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本文引用的文献

1
Folylpoly-glutamate synthetase expression is associated with tumor response and outcome from pemetrexed-based chemotherapy in malignant pleural mesothelioma.叶酸多聚谷氨酸合酶表达与培美曲塞为基础的化疗治疗恶性胸膜间皮瘤的肿瘤应答和预后相关。
J Thorac Oncol. 2012 Sep;7(9):1440-8. doi: 10.1097/JTO.0b013e318260deaa.
2
Significance of thymidylate synthase and thyroid transcription factor 1 expression in patients with nonsquamous non-small cell lung cancer treated with pemetrexed-based chemotherapy.胸苷酸合成酶和甲状腺转录因子 1 表达对接受培美曲塞为基础化疗的非鳞状非小细胞肺癌患者的意义。
J Thorac Oncol. 2011 Aug;6(8):1392-9. doi: 10.1097/JTO.0b013e3182208ea8.
3
Thymidylate synthase and dihydrofolate reductase expression in non-small cell lung carcinoma: the association with treatment efficacy of pemetrexed.胸苷酸合成酶和二氢叶酸还原酶在非小细胞肺癌中的表达:与培美曲塞治疗疗效的关系。
Lung Cancer. 2011 Oct;74(1):132-8. doi: 10.1016/j.lungcan.2011.01.024. Epub 2011 Mar 1.
4
Thymidylate synthase and excision repair cross-complementing group-1 as predictors of responsiveness in mesothelioma patients treated with pemetrexed/carboplatin.胸苷酸合成酶和切除修复交叉互补组 1 作为预测培美曲塞/卡铂治疗间皮瘤患者反应的标志物。
Clin Cancer Res. 2011 Apr 15;17(8):2581-90. doi: 10.1158/1078-0432.CCR-10-2873. Epub 2011 Jan 24.
5
Treatment-by-histology interaction analyses in three phase III trials show superiority of pemetrexed in nonsquamous non-small cell lung cancer.三项 III 期临床试验的组织学分层治疗分析显示培美曲塞在非鳞状非小细胞肺癌中的优势。
J Thorac Oncol. 2011 Jan;6(1):64-70. doi: 10.1097/JTO.0b013e3181f7c6d4.
6
Thymidylate synthase but not excision repair cross-complementation group 1 tumor expression predicts outcome in patients with malignant pleural mesothelioma treated with pemetrexed-based chemotherapy.胸苷酸合成酶而非切除修复交叉互补组 1 肿瘤表达可预测培美曲塞为基础化疗治疗的恶性胸膜间皮瘤患者的结局。
J Clin Oncol. 2010 Mar 20;28(9):1534-9. doi: 10.1200/JCO.2009.25.9275. Epub 2010 Feb 22.
7
Maintenance pemetrexed plus best supportive care versus placebo plus best supportive care for non-small-cell lung cancer: a randomised, double-blind, phase 3 study.培美曲塞维持治疗联合最佳支持治疗与安慰剂联合最佳支持治疗用于非小细胞肺癌:一项随机、双盲、3期研究
Lancet. 2009 Oct 24;374(9699):1432-40. doi: 10.1016/S0140-6736(09)61497-5. Epub 2009 Sep 18.
8
The differential efficacy of pemetrexed according to NSCLC histology: a review of two Phase III studies.培美曲塞根据非小细胞肺癌组织学类型的疗效差异:两项III期研究的综述
Oncologist. 2009 Mar;14(3):253-63. doi: 10.1634/theoncologist.2008-0232. Epub 2009 Feb 16.
9
Effects of folate and folylpolyglutamyl synthase modulation on chemosensitivity of breast cancer cells.叶酸及叶酸多聚谷氨酰合成酶调节对乳腺癌细胞化学敏感性的影响
Mol Cancer Ther. 2007 Nov;6(11):2909-20. doi: 10.1158/1535-7163.MCT-07-0449.
10
Derivation and characterization of monoclonal antibodies against human folypolyglutamate synthetase.抗人叶酸多聚谷氨酸合成酶单克隆抗体的制备与鉴定
Hybridoma (Larchmt). 2007 Jun;26(3):155-61. doi: 10.1089/hyb.2007.004.

胸苷酸合成酶和叶酰多聚谷氨酸合成酶不是预测恶性胸膜间皮瘤患者对培美曲塞治疗反应的有临床意义的标志物。

Thymidylate synthase and folyl-polyglutamate synthase are not clinically useful markers of response to pemetrexed in patients with malignant pleural mesothelioma.

机构信息

Pulmonary Associates, Lehigh Valley Health Network, Allentown, PA, USA.

出版信息

J Thorac Oncol. 2013 Apr;8(4):469-77. doi: 10.1097/JTO.0b013e318283da3e.

DOI:10.1097/JTO.0b013e318283da3e
PMID:23486267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3601580/
Abstract

PURPOSE

Thymidylate synthase (TS) is a potential predictor of outcome after pemetrexed (Pem) in patients with malignant pleural mesothelioma (MPM), and assays measuring TS levels are commercially marketed. The goal of this study was to further evaluate the value of TS and to study another potential biomarker of response, the enzyme, folyl-polyglutamate synthase (FPGS), which activates Pem intracellularly.

METHODS

Levels of TS and FPGS were semi-quantitatively determined immunohistochemically using H-scores on tissue samples from 85 MPM patients receiving Pem as primary therapy. H-score was correlated with radiographic disease control rate (DCR), time to progression (TTP) and overall survival (OS). In addition, expression levels of TS and FPGS in MPM cell lines were determined using immunoblotting and correlated with their sensitivity to Pem-induced cell death.

RESULTS

H-scores from patients with disease control versus progressive disease showed extensive overlap. There were no significant correlations of DCR, TTP, or OS to either TS levels (p = 0.73, 0.93, and 0.59, respectively), FPGS levels (p = 0.95, 0.77, and 0.43, respectively) or the ratio of FPGS/TS using the median scores of each test as cutoffs. There was no correlation between TS or FPGS expression and chemosensitivity of mesothelioma cells to Pem in vitro.

CONCLUSIONS

Although previous retrospective data suggest that TS and FPGS expression might be potential markers of Pem efficacy in MPM, our data indicate these markers lack sufficient predictive value in individual patients and should not be used to guide therapeutic decisions in the absence of prospective studies.

摘要

目的

胸苷酸合成酶(TS)是预测培美曲塞(Pem)治疗恶性胸膜间皮瘤(MPM)患者预后的潜在标志物,并且有测量 TS 水平的商业检测方法。本研究的目的是进一步评估 TS 的价值,并研究另一种潜在的反应生物标志物,即酶叶酸多聚谷氨酸合酶(FPGS),它可使培美曲塞在细胞内激活。

方法

使用组织样本的 H 评分,对 85 名接受培美曲塞作为一线治疗的 MPM 患者的 TS 和 FPGS 水平进行半定量免疫组化检测。H 评分与放射学疾病控制率(DCR)、无进展生存期(TTP)和总生存期(OS)相关。此外,还使用免疫印迹法测定了 MPM 细胞系中 TS 和 FPGS 的表达水平,并将其与培美曲塞诱导的细胞死亡敏感性相关联。

结果

疾病控制与疾病进展患者的 H 评分显示出广泛的重叠。DCR、TTP 或 OS 与 TS 水平(p = 0.73、0.93 和 0.59)、FPGS 水平(p = 0.95、0.77 和 0.43)或中位数作为截断值的每个测试的 FPGS/TS 比值均无显著相关性。TS 或 FPGS 表达与间皮瘤细胞对培美曲塞的体外化疗敏感性之间无相关性。

结论

尽管之前的回顾性数据表明 TS 和 FPGS 表达可能是培美曲塞治疗 MPM 疗效的潜在标志物,但我们的数据表明,这些标志物在个体患者中缺乏足够的预测价值,在缺乏前瞻性研究的情况下,不应用于指导治疗决策。