Nintedanib-docetaxel治疗前非小细胞肺癌癌症患者的预后因素

L. Cabezón-Gutiérrez, S. Custodio-Cabello, V. Pacheco-Barcia, Magda Palka-Kotlowska, Catalina Saez-Bertrand, Marta Blasco-Guerrero
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It is therefore necessary to identify new biomarkers/prognostic factors that select the patients who benefit from this type of treatment.\n\nPatients and Methods: In this single-center retrospective study, we included patients treated NSCLC with nintedanib plus docetaxel in the second/third line and analyzed potential prognostic factors, many of them related to the inflammatory environment; PD-L1 expression levels, Lung Immune Prognostic Index (LIPI), derived neutrophil/lymphocytes ratio (dNLR), etc.\n\nResults: Among 16 patients included in this analysis, the overall response rate was 12.5%, median progression-free survival was 2 months (95% CI, 1.22-2.78) and median overall survival was 6 months (95% CI, 2.11-9.89). LDH level is the only variable related to the disease control rate (70% in normal versus 0% in elevated LDH). 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摘要

背景:在晚期非小细胞肺癌癌症(NSCLC)中,与多西他赛相比,nintedanib联合多西他塞尔的二线治疗提高了生存率,尤其是在开始一线治疗后9个月内进展的腺癌组织学患者。因此,有必要确定新的生物标志物/预后因素,以选择从这种类型的治疗中受益的患者。患者和方法:在这项单中心回顾性研究中,我们纳入了第二/第三线使用宁替达尼联合多西他赛治疗NSCLC的患者,并分析了潜在的预后因素,其中许多因素与炎症环境有关;PD-L1表达水平、肺免疫预后指数(LIPI)、衍生中性粒细胞/淋巴细胞比率(dNLR)等。结果:在纳入本分析的16例患者中,总有效率为12.5%,中位无进展生存期为2个月(95%CI,1.22-2.78),中位总生存期为6个月(95%可信区间,2.11-9.89)。LDH水平是与疾病控制率相关的唯一变量(正常组为70%,LDH升高组为0%)。具有预后意义的变量分析为:;无脑转移(HR 0.33,95%CI 0.14-0.78;p=0.011),少于3个转移部位(HR 0.33,95%CI 014-0.78;p=0.011),一线未使用抗血管生成药物(HR 0.53,95%CI:0.29-0.98;p=0.043),治疗开始时LDH升高的缺失(HR 0.55,95%CI:0.3-1;p=0.051)和肝转移的缺失(HR0.55,95%CI:0.29-1;p=0.05)。结论:在转移部位少于三个的NSCLC患者中,没有脑或肝转移,LDH值正常且先前未在第一线中用抗血管生成药物治疗的患者在用宁替达尼加多西他赛的第二/第三线治疗时显示出更好的预后。
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Prognostic Factors of Nintedanib-docetaxel in Patients with Previously Treated Non-small-cell Lung Cancer
Background: In advanced non-small-cell lung cancer (NSCLC), second-line treatment with nintedanib plus docetaxel improves survival compared with docetaxel, especially in patients with adenocarcinoma histology who progressed within 9 months after the start of firstline treatment. It is therefore necessary to identify new biomarkers/prognostic factors that select the patients who benefit from this type of treatment. Patients and Methods: In this single-center retrospective study, we included patients treated NSCLC with nintedanib plus docetaxel in the second/third line and analyzed potential prognostic factors, many of them related to the inflammatory environment; PD-L1 expression levels, Lung Immune Prognostic Index (LIPI), derived neutrophil/lymphocytes ratio (dNLR), etc. Results: Among 16 patients included in this analysis, the overall response rate was 12.5%, median progression-free survival was 2 months (95% CI, 1.22-2.78) and median overall survival was 6 months (95% CI, 2.11-9.89). LDH level is the only variable related to the disease control rate (70% in normal versus 0% in elevated LDH). The variables analyzed with prognostic significance were; no brain metastases (HR 0.33, 95% CI 0.14-0.78; p=0.011), less than 3 metastatic sites (HR 0.33, 95% CI 0.14-0.78; p=0.011), the non-use of antiangiogenic drugs in the first line (HR 0.53, 95% CI: 0.29-0.98; p=0.043), the absence of elevated LDH at the start of treatment (HR 0.55, 95% CI: 0.3-1; p=0.051) and the absence of liver metastases (HR 0.55, 95% CI: 0.29-1; p=0.05). Conclusions: In NSCLC patients with less than three metastatic sites, no brain or liver metastases, normal LDH values and not previously treated with antiangiogenic drugs in the first line showed a better prognosis when treated with second/third line with nintedanib plus docetaxel.
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