Comparative survival outcomes among histological subtypes of pulmonary adenocarcinoma: A nationwide study.

e20066 Background: Adenocarcinoma of the lung is a heterogeneous malignancy with multiple histological subtypes. In the US, population survival outcomes across these subtypes remain underexplored. Methods: A retrospective analysis of patients with various Lung Adenocarcinomas (Acinar, Lepidic, Papillary, Solid & solid type, Invasive mucinous, Mixed mucinous/non-mucinous, Colloid, Fetal, and Enteric type), diagnosed between 2010 and 2017, was conducted using the National Cancer Database in accordance with STROBE guidelines. Unadjusted median overall survival (mOS) was estimated using Kaplan-Meier survival analysis. Multivariate regression analysis was performed using accelerated failure time model to estimate covariate-adjusted hazard ratios (HR). Covariates included age, sex, race, tumor grade, TNM stage, Charlson Comorbidity Index, insurance status, year of diagnosis, facility type, and treatment modality. Lepidic carcinoma served as the reference arm for HR calculations. Results: A total of 46,218 patients were included in this large cohort study. 39,865 patients (86.3%) were white, 27,094 (58.6%) were female, 31,827 (69%) were aged ≥65 years, 29,843 (64.57%) had Medicare insurance, and 18,788 (40.65%) were treated in academic or research institutions. For unadjusted mOS, Acinar adenocarcinoma (n=15,877; 34.35%) demonstrated the best outcomes (mOS: 97.84 months, p<0.05). After covariate adjustment, Solid adenocarcinoma (n=1,736; 3.76%) had the most favorable prognosis (HR = 0.85, p<0.01). In contrast, Enteric type adenocarcinoma (n=33; 0.07%) exhibited the poorest survival, with an mOS of only 27.24 months (HR = 1.63, p<0.05). Lepidic adenocarcinoma (n=8,923; 19.31%), the reference group, demonstrated an mOS of 73.03 months with HR of 1. Other subtypes, such as Mixed/non mucinous adenocarcinoma (n=195; 0.42%; mOS: 85.22 months, HR = 0.91, p = 0.377) and Papillary adenocarcinoma (n=6,094; 13.19%; mOS: 64.79 months, HR = 0.97, p = 0.236), showed intermediate survival, with no statistically significant differences. On the other hand, significant differences were observed for Fetal adenocarcinoma (n=46; 0.10%; mOS: 39.82 months, HR = 1.17, p = 0.467), Invasive mucinous adenocarcinoma (n=1,254; 2.71%; mOS: 51.81 months, HR = 1.17, p<0.01), and Colloid adenocarcinoma (n=12,060; 26.09%; mOS: 44.09 months, HR = 1.29, p<0.01). Conclusions: This study highlights marked differences in survival across lung adenocarcinoma subtypes. These results stress the importance of further research to develop therapies tailored to specific histological variants. Adenocarcinoma subtype HR CI P value Lepidic ref Acinar 0.90 0.86–0.94 <0.01 Solid 0.85 0.78–0.92 <0.01 Enteric type 1.63 1.05–2.53 <0.05 Mixed/non mucinous 0.91 0.75–1.11 0.37 Papillary 0.97 0.93–1.02 0.23 Fetal 1.17 0.78–1.74 0.46 Invasive mucinous 1.17 1.08– 1.26 <0.01 Colloid 1.29 1.24–1.34 <0.01

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Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.e20066
Primary Topic
Lung Cancer Treatments and Mutations
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article
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article

Comparative survival outcomes among histological subtypes of pulmonary adenocarcinoma: A nationwide study.

Adnan Bhat, Ahmad Basharat, Junaid Anwar, Nadia Akbar et al.
Journal of Clinical Oncology
Lung Cancer Treatments and Mutations
article

Comparative survival outcomes among histological subtypes of pulmonary adenocarcinoma: A nationwide study.

Adnan Bhat, Ahmad Basharat, Junaid Anwar, Nadia Akbar, Usman Ilyas, Ali Usama, Haseeb Tareen, Edward F. LaBelle, Muhammad Salman Faisal, Waseem Nabi, Rana Uzair Ahmad, Moazzam Shahzad, Muzamil Khan, Nouman Aziz, Mir Wajid Majeed, Ali Cheema, Muhammad Jawad Javed, Sukhrob Makhkamov, Muhammad Mudassar
article en

Abstract

e20066 Background: Adenocarcinoma of the lung is a heterogeneous malignancy with multiple histological subtypes. In the US, population survival outcomes across these subtypes remain underexplored. Methods: A retrospective analysis of patients with various Lung Adenocarcinomas (Acinar, Lepidic, Papillary, Solid & solid type, Invasive mucinous, Mixed mucinous/non-mucinous, Colloid, Fetal, and Enteric type), diagnosed between 2010 and 2017, was conducted using the National Cancer Database in accordance with STROBE guidelines. Unadjusted median overall survival (mOS) was estimated using Kaplan-Meier survival analysis. Multivariate regression analysis was performed using accelerated failure time model to estimate covariate-adjusted hazard ratios (HR). Covariates included age, sex, race, tumor grade, TNM stage, Charlson Comorbidity Index, insurance status, year of diagnosis, facility type, and treatment modality. Lepidic carcinoma served as the reference arm for HR calculations. Results: A total of 46,218 patients were included in this large cohort study. 39,865 patients (86.3%) were white, 27,094 (58.6%) were female, 31,827 (69%) were aged ≥65 years, 29,843 (64.57%) had Medicare insurance, and 18,788 (40.65%) were treated in academic or research institutions. For unadjusted mOS, Acinar adenocarcinoma (n=15,877; 34.35%) demonstrated the best outcomes (mOS: 97.84 months, p<0.05). After covariate adjustment, Solid adenocarcinoma (n=1,736; 3.76%) had the most favorable prognosis (HR = 0.85, p<0.01). In contrast, Enteric type adenocarcinoma (n=33; 0.07%) exhibited the poorest survival, with an mOS of only 27.24 months (HR = 1.63, p<0.05). Lepidic adenocarcinoma (n=8,923; 19.31%), the reference group, demonstrated an mOS of 73.03 months with HR of 1. Other subtypes, such as Mixed/non mucinous adenocarcinoma (n=195; 0.42%; mOS: 85.22 months, HR = 0.91, p = 0.377) and Papillary adenocarcinoma (n=6,094; 13.19%; mOS: 64.79 months, HR = 0.97, p = 0.236), showed intermediate survival, with no statistically significant differences. On the other hand, significant differences were observed for Fetal adenocarcinoma (n=46; 0.10%; mOS: 39.82 months, HR = 1.17, p = 0.467), Invasive mucinous adenocarcinoma (n=1,254; 2.71%; mOS: 51.81 months, HR = 1.17, p<0.01), and Colloid adenocarcinoma (n=12,060; 26.09%; mOS: 44.09 months, HR = 1.29, p<0.01). Conclusions: This study highlights marked differences in survival across lung adenocarcinoma subtypes. These results stress the importance of further research to develop therapies tailored to specific histological variants. Adenocarcinoma subtype HR CI P value Lepidic ref Acinar 0.90 0.86–0.94 <0.01 Solid 0.85 0.78–0.92 <0.01 Enteric type 1.63 1.05–2.53 <0.05 Mixed/non mucinous 0.91 0.75–1.11 0.37 Papillary 0.97 0.93–1.02 0.23 Fetal 1.17 0.78–1.74 0.46 Invasive mucinous 1.17 1.08– 1.26 <0.01 Colloid 1.29 1.24–1.34 <0.01

Journal of Clinical OncologyVol. 43(16_suppl)
Rocky Vista University (US), Marshfield Clinic (US), Government Medical College (IN), George Washington University (US), University of South Florida (US), Wyckoff Heights Medical Center (US), Saint Thomas Midtown Hospital (US), Jackson Memorial Hospital (US), Moffitt Cancer Center (US), University of Florida (US), Queens Hospital Center (US), Mount Sinai Queens (US), Mayo Hospital (PK), Baptist Hospital (US), University of Oklahoma Health Sciences Center (US), Albany Medical Center Hospital (US), Parker Hannifin (United States) (US)
Openalex Percentile: Top 80%
Lung Cancer Treatments and Mutations
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