首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Thymidylate synthase and dihydrofolate reductase expression in non-small cell lung carcinoma: the association with treatment efficacy of pemetrexed.
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Thymidylate synthase and dihydrofolate reductase expression in non-small cell lung carcinoma: the association with treatment efficacy of pemetrexed.

机译:胸苷酸合酶和二氢叶酸还原酶在非小细胞肺癌中的表达:与培美曲塞的疗效相关。

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摘要

Thymidylate synthase (TS) and dihydrofolate reductase (DHFR) are target enzymes of inhibition by pemetrexed, an antifolate for treatment of advanced non-small-cell lung cancer (NSCLC). This study is to evaluate the association of TS and DHFR expressions and the treatment efficacy of pemetrexed in NSCLC patients. From January 2006 to October 2008, patients with advanced NSCLC treated with pemetrexed after prior chemotherapy were included. The TS and DHFR expressions in tumor tissues were examined by immunohistochemistry and evaluated by a semiquantitative histologic score (H-score). The H-score was derived from the degrees of intensity of tumor cells multiplied by the percentage of positive neoplastic cells. The medical records were reviewed and analyzed with respect to patients' characteristics, histology types, treatment responses and survivals. Among 268 NSCLC patients treated with pemetrexed, 49 had tumor specimens available for TS and DHFR evaluation. The TS expression was positively correlated with DHFR expression (r(2)=0.11, p=0.02). Patients with low TS (150) expression (4.8 vs. 3.4 months; p=0.01). Patients with low DHFR expression (120), which was not statistically significant (5.8 vs. 3.6 months; p=0.33). In patients with adenocarcinoma, the low TS patient group also had a longer median PFS and a longer median overall survival (OS) as compared with patients with high TS expression (PFS, 4.8 vs. 3.8 months, p=0.03; OS, 21.4 vs. 10.0 months, p=0.03). Nevertheless, the association of DHFR expression level and median PFS as well as OS were not statistically significant. TS expression, rather than DHFR, may be an important predictive factor for treatment efficacy of pemetrexed in NSCLC patients.
机译:胸苷酸合酶(TS)和二氢叶酸还原酶(DHFR)是被培美曲塞(pemetrexed)抑制的目标酶,培美曲塞是一种抗叶酸药物,用于治疗晚期非小细胞肺癌(NSCLC)。本研究旨在评估TS和DHFR表达的关联以及培美曲塞在NSCLC患者中的治疗效果。从2006年1月至2008年10月,纳入了先前化疗后接受培美曲塞治疗的晚期NSCLC患者。通过免疫组织化学检查肿瘤组织中的TS和DHFR表达,并通过半定量组织学评分(H评分)进行评估。 H分数是由肿瘤细胞的强度程度乘以阳性肿瘤细胞的百分比得出的。回顾并分析了患者的病历,组织学类型,治疗反应和生存情况。在268位接受培美曲塞治疗的NSCLC患者中,有49位具有可用于TS和DHFR评估的肿瘤标本。 TS表达与DHFR表达正相关(r(2)= 0.11,p = 0.02)。 TS( 150)表达高的患者具有更高的中位无进展生存期(PFS)(4.8 vs. 3.4个月; p = 0.01)。 DHFR低表达( 120)的患者更长,这在统计学上无统计学意义(5.8 vs. 3.6个月; p = 0.33)。与高TS表达的患者相比,低腺癌患者组中低TS患者组的中位PFS和中位总生存期(OS)也更长(PFS,4.8 vs. 3.8个月,p = 0.03; OS,21.4 vs. 10.0个月,p = 0.03)。然而,DHFR表达水平与中位PFS以及OS的相关性在统计学上不显着。 TS表达而不是DHFR可能是培美曲塞治疗NSCLC患者疗效的重要预测因素。

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