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优化潜在可切除 III 期肺鳞癌的围手术期治疗:替雷利珠单抗联合化疗四周期浓缩方案的有前景结果。

Optimizing perioperative treatment for potentially resectable stage III squamous cell lung carcinoma: promising results of a condensed four-cycle regimen with tislelizumaband chemotherapy.

机构信息

Department of Medical Oncology, The First Affiliated Hospital, Zhejiang University School of Medicine, No. 79 Qingchun Road, Hangzhou, Shangcheng District, China.

Cancer Center, Zhejiang University, Hangzhou, 310058, Zhejiang, China.

出版信息

BMC Med. 2024 Jun 10;22(1):234. doi: 10.1186/s12916-024-03462-4.

Abstract

BACKGROUND

The standard care for resectable non-small cell lung cancer (NSCLC) involves perioperative therapy combining chemotherapy and immune checkpoint inhibitors, typically lasting 6 to 12 months. However, the optimal treatment strategies for potentially resectable squamous cell lung carcinoma (SCC) remain unclear. This Phase 2 trial aimed to assess the efficacy and safety of a condensed four-cycle perioperative treatment regimen with tislelizumab combined with chemotherapy in patients with potentially resectable stage III SCC.

METHODS

Patients with potentially resectable stage IIIA-IIIB (N2) SCC received intravenous tislelizumab, albumin-bound paclitaxel, and carboplatin for up to four cycles. The primary endpoints were major pathologic response (MPR) and incidence of treatment-related adverse events. Safety and potential biomarkers for efficacy prediction were also assessed.

RESULTS

Among 35 enrolled patients, 32 underwent surgery with R0 resection achieved in all cases. MPR was achieved in 24 patients and pathological complete response (pCR) in 14 patients. Radiographic objective response was observed in 31 patients. The 12-month and 24-month event-free survival rate was 85.7 and 61.0%, respectively. Four patients experienced grade 3 or 4 adverse events. Tumor tissue based next-generation sequencing revealed the potential associations between several biomarkers and pathological response, including tumor neoantigen burden score, 18-gene expression profile score, CD8 + T cells, M1/M2 macrophages ratio and interferon-gamma expression level. Besides, circulating tumor DNA (ctDNA) dynamics and concentration were also associated with pathological response and the presence of ctDNA at postoperative month 1 was a strong predictor for disease relapse. Furthermore, metagenomic sequencing in bronchoalveolar lavage fluid demonstrated Streptococcus was the most abundant genus in the pCR group.

CONCLUSIONS

A condensed four-cycle perioperative treatment regimen of tislelizumab combined with chemotherapy demonstrated promising efficacy and manageable toxicities in potentially resectable stage III SCC. Specific biomarkers showed potential for predicting treatment efficacy and the mechanism of superior antitumor response of pCR patients was preliminarily and indirectly explored.

TRIAL REGISTRATION

ClinicalTrials.gov, NCT05024266. Registered August 27, 2021.

摘要

背景

可切除非小细胞肺癌(NSCLC)的标准治疗包括围手术期化疗联合免疫检查点抑制剂治疗,通常持续 6-12 个月。然而,潜在可切除的鳞状细胞肺癌(SCC)的最佳治疗策略仍不清楚。这项 2 期试验旨在评估替雷利珠单抗联合化疗的四周期围手术期浓缩治疗方案在潜在可切除 III 期 SCC 患者中的疗效和安全性。

方法

潜在可切除的 IIIA-IIIB(N2)SCC 患者接受静脉注射替雷利珠单抗、白蛋白结合型紫杉醇和卡铂,最多 4 个周期。主要终点是主要病理缓解(MPR)和治疗相关不良事件的发生率。还评估了安全性和潜在的疗效预测生物标志物。

结果

35 例入组患者中,32 例接受了手术,所有病例均达到了 R0 切除。24 例患者达到 MPR,14 例患者达到病理完全缓解(pCR)。31 例患者观察到影像学客观缓解。12 个月和 24 个月无事件生存率分别为 85.7%和 61.0%。4 例患者发生 3 级或 4 级不良事件。肿瘤组织下一代测序揭示了几种生物标志物与病理反应之间的潜在关联,包括肿瘤新生抗原负荷评分、18 基因表达谱评分、CD8+T 细胞、M1/M2 巨噬细胞比值和干扰素-γ表达水平。此外,循环肿瘤 DNA(ctDNA)动态和浓度与病理反应相关,术后 1 个月存在 ctDNA 是疾病复发的强烈预测因子。此外,支气管肺泡灌洗液的宏基因组测序显示,肺炎链球菌是 pCR 组中最丰富的属。

结论

替雷利珠单抗联合化疗的四周期围手术期浓缩治疗方案在潜在可切除的 III 期 SCC 中显示出有希望的疗效和可管理的毒性。特定的生物标志物显示出预测治疗效果的潜力,并初步和间接探索了 pCR 患者抗肿瘤反应优势的机制。

试验注册

ClinicalTrials.gov,NCT05024266。2021 年 8 月 27 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeb8/11163755/eb9ce22b829f/12916_2024_3462_Fig1_HTML.jpg

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