Neoadjuvant Sunitinib Treatment for Metastatic Clear Cell Renal Cell Carcinoma (RCC)

This is an interventional treatment trial for Clear Cell Renal Cell Carcinoma focused on measuring Neoadjuvant Therapy, Sunitinib, Clear Cell Renal Cell Carcinoma, Metastasis Read More

Inclusion Criteria:

• Biopsy proven RCC with a component of clear cell type histology
• Clinical stage TxNxM+
• At least one site of measurable disease as defined by RECIST criteria
• Potential candidates for cytoreductive nephrectomy
• Favorable or intermittent risk group according to MSKCC risk factor model
• ECOG performance status 0 or 1

• Adequate organ function as defined by:

  • AST or ALT less than or equal to 2.5 times the upper limit of normal
  • Bilirubin less than or equal to 1.5 times the upper limit of normal
  • Absolute neutrophil count (ANC) greater than or equal to 1500/mL
  • Platelets greater than or equal to 100,000/mL
  • Hemoglobin greater than or equal to 9.0 g/dL
  • Serum calcium less than or equal to 12.0 mg/dL
  • Serum creatinine less than or equal to 1.5 times the upper limit of normal
• Male or female, 18 years of age or older
• Women of childbearing potential must NOT be pregnant (as confirmed by a negative pregnancy test)
• Signed informed consent form indicating that the patient or acceptable representative has been informed of all parts of the trial prior to Sunitinib administration (enrollment)
• Willingness and ability to comply with study procedures

Exclusion Criteria:

• History of another primary malignancy within 5 years, with the exception of non-melanoma skin cancer and in situ carcinoma of the uterine cervix.
• NCI CTCAE grade 3 hemorrhage within 4 weeks of commence of Sunitinib therapy.
• Presence of brain metastases during screening period
• Ongoing cardiac dysrhythmias of NCI CTCAE grade of 2 or more, atrial fibrillation of any grade or prolongation of QTc interval to more than 450 millisecond (msec) for male or more than 470 msec for female
• Hypertension that cannot be controlled by medications
• Concurrent treatment with therapeutic doses of coumadin but low dose of coumadin up to 2 mg orally daily for deep vein thrombosis prophylaxis is allowed.
• Current treatment on another therapeutic clinical trial. Supportive care trials or non-treatment trials are allowed.
• Inability to swallow oral medications, or presence of active inflammatory bowel disease, partial or complete bowel obstruction or chronic diarrhea.
• Concurrent medication with known potent CYP3A4 inhibitors and inducers and/or dosing before 7 and 12 days before date of randomization.
• Other severe acute or chronic medical or psychiatric condition of laboratory abnormality that may increase the risk associated with study participation or study drug administration, or may interfere with the interpretation of study results, and in the judgment of the investigator would make the subject inappropriate for entry into this study.
• Any of the following within 12 months prior to study drug administration:

severe/unstable angina, myocardiac infarction, coronary artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident, including transient ischemic attack, or pulmonary embolism.

• Known hypersensitivity to Sunitinib
• Women who are breast-feeding ※ Note At screening, resectability of primary tumor itself does not influence on patients enrollment. Physicians only have to describe about the resectability ("resectable" or "unresectable") at screening on their own discretion, but if they decide that primary tumor is "unresectable", the should specify reasons for unresectable status as follows: invasion into neighboring organs, proximity to vital structure or vessels, bulky regional lymph nodes, vascular invasion, burden of metastatic disease, and others.