Literature DB >> 30551856

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

Tom van den Ende1, Elizabeth Smyth2, Maarten C C M Hulshof3, Hanneke W M van Laarhoven4.   

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. Crown
Copyright © 2018. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Chemoradiotherapy; Esophageal Neoplasms; Immunotherapy; Neoadjuvant Therapy

Mesh:

Year:  2018        PMID: 30551856     DOI: 10.1016/j.bpg.2018.11.005

Source DB:  PubMed          Journal:  Best Pract Res Clin Gastroenterol        ISSN: 1521-6918            Impact factor:   3.043


  4 in total

1.  Dual Erb B Inhibition in Oesophago-gastric Cancer (DEBIOC): A phase I dose escalating safety study and randomised dose expansion of AZD8931 in combination with oxaliplatin and capecitabine chemotherapy in patients with oesophagogastric adenocarcinoma.

Authors:  Anne Thomas; Pradeep S Virdee; Martin Eatock; Simon R Lord; Stephen Falk; D Alan Anthoney; Richard C Turkington; Matthew Goff; Leena Elhussein; Linda Collins; Sharon Love; Joanna Moschandreas; Mark R Middleton
Journal:  Eur J Cancer       Date:  2019-11-22       Impact factor: 9.162

2.  The Depletion of ABI3BP by MicroRNA-183 Promotes the Development of Esophageal Carcinoma.

Authors:  Hongfei Cai; Yang Li; Da Qin; Rui Wang; Ze Tang; Tianyu Lu; Youbin Cui
Journal:  Mediators Inflamm       Date:  2020-07-26       Impact factor: 4.711

3.  AKR1C2 acts as a targetable oncogene in esophageal squamous cell carcinoma via activating PI3K/AKT signaling pathway.

Authors:  Zhan-Fei Zhang; Tie-Jun Huang; Xin-Ke Zhang; Yu-Jie Xie; Si-Ting Lin; Fei-Fei Luo; Dong-Fang Meng; Hao Hu; Jing Wang; Li-Xia Peng; Chao-Nan Qian; Chao Cheng; Bi-Jun Huang
Journal:  J Cell Mol Med       Date:  2020-07-17       Impact factor: 5.310

Review 4.  The Anti-PD-1/PD-L1 Immunotherapy for Gastric Esophageal Cancer: A Systematic Review and Meta-Analysis and Literature Review.

Authors:  Ke Chen; Xiao Wang; Liu Yang; Zheling Chen
Journal:  Cancer Control       Date:  2021 Jan-Dec       Impact factor: 3.302

  4 in total

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