Palbociclib and Cetuximab Versus Cetuximab Monotherapy for Patients With CDKN2A-altered, HPV-unrelated Head and Neck Squamous Cell Carcinoma Who Experienced Disease Progression on a PD-1/L1 Inhibitor: A Multicenter, Open-Label, Randomized Phase 3 Trial

Who is this study for? Patients with HPV-unrelated Head and Neck Squamous Cell Carcinoma
What treatments are being studied? Cetuximab
Status: Recruiting
Location: See all (4) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This multicenter, open-label, randomized phase 3 trial will determine if palbociclib and cetuximab (Arm 1) improves overall survival (OS) in comparison to cetuximab monotherapy (Arm 2) in patients with CDKN2A-altered, HPV-unrelated recurrent or metastatic head and neck squamous cell carcinoma (HNSCC) who experienced disease progression on a PD-1/L1 inhibitor (given as monotherapy or in combination with other therapy).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologically or cytologically confirmed RM-HNSCC that is HPV-unrelated disease; defined as SCC of the oral cavity, larynx, or hypopharynx and p16 negative SCC of the oropharynx or p16 negative non-cutaneous SCC unknown primary of the neck.

• CDKN2A loss-of-function (LOF) alteration: mutation or homozygous deletion described on genomic sequencing report.

• Measurable disease defined as lesions that can be accurately measured in at least one dimension (longest diameter to be recorded) as ≥ 10 mm with CT scan, as ≥ 20 mm by chest x-ray, or ≥ 10 mm with calipers by clinical exam, per RECIST 1.1.

• Disease progression on a PD-1/L1 inhibitor-containing regimen (given as monotherapy or in combination with other therapy).

• Received no more than three lines of prior therapy for RM-HNSCC.

• At least 18 years of age.

• ECOG performance status ≤ 1.

• Normal bone marrow and organ function as defined below:

‣ Hemoglobin ≥ 8 g/L

⁃ Absolute neutrophil count ≥ 1,000/mcl

⁃ Platelets ≥ 100,000/mcl

⁃ Total bilirubin ≤ 3 x institutional upper limit of normal (IULN)

⁃ AST(SGOT)/ALT(SGPT) ≤ 5 x IULN (for cases involving liver metastases, AST/ALT ≤ 10 x IULN)

⁃ Serum creatinine \< 3 x IULN or creatinine clearance \> 30 mL/min by Cockcroft-Gault

• The effects of palbociclib and cetuximab on the developing human fetus are unknown. For this reason and because CDK 4/6 inhibitors are known to be teratogenic, women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately. Men treated or enrolled on this protocol must also agree to use adequate contraception prior to the study, for the duration of the study, and 3 months days after completion of the study

• Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).

Locations
United States
Missouri
Saint Luke's Hospital
RECRUITING
Kansas City
Washington University School of Medicine
RECRUITING
St Louis
North Dakota
Sanford Roger Maris Cancer Center
RECRUITING
Fargo
South Dakota
Sanford Medical Center
RECRUITING
Sioux Falls
Contact Information
Primary
Douglas Adkins, M.D.
dadkins@wustl.edu
314-747-8475
Time Frame
Start Date: 2022-04-06
Estimated Completion Date: 2028-02-28
Participants
Target number of participants: 81
Treatments
Experimental: Arm 1: Palbociclib + Cetuximab
* Palbociclib by mouth 125 mg/daily on Days 1-21 of each 28 day cycle~* Cetuximab: Initial dose 400mg/m\^2 intravenous (IV); Subsequent doses 250 mg/m\^2 IV, weekly
Active_comparator: Arm 2: Cetuximab
-Cetuximab: Initial dose 400mg/m\^2 intravenous (IV); Subsequent doses 250 mg/m\^2 IV, weekly
Sponsors
Leads: Washington University School of Medicine
Collaborators: Pfizer, The Joseph Sanchez Foundation

This content was sourced from clinicaltrials.gov

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