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2023 World Conference on Lung Cancer (Posters)
P1.28. Korean Real-world Data on Unresectable Stag ...
P1.28. Korean Real-world Data on Unresectable Stage III Non-Small Cell Lung Cancer Patients Treated with Durvalumab after Chemoradiotherapy - PDF(Abstract)
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This study investigated the use of durvalumab consolidation (DC) after chemoradiotherapy (CRT) in patients with unresectable stage III non-small cell lung cancer (NSCLC). The study included 157 patients treated at five tertiary hospitals in Korea. The primary endpoint was real-world progression-free survival (rwPFS), and secondary endpoints included overall survival (OS), objective response rate (ORR), and adverse events. <br /><br />At a median follow-up of 19.1 months, the median rwPFS for DC was 25.9 months, with 1-, 2-, and 3-year rwPFS rates of 59.4%, 51.8%, and 43.5%, respectively. The median OS was not matured, and the ORR of DC was 51.0%. High PD-L1 expression (50%) and the development of radiation pneumonitis (RP) requiring steroid treatment were associated with longer and shorter rwPFS, respectively. RP, RP requiring steroid treatment, and immune-related adverse events (irAEs) occurred in 36.3%, 26.8%, and 33.8% of patients, respectively. <br /><br />The study found that a high derived monocyte-to-lymphocyte ratio (dMLR) at the initiation of DC was the most significant risk factor for the development of RP requiring steroid treatment and irAEs. <br /><br />The study concluded that DC after CRT demonstrated favorable survival benefits in patients with unresectable stage III NSCLC compared to the results of the PACIFIC trial. It also suggested that blood-based biomarkers could predict the development of higher-grade RP and irAEs before the initiation of DC.
Asset Subtitle
Hyung-Joo Oh
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Speaker
Hyung-Joo Oh
Topic
Local-Regional NSCLC
Keywords
durvalumab consolidation
chemoradiotherapy
unresectable stage III non-small cell lung cancer
real-world progression-free survival
overall survival
objective response rate
adverse events
PD-L1 expression
radiation pneumonitis
immune-related adverse events
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