Immunotherapy-Boosted Stereotactic Ablative Radiotherapy in Inoperable Early-Stage Non-Small Cell Lung Cancer

被引:0
作者
Lian, Jie [1 ]
Sun, Li [1 ]
Zhang, Shuling [1 ]
Huang, Letian [1 ]
Ma, Jietao [1 ]
Han, Chengbo [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Oncol, Shenyang, Peoples R China
关键词
Inoperable; Early-stage; Non-small cell lung cancer; Stereotactic ablative Radiotherapy; Immune checkpoint inhibitors; Meta-analysis; BODY RADIATION-THERAPY; PHASE-II TRIAL; NSCLC PATIENTS; SURVIVAL; SAFETY; COMBINATION; DURVALUMAB; PATTERNS; EFFICACY; SBRT;
D O I
10.1007/s11864-025-01324-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The combination of stereotactic ablative radiotherapy (SABR) with immune checkpoint inhibitors, known as iSABR, marks a significant evolution in treating early-stage, inoperable non-small cell lung cancer (NSCLC). Managing these cases requires a multidisciplinary approach involving radiation and medical oncologists. Clinical evidence from a meta-analysis of seven studies, including 462 patients, indicates that iSABR may offer better outcomes than SABR alone. The analysis showed significantly improved progression-free survival (PFS) rates at 1-, 2-, and 3-year follow-ups for iSABR compared to SABR. There was also a trend toward better overall survival (OS) with iSABR. Subgroup analyses highlighted enhanced 3-year PFS with programmed death-1 (PD-1) inhibitors and doses per fraction >= 12.5 Gy. While iSABR slightly increased the risk of grade >= 3 adverse events like pneumonitis, fatigue, and skin reactions, these risks are generally manageable within a multidisciplinary treatment framework. In conclusion, iSABR demonstrates potential benefits and manageable risks in phase I/II trials for early-stage, inoperable NSCLC, with improved PFS and acceptable toxicity. These findings warrant further investigation in a larger phase III prospective randomized controlled trial to validate efficacy, optimize protocols, and establish long-term safety.
引用
收藏
页码:500 / 515
页数:16
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