File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Book Chapter: Cancer Management by Tyrosine Kinase Inhibitors: Efficacy, Limitation, and Future Strategies

TitleCancer Management by Tyrosine Kinase Inhibitors: Efficacy, Limitation, and Future Strategies
Authors
Keywordstyrosine kinase inhibitors
targeted therapy
cancer management
clinical efficacy
limitations
Issue Date2019
PublisherIntechOpen
Citation
Cancer Management by Tyrosine Kinase Inhibitors: Efficacy, Limitation, and Future Strategies. In Ren, H (Ed.), Tyrosine Kinases as Druggable Targets in Cancer. London: IntechOpen, 2019 How to Cite?
AbstractTyrosine kinase inhibitors are taking up an increasingly significant role in treating cancers. There are different types of TKIs currently used in clinical settings. However, TKI-associated limitations such as resistance and adverse effects are frequently reported. In this chapter, we would comprehensively review the clinical efficacy of current TKIs using the currently available clinical trial data. Significant limitations of TKIs on cancer treatment will be further summarized and discussed. The strategies on overcoming the limitations of TKIs to maximize their clinical effectiveness and efficiency, such as complementary use of Chinese medicine or development of novel TKIs, will be proposed. In conclusion, an overall picture of the clinical use and limitation of the current TKIs will be drawn and the prospective development in overcoming the limitations will be discussed. Evaluation of clinical efficacy of TKIs, evaluation of limitations of TKIs, strategies in overcoming the limitations of TKIs, and conclusion (including prospective development of TKIs) are discussed below.
Persistent Identifierhttp://hdl.handle.net/10722/293841
ISBN

 

DC FieldValueLanguage
dc.contributor.authorHo, VWT-
dc.contributor.authorTan, HYH-
dc.contributor.authorWang, N-
dc.contributor.authorFeng, Y-
dc.date.accessioned2020-11-23T08:22:34Z-
dc.date.available2020-11-23T08:22:34Z-
dc.date.issued2019-
dc.identifier.citationCancer Management by Tyrosine Kinase Inhibitors: Efficacy, Limitation, and Future Strategies. In Ren, H (Ed.), Tyrosine Kinases as Druggable Targets in Cancer. London: IntechOpen, 2019-
dc.identifier.isbn9781789848083-
dc.identifier.urihttp://hdl.handle.net/10722/293841-
dc.description.abstractTyrosine kinase inhibitors are taking up an increasingly significant role in treating cancers. There are different types of TKIs currently used in clinical settings. However, TKI-associated limitations such as resistance and adverse effects are frequently reported. In this chapter, we would comprehensively review the clinical efficacy of current TKIs using the currently available clinical trial data. Significant limitations of TKIs on cancer treatment will be further summarized and discussed. The strategies on overcoming the limitations of TKIs to maximize their clinical effectiveness and efficiency, such as complementary use of Chinese medicine or development of novel TKIs, will be proposed. In conclusion, an overall picture of the clinical use and limitation of the current TKIs will be drawn and the prospective development in overcoming the limitations will be discussed. Evaluation of clinical efficacy of TKIs, evaluation of limitations of TKIs, strategies in overcoming the limitations of TKIs, and conclusion (including prospective development of TKIs) are discussed below.-
dc.languageeng-
dc.publisherIntechOpen-
dc.relation.ispartofTyrosine Kinases as Druggable Targets in Cancer-
dc.subjecttyrosine kinase inhibitors-
dc.subjecttargeted therapy-
dc.subjectcancer management-
dc.subjectclinical efficacy-
dc.subjectlimitations-
dc.titleCancer Management by Tyrosine Kinase Inhibitors: Efficacy, Limitation, and Future Strategies-
dc.typeBook_Chapter-
dc.identifier.emailTan, HYH: hyhtan@hku.hk-
dc.identifier.emailWang, N: ckwang@hku.hk-
dc.identifier.emailFeng, Y: yfeng@hku.hk-
dc.identifier.authorityWang, N=rp02075-
dc.identifier.authorityFeng, Y=rp00466-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.5772/intechopen.82513-
dc.identifier.hkuros320056-
dc.publisher.placeLondon-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats