20 Participants NeededMy employer runs this trial

Personalized Treatment for Brain Cancer

(SUPERNOVA-RBT Trial)

RR
HL
Overseen ByHope Lovell
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial seeks to identify the best personalized treatment for children and young adults with rare brain tumors that have recurred after treatment. By analyzing the unique characteristics of each person's tumor, researchers aim to recommend the most effective and least harmful treatment options. The trial seeks participants who have experienced a recurrence of a rare brain tumor and are candidates for surgery or biopsy. If successful, this approach could enhance treatments for other types of cancer in the future. As an unphased trial, it offers participants the chance to contribute to groundbreaking research that could lead to improved, personalized cancer treatments.

What prior data suggests that this personalized treatment recommendation is safe for brain cancer patients?

Research has shown that personalized treatments for brain cancer are generally well-tolerated. In one study on treatments for recurring brain tumors, patients received bevacizumab—a drug commonly used in cancer treatment—and found it safe, with most managing the side effects well. Another study discovered that fractionated radiotherapy, a type of targeted radiation, improved survival rates and was preferred over chemotherapy due to fewer severe side effects.

These examples demonstrate that personalized treatments, tailored to the specific characteristics of a person's tumor, aim to be both effective and safe. While side effects can occur, they are usually less severe than those from traditional treatments. This approach focuses on finding the safest and most effective way to treat each unique case of brain cancer.12345

Why are researchers excited about this trial?

Researchers are excited about the Personalized Treatment Recommendation for brain cancer because it tailors therapies based on the unique genetic makeup of each patient's tumor. Unlike the standard treatments, which often include surgery, radiation, and chemotherapy, this approach uses real-time high-throughput drug screening, RNA sequencing, and whole genome sequencing to design a treatment plan specifically for each individual's cancer profile. This personalized approach has the potential to improve treatment effectiveness and reduce side effects by specifically targeting the cancer's unique characteristics.

What evidence suggests that this personalized treatment might be effective for brain cancer?

Research has shown that personalized treatments for brain cancer, like the one in this trial, hold promise. This trial provides participants with a personalized treatment recommendation based on their tumor's unique features, potentially leading to better outcomes. Studies have found that combining personalized treatments with traditional methods, such as surgery and radiation, can improve survival rates. For instance, personalized vaccines for brain cancer have shown potential in extending the time before cancer returns. Additionally, gene therapy, another type of personalized treatment, is advancing rapidly and offers new hope for better outcomes. Overall, these personalized strategies represent a significant advancement in treating brain tumors.678910

Who Is on the Research Team?

AF

Adriana Fonseca, MD

Principal Investigator

Children's National Research Institute

Are You a Good Fit for This Trial?

This trial is for children and young adults with rare brain tumors that have come back or worsened after previous treatment. Participants must be able to undergo surgery to provide tumor tissue for testing.

Inclusion Criteria

I have a rare brain tumor that has come back after at least one prior treatment.
I have fully recovered from side effects of my previous cancer treatments.
I am able to have surgery or a biopsy for my condition.
See 6 more

Exclusion Criteria

Women of childbearing potential must not be pregnant or breast-feeding; a negative serum or urine pregnancy test is required prior to start of therapy
I do not have any uncontrolled illnesses or active infections.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment Recommendation

Participants receive a personalized treatment recommendation based on real-time drug screening and molecular profiling within 28 days from tissue acquisition

4 weeks

Treatment

Participants receive treatment based on tumor board recommendations, with monitoring for adverse events and clinical activity

Up to 2 years

Follow-up

Participants are monitored for safety and effectiveness after treatment, including adverse events and radiographic response

Up to 1 year

What Are the Treatments Tested in This Trial?

Interventions

  • Personalized Treatment Recommendation

Trial Overview

Researchers will analyze each person's tumor in the lab, test different drugs on it, and use genetic information to recommend a personalized treatment plan. The goal is to find the most effective and least toxic therapy for each participant.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Personalized Treatment RecommendationExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Adriana Fonseca

Lead Sponsor

Children's National Research Institute

Collaborator

Trials
227
Recruited
258,000+

Citations

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