Real-World Experience With Multimodal Treatment of Resectable Stage II-III Non-Small Cell Lung Cancer: A Single Institutional Analysis.

IF 4.9 2区 医学 Q1 ONCOLOGY
Raffaella Griffo, Benedikt Niedermaier, Laura V Klotz, Marc Schneider, Michael Allgäuer, Marc Kriegsmann, Romina M Roesch, Lena Brendel, Henrike Deissner, Farastuk Bozorgmehr, Petros Christopoulos, Michael Thomas, Hauke Winter, Martin E Eichhorn, Florian Eichhorn
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引用次数: 0

Abstract

Neoadjuvant therapy has recently become an integral component of multimodal treatment for resectable lung cancer. However, real-world data on perioperative morbidity and treatment adherence remain limited. This study aimed to assess the feasibility and safety of different neoadjuvant treatment approaches applied within daily clinical routine. We retrospectively analyzed patients with resectable stage II-III non-small cell lung cancer undergoing either neoadjuvant chemoimmunotherapy or chemotherapy/chemoradiotherapy followed by curative surgical resection. Treatment groups were compared with respect to perioperative outcomes, radiologic and pathologic downstaging, and pathologic response. A total of 143 patients met the inclusion criteria, of whom 46 (32.2%) received chemoimmunotherapy and 97 (67.8%) were treated with chemotherapy prior to surgery. Adverse events leading to treatment discontinuation occurred in only two patients in the chemoimmunotherapy group and four patients in the chemotherapy group. Chemoimmunotherapy was associated with significantly higher rates of pathologic complete response (37.0% vs. 4.1%) and more pronounced nodal downstaging, with a higher proportion of patients achieving ypN0 status (76.1% vs. 34.0%). High tumoral PD-L1 expression (≥ 50%) and squamous cell carcinoma histology were independently associated with pathologic complete response. Real-world treatment with neoadjuvant chemoimmunotherapy was feasible and resulted in improved response rates compared with chemotherapy, without increasing perioperative morbidity. Histology and high PD-L1 expression may serve as predictors for complete pathologic response, although the predictive value of PD-L1 requires confirmation in larger cohorts with more complete biomarker data.

多模式治疗可切除II-III期非小细胞肺癌的现实经验:单一机构分析。
新辅助治疗最近已成为可切除肺癌的多模式治疗的一个组成部分。然而,关于围手术期发病率和治疗依从性的真实数据仍然有限。本研究旨在评估不同新辅助治疗方法在日常临床应用的可行性和安全性。我们回顾性分析了可切除的II-III期非小细胞肺癌患者,他们要么接受新辅助化疗免疫治疗,要么接受化疗/放化疗,然后进行根治性手术切除。比较各治疗组围手术期预后、放射学和病理降分期以及病理反应。143例患者符合纳入标准,其中46例(32.2%)接受了化疗免疫治疗,97例(67.8%)术前接受了化疗。导致治疗中断的不良事件仅发生在化疗免疫治疗组的2例患者和化疗组的4例患者中。化疗免疫治疗与更高的病理完全缓解率(37.0%对4.1%)和更明显的淋巴结降分期相关,达到ypN0状态的患者比例更高(76.1%对34.0%)。肿瘤PD-L1高表达(≥50%)和鳞状细胞癌组织学与病理完全缓解独立相关。在现实世界中,新辅助化疗免疫治疗是可行的,与化疗相比,可以提高反应率,而不会增加围手术期的发病率。组织学和高PD-L1表达可以作为完全病理反应的预测因素,尽管PD-L1的预测价值需要在更大的队列中得到更完整的生物标志物数据的证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
13.40
自引率
3.10%
发文量
460
审稿时长
2 months
期刊介绍: The International Journal of Cancer (IJC) is the official journal of the Union for International Cancer Control—UICC; it appears twice a month. IJC invites submission of manuscripts under a broad scope of topics relevant to experimental and clinical cancer research and publishes original Research Articles and Short Reports under the following categories: -Cancer Epidemiology- Cancer Genetics and Epigenetics- Infectious Causes of Cancer- Innovative Tools and Methods- Molecular Cancer Biology- Tumor Immunology and Microenvironment- Tumor Markers and Signatures- Cancer Therapy and Prevention
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