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新辅助与辅助化疗免疫治疗 II-IIIB 期非小细胞肺癌。

Neoadjuvant vs Adjuvant Chemoimmunotherapy for Stage II-IIIB Non-Small Cell Lung Cancer.

机构信息

Division of Thoracic Surgery, Department of Surgery, JFK University Medical Center, Hackensack Meridian Health, Edison, New Jersey.

Division of Cardiothoracic Surgery, The DeWitt Daughtry Department of Surgery, University of Miami Miller School of Medicine, Miami, Florida.

出版信息

Ann Thorac Surg. 2024 Sep;118(3):672-681. doi: 10.1016/j.athoracsur.2024.01.004. Epub 2024 Jan 28.

Abstract

BACKGROUND

In patients with resectable non-small cell lung cancer (NSCLC), recent trials demonstrate survival benefit of chemoimmunotherapy over chemotherapy alone in both the neoadjuvant and adjuvant settings. To date, there is no direct comparison between neoadjuvant and adjuvant protocols. We compared neoadjuvant vs adjuvant chemoimmunotherapy for resectable stage II-IIIB NSCLC.

METHODS

We queried the National Cancer Database for patients who had undergone an operation for stage II-IIIB NSCLC and who had received neoadjuvant or adjuvant chemoimmunotherapy between 2015 and 2020. We used inverse probability weighting to adjust for confounding variables and used Kaplan-Meier survival curves and Cox regression to explore the relationship between treatment groups and overall survival (OS) at 3 years postoperatively.

RESULTS

The inverse probability-weighted cohort represented 2119 weighted patient cases (neoadjuvant, 1034; adjuvant, 1085). Kaplan-Meier analysis demonstrated a significant OS benefit for neoadjuvant chemoimmunotherapy compared with adjuvant chemoimmunotherapy in the weighted cohort (3-year OS: 77% [95% CI, 71%-83%] vs 68% [95% CI, 64%-72%]; P = .035). On adjusted Cox regression, neoadjuvant chemoimmunotherapy was associated with a significant OS benefit (hazard ratio, 0.70; 95% CI, 0.50-0.96; P = .027). Among patients for whom pathologic stage data were available, 25% of patients receiving neoadjuvant chemoimmunotherapy had a pathologic complete response, with an additional 32.5% being downstaged.

CONCLUSIONS

Neoadjuvant chemoimmunotherapy confers a significant OS benefit over adjuvant chemoimmunotherapy for patients with resectable stage II-IIIB NSCLC. Although randomized trials are needed to confirm our findings, strong consideration should be given to administering neoadjuvant chemoimmunotherapy to patients who are predetermined to receive systemic treatment.

摘要

背景

在可切除的非小细胞肺癌(NSCLC)患者中,最近的试验表明,与单独化疗相比,新辅助和辅助化疗免疫治疗在新辅助和辅助治疗环境中均能提高生存率。迄今为止,新辅助和辅助方案之间尚无直接比较。我们比较了可切除的 II 期-IIIB 期 NSCLC 的新辅助与辅助化疗免疫治疗。

方法

我们在国家癌症数据库中查询了在 2015 年至 2020 年间接受过 II 期-IIIB 期 NSCLC 手术并接受过新辅助或辅助化疗免疫治疗的患者。我们使用逆概率加权来调整混杂变量,并使用 Kaplan-Meier 生存曲线和 Cox 回归来探讨治疗组与术后 3 年总生存率(OS)之间的关系。

结果

逆概率加权队列代表了 2119 例加权患者病例(新辅助组 1034 例,辅助组 1085 例)。Kaplan-Meier 分析表明,在加权队列中,与辅助化疗免疫治疗相比,新辅助化疗免疫治疗具有显著的 OS 获益(3 年 OS:77% [95% CI,71%-83%] vs 68% [95% CI,64%-72%];P=.035)。在调整后的 Cox 回归中,新辅助化疗免疫治疗与 OS 获益显著相关(风险比,0.70;95% CI,0.50-0.96;P=.027)。在有病理分期数据的患者中,25%接受新辅助化疗免疫治疗的患者有病理完全缓解,另有 32.5%患者降期。

结论

与辅助化疗免疫治疗相比,新辅助化疗免疫治疗可为可切除的 II 期-IIIB 期 NSCLC 患者带来显著的 OS 获益。尽管需要随机试验来证实我们的研究结果,但应强烈考虑对预计接受全身治疗的患者进行新辅助化疗免疫治疗。

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