BAY 1895344 + Radiation + Pembrolizumab for Head and Neck Cancer

Not currently recruiting at 13 trial locations
Age: 18+
Sex: Any
Trial Phase: Phase 1
Sponsor: National Cancer Institute (NCI)
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 tests a new treatment combination to manage head and neck cancer that has recurred and cannot be surgically removed. The treatment includes elimusertib, an experimental drug that might block enzymes aiding cancer growth; precise radiation targeting tumors; and pembrolizumab, which boosts the immune system to fight cancer. It targets individuals with recurrent, inoperable squamous cell head and neck cancer who have previously undergone treatments like chemotherapy or radiation. The trial aims to determine the best dose and assess any benefits or side effects. As a Phase 1 trial, this research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new treatment combination.

Do I need to stop my current medications for the trial?

The trial protocol does not specify if you need to stop your current medications. However, if you are taking medications that interact with CYP3A4, you may need to switch to alternatives. It's best to discuss your current medications with the study team.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that pembrolizumab, one of the treatments in this trial, has been used successfully in patients with head and neck cancer. One study found it improved the time patients lived without the cancer worsening, without causing new safety problems. This suggests that pembrolizumab is generally safe, with no unexpected side effects reported.

For elimusertib, detailed information about its safety in humans is limited. However, as the trial is in an early stage, researchers are closely monitoring its safety and determining the best dose.

Stereotactic body radiation therapy is another part of this trial. This precise type of radiation treatment aims to protect healthy tissues and is generally well-tolerated by patients.

Overall, this combination of treatments is being tested for safety and effectiveness in the trial, with researchers carefully monitoring patient responses to ensure safety.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about this treatment combination for head and neck cancer because it integrates Elimusertib, a new active ingredient, with Pembrolizumab and Stereotactic Body Radiation Therapy (SBRT). Elimusertib targets cancer cells by inhibiting a specific enzyme involved in DNA repair, potentially enhancing the effectiveness of radiation therapy. This approach is different from standard treatments like surgery or chemotherapy, which don't target the DNA repair mechanism. By combining Pembrolizumab, an immune checkpoint inhibitor, with targeted DNA repair disruption and precise radiation, this treatment could improve outcomes by more effectively attacking cancer cells while sparing healthy tissue.

What evidence suggests that this trial's treatments could be effective for head and neck cancer?

Research shows that pembrolizumab, one of the treatments in this trial, effectively treats head and neck squamous cell cancer (HNSCC). Studies have found that pembrolizumab can extend patients' lives, particularly when used as the initial treatment, making it a common first choice for this condition. Pembrolizumab has also proven effective in real-life situations for patients with recurrent or difficult-to-remove HNSCC. In this trial, participants will receive pembrolizumab alongside elimusertib and stereotactic body radiation therapy (SBRT). Although less information exists about elimusertib, it likely works by blocking certain enzymes that cancer cells need to grow. Overall, combining these treatments with precise radiation aims to effectively target and manage cancer in these patients.15678

Who Is on the Research Team?

YM

Yvonne M. Mowery

Principal Investigator

University of Pittsburgh Cancer Institute LAO

Are You a Good Fit for This Trial?

Adults with recurrent, unresectable head and neck squamous cell carcinoma are eligible for this trial. They must have had disease progression on or after anti-PD-1/L1/L2 therapy or be new to such treatment. Prior radiotherapy should be completed at least 6 months before joining, and they should not have contraindications to pembrolizumab. Participants need a negative HIV test under certain conditions, no severe cardiac issues, agree to contraception if applicable, and meet specific health criteria.

Inclusion Criteria

I can care for myself and doctors expect me to live for at least 3 more months.
Patients must have a way to measure their disease according to specific guidelines.
I have had brain metastases treated and they are now stable.
See 13 more

Exclusion Criteria

My cancer has spread extensively.
I have specific allergies or an active autoimmune disease.
I have received a blood transfusion within a specific timeframe.
See 17 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive pembrolizumab IV on day 1 of each cycle, BAY 1895344 orally on specified days, and undergo SBRT during cycle 2

6 weeks
Multiple visits for IV administration and SBRT

Follow-up

Participants are monitored for safety and effectiveness after treatment

24 months
Follow-up every 13 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Elimusertib
  • Pembrolizumab
  • Stereotactic Body Radiation Therapy
Trial Overview The trial is testing the combination of BAY 1895344 (elimusertib), stereotactic body radiation therapy, and pembrolizumab in patients with advanced head and neck cancer. It aims to find the optimal dose while assessing the potential benefits and side effects of this regimen compared to standard treatments involving radiation and immunotherapy without elimusertib.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Treatment (pembrolizumab, BAY 1895344, SBRT)Experimental Treatment7 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

National Cancer Institute (NCI)

Lead Sponsor

Trials
14,080
Recruited
41,180,000+

Published Research Related to This Trial

The Phase III trial KEYNOTE-412 is designed to evaluate the efficacy and safety of pembrolizumab, an immune checkpoint inhibitor, when used alongside chemoradiation therapy (CRT) in patients with locally advanced head and neck squamous cell carcinoma (HNSCC).
Previous Phase Ib studies have indicated that combining pembrolizumab with CRT is safe and feasible, supporting its potential use in this larger trial to improve treatment outcomes for patients with locally advanced HNSCC.
Pembrolizumab given concomitantly with chemoradiation and as maintenance therapy for locally advanced head and neck squamous cell carcinoma: KEYNOTE-412.Machiels, JP., Tao, Y., Burtness, B., et al.[2021]
In a study of 38 patients with p16+ oropharyngeal squamous cell carcinoma, there was a 76% agreement in PD-L1 combined positive scores (CPS) between primary tumors and lymph node metastases, indicating variability in scoring between these specimens.
The interobserver agreement for CPS scoring was fair to substantial, suggesting that additional evaluations may be necessary to ensure accurate scoring, especially for patients who might benefit from immunotherapy.
Programmed Death Ligand-1 Combined Positive Score Concordance and Interrater Reliability in Primary Tumors and Synchronous Lymph Node Metastases in Resected Cases of p16+ Oropharyngeal Squamous Cell Carcinoma.Kaur, A., Kuchta, K., Watkin, W., et al.[2023]
In a phase IB study involving 59 patients with locally advanced head and neck squamous cell carcinoma, the combination of pembrolizumab with cisplatin-based chemoradiotherapy was found to be safe, with a high completion rate of treatment and only 8.8% of patients experiencing immune-related adverse events.
The treatment showed promising efficacy, with complete response rates of 85.3% for HPV-positive and 78.3% for HPV-negative patients, suggesting that this combination warrants further investigation.
Safety and Efficacy of Pembrolizumab With Chemoradiotherapy in Locally Advanced Head and Neck Squamous Cell Carcinoma: A Phase IB Study.Powell, SF., Gold, KA., Gitau, MM., et al.[2022]

Citations

Real-World Evidence on the Effectiveness of Pembrolizumab ...The study showed some beneficial effects of pembrolizumab monotherapy in recurrent/metastatic/unresectable HNSCC patients in real-world scenarios.
Neoadjuvant and Adjuvant Pembrolizumab in Locally ...The addition of neoadjuvant and adjuvant pembrolizumab to standard care significantly improved event-free survival among participants with locally advanced ...
Updated Results of the Phase III KEYNOTE-048 StudyOverall survival improved with pembrolizumab-chemotherapy in the PD-L1 CPS ≥ 20 (HR, 0.62; 95% CI, 0.46 to 0.84), CPS ≥ 1 (HR, 0.64; 95% CI, ...
Study Details | NCT02252042 | Pembrolizumab (MK-3475) ...The primary study hypothesis is that pembrolizumab treatment prolongs Overall Survival (OS) when compared to standard treatment.
Merck's KEYTRUDA (pembrolizumab) Significantly ...“In this study, KEYTRUDA showed the potential to significantly prolong survival when used as first-line therapy for patients whose head and neck cancer had ...
Study Results | Pembrolizumab (MK-3475) Versus ...Serious AEs and Other AEs were reported according to treatment course for all randomized participants who received ≥1 dose of study treatment. Per protocol, ...
KEYTRUDA® (pembrolizumab) as Perioperative Treatment ...Results at the first interim analysis of the trial showed KEYTRUDA significantly improved event-free survival (EFS) as part of a perioperative treatment regimen ...
MSD reports outcomes from trial of Keytruda combination ...After a median follow-up at 38.3 months, the therapy had decreased the EFS event risk by 34% in subjects whose combined positive score (CPS) was ...
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security