Erlotinib versus radiation therapy for brain metastases in patients with EGFR-mutant lung adenocarcinoma
Open accessAbstract
Purpose/objectives Radiation therapy (RT) is the principal modality in the treatment of patients with brain metastases (BM). However, given the activity of EGFR tyrosine kinase inhibitors in the central nervous system, it is uncertain whether upfront brain RT is necessary for patients with EGFR-mutant lung adenocarcinoma with BM.Methods and materials Patients with EGFR-mutant lung adenocarcinoma and newly diagnosed BM were identified.Results 222 patients were identified. Exclusion criteria included prior erlotinib use, presence of a de novo erlotinib resistance mutation, or incomplete data. Of the remaining 110 patients, 63 were treated with erlotinib, 32 with whole brain RT (WBRT), and 15 with stereotactic radiosurgery (SRS). The median overall survival (OS) for the whole cohort was 33 months. There was no significant difference in OS between the WBRT and erlotinib groups (median, 35 vs 26 months; P=.62), whereas patients treated with SRS had a longer OS than did those in the erlotinib group (median, 64 months; P=.004). The median time to intracranial progression was 17 months. There was a longer time to intracranial progression in patients who received WBRT than in those who received erlotinib upfront (median, 24 vs 16 months, P=.04). Patients in the erlotinib or SRS group were more likely to experience intracranial failure as a component of first failure, whereas WBRT patients were more likely to experience failure outside the brain (P=.004).Conclusions The survival of patients with EGFR-mutant adenocarcinoma with BM is notably long, whether they receive upfront erlotinib or brain RT. We observed longer intracranial control with WBRT, even though the WBRT patients had a higher burden of intracranial disease. Despite the equivalent survival between the WBRT and erlotinib group, this study underscores the role of WBRT in producing durable intracranial control in comparison with a targeted biologic agent with known central nervous system activity.
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Patients with EGFR-mutant NSCLC who harbor brain metastases have been reported to have median survival times as long as 2 to 3 years.
“patients with EGFR-mutant NSCLC who are harboring brain metastases have been reported as having median survival times as long as 2 to 3 years.108,109”
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References 25 · Cited by 96
- Authors
- Gerber, N. K., Yamada, Y., Rimner, A., Shi, W., Riely, G. J., Beal, K., Yu, H. A., Chan, T. A., Zhang, Z., & Wu, A. J.
- Affiliations
- Memorial Sloan Kettering Cancer Center (US)
- Corresponding author
- Wu, Abraham J.
- ORCID
- Venue
- International Journal of Radiation Oncology*Biology*Physics
- Publisher
- Elsevier BV
- Published
- 2014-06
- Volume
- 89
- Issue
- 2
- Pages
- 322-329
- ISSN
- 0360-3016 (ISSN-L)
- PMC
- PMC5691362
- OpenAlex
- W2052185432
- Cited by
- 96
- References
- 25
- Citations by year
- 2025: 2 · 2024: 1 · 2023: 2 · 2022: 4 · 2021: 6 · 2020: 2 · 2019: 13 · 2018: 16 · 2017: 16 · 2016: 16 · 2015: 16 · 2014: 2
- FWCI
- 13.37
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- International Journal of Radiation Oncology*Biology*Physics (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (P30CA008748)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Brain Metastases and Treatment
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
- Health Sciences › Medicine › Genetics › Glioma Diagnosis and Treatment
- Keywords
- erlotinib, brain metastases, EGFR-mutant lung adenocarcinoma, whole brain radiotherapy, stereotactic radiosurgery, EGFR tyrosine kinase inhibitors, intracranial control, overall survival, intracranial progression, central nervous system activity
- MeSH terms
- Erlotinib Hydrochloride, Adenocarcinoma, Brain Neoplasms, Female, Humans, Lung Neoplasms, Male, Middle Aged, Mutation, Quinazolines, Retrospective Studies, Survival Analysis, Cranial Irradiation, Radiosurgery, Disease Progression, Drug Resistance, Neoplasm, Protein Kinase Inhibitors, ErbB Receptors
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