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

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机构： [1]Thoraxklinik at University Hospital of Heidelberg, Heidelberg, Germany [2]Translational Lung Research Center (TLRC) Heidelberg, German Center for Lung Research (DZL), Heidelberg, Germany [3]Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China [4]University Hospital Bonn, Bonn, Germany [5]The Netherlands Cancer Institute, Amsterdam, The Netherlands [6]Xuanwu Hospital, Capital Medical University, Beijing, China [7]Hospital Clinic, University of Barcelona, Barcelona, Spain [8]Radboud University Medical Center, Nijmegen, The Netherlands [9]Roche Diagnostics GmbH, Penzberg, Germany [10]Roche Diagnostics International, Rotkreuz, Switzerland [11]University of California, Irvine, Irvine, CA, USA

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关键词： Biomarker progastrin-releasing peptide ProGRP small-cell lung cancer therapy monitoring

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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. © The Author(s) 2020.

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第一作者机构： [1]Thoraxklinik at University Hospital of Heidelberg, Heidelberg, Germany [2]Translational Lung Research Center (TLRC) Heidelberg, German Center for Lung Research (DZL), Heidelberg, Germany

通讯作者：

通讯机构： [*1]Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Dongdan 3rd Alley 9, Beijing 100730, China.

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

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