Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Chicago
With
National Cancer Institute (NCI)
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients must have histologically or cytologically confirmed metastatic or recurrent RCC (any histologic subtype)
Patients must have between 1 to 5 new or recurrent lesions suspicious for metastatic RCC on diagnostic imaging
* Each extracranial lesion must be =\< 6 cm and amenable to SBRT or surgical excision
* Patients must have 3 or fewer brain metastases, of size =\< 4 cm
* Brain metastases must be treated prior to enrollment in the study; the modality of treatment of brain metastases can include surgical resection, whole brain radiotherapy, stereotactic radiosurgery, or any combination of the above
You may not be if
Patients must have had at least a computed tomography (CT) of the chest, abdomen, and pelvis within 4 weeks of registration in the trial; CT or magnetic resonance imaging (MRI) of the brain is only required in the presence of neurologic symptoms
Patients must have had no radiotherapy, immunotherapy, chemotherapy or therapy with targeted agents within the last 1 month
Patients may not have had prior bevacizumab, based on case reports of tracheoesophageal fistula in patients treated with bevacizumab and radiotherapy
Eastern Cooperative Oncology Group (ECOG) performance status =\<2
Age 18 years or older
Life expectancy of \>= 3 months
Patients must have normal organ and marrow function within 30 days of registration, as defined below:
* Absolute neutrophil count \>= 500/mcL
* Hemoglobin \>= 8.0 g/dL
* Platelets \>= 50,000/mcL
* Total bilirubin within normal institutional limits
* Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase \[SGOT\])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase \[SGPT\]) =\< 3 X institutional upper limit of normal if liver metastases are present
Women of childbearing potential must have a negative pregnancy test within 14 days of registration
Patients must have the ability to understand and the willingness to sign a written informed consent document
Patients who have had prior chemotherapy, immunotherapy, targeted therapy, or radiotherapy within 1 month of enrollment
Patients who have had any prior bevacizumab, due to case reports suggesting a possible risk of severe toxicity in combination with radiotherapy
Patients with radiographic or clinical findings of spinal cord compression or cauda equina syndrome with neurologic deficit thought to be due to malignancy
Patients may not be receiving any systemic anti-cancer agents or other investigational agents during radiation therapy
Patients may not have received prior radiation therapy to a site of recurrence which would require overlap of appreciable radiation dose
Known active invasive malignancy except for renal cell carcinoma and/or non-melanoma skin cancer
Severe, active co-morbidity, defined as follows:
* Unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months prior to registration;
* Transmural myocardial infarction within the last 6 months prior to registration;
* Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration;
* Chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days prior to registration;
* Severe hepatic disease, defined as a diagnosis of Child-Pugh class B or C hepatic disease if the liver is involved with metastatic disease;
* Human immunodeficiency virus (HIV) positive with cluster of differentiation (CD)4 count \< 200 cells/microliter; note that patients who are HIV positive are eligible, provided they are under treatment with highly active antiretroviral therapy (HAART) and have a CD4 count \>= 200 cells/microliter within 30 days prior to registration; note also that HIV testing is not required for eligibility for this protocol
Pregnancy or women of childbearing potential who are sexually active and not willing/able to use medically acceptable forms of contraception during protocol treatment or for at least 6 months following treatment
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