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可切除食管和胃食管交界处癌症的化疗和新型靶向治疗。

Chemotherapy and novel targeted therapies for operable esophageal and gastroesophageal junctional cancer.

机构信息

Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam University Medical Centers (UMC) Location AMC, University of Amsterdam, Amsterdam, the Netherlands.

Department of Medical Oncology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, Great Britain, UK.

出版信息

Best Pract Res Clin Gastroenterol. 2018 Oct-Dec;36-37:45-52. doi: 10.1016/j.bpg.2018.11.005. Epub 2018 Nov 22.

Abstract

During the past decades, several treatment strategies such as neoadjuvant chemotherapy, neoadjuvant chemoradiotherapy and perioperative chemotherapy have been shown to improve the prognosis of resectable esophageal cancer. Patients with squamous cell tumors respond better to neoadjuvant chemoradiotherapy compared to adenocarcinoma. Therefore, in squamous tumors neoadjuvant chemoradiotherapy is the preferred strategy. Neoadjuvant chemoradiotherapy and perioperative chemotherapy are both effective in patients with adenocarcinoma. Chemoradiotherapy trials have shown higher rates of pCR, pN0 and R0 resection rates compared to neoadjuvant chemotherapy trials. Nonetheless, it is still unclear whether one strategy should be preferred over the other in terms of overall survival for adenocarcinoma. Based on the currently available evidence, the addition of targeted agents, such as VEGF and EGFR inhibitors, to the aforementioned strategies does not lead to survival benefit. Novel targeted treatment strategies that are currently being investigated include inhibition of HER2, PD-1 or the PD-1 ligand. Molecular subgroup analysis can contribute to better understanding of disease pathogenesis and prediction of response to treatment.

摘要

在过去几十年中,新辅助化疗、新辅助放化疗和围手术期化疗等治疗策略已被证明可改善可切除食管癌的预后。与腺癌相比,鳞状细胞肿瘤患者对新辅助放化疗的反应更好。因此,在鳞状肿瘤中,新辅助放化疗是首选策略。新辅助放化疗和围手术期化疗在腺癌患者中均有效。化疗放疗试验显示,与新辅助化疗试验相比,pCR、pN0 和 R0 切除率更高。尽管如此,在腺癌的总生存方面,哪种策略更优仍不清楚。基于目前的证据,将靶向药物(如 VEGF 和 EGFR 抑制剂)添加到上述策略中并不能带来生存获益。目前正在研究的新型靶向治疗策略包括抑制 HER2、PD-1 或 PD-1 配体。分子亚组分析有助于更好地了解疾病发病机制和预测治疗反应。

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