Lung Cancer Clinical Trial
Official title:
Impact of Fat-free Mass in the Carboplatin Calculated Dose and Chemotherapeutic Toxicity in Patients With Advanced Non-Small Cell Lung Cancer (NSCLC)
NCT number | NCT02734069 |
Other study ID # | INCAN/TOX/CBP |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | February 2016 |
Est. completion date | December 2025 |
This study evaluate the association of body composition (mainly free-fat mass), clinical and biochemical parameters with development of toxicity in patients under treatment with Carboplatin/Paclitaxel in advanced NSCLC.
Status | Recruiting |
Enrollment | 132 |
Est. completion date | December 2025 |
Est. primary completion date | July 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Diagnosis of NSCLC Stage IV (stratification according to the American Joint Committee on Cancers - 7th edition) - Candidates for treatment with carboplatin plus paclitaxel 1st line - Performance status (ECOG 0-2) - Laboratory studies that demonstrate adequate renal, hepatic and hematologic function (blood chemistry and blood count) - Normal renal ultrasound prior to initiation of treatment Exclusion Criteria: - Patients with renal impairment (KDOQI 3-5) - Patients who do not have computed tomography study at baseline - Uncontrolled blood pressure (> 140 mmHg) - Uncontrolled diabetes (> 130 mg / dL) - Obstruction in kidney (s) or ureter (s) - Dehydrated patients - Patients with high consumption of NSAIDs (aspirin, ibuprofen, etc.> 1 month) |
Country | Name | City | State |
---|---|---|---|
Mexico | Instituto Nacional de Cancerologia | Mexico City |
Lead Sponsor | Collaborator |
---|---|
Instituto Nacional de Cancerologia de Mexico |
Mexico,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 | Determine if the dose of carboplatin-based chemotherapy in patients according to the amount of fat-free mass is directly associated with toxicity | Three weeks after the application of chemotherapy to detect changes from Baseline | |
Primary | Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 | Determine if the dose of carboplatin-based chemotherapy in patients according to the amount of fat-free mass is directly associated with toxicity | Six weeks after the application of chemotherapy to detect changes from Baseline | |
Secondary | Compare different formulas to calculate Glomerular Filtration Rate taking as gold standard cystatin c | Calculate the glomerular filtration rate given the amount of fat-free mass (MSA-eCrCl) and correlate with cystatin C and formulas as Cockroft-Gault, Levey, The Modification of Diet in Renal Disease (MDRD) and Chronic kidney disease epidemiology collaboration (CKD-EPI). | Basal evaluation |
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