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What
is Insulin Potentiation Therapy (IPT)?
Insulin Potentiation Therapy is a protocol for administering
traditional chemotherapeutic drugs using Insulin to transport
the chemotherapeutic drugs across the cell membrane into the
cancer cells. A much
lower dose of the highly toxic drugs is required, because IPT treatment
targets only the cancer cells, sparing the good cells. The cancer
cells get the chemotherapeutic drugs, not the normal cells. Therefore,
the patient does notsuffer the severe side effects so common with
conventional chemotherapy – no hair loss, vomiting, or fevers.
The quality of life remains high during treatment.
What cancers respond to IPT?
IPT treatment has beenreported to work well for many different types
of cancers. There are also reports of IPT bringing responses and
remissions to patients with some very difficult cancers, even cancers
in late stages. Of
course, each patient is evaluated anew, depending upon the type of
cancer, the virulence of the individual cancer cells, and the stage
of development of the cancer when the patient first comes for treatment.
Why is IPT needed?
Over time, regular chemotherapy dosages may so compromise the patient's
blood counts, immune system, and organ function as to preclude further
treatment or even cause organ damage resulting in the patient's death.
IPT eliminates the "lesser of two evils" decision all
cancer patients face when diagnosed. Patients fare well as they experience
a gentle and effective answer to cancer.
Is IPT just as effective as the chemotherapy my oncologist
would prescribe?
It does appear that the percentages for remission and survival
are at least as good as with conventional chemotherapy, and probably
much better. IPT has been used successfully in foreign countries
for over 70 years. It has only recently been used in the USA, and
there are many happy patients who now support this modified form
of chemotherapy. They do say that IPT is not only more effective
than conventional chemotherapy, but also that it is certainly more
comfortable than the suffering they experienced with regular chemotherapy.
What are the dangers of regular/conventional chemotherapy?
Cancer cells are voracious in fighting for the life-sustaining glucose
found in the blood stream. With 16 times the number of insulin and
insulin-like receptors of a healthy cell, cancer cells steal any
and all essential nutrients from the blood stream before the good
cells can get any. This is why, in advanced stages of cancer, the
tumor continues to grow while the patient becomes emaciated and simply
wastes away. Added to this, because of the cancer cell’s amazing
internal protection against toxins, standard administered chemotherapy
must be in large enough quantities to force its penetration into
the cancer cells. This results in the indiscriminate penetration
and killing of healthy cells as well, frequently leaving the patient
with fever, nausea, vomiting, hair loss, and a substantially diminished
quality of life.
Are there any side effects of IPT treatment ?
Almost none. There is certainly no hair loss, no going home to shiver
in bed for a day or two, and no severe vomiting. There is occasional
constipation, which is easily controlled by simple medications. Some
nausea is occasionally encountered for a few hours after the first
couple of treatments, but this is also easily managed.
What are the benefits of IPT?
• IPT can be very tough
against tumors while being very gentle for the patient, who continues
to live a normal, vital lifestyle while being treated. Treatments
require only approximately 1 ¼ hours, so many patients
are able to continue to work at their customary vocations while undergoing
these weekly treatments.
• If there is a chemotherapy drug that works
against a particular type of tumor, it is likely to work better if potentiated
with insulin.
• Gentle treatment sometimes precludes
the need for surgery or radiation. But when surgery or radiation is required,
IPT can be administered simultaneously, unlike conventional chemotherapy.
• Treatments costs are significantly
less than standard chemotherapy, and most insurance carriers do pay a significant
portion of the fees.
• As compared to conventional
chemotherapy, there are no severe and debilitating side effects.
The patient can easily continue with normal daily activities, enjoying
a high quality of life while avoiding severe vomiting, hair loss,
or fevers.
Are there any dangers in IPT treatment?
Unlike with conventional chemotherapy, there have been
no reported deaths as a result of IPT. In brief, there is no
danger. The worst side effect encountered is easily managed constipation.
Unlike conventional chemotherapy, anemia and decreased platelet
counts are unusual and usually not so severe as to require transfusions.
What should I expect when being treated?
We usually advise that 18-22 treatments are required
to achieve remission. However, we have observed complete remissions
after only six treatments, and occasionally more than 22 treatments
are required. It all depends on the type of cancer cell and how
far it has advanced in the patient’s body.
IPT is administered in the same manner as traditional
chemotherapy—the patient rests in a recliner while the
chemotherapeutic agent is received through an IV. The procedure
takes about 1 1/4 hours. The number and frequency of treatments
vary with each patient.
Insullin Potentiation Therapy: A More
In Depth Look
Chemotherapy drugs are powerful
cell-killing agents. In current medical practice, getting these
drugs into the inside of cells where they do their work requires
that they be administered in doses high enough to force them across
the membranes of cancer cells.
A major drawback to this dosing
strategy is a serious dose-related side effect profile frequently
seen with anticancer drugs. This happens because chemotherapy agents
do not discriminate between cancer cells and other normal cells
in the patient's body. They kill both kinds of cells, therefore
there are side effects.
With recent advances in our understanding
of the inner workings of cancer cells, it is now possible to avoid
the dose-related side effects of chemotherapy, while at the same
time increasing the effectiveness and specificity of these agents
in killing cancer cells. The key to this is an innovative strategy
for drug delivery called Insulin Potentiation Therapy (IPT).
Readers will recognize insulin
as being the hormone used to treat diabetes. Secreted by the pancreas
in healthy people, insulin is a powerful hormone with many actions
in the human body, a principal one being to manage the delivery
of glucose across cell membranes into cells. Insulin communicates
its messages to cells by joining up with specific insulin receptors
scattered on the outer surface of the cell membranes. Every cell
in the human body has some of these receptors, with there being
from one hundred to one hundred thousand of them per cell.
One might well ask, "What
does any of this have to do with cancer cells?" It is a well-known
scientific fact that cancer cells have a voracious appetite for
glucose. Glucose is their unique source of energy, and because
of the relatively inefficient way cancer cells burn this fuel,
they use up a great deal of it. This is one reason why cancer patients
lose so much weight. Because cancer cells require so much glucose,
they virtually steal it away from the body's normal cells, thus
starving them.
The interesting connection between
cancer cells and insulin is that recent findings published in the
scientific medical literature report that cancer cells
actually manufacture and secrete their own insulin. That
cancer cells should be able to do this makes good sense, knowing
of their requirements for large amounts of glucose to fuel their
processes of uncontrolled growth. Related to this insulin secretion,
and central to the operation of Insulin Potentiation Therapy, is
the even more interesting fact that cancer cells have ten
times more insulin receptors per cell than any of the
normal cells in the body. This fact creates a valuable opportunity
for the chemotherapy of cancer because it significantly differentiates
normal cells from the cancerous ones.
Having ten times more insulin
receptors than normal cells means that the effect of administered
insulin will be ten times greater on cancer cells than on normal
cells. With this difference, combined with actions of insulin in
Insulin Potentiation Therapy, we are able to deliver an effective
dose intensity of chemotherapy drugs to the inside of cancer cells
- selectively, with a sparing of normal tissues - and this can
be accomplished using greatly reduced doses of the drugs, effectively
eliminating all their dose-related side effects.
There is a kind of poetic justice
in this wonderful coincidence of cancer cell biology. The mechanisms
that cancer cells use to kill people are the same ones manipulated
in IPT to selectively potentiate chemotherapy effects in them,
and to more safely and effectively kill the cancer cells. A published
article about cancer cells in tissue culture reported that the
addition of insulin to the culture medium enhanced the cell-killing
effect of methotrexate - a commonly used chemotherapy drug - by
a factor of up to ten thousand. This striking
result was attributed to two effects on the cancer cells.
One was an effect of insulin
to increase the trans-membrane transport of the methotrexate into
the cell. The other was what the authors called "metabolic
modification by insulin" within the cancer cells. There is
yet another wonderful and powerful coincidence of cancer cell biology
involved in this factor of "metabolic modification" -
one that fits right in with the workings of Insulin Potentiation
Therapy.
Just as cancer cells have their
own independent secretion of insulin for unlimited access to the
fuel they require, they also have their own independent secretion
of something called insulin-like growth-factor to provide them
with an unlimited stimulus for growth. Cancer cells also have ten
times more of the receptors for insulin-like growth-factor on
their cell membranes - just as for the insulin receptors.
The metabolic modification by
insulin mentioned above results from the fact that not only can
it join up with its own specific receptors on cell membranes, but insulin
is also able to join up with the receptors for insulin-like growth-factor,
and to communicate messages about growth to these cells. While
it may seem highly undesirable for a cancer therapy to actually
promote cancer cell growth, this is in fact a valuable effect of
insulin here.
Chemotherapy side-effects result
from actions on the cells of patient's hair follicles, their bone
marrow, and the cells lining the stomach and intestines. This is
what causes the hair loss, low blood cell counts, and the nausea
and vomiting. What these different cell types all have in common
- along with cancer cells - is that they are all rapidly
dividing cells.
Chemotherapy drugs like to attack
rapidly dividing cells, indiscriminately. In a tumor, not all the
cancer cells are in this rapidly dividing stage all at once. They
take turns. When insulin joined up with the excess of insulin-like
growth-factor receptors on those cancer cells in the tissue culture,
it stimulated growth in many of the cells that were not in this
growth phase. This "metabolic modification by insulin" rendered
more of these cells susceptible to chemotherapy attack, contributing
to their increased death rate as observed in the experiment.
In Insulin Potentiation Therapy,
insulin administration does cause the blood glucose to go down.
This is called hypoglycemia. This hypoglycemia is an anticipated
side-effect of the insulin, one rapidly and effectively controllable
with intravenous glucose infusions at an appropriate time, according
to the IPT protocol. The principal role insulin plays in IPT is
that of a biologic response modifier. It modifies
the biologic response of cancer cells in such a way that lowered
doses of anticancer drugs, administered in conjunction with insulin,
will kill the cancer cells more effectively. Insulin modifies
the cell membrane allowing more anticancer drugs into
the cell. It also modifies the growth characteristics in
tumors making more of the cancer cells vulnerable to anticancer
drug effects.
Due to the great excess
of insulin-sensitive receptors on cancer cell membranes, we are
now able to create a clear differentiation between cancer and
normal cells using insulin.
Because of this important element
of differentiation, along with the biologic response modification
insulin produces, conventional chemotherapy drugs get targeted
more specifically and more effectively inside the cancer cells
only, and this can occur with the use of greatly reduced doses
of these cell-killing drugs. Cancer cells die, tumors shrink, and
no side-effects are caused in any other tissues. Insulin Potentiation
Therapy appears to be a wonderful new way of treating cancer using
nothing other than conventional chemotherapy drugs.
Please feel
free to contact us with any questions you may have at info@lesbreitmanmd.com
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