Subgroup analyses showed a trend toward a greater PFS and OS benefit for patients randomized early after completion of radiotherapy (<14 days). 48 – 50 The safety profiles were similar between arms, with 30.5% vs 26.1% grade ≥3 AEs, including pneumonitis (3.6% vs 2.4%); 15.4% durvalumab and 9.8% placebo treated patients discontinued the regimen due to AEs. 48 , 49 Treatment exposure was similar in patients with or without pneumonitis across both arms as was median time to onset of pneumonitis from treatment start (55.0 days).
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Update on Targeted Therapies for Advanced Non-Small Cell Lung Cancer: Durvalumab in Context.
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