Abstract 906: Sex-based differences in lung cancer survival: A competing risks model using the PLCO trial.

Abstract Purpose: Lung cancer causes more than 130,000 deaths each year in the United States. Although females with non-small cell lung cancer (NSCLC) appear to have better survival than males, many prior studies did not fully account for key confounders, including smoking history and competing causes of mortality. Moreover, large cohort analyses often relied on Cox models, which may overestimate cause-specific risks when competing mortality is substantial. Hence, in this study, we assessed whether sex-based survival differences in NSCLC persist after adjusting for these confounders and applied competing risk regression to adequately account for competing causes of death and more accurately quantify lung cancer-specific mortality. Methods: Using data from the Prostate, Lung, Colorectal, and Ovarian (PLCO) trial, we selected patients whose first-ever malignancy was primary NSCLC, excluding anyone with a prior other cancer diagnosis or secondary/metastatic lung tumors. Lung cancer-specific survival for females versus males was evaluated using Fine and Gray competing risk models, adjusting for sociodemographic factors, cancer location, histology, treatment, smoking status, and comorbidities. Because patients with NSCLC experience substantial mortality from non-cancer-related causes, we applied a competing risk model to accurately account for this. This approach avoids the more than twofold (2.25-fold) overestimation of cause-specific risk that can occur when Cox models are used in elderly populations. All analyses were performed using SAS 9.4. Results: Among 2,793 patients (59% male, 41% female), 2,006 (72%) experienced lung cancer-related death, 531 (19%) died from other causes, and 256 (9%) were alive at last follow-up. Female patients were more likely to be never smokers (14% vs 5%, p<0.0001), have adenocarcinoma (55% vs 42%, p<0.0001), and less likely to have cardiovascular disease (heart failure: 7% vs 18%, p<0.0001). Unadjusted Fine and Gray models showed (hazard ratio [HR]: 0.81, 95% confidence interval [CI]: 0.74-0.88) lower lung cancer-specific mortality among women. Adjusted analyses demonstrated that female sex (HR: 0.85, 95% CI: 0.74-0.98) was associated with decreased risk of lung cancer-specific death. A significant interaction between female sex and stage IV disease (b coefficient: 0.18, 95% CI: 0.99-1.45) showed that lung cancer-specific survival of women and men was similar among patients with advanced disease. Conclusions: Females with NSCLC demonstrate reduced lung cancer-specific mortality after adjustment for competing risks and confounders. These results could be suggestive of sex-based disparities in inherent biological differences in tumor biology, natural disease progression, or overall increased life expectancy in females, further supporting investigating molecular pathways including hormonal signaling and immune responses to guide optimal treatment strategies. Citation Format: Veer N. Shah, Grace Mhango, Darshi Shah, Paolo Boffetta, Juan P. Wisnivesky. Sex-based differences in lung cancer survival: A competing risks model using the PLCO trial [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 906.

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Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-906
Primary Topic
Cardiovascular Health and Risk Factors
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article

Abstract 906: Sex-based differences in lung cancer survival: A competing risks model using the PLCO trial.

J.P. Wisnivesky, Veer Shah, Darshi Shah, Grace Mhango et al.
Cancer Research
Cardiovascular Health and Risk Factors
article

Abstract 906: Sex-based differences in lung cancer survival: A competing risks model using the PLCO trial.

J.P. Wisnivesky, Veer Shah, Darshi Shah, Grace Mhango, Paolo Boffetta
article en

Abstract

Abstract Purpose: Lung cancer causes more than 130,000 deaths each year in the United States. Although females with non-small cell lung cancer (NSCLC) appear to have better survival than males, many prior studies did not fully account for key confounders, including smoking history and competing causes of mortality. Moreover, large cohort analyses often relied on Cox models, which may overestimate cause-specific risks when competing mortality is substantial. Hence, in this study, we assessed whether sex-based survival differences in NSCLC persist after adjusting for these confounders and applied competing risk regression to adequately account for competing causes of death and more accurately quantify lung cancer-specific mortality. Methods: Using data from the Prostate, Lung, Colorectal, and Ovarian (PLCO) trial, we selected patients whose first-ever malignancy was primary NSCLC, excluding anyone with a prior other cancer diagnosis or secondary/metastatic lung tumors. Lung cancer-specific survival for females versus males was evaluated using Fine and Gray competing risk models, adjusting for sociodemographic factors, cancer location, histology, treatment, smoking status, and comorbidities. Because patients with NSCLC experience substantial mortality from non-cancer-related causes, we applied a competing risk model to accurately account for this. This approach avoids the more than twofold (2.25-fold) overestimation of cause-specific risk that can occur when Cox models are used in elderly populations. All analyses were performed using SAS 9.4. Results: Among 2,793 patients (59% male, 41% female), 2,006 (72%) experienced lung cancer-related death, 531 (19%) died from other causes, and 256 (9%) were alive at last follow-up. Female patients were more likely to be never smokers (14% vs 5%, p<0.0001), have adenocarcinoma (55% vs 42%, p<0.0001), and less likely to have cardiovascular disease (heart failure: 7% vs 18%, p<0.0001). Unadjusted Fine and Gray models showed (hazard ratio [HR]: 0.81, 95% confidence interval [CI]: 0.74-0.88) lower lung cancer-specific mortality among women. Adjusted analyses demonstrated that female sex (HR: 0.85, 95% CI: 0.74-0.98) was associated with decreased risk of lung cancer-specific death. A significant interaction between female sex and stage IV disease (b coefficient: 0.18, 95% CI: 0.99-1.45) showed that lung cancer-specific survival of women and men was similar among patients with advanced disease. Conclusions: Females with NSCLC demonstrate reduced lung cancer-specific mortality after adjustment for competing risks and confounders. These results could be suggestive of sex-based disparities in inherent biological differences in tumor biology, natural disease progression, or overall increased life expectancy in females, further supporting investigating molecular pathways including hormonal signaling and immune responses to guide optimal treatment strategies. Citation Format: Veer N. Shah, Grace Mhango, Darshi Shah, Paolo Boffetta, Juan P. Wisnivesky. Sex-based differences in lung cancer survival: A competing risks model using the PLCO trial [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 906.

Cancer ResearchVol. 86(7_Supplement)
Stony Brook School (US), Stony Brook University (US), Icahn School of Medicine at Mount Sinai (US)
Good health and well-being
Openalex Percentile: Top 5%
Cardiovascular Health and Risk Factors
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