Skip NavigationSkip to Content

Real-World Studies Link Nonsteroidal Anti-inflammatory Drug Use to Improved Overall Lung Cancer Survival

  1. Author:
    Roszik, Jason
    Lee, J Jack
    Wu, Yi-Hung
    Liu,Xi
    Kawakami, Masanori
    Kurie, Jonathan M
    Belouali, Anas
    Boca, Simina M
    Gupta, Samir
    Beckman, Robert A
    Madhavan, Subha
    Dmitrovsky,Ethan
  2. Author Address

    Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030., Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030., Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030., Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030., Frederick National Laboratory for Cancer Research, Frederick, MD 21702-1201., Georgetown Lombardi Comprehensive Cancer Center and Innovation Center for Biomedical Informatics, Georgetown University Medical Center, Washington DC, 20007., Current address: AstraZeneca, Gaithersburg, MD 20878., Department of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030.,
    1. Year: 2022
    2. Date: Jul
    3. Epub Date: 2022 07 06
  1. Journal: Cancer Research Communications
    1. 2
    2. 7
    3. Pages: 590-601
  2. Type of Article: Article
  1. Abstract:

    Inflammation is a cancer hallmark. Nonsteroidal anti-inflammatory drugs (NSAIDs) improve overall survival (OS) in certain cancers. Real-world studies explored here if NSAIDs improve non-small cell lung cancer (NSCLC) OS. Analyses independently interrogated clinical databases from The University of Texas MD Anderson Cancer Center (MDACC cohort, 1987 to 2015; 33,162 NSCLCs and 3,033 NSAID users) and Georgetown-MedStar health system (Georgetown cohort, 2000 to 2019; 4,497 NSCLCs and 1,993 NSAID users). Structured and unstructured clinical data were extracted from electronic health records (EHRs) using natural language processing (NLP). Associations were made between NSAID use and NSCLC prognostic features (tobacco use, gender, race, and body mass index, BMI). NSAIDs were statistically-significantly (P < 0.0001) associated with increased NSCLC survival (5-year OS 29.7% for NSAID users versus 13.1% for non-users) in the MDACC cohort. NSAID users gained 11.6 months over nonusers in 5-year restricted mean survival time. Stratified analysis by stage, histopathology and multicovariable assessment substantiated benefits. NSAID users were pooled independent of NSAID type and by NSAID type. Landmark analysis excluded immortal time bias. Survival improvements (P < 0.0001) were confirmed in the Georgetown cohort. Thus, real-world NSAID usage was independently associated with increased NSCLC survival in the MDACC and Georgetown cohorts. Findings were confirmed by landmark analyses and NSAID type. The OS benefits persisted despite tobacco use and did not depend on gender, race, or BMI (MDACC cohort, P < 0.0001). These real-world findings could guide future NSAID lung cancer randomized trials.

    See More

External Sources

  1. DOI: 10.1158/2767-9764.crc-22-0179
  2. PMID: 35832288
  3. PMCID: PMC9273107

Library Notes

  1. Fiscal Year: FY2021-2022
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel