Phase II Study of Concurrent C225, Cisplatin and Radiation in Stage IV Squamous Cell Carcinoma of the Head and Neck

Eastern Cooperative Oncology Group

Status and phase: Completed; Phase 2

Conditions: Head and Neck Cancer

Treatments: Biological: cetuximab C225; Radiation: radiation therapy; Drug: cisplatin

Study type: Interventional

Funder types: NETWORK; NIH

Identifiers

NCT00096174

E3303 (Other Identifier)

U10CA021115 (U.S. NIH Grant/Contract)

CDR0000390923

Details and patient eligibility

About

RATIONALE: Monoclonal antibodies such as cetuximab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Cetuximab may make the tumor cells more sensitive to radiation therapy and chemotherapy. Giving monoclonal antibody therapy together with chemoradiotherapy may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving cetuximab and cisplatin together with radiation therapy works in treating patients with locally advanced or regional stage IV head and neck cancer that cannot be removed by surgery.

Full description

OBJECTIVES:

Primary

• Determine 2-year progression-free survival in patients with unresectable locally advanced or regional stage IV squamous cell or undifferentiated carcinoma of the head and neck treated with cetuximab, cisplatin, and definitive radiotherapy.

Secondary

• Determine response rate and overall survival in patients treated with this regimen.
• Determine the toxic effects of this regimen in these patients.
• Correlate epidermal growth factor receptor (EGFR) expression by immunohistochemistry, EGFR phosphorylation, map kinase, Akt, signal transducer and activator of transcription 3 (STAT3), and other tissue and serum tests with toxicity of this regimen and outcomes in these patients.

OUTLINE: This is a multicenter study. Patients are stratified according to tumor site (hypopharynx vs. oropharynx vs. oral cavity vs. larynx), primary tumor stage (T1-3 vs. T4), and nodal status (N0 vs. N1 vs. N2-3).

• Cetuximab therapy: Patients receive an initial loading dose of cetuximab IV over 2 hours on day 1. Patients then receive cetuximab IV over 1 hour on days 8, 15, 22, 29, 36, 43, 50, and 57.
• Chemoradiotherapy: Beginning on day 15 of cetuximab therapy, patients undergo radiotherapy once daily, 5 days a week, for at least 7 weeks. Patients also receive cisplatin IV over 1-2 hours on days 15, 36, and 57.
• Cetuximab maintenance therapy: After the completion of chemoradiotherapy, patients continue to receive cetuximab IV over 1 hour once weekly for 6-12 months.

Treatment continues in the absence of disease progression or unacceptable toxicity.

Patients are followed every 6 months for 10 years.

ACCRUAL: A total of 69 patients were accrued for this study.

Enrollment: 69 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histologically confirmed squamous cell or undifferentiated carcinoma of the head and neck (excluding nasopharynx, paranasal sinus, and parotid gland)

  • Unresectable locally advanced or regional stage IV disease
  • No evidence of distant metastases

• Must have demonstrable primary tumor site

• Measurable disease

• Unresectable disease

  • Meets the following criteria for unresectable disease by tumor site:

    • Hypopharynx, meeting 1 of the following criteria:

      • Extension across the midline of the posterior pharyngeal wall
      • Any evidence of fixation to the cervical spine

    • Larynx

      • Direct subglottic extension (>3cm) into surrounding muscle or skin

    • Oral cavity

      • Lesion precluding functional reconstruction

    • Base of tongue, meeting 1 of the following criteria:

      • Extension into the root of the tongue
      • Patient refuses total glossectomy

    • Tonsillar area, meeting 1 of the following criteria:

      • Extension into pterygoid area as manifested by x-ray or trismus
      • Extension across midline of pharyngeal wall
      • Direct extension into soft tissue of the neck

    • Unilateral neck node metastases fixed to carotid artery, mastoid, base of skull, or cervical spine with any of the above tumors

• Patients requiring total glossectomy are eligible

• Age>=18 years

• ECOG Performance status of 0-1

• Adequate hematologic, renal, and hepatic function obtained <=4 weeks prior to registration

  • Absolute neutrophil count ≥ 2,000/mm^3
  • Platelet count ≥ 100,000/mm^3
  • Hemoglobin ≥ 9.0 g/dL
  • Alkaline phosphatase ≤ 3 times normal
  • Aspartate aminotransferase (AST) or Alanine aminotransferase (ALT) ≤ 3 times normal
  • Bilirubin ≤ 1.5 mg/dL
  • Creatinine ≤ 1.2 mg/dL OR creatinine clearance ≥ 50 mL/min

• Able to tolerate fluid load

• At least 14 days since major surgery (including dental extraction) except percutaneous endoscopic gastrostomy (PEG) placement or mediport placement

Exclusion criteria

• Pregnant or nursing
• Fertile patients do not use effective contraception
• Patients who refuse surgery but whose tumors are technically resectable OR whose tumors are unresectable for medical reasons are not eligible
• Disease metastases below the clavicles or elsewhere (M1) or with a postoperative recurrence
• Prior excisional surgery of head and neck tumor
• Prior radiotherapy to the head and neck region
• Prior chemotherapy
• Prior drugs that target the epidermal growth factor receptor pathway
• Prior chimerized or murine monoclonal antibody
• Active systemic infection
• Known allergy to murine proteins
• Severe chronic obstructive pulmonary disease requiring ≥ 3 hospitalizations within the past year
• Myocardial infarction within the past 3 months
• Uncontrolled congestive heart failure
• Unstable or uncontrolled angina
• Clinically apparent jaundice
• Postoperative recurrence
• Other malignancy within the past 3 years except resected basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or other in situ tumors

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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69 participants in 1 patient group

Cisplatin, C225, Radiation

Experimental group

Description:

* Cetuximab therapy: Patients receive an initial loading dose of cetuximab intravenously (IV) over 2 hours on day 1. Patients then receive cetuximab IV over 1 hour on days 8, 15, 22, 29, 36, 43, 50, and 57. * Chemoradiotherapy: Beginning on day 15 of cetuximab therapy, patients undergo radiotherapy once daily, 5 days a week, for at least 7 weeks. Patients also receive cisplatin IV over 1-2 hours on days 15, 36, and 57. * Cetuximab maintenance therapy: After the completion of chemoradiotherapy, patients continue to receive cetuximab IV over 1 hour once weekly for 6-12 months.

Treatment:

Biological: cetuximab C225

Drug: cisplatin

Radiation: radiation therapy