Acute Myelogenous Leukemia Clinical Trial
Official title:
Open Label, Phase II Dosing Study of Ara-C Chemotherapy in Combination With EL625 and Idarubicin in Refractory and Relapsed Acute Myelogenous Leukemia (AML)
The principal goal of this clinical trial is to assess the ability of cenersen sodium
(EL625) to improve cancer responsiveness to the established AML therapeutic agent Idarubicin
used alone or in combination with Cytarabine (Ara-C).
Cenersen sodium is a drug that is designed to block the effects of a protein called p53.
Laboratory evidence shows that blocking p53 will make many types of cancer, including acute
myelogenous leukemia (AML), more sensitive to a variety of established cancer therapeutics
while making normal tissues more resistant to the toxic effects of these agents.
This clinical trial is designed to assess the ability of cenersen sodium (EL625) in
combination with Idarubicin alone or with Cytarabine to either: (1) induce remissions in
patients who have previously failed to go into remission in response to chemotherapy; or (2)
provide patents who have relapsed after going into a chemotherapy-induced remission with a
longer remission.
Cenersen sodium is one of a new class of drugs called antisense oligonucleotides (oligos).
Oligos are designed to block the production of specific proteins and thereby inhibit their
function. Cenersen sodium targets p53, a widely studied protein.
In cancer, p53 occurs either in the un-mutated ("normal") or mutated forms. The majority of
participants in this trial are expected to have un-mutated p53. Cenersen sodium is
anticipated to sensitize cancers with un-mutated p53 to most established cancer
therapeutics.
p53 has a pivotal role in protecting the body from cells that have suffered genetic damage
and, as a result, do not function properly. The protein first senses the level of the damage
and then forces the damaged cell to respond to the damage either by repairing itself or
committing suicide. In general, the greater the level of damage the more likely the cellular
response will be suicide.
Many cancer therapeutics, including both chemotherapy and radiation, cause the types of
genetic damage that activate p53 and, consequently, cause either damage repair or cellular
suicide. Laboratory studies suggest that cancer cells have a host of defenses that reduce
the chances that these cells will respond to genetic damage by committing suicide. So
compared to normal cells, cancer cells are more likely to repair the damage caused by cancer
therapeutics while normal cells are more likely to commit suicide. Thus, blocking un-mutated
p53 is more likely to prevent repair in cancer cells while preventing suicide in normal
cells. This provides the basis for a differential effect of cenersen sodium on cancer cells
verses normal cells.
When p53-dependent repair is prevented in cancer cells they begin to copy their damaged
genetic information in preparation for cell division. This copying of the genetic damage
triggers a p53-independent backup suicide mechanism and, as a result, the cancer cells are
eliminated. This is the presumed mechanism whereby cenersen sodium is able to sensitize
cancer cells with normal p53 function to numerous cancer therapeutics.
At higher doses however, chemotherapy sometimes blocks cells from copying their genes in
preparation for division. Thus, it is possible that a chemotherapeutic agent used at a high
dose could block any sensitizing effect that cenersen sodium might otherwise have on the
cancer.
The chemotherapeutic agent Idarubicin is known to produce the type of genetic damage that
effects p53 expression, causes p53-dependent responses and has been shown to be made more
effective at killing cancer cells by cenersen sodium. Cytarabine (Ara-C) is the most widely
used chemotherapeutic agent for AML. Cenersen sodium does not appear to sensitize cancer
cells to Cytarabine and at higher doses Cytarabine may reduce the capacity of cenersen
sodium to sensitize cancer cells.
Hence, this AML study will examine the effects of Cenersen sodium used in combination with
Idarubicin and one of three different doses of Cytarabine (i.e. 0, 0.1 and 1.0 gm/m2/day),
on the responsiveness of participants to these chemotherapeutic agents.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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