Dovitinib for Imatinib/Sumitinib-failed Gastrointestinal Stromal Tumors (GIST)
With discovery of KIT mutations and the advent of KIT tyrosine kinase inhibitor imatinib (GlivecTM, Novartis), there has been substantial improvement in overall survival in patients with advanced and/or metastatic gastrointestinal tumors (GIST). Recently, sunitinib (SuteneTM, Pfizer) showed activity as second-line therapy in GIST patients after failure with imatinib. However, virtually all patients will eventually progress or become intolerable after the first-line imatinib and the second-line sunitinib. Dovitinib (TKI258, Novartis) is a multi-kinase inhibitor. TKI258 is a potent inhibitor of the VEGFR 1, 2, and 3, FGFR1, 2 and 3, PDGFRβ, Kit, RET, TrkA, CSF 1R, and FLT3 with inhibitory concentration 50% (IC50s) of less than 40nM. Stem cell factor (SCF) also termed KIT ligand, or steel factor has been shown to modulate tumor angiogenesis. In cultured human endothelial cells and Kit expressing cancer cells, TKI258 inhibits VEGF- and SCF-stimulated mitogenesis. .
|Study Design:||Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
|Official Title:||A Phase II Trial of TKI258 in Patients With Metastatic or Advanced Gastrointestinal Stromal Tumors (GIST) After Failure to Imatinib and Sunitinib(CTKI258AKR01T)|
- Disease control rate (DCR; response + stable disease) [ Time Frame: Up to 24 weeks ] [ Designated as safety issue: No ]evaluated with abdominal and pelvic dynamic CT scan every 4 weeks for the initial 8 weeks, and then every 8 weeks, using RECIST version 1.0
- Overall response rate using both CT and PET scans [ Time Frame: Up to 24 weeks ] [ Designated as safety issue: No ]PET scan will be performed at baseline and at 4 weeks of treatment. Choi criteria will be used for determination of response
- Efficacy according to the primary mutation type [ Time Frame: Up to 24weeks ] [ Designated as safety issue: No ]Correlation between efficacy results such as response, progression-free survival and overall survival, and primary mutation type including KIT exons 9, 11, 13, and 17 and PDGFRα exons 12 and 18.
- Efficacy according to the concentrations of circulating growth factors [ Time Frame: Up to 24weeks ] [ Designated as safety issue: No ]Correlation between efficacy results, such as response, progression-free survival, and overall survival andcirculating growth factors (including vascular endothelial growth factor, fibroblast growth factor, interleukin‐8, placental growth factor, and fibroblast growth factor23), and soluble receptors (including soluble form of membrane bound vascular endothelial growth factor receptor-1 and -2).
- Number of participants with adverse events [ Time Frame: Monitoring of adverse events will be continued for at least 28 days following the last dose of study treatment. ] [ Designated as safety issue: Yes ]Adverse events will be graded according to Common Terminology Criteria for Adverse events version 3.0
- Progression-free survival [ Time Frame: Up to 3 years ] [ Designated as safety issue: Yes ]Progression-free survival is defined as the time from the first treatment to the onset of progressive disease per RECIST criteria or to the date of death whichever comes first. For patients who do not experience progressive disease or death, the progression-free survival duration will be right censored on the last disease assessment date.
- Overall survival [ Time Frame: Up to 3 years ] [ Designated as safety issue: No ]Overall survival duration is calculated as time from the first treatment to the date of death. For patients who are still alive at the cut‐off date for statistical reporting, the overall survival duration will be right censored on the last known alive date.
|Study Start Date:||September 2011|
|Estimated Study Completion Date:||March 2013|
|Estimated Primary Completion Date:||September 2012 (Final data collection date for primary outcome measure)|
It is well known that KIT and PDGFR which can be inhibited by TKI258 have a crucial role in the development and proliferation of GIST, and in general FGFR has an important role in angiogenesis and tumor proliferation in many cancers. We assume that TKI258 can be also effective in patients with GIST. The objective of this study is to evaluate the safety and activity of TKI258 given as salvage treatment for GIST after failure to standard imatinib and sunitinib.
|Contact: Yoon-Koo Kang, Md, PhDfirstname.lastname@example.org|
|Contact: Min-Hee Ryu, MD, PhDemail@example.com|
|Korea, Republic of|
|Asan Medical Center, University of Ulsan College of Medicine||Recruiting|
|Seoul,, Korea, Republic of, 138-736|
|Contact: Yoon-Koo Kang, MD, PhD +82-2-3010-3230 firstname.lastname@example.org|
|Contact: Min-Hee Ryu, MD,PhD +82-2-3010-5935 email@example.com|
|Principal Investigator: Yoon-Koo Kang, MD, PhD|
|Principal Investigator:||Yoon-Koo Kang, MD, PhD||Asan Medical Center|