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  3. Heat shock protein 90 (HSP90) inhibitors in gastrointestinal cancer: where do we currently stand?-A systematic review.
 

Heat shock protein 90 (HSP90) inhibitors in gastrointestinal cancer: where do we currently stand?-A systematic review.

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BORIS DOI
10.48350/180693
Date of Publication
August 2023
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Universitätsklinik fü...

Universitätsklinik fü...

Contributor
Magyar, Christian Tibor Josef
Universitätsklinik für Viszerale Chirurgie und Medizin
Vashist, Yogesh K
Keogh-Stroka, Deborah M.orcid-logo
Universitätsklinik für Viszerale Chirurgie und Medizin - Viszeral- und Transplantationschirurgie
Kim-Fuchs, Corina
Universitätsklinik für Viszerale Chirurgie und Medizin - Viszeral- und Transplantationschirurgie
Berger, Martin Dave
Universitätsklinik für Medizinische Onkologie
Banz Wüthrich, Vanessa
Universitätsklinik für Viszerale Chirurgie und Medizin - Viszeral- und Transplantationschirurgie
Subject(s)

600 - Technology::610...

Series
Journal of cancer research and clinical oncology
ISSN or ISBN (if monograph)
1432-1335
Publisher
Springer
Language
English
Publisher DOI
10.1007/s00432-023-04689-z
PubMed ID
36966394
Uncontrolled Keywords

Cancer HSP inhibitors...

Description
PURPOSE

Dysregulated expression of heat shock proteins (HSP) plays a fundamental role in tumor development and progression. Consequently, HSP90 may be an effective tumor target in oncology, including the treatment of gastrointestinal cancers.

METHODS

We carried out a systematic review of data extracted from clinicaltrials.gov and pubmed.gov, which included all studies available until January 1st, 2022. The published data was evaluated using primary and secondary endpoints, particularly with focus on overall survival, progression-free survival, and rate of stable disease.

RESULTS

Twenty trials used HSP90 inhibitors in GI cancers, ranging from phase I to III clinical trials. Most studies assessed HSP90 inhibitors as a second line treatment. Seventeen of the 20 studies were performed prior to 2015 and only few studies have results pending. Several studies were terminated prematurely, due to insufficient efficacy or toxicity. Thus far, the data suggests that HSP90 inhibitor NVP-AUY922 might improve outcome for colorectal cancer and gastrointestinal stromal tumors.

CONCLUSION

It currently remains unclear which subgroup of patients might benefit from HSP90 inhibitors and at what time point these inhibitors may be beneficial. There are only few new or ongoing studies initiated during the last decade.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/165629
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s00432-023-04689-z.pdftextAdobe PDF729.56 KBpublishedOpen
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