Intensity-Modulated Radiation Therapy, Pemetrexed, and Erlotinib in Treating Patients With Recurrent or Second Primary Head and Neck Cancer

NCT ID: NCT00573989

Last Updated: 2019-01-03

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 27 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-03-31
• Study Completion Date: 2017-03-31

Brief Summary

RATIONALE: Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Drugs, such as pemetrexed and erlotinib, may make tumor cells more sensitive to radiation therapy. Erlotinib and pemetrexed may also stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving intensity-modulated radiation therapy together with pemetrexed and erlotinib may kill more tumor cells.

PURPOSE: This phase I/II trial is studying the side effects and best dose of erlotinib when given together with intensity-modulated radiation therapy and pemetrexed and to see how well they work in treating patients with recurrent or second primary head and neck cancer.

Detailed Description

OBJECTIVES:

Primary

• Evaluate the acute toxicity and feasibility of intensity modulated radiotherapy (IMRT) in combination with radiosensitizing drugs pemetrexed disodium and erlotinib hydrochloride in patients with recurrent or second primary squamous cell carcinoma of the head and neck. (Phase I)
• Determine the maximum tolerated dose and recommended phase II dose of erlotinib hydrochloride in these patients. (Phase I)
• Determine progression-free survival (PFS) at 1 year in these patients. (Phase II)

Secondary

• Determine median PFS, median overall survival (OS), and OS at 1 and 2 years in these patients.
• Determine objective tumor response as measured by CT scan or MRI in these patients.
• Evaluate the acute and chronic toxicity of IMRT in combination with radiosensitizing drugs pemetrexed disodium and erlotinib hydrochloride in these patients.
• Evaluate the impact of treatment on quality of life as measured by FACT-H&N, PSS-HN, MD Anderson Dysphagia Inventory (MDADI), and swallowing by direct functional measurements at different time points.
• Evaluate the level of phosphorylation of different tyrosine residues within the cytoplasmic domain of EGFR, bound adaptors, as well as markers of downstream pathways activation by nano LC-MS/MS in tumor tissue and correlate with levels of P-AKT and P-ERK by immunohistochemistry and with response to treatment.
• Measure the levels of TS and p53 and correlate with treatment response.

OUTLINE: This is a phase I, dose-escalation study of erlotinib hydrochloride followed by a phase II study.

• Phase I: Patients undergo intensity modulated radiotherapy (IMRT) once daily, 5 days a week, for 6 weeks. Patients receive pemetrexed disodium IV over 10 minutes on day 1 of radiotherapy. Treatment with pemetrexed disodium repeats every 21 days for 2 courses in the absence of disease progression or unacceptable toxicity. Patients also receive oral erlotinib hydrochloride once daily beginning on day 1 of radiotherapy and continuing for up to 2 years in the absence of disease progression or unacceptable toxicity.
• Phase II: Patients undergo IMRT and receive pemetrexed sodium as in phase I. Patients also receive erlotinib hydrochloride at the maximum tolerated dose determined in phase I.

Quality of life is assessed at baseline, weekly during treatment, at 1, 6, and 12 months, and then annually thereafter.

After completion of study treatment, patients are followed every 3 months for 2 years, every 6 months for 1 year, and then annually thereafter.

Conditions

Head and Neck Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Erlotinib

Erlotinib

Group Type: EXPERIMENTAL

erlotinib hydrochloride

Intervention Type: DRUG

pemetrexed disodium

Intervention Type: DRUG

quality-of-life assessment

Intervention Type: PROCEDURE

intensity-modulated radiation therapy

Intervention Type: RADIATION

Interventions

erlotinib hydrochloride

Intervention Type: DRUG

pemetrexed disodium

Intervention Type: DRUG

quality-of-life assessment

Intervention Type: PROCEDURE

intensity-modulated radiation therapy

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

• Histologically or cytologically confirmed diagnosis of recurrent or second primary squamous cell carcinoma (SCC) of the head and neck, including any of the following:

• Oral cavity
• Oropharynx
• Hypopharynx
• Larynx
• Recurrent neck metastases with unknown primary

Exception from pathology confirmation of tumor recurrence is accepted for patients who originally had pathologically confirmed SCC of the Head and Neck, the new tumor is located in the head and neck area and it is clinically considered as a recurrence of the original tumor, and a tumor biopsy is technically difficult and would expose the patient to unjustified risk. The treating physicians should agree and document the clinical definition of tumor recurrence and should document the increased risk for biopsy.

• Measurable disease by CT scan or MRI OR evaluable disease
• No definitive evidence of distant metastasis
• Unresectable disease by a preliminary ENT evaluation OR refused surgery
• Patients may have received chemotherapy as a component of their primary tumor treatment but not for recurrent or metastatic disease. No prior treatment with systemic anti-EGFR inhibitors or Pemetrexed is permitted
• Has undergone prior head and neck radiotherapy (for SCC of the head and neck) to a dose of ≤ 72 Gy that involved most of the recurrent tumor (> 75%) OR has a second primary tumor volume in areas previously irradiated to > 45 Gy
• The entire tumor volume must be included in a treatment field that limits the total spinal cord dose to 54 Gy (prior plus planned dose)
• Must have disease recurrence or persistence for ≥ 6 months after completion of prior radiotherapy
• ECOG performance status 0-1
• Age ≥ 18 years
• ANC > 1,500/µL
• Platelet count > 100,000/µL
• Total bilirubin < 1.5 times upper limit of normal (ULN)
• AST/ALT < 2 times ULN
• Creatinine < 1.5 times ULN
• Willing and able to take folic acid and vitamin B12 supplementation
• Recovered from prior surgery, chemotherapy, or radiotherapy
• At least 6 months since prior radiotherapy
• At least 5 days since prior aspirin or other non-steroidal anti-inflammatory agents (8 days for long acting agents [e.g., piroxicam])
• Fertile patients must use effective contraception

Exclusion:

• Nasopharyngeal carcinoma
• Concurrent uncontrolled illness, including, but not limited to, any of the following:

• Ongoing or active infection
• Psychiatric illness or social situation that would limit compliance with study requirements
• Significant history of uncontrolled cardiac disease (i.e., uncontrolled hypertension; unstable angina; recent myocardial infarction [within the past 3 months]; uncontrolled congestive heart failure; or cardiomyopathy with decreased ejection fraction)
• Active interstitial lung disease
• Presence of third space fluid that cannot be controlled by drainage
• Other concurrent investigational agents
• Pregnant or nursing
• HIV positive

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 120 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Wake Forest University Health Sciences

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Mercedes Porosnicu, MD

Role: PRINCIPAL_INVESTIGATOR

Wake Forest University Health Sciences

Kathryn M. Greven, MD

Role: PRINCIPAL_INVESTIGATOR

Wake Forest University Health Sciences

Locations

UNC Linberger Comprehensive Cancer Center

Chapel Hill, North Carolina, United States

Wake Forest University Comprehensive Cancer Center

Winston-Salem, North Carolina, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

P30CA012197

Identifier Type: NIH

Identifier Source: secondary_id

View Link

CCCWFU-60107

Identifier Type: -

Identifier Source: secondary_id

IRB00003457

Identifier Type: -

Identifier Source: org_study_id

NCT01580449

Identifier Type: -

Identifier Source: nct_alias