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化疗后晚期非小细胞肺癌患者血清 M30 和 M65 值变化的预后意义。

The prognostic importance of changing serum M30 and M65 values after chemotherapy in patients with advanced-stage non-small-cell lung cancer.

机构信息

Department of Medical Oncology, Dr. Lutfi Kirdar Kartal Education and Research Hospital, Istanbul, Turkey.

出版信息

Med Oncol. 2013 Jun;30(2):551. doi: 10.1007/s12032-013-0551-6. Epub 2013 Mar 28.

Abstract

Although oncological treatments are improving, the prognosis of non-small-cell lung cancer (NSCLC) patients has not. Several biomarkers related to prognosis have been evaluated, and M30 and M65 have been reported to be higher in patients with NSCLC than in healthy people. In the current study, we evaluated the clinical importance of the change in serum M30 and M65 values after chemotherapy in patients with NSCLC. Serum M30 and M65 values were measured before and 48 h after chemotherapy in thirty-two patients with advanced NSCLC. The importance of the change in the levels of these markers after chemotherapy was analyzed by univariate analysis. The median serum M65 and M30 values increased significantly after chemotherapy (p < 0.001). The median M30 value after chemotherapy was an important prognostic factor for both overall survival (OS) (p = 0.002) and progression-free survival (PFS) (p = 0.002). Stage and histopathological type were significant both for PFS and OS. Multivariate analysis showed that the median M30 value after chemotherapy was the only independent prognostic factor for PFS (p = 0.04, HR 5.4) and OS (p = 0.02, HR 11.49). Our results indicated that both serum M30 and M65 values increased after chemotherapy in patients with advanced NSCLC, and an elevated serum M30 value was an independent prognostic factor for both PFS and OS.

摘要

尽管肿瘤治疗在不断进步,但非小细胞肺癌(NSCLC)患者的预后并未得到改善。已经评估了几种与预后相关的生物标志物,据报道,M30 和 M65 在 NSCLC 患者中的水平高于健康人群。在本研究中,我们评估了 NSCLC 患者化疗后血清 M30 和 M65 值变化的临床意义。我们在 32 例晚期 NSCLC 患者化疗前和化疗后 48 小时测量了血清 M30 和 M65 值。通过单因素分析来分析这些标志物水平在化疗后的变化的重要性。化疗后血清 M65 和 M30 值中位数显著升高(p < 0.001)。化疗后 M30 值是总生存期(OS)(p = 0.002)和无进展生存期(PFS)(p = 0.002)的重要预后因素。分期和组织病理学类型对 PFS 和 OS 均有显著影响。多因素分析显示,化疗后 M30 值中位数是 PFS(p = 0.04,HR 5.4)和 OS(p = 0.02,HR 11.49)的唯一独立预后因素。我们的结果表明,晚期 NSCLC 患者化疗后血清 M30 和 M65 值均升高,血清 M30 值升高是 PFS 和 OS 的独立预后因素。

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