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非小细胞肺癌患者接受新辅助化疗的主要病理反应评估协议。

Agreement on Major Pathological Response in NSCLC Patients Receiving Neoadjuvant Chemotherapy.

机构信息

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX.

出版信息

Clin Lung Cancer. 2020 Jul;21(4):341-348. doi: 10.1016/j.cllc.2019.11.003. Epub 2020 Mar 4.

Abstract

INTRODUCTION

We have suggested that major pathologic response (MPR) could serve as a surrogate endpoint for survival and provide rapid means of comparing different neoadjuvant treatment regimens. Here, we confirm that MPR is predictive of long-term overall survival (OS) in patients with non-small-cell lung cancer (NSCLC) who underwent neoadjuvant chemotherapy and surgical resection, to assess agreement on MPR between 2 observers, and to determine the minimum number of slides needed to obtain an accurate determination of MPR.

PATIENTS AND METHODS

We identified 151 patients with NSCLC who had been treated with neoadjuvant chemotherapy followed by complete surgical resection from 2008 to 2012. Tissue specimens were retrospectively evaluated by 2 pathologists who had been blinded to patients' treatment and outcome. We assessed the relationships between MPR and OS, the levels of agreement between the pathologists, and determined the number of slides needed to obtain an accurate determination of MPR.

RESULTS

Our results reveal that MPR examined by either observer 1 (experienced) or by observer 2 (trained) was significantly predictive of long-term OS after neoadjuvant chemotherapy. MPR was associated with long-term OS in patients with NSCLC undergoing neoadjuvant chemotherapy on multivariable analysis (hazard ratio 2.68; P = .01). The levels of agreement between 2 pathologists were high after direct in-person training by one pathologist or the other (R = 0.994). Our data suggest that at least 3 slides should be read to accurately determine MPR.

CONCLUSIONS

MPR is significantly predictive of long-term OS in neoadjuvant chemotherapy-treated patients with NSCLC. MPR may serve as a surrogate endpoint for evaluating novel chemotherapies and immunotherapy response in biomarker-driven translational clinical trials.

摘要

简介

我们曾提出,主要病理反应(MPR)可以作为生存的替代终点,并提供比较不同新辅助治疗方案的快速方法。在这里,我们证实 MPR 可预测接受新辅助化疗和手术切除的非小细胞肺癌(NSCLC)患者的长期总生存期(OS),评估 2 位观察者对 MPR 的一致性,并确定获得 MPR 准确判断所需的最少切片数。

患者和方法

我们从 2008 年至 2012 年确定了 151 名接受新辅助化疗后完全手术切除的 NSCLC 患者。组织标本由 2 位对患者治疗和结果均不知情的病理学家进行回顾性评估。我们评估了 MPR 与 OS 之间的关系、病理学家之间的一致性水平,并确定了获得 MPR 准确判断所需的切片数。

结果

我们的结果表明,由观察者 1(经验丰富)或观察者 2(受过培训)检查的 MPR 均显著预测新辅助化疗后 NSCLC 患者的长期 OS。多变量分析显示,MPR 与新辅助化疗 NSCLC 患者的长期 OS 相关(风险比 2.68;P =.01)。在经过一位病理学家直接面对面培训或另一位病理学家培训后,2 位病理学家之间的一致性水平很高(R = 0.994)。我们的数据表明,至少应读取 3 个切片才能准确判断 MPR。

结论

MPR 可显著预测新辅助化疗治疗的 NSCLC 患者的长期 OS。MPR 可能作为评估新型化疗药物和免疫疗法在生物标志物驱动的转化临床试验中反应的替代终点。

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