Pencil Beam Scanning for Renal Tumors in Children and Young Adults
This study is looking at a special type of radiation called proton beam radiation using pencil beam scanning for patients with kidney tumors, specifically Wilms tumor or clear cell sarcoma. This treatment aims to deliver radiation more precisely to the tumor area. The main goal is to see if this treatment causes fewer side effects, especially stomach and gut problems, within 90 days after starting radiation. It also aims to see if it can shorten the total time you need radiation therapy and deliver lower doses to healthy organs. This study is for patients aged 0 to 30 years who need radiation for their kidney tumor. The current status of the study is unclear, and it plans to enroll 28 patients.
- Study design
- This is a pilot study, meaning it's an early look at this treatment. It plans to enroll 28 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study will assess side effects for 90 days after the start of proton therapy.
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Pencil Beam Scanning in Patients With Renal Tumors
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Christine Hill-Kayser, MD · PRINCIPAL_INVESTIGATOR · Children's Hospital of Philadelphia
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Occurrence of any non-hematologic toxicity that occurs within 90 days following the start of proton therapy assessed with with NCI Common toxicity criteria (CTC Version 4.0) grades].90 days
Acute toxicity in patients receiving flank irradiation using proton therapy for renal tumors. Acute toxicity is defined as any non-hematologic toxicity that occurs within 90 days following the start of proton therapy. NCI Common toxicity criteria (CTC Version 4.0) grades will be employed. Individual category content listings are available to investigators at http://ctep.cancer.gov, with attention to the following System Organ Classes and CTCAE Adverse Events: General Disorders and Administration Site Conditions, Hepatobiliary Disorders, Blood and Lymphatic System Disorders, Gastrointestinal Disorders, Renal and Urinary Disorders, Injury, poisoning, or procedural complications, Metabolism and nutrition disorders, and Benign, Malignant, and Unspecified Neoplasms.