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使用正电子发射断层扫描(PET)放射性标记的 3'-脱氧-3'-氟代胸苷监测地塞米松对非小细胞肺癌的作用。

Using Radiolabeled 3'-Deoxy-3'-F-Fluorothymidine with PET to Monitor the Effect of Dexamethasone on Non-Small Cell Lung Cancer.

机构信息

Wayne State University School of Medicine, Detroit, Michigan.

Karmanos Cancer Institute, Detroit, Michigan; and.

出版信息

J Nucl Med. 2018 Oct;59(10):1544-1550. doi: 10.2967/jnumed.117.207258. Epub 2018 Apr 19.

DOI:10.2967/jnumed.117.207258
PMID:29674424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6167537/
Abstract

Non-small cell lung cancer (NSCLC) is a leading cause of cancer mortality in the United States, and pemetrexed-based therapies are regularly used to treat nonsquamous NSCLC. Despite widespread use, pemetrexed has a modest effect on progression-free survival, with varying efficacy between individuals. Recent work has indicated that dexamethasone, given to prevent pemetrexed toxicity, is able to protect a subset of NSCLC cells from pemetrexed cytotoxicity by temporarily suppressing the S phase of the cell cycle. Therefore, dexamethasone might block treatment efficacy in a subpopulation of patients and might be contributing to the variable response to pemetrexed. Differences in retention of the experimental PET tracer 3'-deoxy-3'-fluorothymidine (FLT) were used to monitor S-phase suppression by dexamethasone in NSCLC cell models, animals with tumor xenografts, and patients with advanced cancer. Significant reductions in tracer uptake were observed after 24 h of dexamethasone treatment in NSCLC cell lines and xenograft models expressing high levels of glucocorticoid receptor α, coincident with pemetrexed resistance visualized by attenuation of the flare effect associated with pemetrexed activity. Two of 4 patients imaged in a pilot study with F-FLT PET after dexamethasone treatment demonstrated reductions in tracer uptake from baseline, with a variable response between individual tumor lesions. F-FLT PET represents a useful method for the noninvasive monitoring of dexamethasone-mediated S-phase suppression in NSCLC and might provide a way to individualize chemotherapy in patients receiving pemetrexed-based regimens.

摘要

非小细胞肺癌(NSCLC)是美国癌症死亡的主要原因,培美曲塞为基础的治疗方案常用于治疗非鳞状 NSCLC。尽管广泛应用,但培美曲塞对无进展生存期的影响有限,个体间疗效差异较大。最近的研究表明,地塞米松可预防培美曲塞毒性,通过暂时抑制细胞周期的 S 期,使一部分 NSCLC 细胞免受培美曲塞细胞毒性。因此,地塞米松可能会阻止一部分患者的治疗效果,并可能导致对培美曲塞的反应不一致。差异保留实验性 PET 示踪剂 3'-脱氧-3'-氟胸苷(FLT)用于监测地塞米松对 NSCLC 细胞模型、肿瘤异种移植动物和晚期癌症患者中 S 期抑制的作用。在高表达糖皮质激素受体α的 NSCLC 细胞系和异种移植模型中,地塞米松治疗 24 小时后观察到示踪剂摄取显著减少,与培美曲塞活性相关的闪光效应减弱,提示培美曲塞耐药。在 4 例接受培美曲塞治疗的患者的初步研究中,2 例患者在接受地塞米松治疗后 F-FLT PET 显示示踪剂摄取减少,个体肿瘤病变之间存在可变反应。F-FLT PET 是一种用于监测 NSCLC 中地塞米松介导的 S 期抑制的非侵入性方法,可能为接受培美曲塞为基础的方案的患者提供化疗个体化的方法。

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Early detection of thymidylate synthase resistance in non-small cell lung cancer with FLT-PET imaging.利用FLT-PET成像早期检测非小细胞肺癌中的胸苷酸合成酶耐药性。
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Glucocorticoid receptor status is a principal determinant of variability in the sensitivity of non-small-cell lung cancer cells to pemetrexed.糖皮质激素受体状态是非小细胞肺癌细胞对培美曲塞敏感性差异的主要决定因素。
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PointBreak: a randomized phase III study of pemetrexed plus carboplatin and bevacizumab followed by maintenance pemetrexed and bevacizumab versus paclitaxel plus carboplatin and bevacizumab followed by maintenance bevacizumab in patients with stage IIIB or IV nonsquamous non-small-cell lung cancer.**点破**:培美曲塞联合卡铂和贝伐珠单抗加培美曲塞和贝伐珠单抗维持治疗对比紫杉醇联合卡铂和贝伐珠单抗加贝伐珠单抗维持治疗用于 IIIB 或 IV 期非鳞状非小细胞肺癌患者的随机 III 期研究。
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Expression of thymidylate synthase predicts clinical outcomes of pemetrexed-containing chemotherapy for non-small-cell lung cancer: a systemic review and meta-analysis.胸苷酸合成酶的表达预测含培美曲塞化疗治疗非小细胞肺癌的临床结局:系统评价和荟萃分析。
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