Palbociclib With Cetuximab and IMRT for Locally Advanced Squamous Cell Carcinoma

  • STATUS
    Recruiting
  • End date
    Dec 25, 2026
  • participants needed
    33
  • sponsor
    Mahidol University
Updated on 25 January 2021
carcinoma
squamous cell carcinoma
dental caries
definitive treatment
cetuximab
squamous cell carcinoma of head and neck
intensity-modulated radiation therapy
squamous cell carcinoma of the oral cavity
head and neck carcinoma
mouth cancer
locally advanced squamous cell carcinoma

Summary

Cyclin D kinase 4 (CDK4) is a key regulator of the G1-S transition in the cell cycle. Alterations in CDK4-cyclin D-retinoblastoma (Rb) pathway may lead to carcinogenesis in many cancers. Several mechanisms have been described: (i) Amplification or overexpression of cyclin D1, (ii) Amplification of CDK4, (iii) Activating mutation of CDK4, and (iv) Loss of the CDK4 inhibitor, p16 (CDKN2A). Human Papilloma Virus (HPV) plays a major role in squamous cell carcinoma of head and neck (SCCHN) carcinogenesis. It induces many alterations in the CDK4-Cyclin D-Rb and apoptotic pathways such as up-regulation of p16, loss of Rb and p53 functions. A novel therapy for HPV-negative SCCHN is clearly an unmet medical need.

Palbociclib (PD 0332991) is an orally active, highly selective inhibitor of the CDK4/6 with ability to block Rb phosphorylation in the low nanomolar range. The most advanced development is in a treatment of metastatic breast cancer. In addition, palbociclib showed a radiosensitization property. Since combination of cetuximab and radiation improved PFS and overall survival (OS) in locally advanced SCCHN when compared with radiation alone, these provide a strong rationale to evaluate a combination of palbociclib, cetuximab, and radiation for locally advanced SCCHN. Because many genetic alterations in SCCHN significantly involve in the CDK4-cyclin D-Rb pathway, predictive biomarker(s) of palbociclib in this combination will be explored.

Thus, the investigators propose a non-randomized, dose escalation, phase I study designed to determine the maximum tolerated dose (MTD) and toxicity of palbociclib, cetuximab, and IMRT for locally advanced SCCHN.

Description

The enrollment of an initial patient cohort of 3 or 6 patients will follow the traditional "3 + 3" dose escalation scheme (see table below). The patients will be treated with palbociclib, cetuximab, and IMRT at starting at Dose Level (DL) 1. Subsequent patient cohort(s) will be enrolled depending on the safety and tolerability of the initial cohort. If <33% patients treated at Dose Level 1 experience DLT (see definition below) by the end of treatment (56 days), then next cohort of 3 patients will be enrolled and treated at Dose Level 2. If 2 treatment-related DLTs are observed at Dose Level 1, patients will be accrued to Dose Level -1. The MTD is defined as the maximum dose level at which 1/6 patients have DLTs.

At the MTD or RP2D, we will accrue up to 15 locally advanced unresectable p16-negative SCCHN patients to allow for definitive evaluation of tolerability, correlative endpoints and preliminary efficacy. CT/PET scan will be performed at 3 months after the last dose of radiation to evaluate residual disease. Patients with residual disease will be considered for salvage surgery following standard of care.

  • IMRT will be administered 5 days on/2 days off with a total dose of 70 Gy for 33-35 fractions.
  • Cetuximab will be administered 400 mg/m2 IV at 7 days before (day -7) starting radiation and then 250 mg/m2 IV weekly for 7 weeks.
  • Palbociclib will be administered orally daily 3 week-on and 1-week of during IMRT (Day 1-21 and Day 29-49).

Details
Condition head and neck cancer, Locally Advanced, cancer of the head and neck
Treatment Cetuximab, Intensity Modulated Radiation Therapy, Palbociclib
Clinical Study IdentifierNCT03024489
SponsorMahidol University
Last Modified on25 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Locally advanced histology or cytology proven squamous cell carcinoma of oral cavity, oropharynx, larynx, and hypopharynx
Locally advanced SCCCH patients who would be considered for concurrent cetuximab and IMRT as a definitive treatment
Age 18 yeas old
Available tissue to determine HPV status and the other biomarkers of interest
ECOG status 1
Adequate bone marrow, liver, and renal functions, defined as
Platelet count 150 x 109/L, Absolute Neutrophile Count (ANC) 1.5 x 109/L, Hgb 9 gm/dL
ALT and AST 1.5 upper limit normal (ULN); serum total bilirubin ULN
Serum creatinine 1.5 x ULN, or calculated or measured creatinine clearance (by Cockcroft-Gault Equation) 50 mL/min
Magnesium the lower limit of normal
Women of childbearing potential must have a negative pregnancy test performed within 7 days prior to the start of study drug
Male and female subjects of child-bearing potential must agree to use double-barrier contraceptive measures, oral contraception, or avoidance of intercourse during the study and for 6 months after last investigational drug dose received
Subject or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure

Exclusion Criteria

Potential subjects who meet ANY of the following exclusion criteria are not
eligible for enrollment into this study
SCCHN patients with distance metastasis
Major surgery < 4 weeks or minor surgery < 2 weeks prior to the first day of study treatment
Patients with previous chemotherapy for cancer treatment and radiation to the head and neck areas
Patients who were previously treated with any CDK4/6 inhibitors or cetuximab
SCCHN with expressed p16 by IHC (only in expansion cohort)
Active cardiac disease described as
Left ventricular ejection fraction (LVEF) < 50% by Multiple Grated acquisition (MUGA) scan or echocardiogram (ECHO)
QTc > 480 msec on screening EKG (using the QTcF formula)
Congenital long QT syndrome
Myocardial infarction or active uncontrolled angina pectoris within the last 6 months prior to the first day of study treatment
Uncontrolled significant cardiac arrhythmias except for benign premature ventricular contractions (PVC) and premature atrial contractions (PAC)
Symptomatic pericarditis
History of cardiomyopathy
Weight loss more than 10% from baseline body weight before illness
Active clinically serious infections or other serious uncontrolled medical conditions
Substance abuse, medical, psychological or social conditions that may, in the opinion of the Investigator, interfere with the patient's participation in the study or evaluation of the study results
Unable to swallow an intact palbociclib tablet
Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of palbociclib
Known HBV, HCV, and/or HIV infection
Patients who are currently treated with drugs known to be strong inhibitors or inducers of isoenzyme CYP3A, and the treatment cannot be discontinued or switched to a different medication prior to starting study drug
Patients who have taken herbal medications and certain fruits within 7 days prior to starting study drug. Herbal medications include, but are not limited to St. John's wort, Kava, ephedra (ma huang), gingko biloba, dehydroepiandrosterone (DHEA), yohimbe, saw palmetto, and ginseng. Fruits include the CYP3A inhibitors Seville oranges, grapefruit, pomelos, or exotic citrus fruits
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

0/250

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note