entry, any ECG abnormality at Screening has to be documented by the investigator as not medically relevant. * Patient has hypersensitivity to VELCADE, boron or mannitol. * Patient has known allergy to any component of Vorinostat (MK-0683) * Female subject is pregnant or breast-feeding. Confirm by a negative serum B-hCG pregnancy test result obtained during screening (not required for post-menopausal or surgically sterilized women). * Patient is participating or has participated in another investigational trial, and has received other investigational drugs/therapies within 30 days of enrollment * Serious medical or psychiatric illness likely to interfere with participation in this clinical study. * Patient has history of GI surgery or other procedures that might, in the opinion of the investigator, interfere with the absorption or swallowing of the study drugs. * Subject is currently taking herbal remedy and/or homeopathic agent which cannot (or the patient is unwilling) be discontinued during the conduct of this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse events | 30 days post surgical resection |
Secondary
| Measure | Time frame |
|---|---|
| Tumor response | Day 22 |
Countries
United States
Outcome results
None listed