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首页> 外文期刊>Journal of chemotherapy >The role of thymidylate synthase in non-small cell lung cancer treated with pemetrexed continuation maintenance therapy
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The role of thymidylate synthase in non-small cell lung cancer treated with pemetrexed continuation maintenance therapy

机译:吡啶基合成酶在培养基继续维持疗法治疗非小细胞肺癌中的作用

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摘要

Pemetrexed continuation maintenance therapy has been proven to be beneficial for patients with advanced non-squamous non-small cell lung cancer (NSCLC). However, the eligibility criteria for maintenance treatment are too simple. This study sought to evaluate thymidylate synthase (TS) as a predicting biomarker for pemetrexed continuation maintenance treatment in NSCLC. Specimens were collected from 87 patients treated with pemetrexed continuation maintenance therapy before and after four-cycle induction chemotherapy. Real-time quantitative PCR was used to detect TS expression in tissues. The TS expression level was correlated with characteristic clinical data, radiographic response, progression-free time (PFS) and overall survival (OS). Low total TS expression(<8.47) was associated with improved PFS (median: 4.7 months vs. 3.5 months, p = 0.034) and improved OS (time from random assignment: 16.4 months vs. 11.7 months, p = 0.026; time from induction: 19.7 months vs. 14.8 months, p = 0.022). Our results indicate that in NSCLC patients treated with pemetrexed continuation maintenance therapy, low TS expression is associated with improved PFS and OS.
机译:已被证明对患有先进的非鳞状非小细胞肺癌(NSCLC)的患者有益的培养基继续维持治疗。但是,维护治疗的资格标准太简单。该研究寻求将胸苷合酶(TS)评估为NSCLC中的磷酸盐延续维持治疗的预测生物标志物。在四循环诱导化疗之前和之后,从87例治疗的87名患者收集标本。实时定量PCR用于检测组织中的TS表达。 TS表达水平与特征临床数据,射线照相响应,无进展时间(PFS)和总存活(OS)相关。低总TS表达(<8.47)与改善的PFS(中位数:4.7个月,3.5个月,P = 0.034)和改进的OS(来自随机分配的时间:16.4个月与11.7个月,P = 0.026;从诱导的时间:19.7个月与14.8个月,P = 0.022)。我们的结果表明,在NSCLC患者中,用培养基继续维持治疗治疗,低TS表达与改善的PFS和OS相关。

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