Women diagnosed with non-small cell lung cancers (NSCLC) live longer than their male counterparts, according to results of a SWOG study presented by Loyola Medicine researcher Kathy Albain, MD, at the International Association for the Study of Lung Cancer’s 19th World Conference on Lung Cancer in Toronto.
Dr. Albain is the Huizenga Family Endowed Chair in Oncology Research at Loyola University Chicago Stritch School of Medicine.
Dr. Albain led the international study, S0424, for SWOG, the cancer clinical trials group that is part of the National Cancer Institute’s National Clinical Trials Network, the nation’s oldest and largest publicly-funded cancer research network. Dr. Albain and her SWOG team studied 981 patients newly diagnosed with stage I, II or III NSCLC. Non-small cell lung cancers account for about 80 to 85 percent of all lung cancers.
Researchers grouped patients into four groups based on sex and smoking history. Then, they analyzed data on cancer stage, patients’ tumor type and mutations, hormonal influences, treatment plans and survival rates. Patients were followed for five years, or until their deaths, in order to determine overall survival, or how long they lived after enrolling in the trial.
The study is the first prospective trial of this scope for NSCLC, designed specifically to follow survival outcomes. It represents collaboration across the clinical trials network, and included researchers from Canada and Japan.
Regardless of smoking history or any other factor, women in S0424 had significantly better overall survival (OS) rates compared to men. The analysis found that female never-smokers (FNS) and female ever-smokers (FES) had significantly better OS compared to male never-smokers (MNS) and male ever-smokers (MES). Five-year estimates reported overall survival at 73 percent for FNS, 69 percent for FES, 58 percent for MNS and 52 percent for MES. Women lived longer, even when adjustments were made for the medical care they received, their smoking history, hormonal factors, or the presence of mutations in their tumors common to NSCLC types.
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