An Open-label, Non-randomized, Multicenter, Two Stage Designed Phase II Study of Axitinib for Downstaging Large Renal Tumors Not Primarily Suitable for Partial Nephrectomy (AXIPAN)
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 21
- 试验地点
- 1
- 主要终点
- The number of patients actually experiencing a partial nephrectomy for a tumor ≤ 7cm
研究概览
简要总结
Axitinib (AXITINIB) is an oral, potent, and selective inhibitor of vascular endothelial growth factor receptors 1, 2, and 3 which has achieved objective response rate of 44.2% in phase II study in cytokine-refractory metastatic renal-cell cancer patients.
Pre-surgical treatment with Axitinib could allow a substantial proportion of patients with large organ confined tumors to benefit from NSS.
The Objective is to determine the efficacy of Axitinib administered prior to surgery in patients with large organ confined tumors not primarily suitable for NSS (cT2aNoNxM0) for shifting from a radical nephrectomy indication to a nephron sparing procedure.
详细描述
Radical nephrectomy (RN) is the current standard of care for large organ confined renal tumors.
Experience and surgical technical improvements have allowed the feasibility of Nephron Sparing Surgery (NSS) in tumors larger than 4 cm and up to 7cm. Very limited data exist regarding the feasibility and safety of NSS in tumors larger than 7cm.
It has been demonstrated that NSS compared to RN offers similar oncological outcome while better preserving renal function and thus improving overall survival.
The purpose of this study is to test the possibility of offering patients with large organ confined renal tumors, candidates for radical nephrectomy according to current guidelines the benefit of partial nephrectomy thanks to axitinib neo-adjuvant treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
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
- •Patients must sign IRB/EC-approved informed consent.
- •Histologically proven clear cell RCC (obtained by CT or US guided biopsy)
- •cT2a N0NxM0 Renal tumor according to 2009 TNM classification (tumor Ø> 7cm; ≤ 10 cm)
- •No evidence of preexisting uncontrolled hypertension as documented by 2 baseline blood pressure readings taken at least 1 hour apart.
- •Normal renal function (MDRD creatinin clearance ≥ 60 ml/min)
- •Patients must have adequate organ function defined as: Platelets ≥ 150 x 109/L, hemoglobin > 9 g/dl, absolute neutrophil count (ANC) >1.5 x 109/L; Bilirubin < 2 mg/dL, aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 2.5 times the upper limit of normal; Total cholesterol ≤ 9.1 mmol/l and triglyceride level ≤ 4.5 mmol/l
- •Urinary protein <2+ by urine dipstick.
- •Patients with reproductive potential must use medically acceptable contraceptive method.
- •Beneficiary of a social coverage (except AME)
排除标准
- •Patients with < 50 % clear cell histology
- •Evidence of locally advanced disease: cT stage≥T2b, N Stage≥1 or metastatic disease (M1)
- •Patients must not be pregnant or lactating.
- •Patients must not have uncompensated coronary artery disease or an history of myocardial infarction or severe or unstable angina within the past six months or severe diabetes mellitus with severe arterial peripheral disease or deep venous or arterial thrombosis or embolism with the past 3 months. Patients must not need curative anticoagulants.
- •Patients must not have any medical/systemic or psychiatric disorder incompatible with the study.
- •Patients must not have a history of significant gastric or small bowel resection, malabsorption syndrome, or other lack of integrity of the upper gastrointestinal tract that may compromise the absorption of Axitinib or an unavailability of the oral route.
研究组 & 干预措施
AXITINIB
干预措施: AXITINIB (Drug)
结局指标
主要结局
The number of patients actually experiencing a partial nephrectomy for a tumor ≤ 7cm
时间窗: At 6 months after beginning of the treatment
次要结局
- Renal function assessed by serum creatinin(At baseline and at 30 months after beginning of the treatment)
- Response rate according to RECIST criteria(At 30 months after beginning of the treatment)
- Number of participants with treatment-related serious adverse events and their grades according to CTCAE V4.0.(At 30 months after beginning of the treatment)
- Renal function assessed by calculated glomerular filtration rate (GFR) according to MDRD formula(At baseline and at 30 months after beginning of the treatment)
- Renal function assessed by renal scintigraphy(At baseline and at 30 months after beginning of the treatment)