Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:10 AM
Ignite Modification Date:
2025-12-25 @ 3:10 AM
NCT ID:
NCT02328105
Eligibility Criteria:
Inclusion Criteria:
* Histologically confirmed stage IV non-small cell lung cancer with predominantly squamous histology
* No prior systemic treatment for metastatic disease. Patients who have received prior adjuvant chemotherapy for early-stage lung cancer are eligible if at least 12 months have elapsed between the date of final chemotherapy administration and the date of consent
* Patients must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded for non-nodal lesions and short axis for nodal lesions) as \>20 mm with conventional techniques or as \>10 mm with CT scan, MRI, or calipers by clinical exam
* Biopsy accessible disease
* Patients with previous radiotherapy as definitive therapy for locally advanced non-small cell lung cancer are eligible, as long as the recurrence is outside the original radiation therapy port. Definitive radiation therapy must have been completed \>4 weeks prior to the date the informed consent is signed
* Age \>18 years
* ECOG performance status less than or equal to 1
* If patient has brain metastasis, the disease must be stable (treated and/or asymptomatic) for at least 4 weeks prior to first dose of study treatment
* Bilirubin \< 1.5 mg/dL
* Adequate liver function: AST and ALT \<= 2.5x upper limit of normal, alkaline phosphatase \<= 2.5x upper limit of normal, unless bone metastasis is present (\< 5x upper limit of normal) in the absence of liver metastasis
* Adequate bone marrow function: Platelets \>100,000 cells/mm3, Hemoglobin \> 9.0g/dL and ANC \> 1,500 cells/mm3
* Adequate renal function with creatinine \<1.5 mg/dL is recommended
* Females of childbearing potential and sexually active males must use an effective contraception method during treatment and for six months after completing treatment
* Negative serum or urine B-hCG pregnancy test at screening for patients of childbearing potential
* Patients must have \< Grade 2 pre-existing peripheral neuropathy (per CTCAE version 4.0)
* Ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria
* Received prior systemic therapy for metastatic disease
* Received limited field radiation for palliation \<= 2 weeks prior to starting study treatment and/or from whom \>= 30% bone marrow was irradiated
* Receiving any other investigational agents
* Known hypersensitivity to either carboplatin or ABRAXANE
* Uncontrolled and current illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
* Pregnant or breast feeding
* Other active malignancies
* Neuropathy greater than or equal to grade 2
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02328105
Study Brief:
Protocol Section:
NCT02328105