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可切除非小细胞肺癌患者中,帕博利珠单抗联合化疗与替雷利珠单抗联合化疗的真实世界比较:治疗结局的回顾性队列研究

Real-world comparison of neoadjuvant pembrolizumab plus chemotherapy versus tislelizumab plus chemotherapy in patients with resectable non-small cell lung cancer: a retrospective cohort study of treatment outcomes.

作者信息

Hu Yan, Ren Siying, Feng Juan, Zeng Chao, Yang Lulu, Liu Jinyou, Wu Fang, Liu Wenliang

机构信息

Department of Thoracic Surgery, the Second Xiangya Hospital of Central South University, Changsha, China.

Department of Respiratory and Critical Care Medicine, the Second Xiangya Hospital of Central South University, Changsha, China.

出版信息

Transl Lung Cancer Res. 2025 Feb 28;14(2):467-479. doi: 10.21037/tlcr-24-721. Epub 2025 Feb 14.

DOI:10.21037/tlcr-24-721
PMID:40114940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11921188/
Abstract

BACKGROUND

Pembrolizumab and tislelizumab have shown substantial clinical benefits in perioperative treatment of resectable non-small cell lung cancer (NSCLC), yet no direct head-to-head trial has established which is optimal. This study, for the first time, aimed to directly compare the efficacy and safety of neoadjuvant pembrolizumab plus chemotherapy versus tislelizumab plus chemotherapy in resectable NSCLC using real-world data.

METHODS

Data of patients with resectable NSCLC treated with neoadjuvant pembrolizumab plus chemotherapy or tislelizumab plus chemotherapy followed by radical resection between December 2017 and August 2023 at the Second Xiangya Hospital of Central South University were retrospectively analyzed. Patients aged 18 years and above, diagnosed with biopsy-proven and treatment-naïve clinical stage II-IIIb NSCLC were included in the study. Patients with autoimmune disease, pulmonary interstitial disease, acute infection, or systemic immunosuppression were excluded. Data that may affect treatment efficacy were collected, including age, sex, body mass index (BMI), smoking history, comorbidities, pulmonary function, pathological type, clinical stage, programmed cell death-ligand 1 (PD-L1) tumor proportion score (TPS), dosage of neoadjuvant therapy, duration from final therapy to surgery and chemotherapy regimens, and compared between the two groups. The follow-up was performed through outpatient visits or telephone calls. The last follow-up was set in June 2024.

RESULTS

A total of 126 patients were included and divided into the pembrolizumab (n=62) and tislelizumab (n=64) groups with a median follow-up time of 26.3 months. The mean age at diagnosis was 59.76 years (standard deviation, 7.05 years) and 103 patients (81.75%) were current or former smoker. Squamous cell carcinoma (SCC) (102, 80.95%) was the most common histological type, followed by adenocarcinoma (18, 14.29%), large cell neuroendocrine carcinoma (2, 1.59%) and sarcomatoid carcinoma (2, 1.59%). Although there was a lower proportion of SCC (72.58% 89.06%, P=0.02) and a lower use of paclitaxel (75.81% 96.88%, P=0.004) in the pembrolizumab group in the overall cohort, the baseline characteristics between two groups were balanced in the SCC cohort. No significant differences in objective response rate, percentage of primary tumors with no viable tumor cells, pathologic and lymph node downstaging, pathological complete response and major pathological response existed between the two groups in both cohorts. Additionally, disease-free survival and overall survival were similar between the two groups in both cohorts. No significant differences in the postoperative complications and grade 3/4 toxicity profiles existed in both cohorts.

CONCLUSIONS

This real-world evidence study supports the non-inferiority of neoadjuvant pembrolizumab plus chemotherapy versus tislelizumab plus chemotherapy in terms of efficacy and safety in patients with resectable NSCLC. We believe that our findings could be an important reference for future studies comparing pembrolizumab- and tislelizumab-based treatment combinations in the neoadjuvant setting.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/079c/11921188/63b79bf017c4/tlcr-14-02-467-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/079c/11921188/160053c72843/tlcr-14-02-467-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/079c/11921188/63b79bf017c4/tlcr-14-02-467-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/079c/11921188/160053c72843/tlcr-14-02-467-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/079c/11921188/63b79bf017c4/tlcr-14-02-467-f2.jpg
摘要

背景

帕博利珠单抗和替雷利珠单抗在可切除非小细胞肺癌(NSCLC)的围手术期治疗中已显示出显著的临床益处,但尚无直接的头对头试验确定哪种药物最佳。本研究首次旨在利用真实世界数据,直接比较新辅助帕博利珠单抗联合化疗与替雷利珠单抗联合化疗在可切除NSCLC中的疗效和安全性。

方法

回顾性分析2017年12月至2023年8月在中南大学湘雅二医院接受新辅助帕博利珠单抗联合化疗或替雷利珠单抗联合化疗后行根治性手术的可切除NSCLC患者的数据。纳入年龄18岁及以上、经活检证实且未经治疗的临床II-IIIb期NSCLC患者。排除患有自身免疫性疾病、肺间质疾病、急性感染或全身免疫抑制的患者。收集可能影响治疗疗效的数据,包括年龄、性别、体重指数(BMI)、吸烟史、合并症、肺功能、病理类型、临床分期、程序性细胞死亡配体1(PD-L1)肿瘤比例评分(TPS)、新辅助治疗剂量、从最后一次治疗到手术的时间以及化疗方案,并在两组之间进行比较。通过门诊就诊或电话进行随访。最后一次随访设定为2024年6月。

结果

共纳入126例患者,分为帕博利珠单抗组(n = 62)和替雷利珠单抗组(n = 64),中位随访时间为26.3个月。诊断时的平均年龄为59.76岁(标准差,7.05岁),103例患者(81.75%)为当前或既往吸烟者。鳞状细胞癌(SCC)(102例,80.95%)是最常见的组织学类型,其次是腺癌(18例,14.29%)、大细胞神经内分泌癌(2例,1.59%)和肉瘤样癌(2例,1.59%)。尽管在整个队列中,帕博利珠单抗组的SCC比例较低(72.58%对89.06%,P = 0.02)且紫杉醇的使用较少(75.81%对96.88%,P = 0.004),但在SCC队列中两组的基线特征是平衡的。在两个队列中,两组之间的客观缓解率、无存活肿瘤细胞的原发性肿瘤百分比、病理和淋巴结降期、病理完全缓解和主要病理缓解均无显著差异。此外,两个队列中两组之间的无病生存期和总生存期相似。两个队列中术后并发症和3/4级毒性反应情况均无显著差异。

结论

这项真实世界证据研究支持新辅助帕博利珠单抗联合化疗与替雷利珠单抗联合化疗在可切除NSCLC患者的疗效和安全性方面非劣效。我们认为,我们的研究结果可能为未来在新辅助治疗中比较基于帕博利珠单抗和替雷利珠单抗的治疗组合的研究提供重要参考。

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Lancet Respir Med. 2025 Feb;13(2):119-129. doi: 10.1016/S2213-2600(24)00269-8. Epub 2024 Nov 21.
2
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