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可切除 N1/N2 NSCLC 的新辅助化疗加免疫治疗。

Neo-adjuvant chemotherapy plus immunotherapy in resectable N1/N2 NSCLC.

机构信息

Department of Thoracic Surgery, the first affiliated hospital, Zhejiang University School, 1367 West Wenyi Rd., Hangzhou, 311121, China.

出版信息

BMC Cancer. 2023 Dec 21;23(1):1260. doi: 10.1186/s12885-023-11745-x.

Abstract

BACKGROUND

Locally advanced non-small cell lung cancer (NSCLC) with N1/N2 lymph node metastasis is challenging with poor survival. Neo-adjuvant chemo-immunotherapy has gained benefits in a proportion of these patients. However no specific biomarker has been proved to predict the effect before therapy. In addition, the relationship of nodal status and survival after neo-adjuvant chemo-immunotherapy is still not well stated.

METHODS

A total of 75 resectable NSCLC patients with N1/N2 stage who received neo-adjuvant chemo-immunotherapy plus surgery were retrospectively studied. The clinical characteristics, surgical information and safety parameters were collected. The correlations of major pathological response (MPR) and pathological complete response (pCR) with clinical data were analyzed. The progression free disease(PFS) and overall survival(OS) were evaluated with pathological response and nodal status.

RESULTS

Of the 75 patients, 69 (92%) patients experienced treatment related adverse effects, while grade 3-4 adverse effects occurred in 8 (10%) patients. All the patients received surgical R0 resection with a MPR rate of 60% and a pCR rate of 36%. 67% of N1 patients and 77% of N2 patients had nodal clearance after neo-adjuvant treatment. A significant difference was observed between pathological response with age, histology and multiple lymph node metastasis. The PFS was better in the MPR cohort. The PFS was 90.1% and 83.6% at the nodal clearance group at the time of 12 and 18 months, compared with 70.1% and 63.7% at the nodal residual group.

CONCLUSIONS

The neo-adjuvant chemo-immunotherapy for locally advanced NSCLC with nodal positive was safe and feasible. The patients with elder age and squamous-cell carcinoma (SCC) were more likely to have better pathological response, while multiple nodal metastasis was a negative predictor. The clearance of lymph node resulted in significantly longer PFS and OS.

摘要

背景

局部晚期非小细胞肺癌(NSCLC)伴 N1/N2 淋巴结转移患者的生存预后较差。新辅助化疗免疫治疗在部分患者中获益。但目前尚无特定的生物标志物能预测治疗前的疗效。此外,新辅助化疗免疫治疗后淋巴结状态与生存的关系尚不清楚。

方法

回顾性分析 75 例接受新辅助化疗免疫治疗加手术的可切除 NSCLC 患者的临床资料。收集患者的临床特征、手术信息和安全性参数。分析主要病理缓解(MPR)和病理完全缓解(pCR)与临床资料的相关性。根据病理反应和淋巴结状态评估无进展疾病(PFS)和总生存(OS)。

结果

75 例患者中,69 例(92%)发生与治疗相关的不良反应,8 例(10%)发生 3-4 级不良反应。所有患者均行 R0 切除手术,MPR 率为 60%,pCR 率为 36%。新辅助治疗后,N1 患者中有 67%,N2 患者中有 77%淋巴结完全清除。病理反应与年龄、组织学和多个淋巴结转移有关,差异有统计学意义。MPR 组的 PFS 更好。在淋巴结清除组,12 个月和 18 个月时的 PFS 分别为 90.1%和 83.6%,而淋巴结残留组的 PFS 分别为 70.1%和 63.7%。

结论

新辅助化疗免疫治疗局部晚期 NSCLC 伴淋巴结阳性是安全可行的。年龄较大和鳞状细胞癌(SCC)的患者更有可能获得更好的病理缓解,而多个淋巴结转移是一个负性预测因素。淋巴结清除可显著延长 PFS 和 OS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a22/10734172/35db8e78073b/12885_2023_11745_Fig1_HTML.jpg

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