Results 41 to 50 of about 694 (96)
ObjectiveThe management of cardiotoxicity concerning the use of oral antineoplastic agents (OAAs) is a challenge for healthcare professionals. Our objective was to create a comprehensive medication management guide with dose adjustment recommendations on
Elena Ramos-Ruperez +26 more
doaj +1 more source
Although KIT-mutant GISTs can be effectively treated with tyrosine kinase inhibitors (TKIs), many patients develop resistance to imatinib mesylate (IM) as well as the FDA-approved later-line agents sunitinib, regorafenib and ripretinib.
Donna M. Lee +14 more
doaj +1 more source
Progression in treatment of advanced gastrointestinal stromal tumors [PDF]
Gain-of-function mutations in KIT or PDGFRA receptor tyrosine kinase are key drivers of most gastrointestinal stromal tumor (GIST). The continuous development of tyrosine kinase inhibitors, such as imatinib, sunitinib, anlotinib, regorafenib, ripretinib ...
TANG Haixiao, ZHANG Yun, HAN Gang, GONG Hangjun
doaj +1 more source
Recent advances in drug therapy for advanced gastrointestinal stromal tumor
Gastrointestinal stromal tumors (GISTs) are rare neoplasms of the gastrointestinal tract associated with high rates of malignant transformation. Tyrosine kinase inhibitors (TKIs) as targeted agents are the backbone for advanced GIST treatment. During the
汪 明, 曹 晖
doaj
Why precision oncology works: lessons from gastrointestinal stromal tumours [PDF]
Gastrointestinal stromal tumours (GISTs) are the clearest solid-tumour model of precision oncology because diagnosis, prognosis, and treatment are strongly shaped by molecular genotype. The discovery of activating mutations in KIT proto-oncogene receptor
Si Ying Adelina Ho +4 more
doaj +1 more source
Background: KIT alterations occur in distinct melanoma subtypes, yet KIT-mutant melanoma remains clinically and biologically heterogeneous and lacks approved KIT-targeted therapy.
Carl Maximilian Thielmann +25 more
doaj +1 more source
The Effect of Yinchenhao Decoction on the Pharmacokinetic Profile of Futibatinib by HPLC-MS/MS
Futibatinib is an excellent fibroblast growth factor receptor 1–4 (FGFR 1–4) inhibitor that exhibits selective anti-tumor activeness against FGFR-deregulated tumors.
Chunfu Wang +5 more
doaj +1 more source
Emerging mechanisms of kinase inhibitor escape and clinical implications of ponatinib in advanced gastrointestinal stromal tumor. [PDF]
Shenoy S.
europepmc +1 more source

