Concurrent use of aspirin with osimertinib is associated with improved survival in advanced EGFR-mutant non-small cell lung cancer
Open accessAbstract
Background Osimertinib is the treatment of choice for advanced EGFR-mutant non-small cell lung cancer (NSCLC). However, novel strategies to improve the duration of disease control are still urgently needed. Aspirin has been shown to decrease cancer incidence and improve outcomes in various malignancies. Therefore, we evaluated a cohort of patients who received osimertinib with or without concurrent use of aspirin to assess whether the addition of aspirin may lead to improved clinical outcomes.Methods MD Anderson Cancer Center GEMINI database was retrospectively queried for EGFR-mutant NSCLC patients who received osimertinib with or without concurrent use of aspirin for progression-free survival (PFS) and overall survival (OS).Results A total of 365 patients were identified including 77 which had concurrent use of aspirin. Patients in the aspirin-osimertinib group had significantly improved PFS (21.3 vs 11.6 months; HR, 0.52; 95 % CI, 0.38-0.70) and OS (Not reached vs 32.3 months; HR, 0.56; 95 % CI, 0.35-0.91) compared to osimertinib group. In subgroup analyses, the aspirin-associated PFS benefit was observed in patients with and without central nervous system (CNS) metastases, as well as in osimertinib first-line setting and in subsequent line setting. The median PFS in EGFR 19Del patients was longer than EGFR L858R patients with osimertinib, and when aspirin was added, the median PFS significantly improved in both groups regardless of lines of therapy. The benefit from aspirin was independent of age, gender, TP53 mutational status, or PD-L1 positivity.Conclusion Concurrent aspirin use with osimertinib in EGFR-mutant NSCLC patients was associated with improved survival, regardless of lines of therapy, CNS metastatic status, EGFR mutation type, age, gender, TP53, and PD-L1 status.
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EGFR mutations were determined from formalin-fixed paraffin-embedded tumours or digital-droplet PCR for blood samples by CLIA-certified methods.
“EGFR mutations were determined from formalin-fixed paraffin-embedded tumours or digital-droplet PCR for blood samples by CLIA-certified methods as previously described18,37.”
From Structure-based classification predicts drug response in EGFR-mutant NSCLC (2021) · cites this paper as [37]
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- Authors
- Liu, X., Hong, L., Nilsson, M., Hubert, S. M., Wu, S., Rinsurongkawong, W., Lewis, J., Spelman, A., Roth, J., Swisher, S., He, Y., Jack Lee, J., Fang, B., Heymach, J. V., Zhang, J., & Le, X.
- Affiliations
- The University of Texas MD Anderson Cancer Center (US)
- Army Medical University (CN)
- Corresponding author
- Zhang, Jianjun
- Le, Xiuning
- ORCID
- Venue
- Lung Cancer
- Publisher
- Elsevier BV
- Published
- 2020-11
- Volume
- 149
- Pages
- 33-40
- ISSN
- 0169-5002 (ISSN-L)
- PMC
- PMC7577964
- OpenAlex
- W3084333151
- Cited by
- 20
- References
- 57
- Citations by year
- 2025: 2 · 2024: 5 · 2023: 5 · 2022: 3 · 2021: 3
- FWCI
- 1.55
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Lung Cancer (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- University of Texas MD Anderson Cancer Center
- American Association for Cancer Research
- Sheikh Khalifa Bin Zayed Al Nahyan Institute for Personalized Cancer Therapy
- Conquer Cancer Foundation
- China Scholarship Council
- National Institutes of Health
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Diagnosis and Treatment
- Health Sciences › Medicine › Oncology › Lung Cancer Research Studies
- Keywords
- aspirin, osimertinib, EGFR-mutant non-small cell lung cancer, progression-free survival, overall survival, central nervous system metastasis, EGFR 19del, L858R mutation, first-line therapy, second-line therapy, TP53 mutation, PD-L1 expression
- MeSH terms
- Acrylamides, Aniline Compounds, Aspirin, Carcinoma, Non-Small-Cell Lung, Humans, Indoles, Lung Neoplasms, Mutation, Pyrimidines, Retrospective Studies, Protein Kinase Inhibitors, ErbB Receptors
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