The goal of this clinical research study is to learn if it is tolerable for patients with NSCLC to receive afatinib before surgery. The safety of this drug will also be studied.
Study Drug Administration: If you are found to be eligible to take part in this study, you will take afatinib by mouth 1 time a day for at least 14 days before your surgery. You should take it at least 1 hour before or 2 hours after a meal. You will sign a separate consent form that describes the surgery and its risks in more detail. You will keep a diary of when you take the pills. You should bring the diary to each visit, along with your pill bottle so the study staff can count any remaining pills. Some side effects, such as diarrhea and skin rash, will occur in almost all patients. If you have severe side effects, your dose may be lowered. Study Visits: One (1) time a week while you are taking afatinib: * You will have a physical exam. * Blood (about 3 teaspoons) will be drawn for routine tests. Within a week before your surgery: * You will have a physical exam. * Blood (about 3 teaspoons) will be drawn for routine tests. * You will have a PET-CT scan to check the status of the disease. * You will have a MUGA scan to check your heart function. On the day of surgery, blood (about 3 teaspoons) will be drawn for research tests, including looking for tumor cells that may be in the blood. Leftover tissue from surgery will be used for biomarker testing. Length of Treatment: You will take your last dose of study drug within 24 hours before your surgery. You will no longer be able to take the study drug if the disease gets worse, if intolerable side effects occur, or if you are unable to follow study directions. Your participation on the study will be over after the follow-up visit. Follow-Up: At about 30 days after surgery: * You will have a physical exam. * Blood (about 3 teaspoons) will be drawn for routine tests. It is possible that the study staff will call you instead of the visit above. You will be asked how you are doing. The call should last about 5 minutes. If you are having side effects from the study drug at the time of the follow-up visit or call, you may have additional follow-up if the doctor thinks it is needed. The follow-up tests, procedures, and schedule will be the doctor's decision depending on the side effects. This is an investigational study. Afatinib is FDA approved and commercially available to be the first treatment for patients with a specific type of NSCLC that has spread. It is currently being used for research purposes only. The study doctor can explain how the study drug is designed to work. Up to 20 participants will be enrolled in this study. All will take part at MD Anderson.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
2
40 mg by mouth daily for a minimum of 14 days, and until the day of surgery.
University of Texas MD Anderson Cancer Center
Houston, Texas, United States
Number of Patients With Treatment "Completed"
A patient is declared to have the treatment "completed" if he completes at least 14 days of neoadjuvant treatment, had a thoracotomy for the planned surgical resection, and 30 days of post operative care.
Time frame: From the start of neoadjuvant treatment to 30 days post operative care
Number of Participants With a Change in Standard Uptake Value (SUV) From Pre to Post Operative PET-CT
To determine whether pre-operative Afatinib treatment affects metabolic tumor labeling, as measured by PET-CT scanning.
Time frame: From the start of neoadjuvant treatment to follow-up, up to 30 days post surgery
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.