Metastatic Breast Cancer Clinical Trial
Official title:
A Phase II Double-Blinded, Randomized, Placebo-Controlled Study of Indoximod in Combination With a Taxane Chemotherapy in Metastatic Breast Cancer
The purpose of this study is to compare the effects, good and/or bad, of standard of care therapy (docetaxel or paclitaxel) with or without the addition of 1-Methyl-D-tryptophan (referred to as indoximod) an experimental drug to find out which treatment is better.
It is estimated that 232,340 US women will be diagnosed with and 40,030 women will die of
breast cancer in 2013. Metastatic breast cancer is a terminal condition and treatments are
palliative in nature. The median survival for patients with metastatic breast cancer is
approximately 2.5 years. The standard therapies currently in use include anti-estrogen
therapies (anastrazole, letrozole, fulvestrant, tamoxifen), chemotherapy agents (taxanes,
capecitabine, navelbine, gemcitabine, eribulin, ixabepilone), targeted therapies
(trastuzumab, lapatinib), and supportive care agents (zolendronic acid, denosumab). While
breast cancer typically responds well to treatment, the response is transient and their
disease becomes more refractory with continued therapy. Also, quality of life is a
significant issue for these patients as many of these therapies are associated with
significant side effects. Well tolerated, novel agents which improve the efficacy of existing
chemotherapy agents would prove quite useful in managing metastatic breast cancer.
Preclinical data derived from MMTV-Neu mice with autochthonous tumors studied the interaction
between indoximod and various chemotherapeutic agents. Mice with 5-10mm tumors were enrolled
into control and treatment groups. Mice were treated with indoximod alone, chemotherapy alone
(paclitaxel, doxorubicin, cyclophosphamide, and others), and the combination of indoximod and
chemotherapy. treatment with indoximod or paclitaxel alone caused retardation of tumor growth
in this model but no regressions were seen. the combination of indoximod plus paclitaxel
caused 30% tumor regression and histologically there was significantly enhanced tumor cell
death with the combination versus either agent alone. This synergism was abrogated when the
mice underwent CD4+ T cell depletion prior to treatment with the combination, suggesting the
immune response played a role in the observed effect. Based on this data and other reports
suggesting systemic immunomodulating drugs like indoximod can synergize with chemotherapy
agents such as taxanes, the decision was made to devise this combination of therapy of
docetaxel or paclitaxel with indoximod in metastatic breast cancer.
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