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Clinical Trial Summary

Given the poor prognosis and limited treatment options available for patients with mucosal or acral/lentiginous melanomas who develop metastatic disease, genetic discoveries of KIT mutations in these cancers present the need to test multi-targeted kinase inhibitors with potent KIT inhibitory activity in this patient population. Imatinib and other tyrosine kinase inhibitors (TKIs) have the potential to be effective in this patient population, but patients may develop resistance to treatment. Therefore, in this study, we propose to test nilotinib in patients with metastatic mucosal, acral, or chronically sun-damaged melanoma following treatment with another TKI.


Clinical Trial Description

OBJECTIVES:

Primary

* To estimate the proportion of patients, with metastatic mucosal, acral, or chronically sun damaged melanomas, whose tumors have KIT aberrations, and who progressed or could not tolerate a KIT targeting tyrosine kinase inhibitor (TKI) (e.g. including but not limited to imatinib mesylate, sunitinib, or dasatanib), who are alive and without progression of disease four months after beginning treatment with nilotinib.

Secondary

- To determine early evidence of biologic and clinical activity by best overall response rate.

- To estimate time to progression of disease and overall survival.

- To determine the tolerability of nilotinib.

- To evaluate the use of FDG-PET scanning in determining early biologic response to therapy.

- To correlate c-kit mutational status and amplification status with response to therapy.

- To evaluate the feasibility of nilotinib.

- To evaluate the tolerability of nilotinib in patients with brain metastases. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00788775
Study type Interventional
Source Dana-Farber Cancer Institute
Contact
Status Completed
Phase Phase 2
Start date January 23, 2009
Completion date March 2014

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