机构地区:[1]Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education),Department of Bone and Soft Tissue Sarcoma,Peking University Cancer Hospital and Research Institute,Beijing,China [2]Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education),Department of Melanoma and Sarcoma,Peking University Cancer Hospital and Research Institute,Beijing,China [3]Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education),Department of Pathology,Peking University Cancer Hospital and Research Institute,Beijing,China [4]Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education),Department of Radiology,Peking University Cancer Hospital and Research Institute,Beijing,China [5]Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education),Department of Genitourinary Oncology,Peking University Cancer Hospital and Research Institute,Beijing,China
出 处:《Signal Transduction and Targeted Therapy》2024年第12期5777-5785,共9页信号转导与靶向治疗(英文)
基 金:supported by the National Key Research and Development Program(2023YFC2506404);National Natural Science Foundation of China(82372869,82272676,and 82073011);Beijing Municipal Administration of Hospitals’Ascent Plan(DFL20220901,QML20231107);Beijing Natural Science Foundation(7242021).
摘 要:Neoadjuvant PD-1 inhibitor is promising in cutaneous melanoma but remains unknown in acral melanoma(AM).This phase Ib trial study(Clinicaltrials.gov NCT04197882)assessed the efficacy and safety of the combination of neoadjuvant oncolytic virus orienX010(ori)and anti-PD-1 toripalimab(tori)for resectable AM.Thirty patients of stage III/IV received neoadjuvant therapy of ori and tori for 12 weeks before surgery,followed by adjuvant treatment with tori for 1 year.Primary endpoints were radiographic and pathological response rates,with secondary endpoints of 1-and 2-year recurrence-free survival(RFS)rates,event-free survival(EFS)rates,and safety.Twenty-seven completed surgery and tori adjuvant treatment and median follow-up was 35.7 months.Radiographic and pathological response rates were 36.7%and 77.8%,with complete response rates of 3.3%and 14.8%,1-and 2-year RFS rates of 85.2%and 81.5%,and 1-and 2-year EFS rates of 83%and 73%,respectively.Adverse events occurred in all patients,mainly grade 1-2.There was no correlation between PET/CT evaluation and pathological response or progression-free survival/overall survival.Patients with pathological response showed tumor beds with high tertiary lymphoid structures(TLSs)and tumor-infiltrating lymphocytes(TILs).Cytokines and chemokines analysis showed the combination therapy significantly increases the secretion of proinflammatory cytokines and chemokines in both responders and non-responders.Therefore,neoadjuvant ori and tori demonstrated promising antitumor activity with high response rates and high 2-year RFS/EFS for AM with acceptable tolerability.
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