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新辅助化疗免疫治疗后袖状切除术治疗局部晚期非小细胞肺癌

Sleeve resection after neoadjuvant chemoimmunotherapy in the treatment of locally advanced non-small cell lung cancer.

作者信息

Dai Jie, Zhu Xinsheng, Li Dianke, Huang Yan, Liu Xiaogang, He Wenxin, Duan Liang, Zhao Deping, Zhu Yuming, Chen Chang, Provencio Mariano, Ramirez Robert A, Antonoff Mara B, Wu Chunyan, Jiang Gening

机构信息

Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.

Department of Pathology, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.

出版信息

Transl Lung Cancer Res. 2022 Feb;11(2):188-200. doi: 10.21037/tlcr-22-56.

Abstract

BACKGROUND

We aimed to characterize the outcomes of sleeve resection after neoadjuvant chemoimmunotherapy for the treatment of non-small cell lung cancer (NSCLC), including perioperative and oncologic outcomes, and to identify any impact of operative approach on resultant findings.

METHODS

We identified patients with NSCLC who underwent sleeve resection after ≥2 cycles of neoadjuvant chemoimmunotherapy between May 2019 and April 2021 and retrospectively reviewed clinical records. Perioperative data were collected and compared between video-assisted thoracoscopic surgery (VATS) (n=8) and thoracotomy (n=15) groups. Immunohistochemistry (IHC) scores were compared between tumors with and without major pathological response (MPR).

RESULTS

Twenty-three patients met inclusion criteria, with clinical stages as follows: IB, 2 (8.7%); IIIA, 14 (60.9%); and IIIB, 7 (30.4%). Treatment-related adverse events (TRAE) were recorded in 17 patients (73.9%), including anemia and neutropenia, with no patients exhibiting serious TRAE. Radiological evaluation revealed 5 (21.7%) patients with complete response (CR), 14 (60.9%) with partial response (PR), and 4 (17.4%) with stable disease (SD). Complete resection was accomplished for all patients. One VATS procedure was converted to thoracotomy due to extensive pleural adhesions. There were no significant differences in intraoperative blood loss (87.5±51.8 193.9±145.3 mL), operative time (198.8±79.7 225.5±55.0 min), number of lymph node examined (16.9±6.6 18.2±6.5), and hospital stay (5.5±2.8 9.2±11.2 days) between the VATS and thoracotomy groups (all P>0.05). Postoperative complications occurred in 3 patients, and 1 patient died of bronchopleural fistula (BPF) in the thoracotomy group. Complete pathological response (CPR) and MPR were achieved in seven (30.4%) and 13 (56.5%) patients, respectively. Both preoperative histopathology (P=0.024) and radiological response (P=0.002) were significantly associated with MPR. In postoperative specimens with MPR, the IHC scores of cluster of differentiation (CD)4, CD8, and CD20 were modestly higher, while programmed cell death receptor 1 (PD-1), lymphocyte-activation gene 3 (LAG3) and T cell immunoglobulin and ITIM domain (TIGIT) were lower compared with non-MPR specimens, albeit insignificantly.

CONCLUSIONS

Sleeve resection after neoadjuvant chemoimmunotherapy was feasible in patients with locally advanced NSCLC. Perioperative outcomes were comparable between the VATS and thoracotomy groups.

摘要

背景

我们旨在描述新辅助化疗免疫治疗后袖状切除术治疗非小细胞肺癌(NSCLC)的结果,包括围手术期和肿瘤学结果,并确定手术方式对结果的影响。

方法

我们纳入了2019年5月至2021年4月期间接受≥2周期新辅助化疗免疫治疗后行袖状切除术的NSCLC患者,并回顾性分析临床记录。收集围手术期数据,并在电视辅助胸腔镜手术(VATS)组(n = 8)和开胸手术组(n = 15)之间进行比较。比较有和无主要病理反应(MPR)的肿瘤之间的免疫组织化学(IHC)评分。

结果

23例患者符合纳入标准,临床分期如下:IB期,2例(8.7%);IIIA期,14例(60.9%);IIIB期,7例(30.4%)。17例患者(73.9%)记录了治疗相关不良事件(TRAE),包括贫血和中性粒细胞减少,无患者出现严重TRAE。影像学评估显示5例(21.7%)患者完全缓解(CR),14例(60.9%)部分缓解(PR),4例(17.4%)疾病稳定(SD)。所有患者均完成了完全切除。1例VATS手术因广泛胸膜粘连转为开胸手术。VATS组和开胸手术组在术中失血(87.5±51.8对193.9±145.3 mL)、手术时间(198.8±79.7对225.5±55.0 min)、检查淋巴结数量(16.9±6.6对18.2±6.5)和住院时间(5.5±2.8对9.2±11.2天)方面均无显著差异(均P>0.05)。3例患者发生术后并发症,开胸手术组1例患者死于支气管胸膜瘘(BPF)。7例(30.4%)和13例(56.5%)患者分别实现了完全病理缓解(CPR)和MPR。术前组织病理学(P = 0.024)和影像学反应(P = 0.002)均与MPR显著相关。在有MPR的术后标本中,分化簇(CD)4、CD8和CD20的IHC评分略高,而程序性细胞死亡受体1(PD - 1)、淋巴细胞激活基因3(LAG3)和T细胞免疫球蛋白和ITIM结构域(TIGIT)与无MPR标本相比略低,尽管差异不显著。

结论

新辅助化疗免疫治疗后袖状切除术在局部晚期NSCLC患者中是可行的。VATS组和开胸手术组的围手术期结果相当。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c4e/8902091/7d11106c602a/tlcr-11-02-188-f1.jpg

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