Literature DB >> 30791774

Oxaliplatin in perioperative chemotherapy for gastric and gastroesophageal junction (GEJ) adenocarcinoma.

Ralph Fritsch1,2,3, Jens Hoeppner2,4,5.   

Abstract

INTRODUCTION: Platinum-based chemotherapy remains standard-of-care for gastric and gastroesophageal junction (GEJ) adenocarcinoma. For locally advanced resectable disease, perioperative treatment with cisplatin-based doublet or triplet chemotherapy regimens had been the predominant approach in Europe and the US, based on pivotal phase III trials including the MAGIC study. Results from more recent landmark studies including the German FLOT4 and the Asian CLASSIC trials have, however, triggered a shift from cisplatin towards oxaliplatin-based chemotherapy protocols in the perioperative setting. Areas covered: This drug profile summarizes current state-of-the-art of perioperative and adjuvant treatment for locally advanced resectable gastric/GEJ cancers with a special focus on the increasingly predominant role of oxaliplatin over cisplatin in this setting. We review pharmacology, clinical efficacy, and safety profile of oxaliplatin and oxaliplatin combination regimens. We highlight recent advances and ongoing developments in the field. Expert opinion: While the adoption of oxaliplatin-containing combination regimens for perioperative therapy of gastric/GEJ cancers represents a significant step ahead, many pivotal questions remain unanswered. At the sample time, the evolution of molecular subtyping and immunotherapy is likely to dramatically change clinical practice in the foreseeable future.

Entities:  

Keywords:  Perioperative chemotherapy; efficacy; esophageal cancer; gastric cancer; gastroesophageal junction adenocarcinoma; oxaliplatin; safety

Mesh:

Substances:

Year:  2019        PMID: 30791774     DOI: 10.1080/17474124.2019.1573143

Source DB:  PubMed          Journal:  Expert Rev Gastroenterol Hepatol        ISSN: 1747-4124            Impact factor:   3.869


  3 in total

1.  Oxidative stress activates NORAD expression by H3K27ac and promotes oxaliplatin resistance in gastric cancer by enhancing autophagy flux via targeting the miR-433-3p.

Authors:  Jizhao Wang; Yuchen Sun; Xing Zhang; Hui Cai; Cheng Zhang; Hangying Qu; Lin Liu; Mingxin Zhang; Junke Fu; Jia Zhang; Jiansheng Wang; Guangjian Zhang
Journal:  Cell Death Dis       Date:  2021-01-18       Impact factor: 8.469

2.  Upregulation of CRABP2 by TET1-mediated DNA hydroxymethylation attenuates mitochondrial apoptosis and promotes oxaliplatin resistance in gastric cancer.

Authors:  Xiaolong Tang; Yahang Liang; Guorui Sun; Qingsi He; Zhenyu Hou; Xingzhi Jiang; Peng Gao; Hui Qu
Journal:  Cell Death Dis       Date:  2022-10-04       Impact factor: 9.685

3.  A Recombinant Human Adenovirus Type 5 (H101) Combined With Chemotherapy for Advanced Gastric Carcinoma: A Retrospective Cohort Study.

Authors:  Ran Zhang; Yanxin Cui; Xin Guan; Xiangjun Jiang
Journal:  Front Oncol       Date:  2021-12-09       Impact factor: 6.244

  3 in total

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