(118) Evaluation of Treatment Tolerability Associated with Carboplatin Dose Based on Actual Body Weight Versus Adjusted Body Weight in Patients with a BMI ≥ 25 mg/m2 with Advanced Ovarian Cancer
PGY2 Oncology Pharmacy Resident Huntsman Cancer Institute COTTONWOOD HEIGHTS, Utah, United States
Poster Abstract:
Background: The National Comprehensive Cancer Network (NCCN) guidelines recommend utilizing carboplatin and paclitaxel with or without bevacizumab as the preferred treatment regimen for patients with stages II-IV epithelial ovarian cancer. Carboplatin is primarily eliminated via urinary excretion; therefore, a patient’s overall exposure to the medication is correlated with renal clearance. The Calvert equation was developed as a formula to allow clinicians to dose carboplatin in a way that targets a specific area under the curve (AUC) based on an individual’s glomerular filtration rate (GFR). There is controversy among treating clinicians and national guidelines about whether it is preferable to use actual body weight or adjusted body weight when calculating GFR for overweight patients with a body mass index (BMI) of 25 kg/m2 or greater. The NCCN and Gynecologic Oncology Group (GOG) guidelines recommend using adjusted body weight to calculate creatinine clearance in patients with a BMI of 25 kg/m2 or greater. However, the American Society of Clinical Oncology (ASCO) recommends using actual body weight when calculating chemotherapy doses in obese patients. ASCO states that using actual weight-based cytotoxic chemotherapy for obese patients does not increase toxicity and may result in decreased efficacy. Both dosing strategies are utilized in clinical practice depending on clinician preference.
Objectives: The aim of this study is to describe the composite incidence of dose reductions, treatment delays or omissions due to toxicity, early discontinuation, or the need for granulocyte colony-stimulating factor (G-CSF) support associated with carboplatin dosing utilizing actual body weight compared with adjusted body weight in patients with advanced epithelial ovarian cancer receiving neoadjuvant or adjuvant carboplatin and paclitaxel with or without bevacizumab.
Methods: This study is a retrospective descriptive analysis. Patients with advanced epithelial ovarian cancer and a BMI ≥ 25 kg/m2 who received treatment with carboplatin and paclitaxel were included. Patient charts were reviewed to determine the incidence of dose reductions, treatment delays due to toxicity, and/or the need for growth factor support associated with carboplatin dosing utilizing actual body weight compared to adjusted body weight. Additionally, data was collected to determine the incidence of grade 3 or higher hematologic toxicity associated with both dosing strategies.
Results: Data collection has been completed; however, data analysis is pending. Discussion/conclusions: The results of this research will contribute to the current body of literature regarding the appropriate dosing of carboplatin in obese patients and help standardize dosing practices.
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