CNS Downstaging: An Emerging Treatment Paradigm for Extensive Brain Metastases in Oncogene-Addicted Lung Cancer

•Newer generation tyrosine kinase inhibitors (TKIs) have demonstrated high CNS objective response rates, opening the door to new multidisciplinary treatment strategies for brain metastases.•For extensive brain metastases presentations, TKIs can downstage the burden of CNS disease allowing for the av...

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Veröffentlicht in:Lung cancer (Amsterdam, Netherlands) Netherlands), 2023-04, Vol.178, p.103-107
Hauptverfasser: Langston, Jacob, Patil, Tejas, Ross Camidge, D., Bunn, Paul A., Schenk, Erin L., Pacheco, Jose M., Jurica, James, Waxweiler, Timothy V., Kavanagh, Brian D., Rusthoven, Chad G.
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Sprache:eng
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Zusammenfassung:•Newer generation tyrosine kinase inhibitors (TKIs) have demonstrated high CNS objective response rates, opening the door to new multidisciplinary treatment strategies for brain metastases.•For extensive brain metastases presentations, TKIs can downstage the burden of CNS disease allowing for the avoidance of whole-brain radiotherapy (WBRT) and the conversion of some patients into candidates for stereotactic radiosurgery (SRS).•CNS downstaging is an emerging multidisciplinary paradigm with the potential to offer encouraging CNS control outcomes and reduced treatment-related toxicity by avoiding upfront WBRT administration. For extensive brain metastases (BrM) presentations arising from oncogene-addicted lung cancer, tyrosine kinase inhibitors (TKIs) with high response rates in the central nervous system (CNS) could potentially downstage the CNS disease burden, allowing for the avoidance of upfront whole-brain radiotherapy (WBRT) and the conversion of some patients into candidates for focal stereotactic radiosurgery (SRS). We describe the outcomes of patients with ALK, EGFR, and ROS1-driven NSCLC with extensive BrM presentations (defined as > 10 BrMs or leptomeningeal disease) treated with upfront newer generation CNS-active TKIs alone, including osimertinib, alectinib, brigatinib, lorlatinib, and entrectinib, from 2012 to 2021 at our institution. All BrMs were contoured at study entry, best CNS response (nadir), and first CNS progression. Twelve patients met criteria including 6 with ALK, 3 with EGFR, and 3 with ROS1-driven NSCLC. The median number and volume of BrMs at presentation were 49 and 19.6 cm3, respectively. Eleven patients (91.7 %) achieved a CNS response by modified-RECIST criteria to upfront TKI (10 partial responses, 1 complete response, 1 stable disease) with nadir observed at a median of 5.1 months. At nadir, the median number and volume of BrMs were 5 (median 91.7 % reduction per-patient) and 0.3 cm3(median 96.5 % reduction per-patient), respectively. Eleven patients (91.6 %) developed subsequent CNS progression (7 local failures, 3 local + distant, 1 distant) at a median of 17.9 months. At CNS progression, the median number and volume of BrMs were 7 and 0.7 cm3, respectively. Seven patients (58.3 %) received salvage SRS and no patients received salvage WBRT. The median overall survival from initiation of TKI for the extensive BrM presentation was 43.2 months. In this initial case series, we describe CNS downstaging as a promising multidis
ISSN:0169-5002
1872-8332
DOI:10.1016/j.lungcan.2023.02.006