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Updated: Apr 22, 2026

Dynamic Lung Tumor Tracking for Stereotactic Ablative Body Radiation Therapy
Published on: June 7, 2015
A Phase II Study of Stereotactic Ablative Radiotherapy plus Atezolizumab plus Tiragolumab in Treatment-Naïve Patients
Jii Bum Lee1, Dong Kwon Kim2, Sang Hoon Lee2,3
1Division of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.
Purpose:
SKYROCKET is a single-center, single-arm phase II study that evaluated whether the addition of stereotactic body radiotherapy (SBRT) to atezolizumab plus tiragolumab enhances antitumor efficacy in PD-L1-positive non-small cell lung cancer (NSCLC).
Patients And Methods:
Patients received SBRT to all metastatic sites and subsequently received atezolizumab and tiragolumab every 3 weeks on day 1 of each 21-day cycle with 7 days of completion of SBRT. The primary endpoint was investigator-assessed progression-free survival (PFS) from the start of SBRT. Exploratory endpoints included single-cell RNA sequencing (scRNA-seq) obtained from tumor biopsies at baseline (BL) and on-treatment (OT) and were further characterized as clinical benefit [CB; partial response or stable disease (SD) ≥ 6 months] and non-clinical benefit (NCB; progressive disease or SD < 6 months).
Results:
Forty-one patients were enrolled. At a median duration of follow-up of 9.8 months, median PFS at the start of SBRT was 9.3 months [95% confidence interval (CI), 6.0-NR]. No new safety signal was observed. scRNA-seq of paired BL and OT (n = 3) and single-time point (n = 2) revealed that CD8 progenitor-exhausted (TPEX) cells markedly expanded after treatment, with high T-cell immunoreceptor with Ig and ITIM (TIGIT) and PD-1 expression in CD8 TPEX/TEX subsets. CD4 regulatory T cells (Treg) were reduced in the CB group but increased in the NCB group. The CB group showed reduced Treg suppression and NECTIN-TIGIT signaling, whereas NCB maintained proliferative CTLA4high/TIGIThigh Treg supported by ICAM/galectin-CTLA4 pathways.
Conclusions:
SBRT followed by atezolizumab plus tiragolumab showed encouraging clinical activity with manageable safety in PD-L1-positive metastatic NSCLC.
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