新辅助化疗免疫治疗前后非小细胞肺癌患者淋巴结状态的预后意义:一项多中心回顾性研究

IF 3.3 3区 医学 Q2 ONCOLOGY
Ran Ma, Haitang Yang, Yong Ge, Tianyue Ma, Jiayi Wang, Shuyuan Li, Tianci Feng, Shoujie Feng, Cheng Zhang, Teng Sun, Feng Yao, Jun Yi, Hao Zhang, Pingping Song
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引用次数: 0

摘要

背景:在接受新辅助化疗免疫治疗的非小细胞肺癌(NSCLC)患者中,淋巴结(LN)状态分为ypN0和ypN+。然而,ypN0包括新辅助治疗前有淋巴结转移的患者(cN+/ypN0)或从未发生淋巴结转移的患者(cN0/ypN0)。这些不同LN状态的预后含义尚未得到很好的理解。方法:回顾性分析2019 - 2022年中国4个中心接受新辅助化疗免疫治疗后手术的非小细胞肺癌患者。根据LN状态将患者分为“自然”N0 (cN0/ypN0)、“下行”N0 (cN+/ypN0)和ypN+ (cN+/ypN+)。结果:在527例初始入组患者中,186例符合纳入标准:34例(18.3%)为“自然”N0, 95例(51.1%)为“降级”N0, 57例(30.6%)为ypN+。中位随访时间为24个月(11-64个月)。与“自然”N0和“降级”N0相比,ypN+患者的无病生存期(DFS)和总生存期(OS)显著降低(DFS: P < 0.001;Os: p < 0.001)。然而,在“自然”N0和“降级”N0之间,DFS (P = .695)和OS (P = .814)均无显著差异。亚组分析显示,MPR/ypN0组的DFS明显优于非MPR/ypN0组(P = 0.008)、MPR/ypN+组(P = 0.028)和非MPR/ypN+组(P < 0.001)。在OS方面,MPR/ypN0组显著优于非MPR/ypN+组(P < 0.001),并有优于非MPR/ypN0组(P = 0.067)和MPR/ypN+组(P = 0.067)的OS趋势。值得注意的是,在非MPR/ypN0组和MPR/ypN+组之间,DFS (P = .908)和OS (P = .943)均无显著差异。非mpr /ypN+组在DFS和OS中生存结果最差。结论:无论前cN状态如何,在新辅助化疗免疫治疗后达到ypN0状态强烈预示着NSCLC患者的有利结局。MPR与LN状态相结合可有效区分患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic Implications of Lymph Node Status in Non-Small-Cell Lung Cancer Patients Before and After Neoadjuvant Chemoimmunotherapy: A Multicenter Retrospective Study.

Background: In patients with non-small-cell lung cancer (NSCLC) treated with neoadjuvant chemoimmunotherapy, lymph node (LN) status is classified as ypN0 and ypN+. However, ypN0 includes patients who either had LN metastasis before neoadjuvant therapy (cN+/ypN0) or those who never developed LN metastasis (cN0/ypN0). The prognostic implications of these different LN statuses are not well understood.

Methods: A retrospective analysis was conducted on patients with NSCLC who underwent surgery after neoadjuvant chemoimmunotherapy at 4 centers in China from 2019 to 2022. Patients were grouped by their LN status into ``natural'' N0 (cN0/ypN0), ``downstaged'' N0 (cN+/ypN0), and ypN+ (cN+/ypN+).

Results: Out of 527 initially enrolled patients, 186 met the inclusion criteria: 34 (18.3%) had ``natural'' N0, 95 (51.1%) had ``downstaged'' N0, and 57 (30.6%) had ypN+. The median follow-up was 24 months (11-64 months). Disease-free survival (DFS) and overall survival (OS) were significantly lower in ypN+ compared to ``natural'' N0 and ``downstaged'' N0 (DFS: P < .001; OS: P < .001). However, no significant difference in either DFS (P = .695) or OS (P = .814) were observed between ``natural'' N0 and ``downstaged'' N0. Subgroup analysis showed that the MPR/ypN0 group had significantly better DFS compared to the non-MPR/ypN0 (P = .008), MPR/ypN+ (P = .028), and non-MPR/ypN+ groups (P < .001). For OS, MPR/ypN0 group was significantly superior to non-MPR/ypN+ (P < .001) and showed a trend toward better OS than non-MPR/ypN0 (P = .067) and MPR/ypN+ (P = .067). Notably, no significant differences were observed in either DFS (P = .908) or OS (P = .943) between non-MPR/ypN0 and MPR/ypN+ groups. The non-MPR/ypN+ group had the poorest survival outcomes in both DFS and OS.

Conclusions: Achieving ypN0 status after neoadjuvant chemoimmunotherapy strongly predicts favorable outcomes in patients with NSCLC, regardless of pretreatment cN status. Combining MPR with LN status effectively differentiates patient prognoses.

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来源期刊
Clinical lung cancer
Clinical lung cancer 医学-肿瘤学
CiteScore
7.00
自引率
2.80%
发文量
159
审稿时长
24 days
期刊介绍: Clinical Lung Cancer is a peer-reviewed bimonthly journal that publishes original articles describing various aspects of clinical and translational research of lung cancer. Clinical Lung Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of lung cancer. The main emphasis is on recent scientific developments in all areas related to lung cancer. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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