Lapatinib and Radiation for Stage III-IV Head and Neck Cancer Patients Who Cannot Tolerate Concurrent Chemotherapy
Stopped early · Phase 2
Conditions studied: Head and Neck Cancer, Carcinoma, Squamous Cell, Head and Neck Cancers
In brief
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).
Key facts
- Study ID
- NCT00490061
- Run by
- Quynh-Thu Le
- People needed
- 17
- Starts
- 2007-07-01
- Expected to finish
- 2016-06-01
- Last updated by the study team
- 2017-03-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- Stanford University School of Medicine — Stanford, California, United States
- University of Florida Shands Cancer Center — Gainsville, Florida, United States
- Beth Israel — New York, New York, United States
- Duke University — Durham, North Carolina, United States
- University of Wisconsin Cancer Center — Madison, Wisconsin, United States
Full record on ClinicalTrials.gov
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