Erdafitinib for Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests erdafitinib (Balversa), a treatment that might stop the growth of cancer cells with specific FGFR mutations. It targets patients with hard-to-treat cancers, such as certain solid tumors and lymphomas, that have spread or returned after other treatments. The trial aims to assess erdafitinib's effectiveness in these cases. Individuals with solid tumors featuring FGFR mutations who have not responded to other treatments might be suitable candidates. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group of participants.
Will I have to stop taking my current medications?
The trial requires that you stop taking certain medications before participating. You cannot be on other anti-cancer agents, investigational drugs, or certain medications that affect specific liver enzymes (CYP3A4 and CYP2C9). If you're on corticosteroids, you need to be on a stable or decreasing dose for at least 7 days before joining the trial.
Is there any evidence suggesting that erdafitinib is likely to be safe for humans?
Research has shown that erdafitinib has been tested in patients with other types of cancer, such as bladder cancer. In these studies, hundreds of patients received the treatment, and results indicated that erdafitinib was generally well-tolerated. Most patients experienced side effects similar to those from other cancer treatments.
The most common side effects included changes in vision and dry mouth, while some patients experienced skin or nail issues. In rare cases, more serious side effects occurred.
Erdafitinib is already approved by the FDA for treating certain cancers with FGFR mutations, indicating it is safe enough for use in these conditions. However, individual experiences can vary, so discussing potential risks with a healthcare provider is important.12345Why do researchers think this study treatment might be promising?
Erdafitinib is unique because it targets specific genetic changes in cancer cells, called FGFR mutations, which are not addressed by most standard treatments like chemotherapy or immunotherapy. This targeted approach could potentially offer more effective results for those with these mutations. Additionally, erdafitinib is taken orally, which may provide a more convenient option compared to treatments that require hospital visits for infusions. Researchers are excited because this precision medicine can lead to better outcomes with potentially fewer side effects for patients with certain types of cancer.
What evidence suggests that erdafitinib might be an effective treatment for cancer?
Research shows that erdafitinib effectively treats cancers with FGFR mutations. Studies have found that erdafitinib can reduce the risk of death by 36% compared to chemotherapy for patients with certain cancers. Specifically, patients with metastatic urothelial carcinoma, a type of bladder cancer, lived longer on average—12.1 months compared to 7.8 months for those receiving chemotherapy. These results suggest that erdafitinib may slow the growth of cancer cells with FGFR mutations by blocking the enzymes they need to grow. While these findings are encouraging, they are based on studies of other cancers, so erdafitinib is still being tested for the specific conditions in this trial. Participants in this trial will receive erdafitinib as part of the study treatment.36789
Who Is on the Research Team?
Alice Lee
Principal Investigator
Children's Oncology Group
Are You a Good Fit for This Trial?
This trial is for children and young adults aged 12 months to 21 years with advanced solid tumors, non-Hodgkin lymphoma, or histiocytic disorders that have FGFR mutations. Participants must be able to swallow tablets, have not been treated with erdafitinib before, and meet specific health criteria like normal bilirubin levels and kidney function.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive erdafitinib orally once daily on days 1-28 of each cycle, repeating every 28 days for up to 26 cycles
Follow-up
Participants are monitored for safety and effectiveness after treatment completion
Exploratory Genomic Profiling
Evaluation of changes in tumor genomics over time through circulating tumor DNA
What Are the Treatments Tested in This Trial?
Interventions
- Erdafitinib
Erdafitinib is already approved in United States, European Union for the following indications:
- Locally advanced or metastatic urothelial carcinoma with susceptible FGFR3 genetic alterations
- Locally advanced or metastatic urothelial carcinoma with susceptible FGFR3 genetic alterations
Find a Clinic Near You
Who Is Running the Clinical Trial?
National Cancer Institute (NCI)
Lead Sponsor