A randomized phase II trial of atezolizumab with or without tiragolumab before and after definitive chemoradiation for unresectable stage III non-small cell lung cancer (NSCLC; AFT-57).

Helen J. Ross Rush University Cancer Center, Chicago, IL info_outline Helen J. Ross, David E. Kozono, Michael D Mix, James John Urbanic, Terence Marques Williams, Taylor O'Donnell, Ilze Bara, Katja Schulze, Xiaofei F. Wang, Garth D. Nelson, Tom Stinchcombe

Authors Helen J. Ross Rush University Cancer Center, Chicago, IL info_outline Helen J. Ross, David E. Kozono, Michael D Mix, James John Urbanic, Terence Marques Williams, Taylor O'Donnell, Ilze Bara, Katja Schulze, Xiaofei F. Wang, Garth D. Nelson, Tom Stinchcombe Organizations Rush University Cancer Center, Chicago, IL, Brigham and Women's Hospital/Dana-Farber Cancer Institute, Boston, MA, SUNY Upstate Medical Center, Syracuse, NY, University of California, San Diego, Ideker Laboratory, Encinitas, CA, City of Hope National Medical Center, Duarte, CA, Alliance Foundation Trials, Boston, MA, Genentech Inc, South San Francisco, CA, Genentech, South San Francisco, CA, Duke University Medical Center, Durham, NC, Mayo Clinic, Rochester, MN, Duke Cancer Institute, Durham, NC Abstract Disclosures Research Funding Alliance Foundation Background: A minority of patients with unresectable stage III non-small cell lung cancer (NSCLC) may be cured by chemoradiotherapy (CRT). Adjuvant checkpoint inhibition through PD-L1 blockade after CRT improved survival compared to placebo in the PACIFIC trial (median progression-free survival (mPFS) 16.9 vs 5.6 months (mo), median overall survival (mOS) 47.5 vs 29.1 mo), but overall survival at 5 years remains below 50% (Spigel D, et al J Clin Oncol 2022, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9015199/. Only patients completing CRT without progression and with good performance status were eligible for this approach. Neoadjuvant checkpoint inhibition would allow more patients the opportunity to benefit from immunotherapy and may attenuate tumor-related immunosuppression via depletion of regulatory T cells and clonal expansion of effector T cells, thereby improving tumor immunogenicity. Neoadjuvant atezolizumab had favorable outcomes compared to historic PACIFIC data in the phase II single arm trial, AFT-16 (mPFS 30 mo and mOS not reached). Whether combination immunotherapy therapy before CRT will improve outcomes in this setting is the question posed in the AFT-57 trial. Methods: This phase II randomized Alliance Foundation Trials study (AFT-57) will evaluate safety and efficacy of atezolizumab with or without the anti-TIGIT monoclonal antibody, tiragolumab, before and after definitive CRT with concurrent atezolizumab. The primary endpoint is PFS in the two experimental arms with a goal to select the most promising regimen for further study. AFT-57 will randomly assign 158 patients with stage III NSCLC (AJCC v8), Eastern Cooperative Oncology Group performance status 0-1, no active autoimmune disease and no underlying organ dysfunction to 2 cycles of neoadjuvant atezolizumab (1200 mg intravenously [IV] every 21 days) with or without tiragolumab (600 mg IV). Non-progressing patients will receive carboplatin and paclitaxel weekly with atezolizumab 1200 mg IV every 21 days concurrent with 60 Gray involved field thoracic radiation in 30 daily fractions (Monday - Friday) followed by atezolizumab with or without tiragolumab on the same schedule as the neoadjuvant doses, with a plan to complete one year of therapy. A pilot cohort of 20 patients for whom tiragolumab will be combined with atezolizumab during chemoradiotherapy is planned toward the end of accrual. Correlative science includes tissue and blood-based immune-related biomarkers at baseline and during therapy. This trial utilizes the Alliance Participant Engagement Portal, a patient-facing site designed to provide information and resources to Alliance clinical trial participants. The trial was activated on 12/7/23 with the first patient screened 1/19/24. Clinical trial information: NCT05798663.

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