Safety and Efficacy of Radiation/Cetuximab Plus EGFR Antisense DNA for Head and Neck Squamous Cell Carcinoma

• To evaluate the toxicities associated with the above treatment. [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]
• Evaluate other efficacy parameters, including the objective response rate, distant control and overall progression-free survival, and overall survival. [ Time Frame: 10 years ] [ Designated as safety issue: No ]
• Determine the effect of EGFR antisense therapy on EGFR and EGFR-related biomarkers. [ Time Frame: 3 years ] [ Designated as safety issue: No ]
• Examine the transfection of the EGFR antisense gene therapy in vivo. [ Time Frame: 3 Years ] [ Designated as safety issue: No ]

The Epidermal Growth Factor Receptor (EGFR) is highly expressed in SCCHN and its overexpression is associated with poor patient outcome. EGFR is a promising target of anticancer therapy. We have developed EGFR antisense DNA as a safe and potentially efficacious treatment for SCCHN as shown in a previous phase I study conducted at the University of Pittsburgh. Cetuximab (Erbitux or C225) is a chimerized EGFR monoclonal antibody that has produced positive results in a phase III trial in SCCHN when added to radiation therapy and was approved by the FDA for the treatment of locally advanced SCCHN. Radiation plus cetuximab is considered a standard treatment, especially for patients who are not good candidates for chemotherapy. In the current study, we plan to evaluate the addition of intratumoral EGFR antisense DNA (EGFR AS) to standard radiation with concurrent cetuximab in the elderly (i.e. 70 years or older) or cisplatin-ineligible patients.

Subject population We will enroll elderly (i.e. 70 years or older) or cisplatin-ineligible patients with SCCHN who are suitable for intratumoral injections of EGFR antisense. Please see section 3 for detailed eligibility criteria.

Treatment plan EGFR AS will be administered by direct intratumoral injection using direct visualization, endoscopy, or imaging-guidance (ultrasound) as clinically determined (see sections 5 and 7 for detailed treatment plan and dose modifications). Patients will receive a total of up to 7 weekly intratumoral injections of EGFR antisense (or less if there is no identifiable tumor) starting 2 weeks prior to radiation (see schema on the next page). Patients will receive standard radiation 70 Gy/200 cGy/daily, 5 days/week, with concurrent cetuximab 250 mg/m2, after a loading dose of 400 mg/m2 2 weeks prior to starting radiation.

Statistical Design and Sample Size The study will be conducted in two-stages. In the first stage, 11 patients with stage IVA-C or recurrent disease will be evaluated for safety. If the regimen is deemed safe, a total of 31 patients with stage III or IVA-B, previously untreated SCCHN will be enrolled in the second stage of the study (see section 11).

Inclusion Criteria:

• First stage Patients with AJCC 6th edition stage IVA-IVC or recurrent or metastatic head and neck cancer will be eligible.

Second stage (phase II part) Patients with AJCC 6th edition stage III-IVB (T1-T4, N1-3M0) head and neck cancer, except WHO type II and III nasopharyngeal cancer, including unknown primary tumors.

• Histologically or cytologically confirmed diagnosis of squamous cell carcinoma or variants or poorly differentiated carcinoma.
• Unidimensionally measurable disease (RECIST criteria).

• Age limits

  • Age 70 or older with performance status 0-2
  • Patients of any age (but 18 years of age or older) with ECOG performance status of 2 (see Appendix for definition)

  • Patients of any age (but 18 years of age or older) unsuitable for concurrent cisplatin due to:

    • calculated creatinine clearance of 20-60 mL/min, or
    • severe cardiopulmonary disease, or
    • other end-organ dysfunction that precludes the use of cisplatin chemotherapy but does not preclude the administration of cetuximab or intratumoral EGFR antisense.
• In the second stage of the study, therapy will be administered with a curative intent and patients should not have recurrent disease or distant metastasis.
• Primary tumor and/or lymphadenopathy should be technically suitable for intratumoral injections. The Otolaryngologist specialist on the head and neck team will determine this feasibility.
• Participating patients should agree to undergo a tumor biopsy at baseline as well as approximately 2 weeks later as specified in study schema.

• Prior treatment

  • First stage: any prior treatment, except prior therapy which specifically and directly targets the EGFR pathway, administered within the last 6 months.
  • Second stage: no prior chemotherapy, biologic/molecular targeted therapy (including any prior therapy which specifically and directly targets the EGFR pathway), or radiotherapy for head and neck cancer.
• Prior surgical therapy will consist only of incisional or excisional biopsy, including tonsillectomy, and organ sparing procedures, including neck dissection. Any non-biopsy surgical procedure for head and neck cancer must have taken place < 3 months of initiating protocol treatment.
• Patients must have organ and marrow function as defined below:

Absolute neutrophil count ≥1,000/µL Platelets ≥75,000/µL Hemoglobin ≥ 10 g/dL Total bilirubin <2 x upper normal institutional limits Creatinine clearance > 20 mL/min

• Age of ≥18 years.
• Because radiation therapy is known to be teratogenic and EFGR inhibitors may have teratogenic potential, women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control) prior to study entry and for the duration of study participation, and for 3 months after completing study treatment. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
• Informed consent must be obtained from all patients prior to beginning therapy. Patients should have the ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

• Severe renal insufficiency (creatinine clearance < 20 mL/min)
• Treatment with anticoagulants, except when used to maintain the patency of a central venous line, or INR >1.5, or PTT ratio >1.5.
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection or psychiatric illness/social situations that would limit compliance with study requirements. Significant history of uncontrolled cardiac disease; i.e., uncontrolled hypertension, unstable angina, uncontrolled congestive heart failure.
• Patients may not be receiving any other investigational agents.
• No history of prior malignancy, with the exception of curatively treated squamous cell or basal carcinoma of the skin or in situ cervical cancer, DCIS or LCIS of the breast, localized early stage prostate cancer, or malignancy that has been treated with a curative intent with a 3-year disease-free survival.
• Pregnant women are excluded from this study because cetuximab, EGFR AS, and radiation have the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with cetuximab and EGFR AS, breastfeeding should be discontinued if the mother is treated with cetuximab. The effects of cetuximab and EGFR AS on the developing human fetus at the recommended therapeutic dose are unknown. For this reason women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while in this study, she should inform her treating physician immediately.
• HIV-positive patients receiving combination anti-retroviral therapy are excluded from the study because of possible drug interactions with cetuximab. Appropriate studies will be undertaken in patients receiving combination anti-retroviral therapy when indicated.
• Prior severe infusion reaction to a monoclonal antibody.
• Patients who are not informed of and are not willing to comply with the investigational nature of the study and have not signed a written informed consent in accordance with institutional and good clinical practice guidelines.