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Phase
II trial of tetrathiomolybdate in patients with advanced kidney cancer
Redman BG, Esper P, Pan Q, Dunn RL, Hussain HK, Chenevert T, Brewer GJ,
Merajver SD
Division of Hematology and Oncology, University of Michigan
Comprehensive Cancer Center, University of Michigan, Ann Arbor 48109-0948,
USA.
Redmanb@umich.edu
Purpose. Tetrathiomolybdate (TM), a copper-lowering agent, has
been shown in preclinical murine tumor models to be antiangiogenic.
We evaluated the antitumor activity of TM in patients with advanced kidney
cancer in a Phase II trial.
Experimental
Design. Fifteen patients with advanced kidney cancer were eligible to
participate in this trial.
TM was initiated p.o. at 40 mg three times a day with meals and 60 mg at bedtime
to deplete copper.
A target serum ceruloplasmin (CP) level of 5-15 mg/dl was defined as copper
depletion.
Doses of TM were reduced for grade 3-4 toxicity and to maintain a CP level in
the target range.
Once copper depletion was attained, patients underwent baseline tumor
measurements and then again every 12 weeks for response assessment.
Patients not exhibiting progressive disease at 12 weeks after copper depletion
continued on treatment.
Serum levels of Interleukin (IL)-6, IL-8, vascular endothelial growth factor
(VEGF) and basic fibroblast growth factor (bFGF) were assayed pretreatment and
at various time points on treatment.
Dynamic contrast enhanced-magnetic resonance imaging (DCE-MRI) was performed on
selected patients in an attempt to assess changes in tumor vascularity.
Results.
All of the patients rapidly became copper depleted.
Thirteen patients were evaluable for response.
No patient had a complete response or PR.
Four patients (31%) had stable disease for at least 6 months during copper
depletion (median, 34.5 weeks).
TM was well tolerated, with dose reductions most commonly occurring for grade
3-4 granulocytopenia of short duration not associated with febrile
episodes.
Serum levels of IL-6, IL-8, VEGF, and bFGF did not correlate with clinical
activity.
Serial DCE-MRI was performed only in four patients, and a decrease in
vascularity seemed to correlate with necrosis of a tumor mass associated with
tumor growth.
Conclusions.
TM is well tolerated and consistently depletes copper as measured by the serum
CP level.
Clinical activity was limited to stable disease for a median of 34.5 weeks in
this Phase II trial in patients with advanced kidney cancer.
Serum levels of proangiogenic factors IL-6, IL-8, VEGF, and bFGF may correlate
with copper depletion but not with disease stability in this small cohort.
TM may have a role in the treatment of kidney cancer in combination with other
antiangiogenic therapies.
PMID: 12738719 [PubMed - in process]
Source: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12738719&dopt=Abstract
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