To gather preliminary safety and outcome data for the multimodality treatment of lung adenocarcinoma in the setting of multifocal BAC.
Lung bronchoalveolar carcinoma (BAC) or adenocarcinoma in situ (AIS) continues to represent a poorly understood clinical entity. A frequent clinical dilemma in lung cancer care is the management of a documented or suspected invasive adenocarcinoma in the setting of multifocal ground glass opacity (GGO) consistent with multifocal AIS. These patients are typically classified as stage IV disease, and treated with palliative chemotherapy. No existing pathologic or molecular test is currently capable of making the distinction between independent primary versus metastatic tumors, a distinction for which substantial treatment impact exists. Many treating physicians suspect that outcomes for this specific patient subgroup are better than norms for stage IV disease, as such patients are frequently node-negative and without distant metastases despite multiple lesions present. To address this issue, we will evaluate a multimodality treatment protocol using aggressive local and targeted systemic therapy for multifocal lung adenocarcinoma, incorporating information from tumor genome sequencing for individualized treatment planning. The results will have significant impact in advancing the biologic understanding and treatment approach for lung adenocarcinoma in the setting of multifocal AIS.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Tissue collection at the time of surgery for genetic testing and blood sample for germ line DNA.
Mayo Clinic in Rochester
Rochester, Minnesota, United States
Overall Survival
Overall survival compared to survival for Stage IV NSCLC on NCCTG trials
Time frame: 2 years
Progressive free survival
Progressive free survival
Time frame: Every 3 months for 2 years
Treatment Morbidity and Mortality
Treatment Morbidity and Mortality
Time frame: 2 years
Post-treatment Pulmonary Function
Post-treatment Pulmonary Function measured by pulmonary function testing (spirometry)
Time frame: 2 years
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