Radiation + Cemiplimab ± Fianlimab for Bladder Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores whether combining radiation therapy with immunotherapy drugs, cemiplimab and possibly fianlimab, can effectively and safely treat muscle-invasive bladder cancer before surgery. The goal is to determine if this approach can improve treatment outcomes for those with this type of bladder cancer. Participants must have a confirmed diagnosis of muscle-invasive bladder cancer and be eligible for surgery but cannot use cisplatin-based therapy due to specific health reasons. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group, offering participants a chance to contribute to potentially groundbreaking advancements in bladder cancer treatment.
Do I need to stop my current medications for the trial?
The trial does not specify if you need to stop taking your current medications. However, you cannot use certain immunosuppressive drugs or systemic corticosteroids above a certain dose, and these must be stopped 14 days before starting the trial treatment. It's best to discuss your specific medications with the study team.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that cemiplimab, already used for some skin cancers, is generally well-tolerated. In a large study, only 0.7% of patients experienced serious kidney-related side effects, with most handling the treatment without major problems.
When combined with fianlimab, early research suggests this combination is usually safe. Studies involving patients with advanced kidney cancer found the combination well-tolerated and effective over time. Most patients did not experience severe side effects, and the treatment remained effective for an extended period.
Both cemiplimab alone and with fianlimab have demonstrated promising safety results in past trials. This suggests these treatments might be safe for those considering participation in the current trial for bladder cancer treatment.12345Why are researchers excited about this trial's treatments for bladder cancer?
Researchers are excited about these treatments for bladder cancer because they combine advanced immunotherapy with radiation. Cemiplimab is a checkpoint inhibitor that helps the immune system recognize and attack cancer cells more effectively. When paired with stereotactic body radiotherapy (SBRT), it may enhance the body's ability to target tumors precisely and aggressively. Adding Fianlimab to the mix could further boost this immune response, offering a potentially more powerful and targeted approach than traditional treatments like chemotherapy or standard radiation alone. This combination could lead to better outcomes by bolstering the body's natural defenses against cancer.
What evidence suggests that this trial's treatments could be effective for muscle-invasive bladder cancer?
Research has shown that cemiplimab, when combined with radiation therapy, yields promising results for treating certain cancers. In earlier studies, it reduced the risk of cancer recurrence or death by 68%. Many patients experienced tumor shrinkage or halted growth, indicating a high response rate. In this trial, one group of participants will receive radiation therapy and cemiplimab, while another group will receive radiation therapy combined with cemiplimab and fianlimab. The combination of cemiplimab and fianlimab has also produced encouraging results. More than half of the patients responded positively, with some achieving complete recovery. These findings suggest that this combination could effectively treat muscle-invasive bladder cancer.46789
Who Is on the Research Team?
Daniel Gorovets, MD
Principal Investigator
Memorial Sloan Kettering Cancer Center
Are You a Good Fit for This Trial?
This trial is for adults (18+) with muscle-invasive bladder cancer confirmed by tests, whose kidneys are working moderately well. They must have no signs of cancer in pelvic lymph nodes and be healthy enough for treatment. People with mostly non-urothelial or small cell cancers cannot join.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Radiation and Immunotherapy Treatment
Participants receive stereotactic body radiotherapy (SBRT) and cemiplimab, with or without fianlimab, as neoadjuvant treatment before cystectomy
Cystectomy
Participants undergo radical cystectomy to remove the bladder and surrounding tissues
Follow-up
Participants are monitored for safety and effectiveness after treatment, including assessment of pathologic downstaging and complete response
What Are the Treatments Tested in This Trial?
Interventions
- Cemiplimab
- Fianlimab
- Stereotactic body radiotherapy
Trial Overview
The study is testing if giving focused radiation therapy (SBRT) along with cemiplimab immunotherapy, either alone or combined with fianlimab, before bladder removal surgery works better and is safe compared to standard approaches.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Stereotactic body radiotherapy (SBRT) and cemiplimab with Fianlimab
Stereotactic body radiotherapy (SBRT) and cemiplimab
Find a Clinic Near You
Who Is Running the Clinical Trial?
Memorial Sloan Kettering Cancer Center
Lead Sponsor
Regeneron Pharmaceuticals
Industry Sponsor
Leonard Schleifer
Regeneron Pharmaceuticals
Chief Executive Officer since 1988
MD and PhD in Medicine
George Yancopoulos
Regeneron Pharmaceuticals
Chief Medical Officer since 1997
MD from Harvard Medical School
Citations
A Study of Radiation Therapy and Cemiplimab With or ...
Within 60 days of completing the 4 cycles of cemiplimab and fianlimab, patients will undergo radical cystectomy which is standard of care. What ...
2.
investor.regeneron.com
investor.regeneron.com/news-releases/news-release-details/libtayor-cemiplimab-plus-chemotherapy-results-five-years/Libtayo® (cemiplimab) Plus Chemotherapy Results at Five ...
Late-breaking data from exploratory analyses at WCLC show Libtayo plus chemotherapy demonstrates a more than double five-year overall ...
3.
targetedonc.com
targetedonc.com/view/positive-responses-are-reported-for-fianlimab-cemiplimab-in-ccrccPositive Responses Are Reported for Fianlimab ...
Twenty-seven percent of patients went from diagnosis to systemic treatment in less than 1 year. All patients in cohort 3 had an ECOG PS of 1.
A phase 2, randomized, open-label study of gemcitabine ...
Fianlimab (anti-LAG-3) in combination with cemiplimab (anti-PD-1) has been previously shown to be both tolerable and effective in patients with ...
AUA 2025: NeoSTOP-IT: A Phase 2, Randomized, Open- ...
The primary objective is to measure the rate of clinical complete response following treatment with neoadjuvant chemotherapy combined with ...
6.
investor.regeneron.com
investor.regeneron.com/news-releases/news-release-details/libtayor-cemiplimab-phase-3-data-adjuvant-treatment-post/Libtayo® (cemiplimab) Phase 3 Data in the Adjuvant ...
Libtayo demonstrated a 68% reduction in the risk of disease recurrence or death, the primary endpoint of the trial (p<0.0001).
Efficacy and Safety of Cemiplimab for the Management of Non ...
4. Basal Cell Carcinoma ... Cemiplimab has received approval as a standalone therapy for managing adult patients with laBCC or mBCC who have ...
LIBTAYO® (cemiplimab-rwlc) Study Results | High-Risk CSCC
Discover study results and possible side effects of the adjuvant treatment of LIBTAYO® (cemiplimab-rwlc) in adults with high-risk CSCC.
Adjuvant Cemiplimab Approval Redefines Management of ...
[Specifically, cemiplimab reduced the risk of recurrence or death by 68% compared with placebo (HR, 0.32), which is among the most impressive ...
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