Clinical Trials Directory

Trials / Terminated

TerminatedNCT00925132

Treatment of Resistant Metastatic Melanoma Using Decitabine, Temozolomide and Panobinostat

Phase Ib/II: Epigenetic Modification of Chemosensitivity and Apoptosis in Metastatic Melanoma: Treatment of a Resistant Disease Using Decitabine, Temozolomide and Panobinostat

Status
Terminated
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
39 (actual)
Sponsor
University of Iowa · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to treat metastatic melanoma with a combination of standard chemotherapy (decitabine and Temozolomide in a dose escalation scheme) with an study drug called panobinostat. This combination is proposed to unlock genes that may contribute to mechanisms that cause tumor growth. The primary objectives of this study are: * To evaluate the safety and tolerability of the proposed schedule of decitabine, temozolomide and panobinostat in the treatment of metastatic melanoma. * To define any Dose Limiting Toxicity (DLT) and maximum tolerated dose (MTD) of the combination of decitabine, temozolomide and panobinostat.

Detailed description

Most chemotherapeutics target rapidly proliferating cells, leaving quiescent cells and those with extended cell cycles unaffected. The investigators propose that this combination of decitabine, temozolomide, and panobinostat will target both melanoma stem cells and rapidly proliferating melanoma cells. The use of two drugs that regulate gene expression epigenetically (panobinostat and decitabine) in combination with a chemotherapeutic agent (temozolomide) is hypothesized to: * induce expression genes (e.g., Apaf-1) that increase chemosensitivity of tumor cells and enhance apoptosis * potentiate the cytotoxic effect of temozolomide by epigenetic modulation, and * induce proliferation and differentiation of tumor stem cells, thus enabling senescence and apoptosis. Secondary objectives: * To measure overall survival * To measure the time to progression of patients treated with this combination in comparison to patients treated historically with DTIC (the current standard of care). * To evaluate treatment response with FDG PET and compare FDG PET with conventional imaging for treatment response assessment.

Conditions

Interventions

TypeNameDescription
DRUGTemozolomide, Decitabine, PanobinostatTemozolomide - given each cycle. Decitabine - 6 cohorts with dose escalation. Panobinostat - 6 cohorts with dose escalation.

Timeline

Start date
2009-12-01
Primary completion
2014-11-01
Completion
2016-12-01
First posted
2009-06-19
Last updated
2017-07-02
Results posted
2017-07-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00925132. Inclusion in this directory is not an endorsement.