The frontier of neoadjuvant therapy in non-small cell lung cancer beyond PD-(L)1 agents

被引:0
作者
Sposito, Marco [1 ,2 ]
Eccher, Serena [1 ,2 ]
Scaglione, Ilaria [1 ,2 ]
Avancini, Alice [1 ,2 ]
Rossi, Antonio [2 ,3 ]
Pilotto, Sara [1 ]
Belluomini, Lorenzo [1 ,2 ]
机构
[1] Univ Verona, Dept Engn Innovat Med DIMI, Sect Innovat Biomed, Oncol Area, Verona, Italy
[2] Verona Univ Hosp Trust, Verona, Italy
[3] Oncol Ctr Excellence, Therapeut Sci & Strategy Unit, Milan, Italy
关键词
Neoadjuvant; antiangionesis; CTLA4; TIGIT; LAG3; lung cancer; immunotherapy; PHASE-II TRIAL; MONOCLONAL-ANTIBODY; PLUS PEMBROLIZUMAB; CTLA4; BLOCKADE; 8TH EDITION; CHEMOTHERAPY; BEVACIZUMAB; TUMOR; ANGIOGENESIS; CARBOPLATIN;
D O I
10.1080/14712598.2024.2408292
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
IntroductionWhile surgical resection is the cornerstone of treatment for resectable lung cancer, neoadjuvant/adjuvant chemotherapy has shown limited improvement in survival rates over the past decades. With the success of immune checkpoint inhibitors (ICIs) in advanced NSCLC, there is growing interest in their application in earlier stages of the disease. Recent approvals for neoadjuvant/adjuvant ICIs in stage II-IIIA NSCLC highlight this shift in treatment paradigms.Areas coveredIn this review, we aim to explore available data regarding alternative agents beyond the PD-(L)1 inhibitors, such as monoclonal antibodies against CTLA4, LAG3, TIGIT, antiangiogenic drugs, and novel therapies (antibody drug conjugates, bispecific antibodies) in neoadjuvant/perioperative regimens.Expert opinionNovel agents and combinations (with or without ICI or/and chemotherapy), guided by molecular profiling and immune phenotyping, showed promise in improving surgical and survival outcomes. Crucial is, also in early setting, to identifying biomarkers predictive of treatment efficacy in order to personalize neoadjuvant/perioperative treatment strategies.
引用
收藏
页码:1025 / 1037
页数:13
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