81 Participants Needed

Palbociclib + Cetuximab for Head and Neck Cancer

Recruiting at 4 trial locations
Douglas R. Adkins profile photo
Overseen ByDouglas R. Adkins
Age: 18+
Sex: Any
Trial Phase: Phase 3
Sponsor: Washington University School of Medicine
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to determine if combining the drugs palbociclib (a cancer treatment) and cetuximab can extend the lives of people with a specific type of head and neck cancer compared to using cetuximab alone. It targets individuals whose cancer has returned or spread and who did not respond to PD-1/L1 inhibitors. Suitable candidates include those with HPV-unrelated head and neck cancer that has progressed despite previous treatments. As a Phase 3 trial, this study represents the final step before FDA approval, providing participants an opportunity to contribute to potentially groundbreaking treatment advancements.

Will I have to stop taking my current medications?

The trial information does not specify if you need to stop taking your current medications. However, it mentions that certain HIV medications may need to be avoided due to potential drug interactions. It's best to discuss your current medications with the trial team.

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

Research has shown that patients generally tolerate the combination of palbociclib and cetuximab well. In one study, researchers could not find a dose too strong for most patients, suggesting that the treatment rarely causes severe side effects. Another study found that 39% of patients who did not respond to platinum treatments responded to this combination, demonstrating its effectiveness and tolerability.

Cetuximab, used in both treatment groups, has FDA approval for certain cancers, indicating its well-established safety. Side effects like skin reactions or tiredness can occur but are usually manageable.

Overall, previous research indicates that both palbociclib and cetuximab, whether used together or separately, have been well-tolerated in other studies.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about the combination of Palbociclib and Cetuximab for head and neck cancer because it offers a novel approach by targeting cancer cell growth differently than the standard treatments. Most current therapies, such as chemotherapy and radiation, broadly attack rapidly dividing cells, which can lead to significant side effects. However, Palbociclib specifically inhibits cyclin-dependent kinases 4 and 6 (CDK4/6), proteins that are crucial for cancer cell division, potentially leading to a more targeted and effective treatment with fewer side effects. Additionally, combining Palbociclib with Cetuximab, which targets the epidermal growth factor receptor (EGFR), may enhance the overall effectiveness against cancer cells, providing a promising new option for patients.

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

Research shows that combining palbociclib and cetuximab yields promising results for head and neck cancer. In earlier studies, 39% of patients saw their tumors shrink or disappear with this combination, meaning it worked for 39 out of every 100 patients. In this trial, one group of participants will receive the combination of palbociclib and cetuximab, which has proven effective even for patients unresponsive to other treatments like platinum or cetuximab alone. Another group will receive cetuximab alone. These findings suggest that the combination might be more effective than cetuximab alone for some patients with head and neck cancer.12346

Who Is on the Research Team?

Douglas R. Adkins, MD - Washington ...

Douglas R. Adkins

Principal Investigator

Washington University School of Medicine

Are You a Good Fit for This Trial?

This trial is for adults with CDKN2A-altered, HPV-unrelated head and neck squamous cell carcinoma who have had disease progression after treatment with a PD-1/L1 inhibitor. They should not have received more than three prior therapies, must be in good physical condition (ECOG ≤ 1), and have proper organ function. Pregnant women are excluded, and participants must agree to use contraception.

Inclusion Criteria

I have had up to three treatments for my head and neck cancer.
My bone marrow and organs are functioning normally.
My throat cancer is not related to HPV and has been confirmed by a lab test.
See 5 more

Exclusion Criteria

QTc >500 msec
I do not have any unmanaged ongoing illnesses.
My cancer has a specific genetic change known as Rb loss.
See 8 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either palbociclib and cetuximab or cetuximab monotherapy

12 weeks
Weekly visits for cetuximab administration

Follow-up

Participants are monitored for safety and effectiveness after treatment

15 months

What Are the Treatments Tested in This Trial?

Interventions

  • Cetuximab
  • Palbociclib
Trial Overview The study compares the effectiveness of combining Palbociclib with Cetuximab versus using Cetuximab alone in improving overall survival rates. Participants will be randomly assigned to one of these two treatments after showing progression on a PD-1/L1 inhibitor.
How Is the Trial Designed?
2Treatment groups
Experimental Treatment
Active Control
Group I: Arm 1: Palbociclib + CetuximabExperimental Treatment2 Interventions
Group II: Arm 2: CetuximabActive Control1 Intervention

Cetuximab is already approved in United States, European Union for the following indications:

🇺🇸
Approved in United States as Erbitux for:
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Approved in European Union as Erbitux for:

Find a Clinic Near You

Who Is Running the Clinical Trial?

Washington University School of Medicine

Lead Sponsor

Trials
2,027
Recruited
2,353,000+

Pfizer

Industry Sponsor

Trials
4,712
Recruited
50,980,000+
Known For
Vaccine Innovations
Top Products
Viagra, Zoloft, Lipitor, Prevnar 13

Albert Bourla

Pfizer

Chief Executive Officer since 2019

PhD in Biotechnology of Reproduction, Aristotle University of Thessaloniki

Patrizia Cavazzoni profile image

Patrizia Cavazzoni

Pfizer

Chief Medical Officer

MD from McGill University

The Joseph Sanchez Foundation

Collaborator

Trials
2
Recruited
220+

Published Research Related to This Trial

Monoclonal antibodies like cetuximab work by promoting receptor endocytosis and activating the immune system to reduce tumor growth in head and neck squamous cell carcinoma (HNSCC).
Different strategies for targeting EGFR, including tyrosine kinase inhibitors and antisense approaches, have unique mechanisms of action, which could lead to more effective treatments and better patient selection for EGFR inhibition.
Investigational EGFR-targeted therapy in head and neck squamous cell carcinoma.Cassell, A., Grandis, JR.[2021]
In a post-marketing surveillance study involving 2126 patients with metastatic colorectal cancer, cetuximab was found to be well tolerated, with a median treatment duration of 15.3 weeks and a high incidence of adverse reactions at 89.6%.
The most common adverse reactions included skin disorders (83.7%) and infusion reactions (5.7%), primarily occurring during the first administration, indicating that while side effects are common, they align with previous reports and suggest that cetuximab is clinically useful in this patient population.
A Japanese post-marketing surveillance of cetuximab (Erbitux®) in patients with metastatic colorectal cancer.Ishiguro, M., Watanabe, T., Yamaguchi, K., et al.[2022]
Cétuximab, a monoclonal antibody targeting EGFR, has been shown to improve overall survival in patients with locally advanced head and neck cancer when used alongside radiotherapy, and is now reimbursed in Belgium under specific conditions.
In metastatic head and neck cancer, adding cétuximab to platinum-based chemotherapy has demonstrated improved overall survival compared to chemotherapy alone, marking a significant advancement in treatment options, although it is not yet available to Belgian patients.
[Monoclonal antibodies for the treatment of head and neck cancer].Sautois, B., Martin, M., Demez, P., et al.[2018]

Citations

Safety And Efficacy Study Of Palbociclib Plus Cetuximab ...The purpose of this study is to determine whether the combination of palbociclib with cetuximab is superior to cetuximab in prolonging overall survival in ...
Promising Activity Seen With Palbociclib/Cetuximab ...An overall response rate of 39% was induced with the combination of the CDK4/6 inhibitor palbociclib (Ibrance) and cetuximab (Erbitux) in ...
3.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/37982827/
A Phase I Study of the CDK4/6 Inhibitor Palbociclib in ...The palbociclib, cetuximab, and IMRT combination was well tolerated. The RP2D was established, while no MTD was determined.
Study Details | NCT04966481 | Palbociclib and Cetuximab ...This multicenter, open-label, randomized phase 3 trial will determine if palbociclib and cetuximab (Arm 1) improves overall survival (OS) in comparison to ...
Palbociclib plus cetuximab shows antitumor activity among ...A combination of palbociclib and cetuximab demonstrated substantial antitumor activity among patients with platinum- or cetuximab-resistant ...
Clinical Study ResultsPalbociclib prevents the CDK4 and CDK6 enzymes from functioning, which stops the cells from dividing and stops cancer growth. What is cetuximab?
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