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Am J Transl Res. 2019 Jan 15;11(1):473-485. eCollection 2019.
2
CYR61/CCN1 Regulates dCK and CTGF and Causes Gemcitabine-resistant Phenotype in Pancreatic Ductal Adenocarcinoma.CYR61/CCN1 调节 dCK 和 CTGF 并导致胰腺导管腺癌对吉西他滨产生耐药表型。
Mol Cancer Ther. 2019 Apr;18(4):788-800. doi: 10.1158/1535-7163.MCT-18-0899. Epub 2019 Feb 20.
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Cancer statistics, 2019.癌症统计数据,2019 年。
CA Cancer J Clin. 2019 Jan;69(1):7-34. doi: 10.3322/caac.21551. Epub 2019 Jan 8.
4
Predictive Early Recurrence Factors of Preoperative Clinicophysiological Findings in Pancreatic Cancer.胰腺癌术前临床生理检查结果的早期复发预测因素
Eur Surg Res. 2018;59(5-6):329-338. doi: 10.1159/000494382. Epub 2018 Nov 19.
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Circulating Tumor Cells Dynamics in Pancreatic Adenocarcinoma Correlate With Disease Status: Results of the Prospective CLUSTER Study.循环肿瘤细胞动力学与胰腺腺癌疾病状态相关:前瞻性 CLUSTER 研究结果。
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Ann Surg. 2018 Oct;268(4):610-619. doi: 10.1097/SLA.0000000000002957.
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Phase 1 trial evaluating cisplatin, gemcitabine, and veliparib in 2 patient cohorts: Germline BRCA mutation carriers and wild-type BRCA pancreatic ductal adenocarcinoma.评估顺铂、吉西他滨和维利帕利在 2 个患者队列中的 1 期临床试验:种系 BRCA 突变携带者和野生型 BRCA 胰腺导管腺癌。
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9
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胰腺导管腺癌新辅助治疗反应的生化预测指标

Biochemical Predictors of Response to Neoadjuvant Therapy in Pancreatic Ductal Adenocarcinoma.

作者信息

Awad Seifeldin, Alkashash Ahmad M, Amin Magi, Baker Samantha J, Rose J Bart

机构信息

Department of Surgical Oncology, University of Alabama in Birmingham, Birmingham, AL, United States.

Department of Gastroenterology, Cairo Fatimid Hospital, Cairo, Egypt.

出版信息

Front Oncol. 2020 May 12;10:620. doi: 10.3389/fonc.2020.00620. eCollection 2020.

DOI:10.3389/fonc.2020.00620
PMID:32477933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7235358/
Abstract

Pancreatic ductal adenocarcinoma (PDAC) is becoming increasingly more common. Treatment for PDAC is dependent not only on stage at diagnosis, but complex anatomical relationships. Recently, the therapeutic approach to this disease has shifted from upfront surgery for technically resectable lesions to a neoadjuvant therapy first approach. Selecting an appropriate regimen and determining treatment response is crucial for optimal oncologic outcome, especially since radiographic imaging has proven unreliable in this setting. Tumor biomarkers have the potential to play a key role in treatment planning, treatment monitoring, and surveillance as an adjunct laboratory test. In this review, we will discuss common chemotherapeutic options, mechanisms of resistance, and potential biomarkers for PDAC. The aim of this paper is to present currently available biomarkers for PDAC and to discuss how these markers may be affected by neoadjuvant chemotherapy treatment. Understanding current chemotherapy regiments and mechanism of resistance can help us understand which markers may be most affected and why; therefore, determining to what ability we can use them as a marker for treatment progression, prognosis, or potential relapse.

摘要

胰腺导管腺癌(PDAC)正变得越来越常见。PDAC的治疗不仅取决于诊断时的分期,还取决于复杂的解剖关系。最近,针对这种疾病的治疗方法已从对技术上可切除病变的 upfront 手术转变为首先采用新辅助治疗的方法。选择合适的治疗方案并确定治疗反应对于实现最佳肿瘤学结果至关重要,特别是因为在这种情况下放射影像学已被证明不可靠。肿瘤生物标志物作为辅助实验室检测手段,有可能在治疗规划、治疗监测和随访中发挥关键作用。在本综述中,我们将讨论PDAC的常见化疗选择、耐药机制和潜在生物标志物。本文的目的是介绍目前可用的PDAC生物标志物,并讨论这些标志物如何可能受到新辅助化疗治疗的影响。了解当前的化疗方案和耐药机制可以帮助我们理解哪些标志物可能受到的影响最大以及原因;因此,确定我们能够在何种程度上使用它们作为治疗进展、预后或潜在复发的标志物。