Abstract
Methods: ES-SCLC pts received atezo IV q3w at 15 mg/kg or 1200 mg as part of a Ph Ia study (NCT01375842). Due to protocol amendments the first 5 pts were PD-L1 selected and the subsequent 12 were not PD-L1 selected. Initially treatment was to last up to 1 y though retreatment at PD was allowed. Later pts were treated until loss of clinical benefit. RECIST v1.1 and irRC assessments were used. PD-L1 expression was centrally evaluated using the VENTANA SP142 IHC assay. Teffector (Teff) gene signature (CD8A, GZMA, GZMB, EOMES, CXCL9, CXCL10, TBX21) and PD-L1 mRNA was measured (iChip).
Cite
CITATION STYLE
Sequist, L. V., Chiang, A., Gilbert, J., Gordon, M., Conkling, P. R., Thompson, D., … Gettinger, S. (2016). Clinical activity, safety and predictive biomarkers results from a phase Ia atezolizumab (atezo) trial in extensive-stage small cell lung cancer (ES-SCLC). Annals of Oncology, 27, vi493. https://doi.org/10.1093/annonc/mdw389.03
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.