Phase II Lapatinib and Radiation for Stage III-IV Head and Neck Cancer Patients Who Cannot Tolerate Concurrent Chemotherapy

• 2-year locoregional control, progression free survival and over all survival rates in these patients [ Time Frame: Two years after completion of study ] [ Designated as safety issue: No ]
• Rate and pattern of late-treatment related toxicity in these patients [ Time Frame: Two years after completion of study ( ] [ Designated as safety issue: Yes ]
• Role of DCE MRI in predicting treatment outcomes in treated patients Outcome Time Frame: [ Time Frame: Two years after completion of study ( ] [ Designated as safety issue: No ]
• Changes in the expression of relevant tumoral and circulating biomarkers [ Time Frame: After completion of treatment (2014) ] [ Designated as safety issue: No ]
• Change in quality of life status relative to baseline [ Time Frame: After completion of study ] [ Designated as safety issue: No ]

• 2-year locoregional control, progression free survival and over all survival rates in these patients [ Time Frame: 2 years, following treatment ]
• Rate and pattern of late-treatment related toxicity in these patients [ Time Frame: Following treatment ]
• Role of DCE MRI in predicting treatment outcomes in treated patients [ Time Frame: Following treatment ]
• Changes in the expression of relevant tumoral and circulating biomarkers [ Time Frame: After one week of lapatinib treatment ]
• Change in quality of life status relative to baseline [ Time Frame: Following treatment ]

We propose to combine lapatinib with RT alone in patients with locally advanced head and neck cancer who cannot tolerate chemotherapy. The main objective of the study is to determine the efficacy of combining concurrent radiation and lapatinib in terms of time-to-progression (TTP) in this group of patients. In addition, we will determine the 2-year locoregional control rate (LRC), progression-free survival (PFS) and overall survival (OS) in these patients. We will also evaluate the profile and frequency of late toxicity, specifically mucosal and dermatologic toxicity, of the combination of lapatinib and RT in patients with locally advanced head and neck squamous cell carcinoma (HNSCC).

There is substantial data to suggest that EGFR and Her-2/neu expressions are important predictors for prognosis in HNSCC. EGFR blockade with a monoclonal antibody in conjunction with radiotherapy has been shown to improve survival over radiotherapy alone in patients with locally advanced HNSCC. Dual inhibition of EGFR and ErbB2 tyrosine kinases results in greater inhibitory effect of the downstream signaling pathways in cancer cells than inhibition of either receptor alone. Phase I studies in HNSCC suggested that the drug is well tolerated when delivered either alone or concurrently with cisplatin based chemoradiotherapy in HNSCC.

We propose to combine lapatinib with RT alone in patients with locally advanced HNSCC who cannot tolerate chemotherapy. The main objective of the study is to determine the efficacy of combining concurrent radiation and lapatinib in terms of time-to-progression (TTP) in this group of patients. In addition, we will determine the 2-year locoregional control rate (LRC), progression-free survival (PFS) and overall survival (OS) in these patients. We will also evaluate the profile and frequency of late toxicity, specifically mucosal and dermatologic toxicity, of the combination of lapatinib and RT in patients with locally advanced HNSCC.

• Head and Neck Cancer
• Carcinoma, Squamous Cell
• Head and Neck Cancers

• Drug: Lapatinib
  1500 mg po daily orally
  Other Names:

  • Tykerb/Tyverb
  • GlaxoSmithKline
• Procedure: Radiotherapy
  Standard of Care
  Other Name: IMRT - Intensity Modulated Radio Therapy
• Device: G.E. Healthcare 1.5T MR, systems revision 12.0 M5
  Standard of Care
  Other Name: G.E. Healthcare MRI Device and Software
• Procedure: Pet/CT
  Standard of Care
  Other Name: Positron emission tomography - computed tomography

Inclusion Criteria:

• Newly diagnosed stage III-IV HNSCC, pathologically confirmed (HNSCC from unknown primary sites are allowed)
• No evidence of distant metastasis
• No prior radiation therapy to the head and neck sites.
• Able to sign a study-specific informed consent form.
• Women of childbearing potential and men with partners capable of producing offspring must be willing to practice acceptable methods of birth control to prevent pregnancy.
• Left ventricular ejection fraction (LVEF) within the institutional normal range as measured by ECHO (If ECHO cannot be performed or if the Investigator feels that it is not conclusive to evaluate LVEF, then a MUGA scan should be performed).

• Having one of the following parameters that would preclude the use of concurrent CRT:

  • ECOG PS > 2.
  • Creatinine > 1.3 or calculate or measure creatinine clearance < 60 ml/min.
  • AST or ALT > 1.5 times normal limit but < 3 times normal limit
  • Total bilirubin > 1.5 mg/dL but < 3mg/dL
  • History of hearing loss that would preclude cisplatin chemotherapy. These would include the existing need of a hearing aid or a >= 25 decibel shift over 2 contiguous frequencies on a pretreatment hearing test.
  • Pre-existing peripheral neuropathy that would preclude cisplatin chemotherapy
  • Refuse or cannot tolerate chemotherapy
• Age 18 years or older

Exclusion Criteria:

• Known hypersensitivity to lapatinib or any of the excipients of this product (quinazolines).
• Uncontrolled angina, arrhythmia or congestive heart failure at the time of HNSCC diagnosis and treatment.
• History of myocardial infarction < 6 months from study entry.
• Treatment with a non-approved or investigational drug within 30 days before Day 1 of study treatment.
• Prior treatment with EGFR or Her2/Neu directed therapies.
• HIV-positive patients receiving combination anti-retroviral therapy are excluded from the study because of possible pharmacokinetic interactions with Lapatinib.
• Absolute neutrophil count < 1500/uL