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[围术期无驱动] 非小细胞肺癌:新辅助化免治疗 vs 新辅助化疗 vs 新辅助化放疗:NCDB大数据

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阳光肺科 发表于 2026-3-21 23:38:21 | 显示全部楼层 |阅读模式

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非小细胞肺癌:新辅助化免治疗 vs 新辅助化疗 vs 新辅助化放疗:NCDB大数据

Caturegli G, Kaminski MF, Canavan M, Ayoade OF, Resio BJ, Boffa DJ. Real-world perioperative outcomes of neoadjuvant chemoimmunotherapy in non-small cell lung cancer. JTCVS Open. 2025 Sep 20;28:554-564. doi: 10.1016/j.xjon.2025.09.016. PMID: 41473080; PMCID: PMC12745116.
Real-world perioperative outcomes of neoadjuvant chemoimmunotherapy in non–small cell lung cancer - PMC
Real-world perioperative outcomes of neoadjuvant chemoimmunotherapy in non–small cell lung cancer - JTCVS Open

Objective: Approximately 30% of non-small cell lung cancers will recur after surgery, highlighting a need for additional perioperative therapies. Several recent clinical trials demonstrated a reduction in non-small cell lung cancer recurrence with the use of neoadjuvant chemoimmunotherapy. Recognizing that trial results may not always be replicated in the general population, our objective was to evaluate perioperative outcomes of immunotherapy in the real-world setting.

Methods: Adult patients diagnosed with clinical stage I to III non-small cell lung cancer in the National Cancer Database between 2018 and 2022 were included. Perioperative outcomes were evaluated in the following groups: neoadjuvant chemoimmunotherapy, neoadjuvant chemotherapy, or neoadjuvant chemoradiotherapy.

Results: Overall, 3956 patients were identified, including 1051 treated with neoadjuvant chemoimmunotherapy (33.2%), 1590 treated with chemotherapy (40.1%), and 1315 treated with neoadjuvant chemoradiotherapy (26.5%). The pneumonectomy rate after induction chemoimmunotherapy was 6.2%, which was lower than after chemotherapy (10.0%, P = .001) but similar to after chemoradiotherapy (7.9%, P = .11). Postoperative 90-day mortality among patients receiving chemoimmunotherapy was less than 1.0%, which was lower than both chemotherapy (2.0%, P < .001) and chemoradiotherapy (3.5%, P < .001). Nodal downstaging was seen in 43.9% of patients receiving chemoimmunotherapy. The pathologic complete response rate was 30.2%, which was higher than chemotherapy (9.1%, P < .001) but comparable to chemoradiotherapy (26.8%, P = .13). Results from adjusted logistic regressions were consistent with findings of unadjusted analyses.

Conclusions: Real-world outcomes suggest that the reassuring safety and impressive downstaging effect of neoadjuvant chemoimmunotherapy seen in clinical trials can be reproduced in the general population with non-small cell lung cancer. Further study to understand the impact of perioperative chemoimmunotherapy in the real-world setting is justified.

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