Esophagogastric Cancer: Integration of Targeted Therapies into Systemic Chemotherapy

2011 ◽  
Vol 11 (6) ◽  
pp. 681-687 ◽  
Author(s):  
M. Moehler ◽  
S. Schwarz ◽  
A. D. Wagner
2017 ◽  
Vol 24 (6) ◽  
pp. R239-R259 ◽  
Author(s):  
Anna Angelousi ◽  
Georgios K Dimitriadis ◽  
Georgios Zografos ◽  
Svenja Nölting ◽  
Gregory Kaltsas ◽  
...  

Tumourigenesis is a relatively common event in endocrine tissues. Currently, specific guidelines have been developed for common malignant endocrine tumours, which also incorporate advances in molecular targeted therapies (MTT), as in thyroid cancer and in gastrointestinal neuroendocrine malignancies. However, there is little information regarding the role and efficacy of MTT in the relatively rare malignant endocrine tumours mainly involving the adrenal medulla, adrenal cortex, pituitary, and parathyroid glands. Due to the rarity of these tumours and the lack of prospective studies, current guidelines are mostly based on retrospective data derived from surgical, locoregional and ablative therapies, and studies with systemic chemotherapy. In addition, in many of these malignancies the prognosis remains poor with individual patients responding differently to currently available treatments, necessitating the development of new personalised therapeutic strategies. Recently, major advances in the molecular understanding of endocrine tumours based on genomic, epigenomic, and transcriptome analysis have emerged, resulting in new insights into their pathogenesis and molecular pathology. This in turn has led to the use of novel MTTs in increasing numbers of patients. In this review, we aim to present currently existing and evolving data using MTT in the treatment of adrenal, pituitary and malignant parathyroid tumours, and explore the current utility and effectiveness of such therapies and their future evolution.


Author(s):  
Christopher Chen ◽  
Maria Di Bartolomeo ◽  
Salvatore Corallo ◽  
John H. Strickler ◽  
Lipika Goyal

Targeted therapies have transformed the treatment paradigm in diseases such as non–small cell lung cancer and melanoma but have shown relatively modest clinical benefit in gastrointestinal malignancies. Anti-EGFR therapy in RAS wild-type colorectal cancer, anti-HER2 therapy in HER2- amplified esophagogastric cancer, and FGFR and isocitrate dehydrogenase 1 (IDH1) inhibitors in FGFR2 fusion-positive and IDH1-mutant biliary tract cancers offer antitumor efficacy, but the clinical benefit and durability of response in each case are typically limited. We review targeted therapies in each of these therapeutic areas and discuss their clinical efficacy, mechanisms of primary and acquired resistance, and strategies to overcome this resistance. We discuss lessons learned that we hope will lead to an expanded role for molecularly targeted therapy options for patients with gastrointestinal cancers.


2017 ◽  
Vol 26 (2) ◽  
pp. 293-312 ◽  
Author(s):  
Steven B. Maron ◽  
Daniel V.T. Catenacci

2019 ◽  
Author(s):  
PI Mester ◽  
E Aschenbrenner ◽  
K Pollinger ◽  
C Kunst ◽  
K Gülow ◽  
...  
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