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一种以胃泌素释放肽作为简单血液检测指标来优化小细胞肺癌临床管理的连续反应者算法。

A continuous responder algorithm to optimize clinical management of small-cell lung cancer with progastrin-releasing peptide as a simple blood test.

作者信息

Muley Thomas, Zhang Xiaotong, Holdenrieder Stefan, Korse Catharina M, Zhi Xiu-Yi, Molina Rafael, Liu Zhongjuan, Hartmann Gunther, van den Heuvel Michel M, Qian Kun, Marrades Ramon, Engel Christine, He Ying, Wehnl Birgit, Dayyani Farshid, Herth Felix

机构信息

Thoraxklinik at University Hospital of Heidelberg, Heidelberg, Germany.

Translational Lung Research Center (TLRC) Heidelberg, German Center for Lung Research (DZL), Heidelberg, Germany.

出版信息

Tumour Biol. 2020 Sep;42(9):1010428320958603. doi: 10.1177/1010428320958603.

Abstract

This study aimed to investigate whether changes in progastrin-releasing peptide (ProGRP) levels correlate with treatment response and can be used to optimize clinical management of patients with small-cell lung cancer. Patients with small-cell lung cancer (any stage) receiving chemotherapy were eligible. ProGRP was measured in serum/plasma at baseline and after each chemotherapy cycle using the Elecsys ProGRP assay (Roche Diagnostics). Treatment response was assessed by computed tomography scan. The primary objective was to examine whether changes in ProGRP levels correlated with computed tomography scan results after two cycles of chemotherapy. The prognostic value of ProGRP among patients receiving first-line chemotherapy was also assessed. Overall, 261 patients from six centers were eligible. Among patients with elevated baseline ProGRP (>100 pg/mL), a ProGRP decline after Cycle 2 was associated with nonprogression (area under the curve: 84%; 95% confidence interval: 72.8-95.1; n = 141). ProGRP changes from baseline to end of Cycle 1 were predictive of response, as determined by computed tomography scan 3 weeks later (area under the curve: 87%; 95% confidence interval: 74.1-99.2; n = 137). This was enhanced by repeat measurements, with a 92% area under the curve (95% confidence interval: 85.3-97.8) among patients with ProGRP data after both Cycles 1 and 2 (n = 123); if a patient experienced a ≥25% decline in ProGRP after Cycle 1, and ProGRP remained stable or decreased after Cycle 2, the probability of finding progression on the interim computed tomography scan at the end of Cycle 2 was almost zero (sensitivity: 100%, specificity: 71%). Both ProGRP levels at baseline and at the end of first-line chemotherapy were prognostic; the latter provided a moderately improved hazard ratio of 2.43 (95% confidence interval: 1.33-4.46; n = 110) versus 1.87 (95% confidence interval: 1.04-3.37; n = 216). In summary, for patients with small-cell lung cancer and elevated baseline ProGRP levels, ProGRP may be a simple, reliable, and repeatable tool for monitoring response to chemotherapy and provide valuable prognostic information.

摘要

本研究旨在调查胃泌素释放肽原(ProGRP)水平的变化是否与治疗反应相关,以及是否可用于优化小细胞肺癌患者的临床管理。纳入接受化疗的各期小细胞肺癌患者。使用罗氏诊断公司的电化学发光免疫分析法(Elecsys ProGRP检测)在基线及每个化疗周期后检测血清/血浆中的ProGRP。通过计算机断层扫描评估治疗反应。主要目的是检查两个化疗周期后ProGRP水平的变化是否与计算机断层扫描结果相关。还评估了ProGRP在接受一线化疗患者中的预后价值。总体而言,来自六个中心的261例患者符合条件。在基线ProGRP升高(>100 pg/mL)的患者中,第2周期后ProGRP下降与疾病无进展相关(曲线下面积:84%;95%置信区间:72.8-95.1;n = 141)。从基线到第1周期末的ProGRP变化可预测反应,这由3周后的计算机断层扫描确定(曲线下面积:87%;95%置信区间:74.1-99.2;n = 137)。重复测量可增强这一预测效果,在第1周期和第2周期后均有ProGRP数据的患者中,曲线下面积为92%(95%置信区间:85.3-97.8)(n = 123);如果患者在第1周期后ProGRP下降≥25%,且在第2周期后ProGRP保持稳定或下降,则在第2周期末的中期计算机断层扫描中发现疾病进展的概率几乎为零(敏感性:100%,特异性:71%)。基线和一线化疗结束时的ProGRP水平均具有预后意义;后者的风险比适度提高,为2.43(95%置信区间:1.33-4.46;n = 110),而前者为1.87(95%置信区间:1.04-3.37;n = 216)。总之,对于基线ProGRP水平升高的小细胞肺癌患者,ProGRP可能是一种简单、可靠且可重复的工具,用于监测化疗反应并提供有价值的预后信息。

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