Unfortunately majority of the cancer patients are
diagnosed in late stages, when there are distinct clinical symptoms.
By this time in most of the cases there are already visible or invisible
metastatic growths which are the main causes for unsuccessful cancer
treatment results – causes for relapses, uncontrollable tumor
spreads and the causes for short life expectancy. Even in those
patients in whom the cancers are found little earlier, by the time
they go through the standard harsh scheme of the traditional cancer
treatments and realize that these methods are no longer effective,
the cancers already outgrow to advance stages.
This is why over last decades, NCI and other cancer
institutions are looking for new methods, which could solve these
problems. Among others the immunotherapy, mainly in the form of
cancer vaccines have been distinguished in this task, achieving
many promising results in the cancer world. The only thing is the
time factor – it takes minimum 10-15 years before any new
medicine could be formulated in the common pharmaceutical market
as the standard therapy.
The anticancer vaccine
Resan can be used to treat the advanced cancers, mobilizing
its anticancer immunotherapeutical potentials. For this we have
elaborated two main approaches utilizing the latest immunotherapeutical
techniques: extracorporal activation of anticancer immunocompetent
cells (EAAIC) and a complex cancer therapy.
A Complex Cancer Therapy
The development of cancers indicates a failure
(due to various reasons) in the complex network of immunological
defense system which is present in every organism. This is why
a correct complex immunotherapy could have considerable positive
effects in the treatment of malignant tumors, which may improve
considerably the life expectancy and in certain cases even achieve
a complete cure. This can make a great sense especially if the tumor
has grown up to 3 and 4 stages.
The complex therapy includes:
1. The maximum resection of the primary tumor and the visible
metastases.
2. Use of antitumor vaccine RESAN.
3. Use of cytokines and immunostimulators (IL-1a,
IL-2, IFN-g).
4. Use of thyroid hormones (L-thyroxine).
5. Prevention and treatments of cachexy.
The maximum resection of tumors
When the immune system is matched against a large
number of tumor cells, it is more likely to be overwhelmed like
an outnumbered army which is one of the main causes for the vaccine
to be ineffective during cancer treatment. On the other hand, when
the immune system has to detect and fight a smaller number of cancerous
cells, it is more likely to be successful in curing cancers, for
example when the tumors have not grown too large sizes or when the
primary tumor has been eliminated by surgery. This is why better
results are obtained when we resect out the primary tumor and the
visible metastases as maximum as possible.
Use of antitumor vaccine RESAN
The most optimum time to inject the vaccine RESAN
is 7-10 days prior the operation, though good results are obtained
when it is injected 7-14 days after the operation too. However,
if the vaccine has been missed to inject with in this period, it
can be injected later too, but it is important to note that earlier
it is injected the better the result you get.
Use of citokines and immunostimulators
Similarly, the use of cytokines has shown a considerable
significance in the complex immunotherapy. The doses and the number
of injections of cytokines needed to administer depend on the immune
status and the moment at which the vaccine is administered.
Interleukin-1a (IL-1a
) helps to restore the weakening antitumoral immunity, decelerates
the tumor growth and reduces its' metastatic potential. IL-1a
should be injected prior to the vaccine administration if CD4 >
350 and CD8 < 280 in order to re-establish the immune system.
IL-1a, in such case, should be injected
5 days continuously through i. v. drip-feed, within 30-40
minutes at the dose of 15 ng per kg mass.
The changes of the immune status after a course of IL-1a
|
cells
|
total number of cells before the course
|
total number of cells after the course
|
|
CD3
|
609±85
|
781±36
|
|
CD4
|
309±44
|
386±42
|
|
CD8
|
278±32
|
352±40
|
|
CD20
|
197±43
|
288±58
|
|
CD25
|
226±39
|
261±47
|
|
CD16
|
189±26
|
249±32
|
The vaccine RESAN is applied after getting the better
parameters of the immunal status. After the injection of vaccines,
a back-up immunotherapy with IL-1a is
applied for 6-12 months. The back-up course is prescribed once in
two months which includes: 2 injections daily at the dose of 15
ng per kg mass, even in the case when CD4 > 350 and CD8 > 280. If
the number of lymphocytes has decreased lower the given margin (CD4
< 350, CD8 < 280) a full course of IL-1a
is prescribed.
During the immunotherapy
of tumors the application of IL-1b
is absolutely contra indicative, as it promotes the tumor
growth and raises its' metastatic potential. In
patients with out metastases, it was noticed that the tumor markers
raised up 2-10 times after a month of IL-1b
application where as in the patients already having metastases,
the tumor markers raised up-to 20-40 times.
Interleukin 2 (IL-2) is used on 10-14 days after
the injection of vaccines at the dose of 100000-125000 IU per m2
surface area of the, daily, through i. v. drip feed within 4 hrs.
A full course therapy consists of 15-60 of such injections. Further,
IL-2 immunotherapy is applied at an interval of 2 months for 6-12
months. A single back-up course of IL-2 consists of 125000
IU per m2 daily for 4 days.
Gamma interferon (IFN-g)
is used according to the following scheme: intramuscular injection
of 1000000 IU IFN-g on every second
day for a month and then once a week for 2 months. Gamma interferon
is started to applied from the next day after the RESAN injections.
Better results were observed when IL-2 and IFN-g
could have been supplied directly into the tumors during the basic
course of immunotherapy.
It is compulsory to use L-thyroxine during
the complex immunotherapy. L-thyroxine is prescribed as 25 mcg (microgram),
under tongue everyday in the morning for 4-6 months. Then, it is
withdrawn slowly reducing 25 mcg (microgram) every week.
Prevention and treatments of
cachexy
During the cancer patient care it is important
to have regular weight checkings (once in 2 months), as in 50-80
% of the patients with advancing cancer growths develops cachexia.
Cachexia is said to be developed when the patients lose more than
5 % of premorbidal weight within six months period. Cachexia - a
word from Greek derivation: "kakos" – poor and "hexis" –
state. The development of a cachexia in cancer patients indicates
a bad prognosis and a considerable decline in the patient's general
health condition. In fact cachexia is the principal cause of deaths
among the cancer patients. The main mechanism is the hypermetabolism
that takes place in most of the cancer patients. The major clinical
signs of the hypermetabolism are fatigue, apathy and depression.
As a whole it affects the protein, fat and carbohydrate metabolisms.
For the prevention and treatments of cachexy the
following therapy is recommended:
1. Peritol (Cyproheptadine) 4 mg, 4 times a day,
daily, constantly.
2. Dexamethasone 4 mg, once a day, daily for one week.
Dexamethasone is better to take in the morning
during breakfast. If the appetite of the patient increases then
dexamethasone is taken constantly; where as if there is no changes
in appetite then dexamethasone is replaced by medroxyprogesterone
at the doses - 500 mg, 2 times a day. If medroxyprogesterone is
not found, it can be replaced by megestrol acetate at the doses
- 40 mg, 4 times a day.
If the necessary effects are not achieved then
the doses of megestrol acetate is increased gradually first 80 mg,
4 times a day then 100 mg 4 times a day. If you still don't get
the effect, then megestrol acetate is prescribed as 200 mg, 4 times
a day.
3. Ibuprofen at a dose of 400 mg, three times,
daily OR indomethacin at a dose of 50 mg twice a daily.
4. Almagel, 1 tea spoon, 20-30 minutes before the intake of ibuprofen
or indomethacin.
5. Activated carbon, 2 g at night, daily.
6. Fish-oil, 1 tea spoon, once a week.
Resan vaccine which can release
intensive pain symptoms
Beside the anticancer specific immune responses,
RESAN increases the number and functional activeness of the natural
killers – CD56 lymphocytes, which secrete beta-endorphins
in large amounts. In our body beta-endorphins are responsible to
block out the pain signals. So more the amount of these substances
in our body the higher the pain threshold.
Due to this, the vaccine administration may release
the pain symptoms (in fact one of the dominant clinical problems
in the late stage cancer patients) considerably. This would
in turn, improve the general life-style of the cancer patients.
Extracorporal Activation of Anticancer
Immune-competent Cells (EAAIC)
The vaccine RESAN can be used in an extra corporal
(outside the organism) activation of immunocompetent blood cells
of cancer patient, specifically sensitive to response against cancer
antigens, which are in turn are returned back to the patient to
destroy cancer cells.
As a result of leucocyte activation, it is possible
to derive autogenous cytokines of an early phase of the immune
answer for a particular patient which then, can be returned back
in optimal, physiologically balanced proportions. Because of the
fact that these cytokines are of own, antibodies against them do
not form, in difference to that when used recombinant cytokines.
This enables to maintain the activity of autogenous cytokines
constantly in a high level increasing the overall efficiency of
the applied immunotherapy.
The production of the cytokines of an early phase of the immune
answer

Fig. 1
Utilizing a vaccine in extracorporal activations
of lymphocytes we can select a particular clone of lymphocytes activated
against a particular tumor of the patient as well. Then, having
multiplied these highly activated lymphocytes we return them back
into the patient which significantly increases the antitumoral immune
answer.
Both of these methods can be used together or separately.
The only thing is that they can be conducted only in clinics equipped
by special equipments for separation of blood cells and cell culture.
The production of the antitumoral
T-lymphocytes |
Fig. 2
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