Evaluation of the Effect of Genetic Polymorphisms in ERCC1 and OCT2 on the Occurrence and Severity of Cisplatin-induced Nephrotoxicity
试验速览
- 阶段
- 不适用
- 入组人数
- 89
- 试验地点
- 1
- 主要终点
- Serum Creatinine
研究概览
简要总结
Approximately one-third of all patients treated with cisplatin develop renal dysfunction after a single dosage of cisplatin. Germline genetic polymorphisms may cause variations in cisplatin pharmacokinetics and in the ability of epithelial kidney cells to take up cisplatin and repair cisplatin-induced Deoxyribonucleic Acid (DNA) damage. Knowledge concerning which genotypes are associated with cisplatin-induced nephrotoxicity may help to identify at-risk patients and initiate strategies, such as using lower or fractionated cisplatin doses or avoiding cisplatin altogether, to prevent Acute Kidney Injury (AKI).
详细描述
Approximately one-third of all patients treated with cisplatin develop renal dysfunction after a single dosage of cisplatin. Germline genetic polymorphisms may cause variations in cisplatin pharmacokinetics and in the ability of epithelial kidney cells to take up cisplatin and repair cisplatin-induced DNA damage. Knowledge concerning which genotypes are associated with cisplatin-induced nephrotoxicity may help to identify at-risk patients and initiate strategies, such as using lower or fractionated cisplatin doses or avoiding cisplatin altogether, to prevent AKI.
Patient written informed consent will be taken prior to study conductance
- Full laboratory evaluation before and after cisplatin administration including:
(Complete Blood Count) CBC, liver and renal functions. glomerular filtration rate (GFR), and estimated glomerular filtration rate (eGFR) Serum electrolytes. Marker of nephrotoxicity: Cystatin C. 2. Sample Collection and single nucleotide polymorphism (SNP) Genotyping:
Venous blood (2 mL) will be collected from each subject into tubes containing 50 mmol of Ethylenediamine tetraacetic acid (EDTA) per liter and genomic DNA will be isolated with the GeneJET Whole Blood Genomic DNA purification Mini kit, according to manufacturer's instructions. Polymorphisms will be assessed using the TaqMan based real-time polymerase chain reaction (PCR) assay.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Males or females aged >18 years receiving cisplatin-containing chemotherapy.
- •A Cisplatin dose starting from 75 mg/m2
- •Various cancer types
- •No history of organ transplantation or kidney dialysis.
- •Patients with normal renal function
排除标准
- •Co-administration of ifosfamide with cisplatin, because of the known risk of nephrotoxicity.
- •Pregnant or lactation.
- •Infection with the human immunodeficiency virus (HIV).
- •Prior administration of cisplatin.
- •Intraperitoneal chemotherapy.
- •Inadequate liver function (bilirubin > 1.5 times upper normal limit (UNL) and alanine transaminase (ALT) or aspartate transaminase (AST) > 3.0 UNL or up to 5.0 UNL in the presence of hepatic metastases).
- •Inadequate renal function (creatinine > 1.25 times UNL, creatinine clearance < 50 mL/min).
- •Serious comorbid systemic disorder incompatible with the study (uncontrolled diabetes mellitus (DM) or hypertension (HTN), myocardial infarction within the last 6 months).
- •Patients diagnosed with kidney cancer.
- •Exposure to any nephrotoxic drugs or agents.
结局指标
主要结局
Serum Creatinine
时间窗: Change from baseline at the end of cycle 2 (each cycle is 28 days)
available in patient profile
次要结局
- cystatin c(Change from baseline at the end of cycle 2 (each cycle is 28 days))