Clinical and Translational Oncology | 2021

Upfront pembrolizumab as an effective treatment start in patients with PD-L1\u2009≥\u200950% non-oncogene addicted non-small cell lung cancer and asymptomatic brain metastases: an exploratory analysis

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Abstract


The efficacy of immune checkpoint inhibitors in patients with brain metastases (BMs) from non-oncogene addicted non-small cell lung cancer (NSCLC) is under investigation. Here, we sought to determine the optimal management of NSCLCs with PD-L1\u2009≥\u200950% and asymptomatic BMs who were treated with first-line pembrolizumab. Thirty patients from 15 institutions with PD-L1\u2009≥\u200950% NSCLC had asymptomatic BMs, and met inclusion criteria. Patients were classified based on whether they had undergone upfront local radiotherapy for BMs as well as on the type of brain radiotherapy received. Nine patients were treated with upfront pembrolizumab alone, 8 patients with whole-brain radiotherapy (WBRT) followed by pembrolizumab and 13 patients with stereotactic radiosurgery (SRS) followed by pembrolizumab. Patients’ characteristics were similar among the three groups of patients except for a higher number of BMs\u2009≥\u20093 in the WBRT group. One complete and 4 partial intracranial responses were observed with upfront pembrolizumab alone. The median survival was not reached for the pembrolizumab and WBRT (n\u2009=\u20098) groups, and it was 7.6 months for the SRS (n\u2009=\u200913) group (P\u2009=\u20090.09), with 12-month survival rates being 55.5%, 62.5%, and 23.0%, respectively. Salvage WBRT was delivered in 1 patient in the upfront pembrolizumab group and in 4 patients in the SRS group. Upfront pembrolizumab showed efficacy in selected patients with PD-L1\u2009≥\u200950% non-oncogene addicted NSCLC and asymptomatic BMs. Prospective studies should address whether pembrolizumab alone, and deferral of radiotherapy, could be pursued in this patient population.

Volume 23
Pages 1818 - 1826
DOI 10.1007/s12094-021-02588-8
Language English
Journal Clinical and Translational Oncology

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