1. What is immunotherapy?
This is a process of enhancement of
the innate immunity present in all individuals. Lymphocytes are the most
important functioning components of this innate immunity, in which a part
of them are Natural Killer (NK) cells and Dentritic Cells (DCs). In
Immunotherapy Lymphocytes, NK cells and DCs are taken from the patients
own blood and then in the laboratory (in vitro) lymphocytes are
activated, the NK cells as well as DCs are expanded, and then transfused
back into their body.
2. How does it work?
The Lymphocytes are the first line of
defence in our body against Cancer cells; specifically the NK cells and
DCs. They are very efficient because they cause direct cell lysis (direct
damage to cancer cells) and do not need activation by antibodies.
Normally
only 5% - 10% of our body’s WBC is Natural killer cells. Here we activate
the lymphocytes in general and expand it many fold so that once infused
they will kill the cancer cells.
3. Can it be used for all cancers?
Yes it is
applicable for all cancers in general. But very good results have been
reported with Renal Cell cancer (Kidney), Malignant Melanoma (Skin),
Advanced Pancreatic Tumours, Leukemias (Blood cancers), Lymphomas, Breast
Cancer, Ovarian Cancer, Liver and Lung Metastasis etc.
4. What are the procedures involved before a patient can receiving
immunotherapy?
a) Blood is collected by a simple puncture of the vein as
is done for any other lab test.
b) The collected blood is then processed in the
specialized lab by specially trained scientists under highly sterile and
aseptic techniques.
c) The application of the famed Japanese technique (Technical
Collaboration M/S Biotherapy Institute of Japan) in the culture of the
cells will result in three events.
i. Activation
of Lymphocytes ii. Expansion of natural killer cells, iii. Passive expansion of stem cells.
d) After the process is completed the cultured cells of the
patient are readministered (Given Back) to the patients as an intravenous
drip some 14-21 days after the blood was collected from him/her.
5. Does the immunotherapy necessitate admission of the
patients to a hospital?
The
patient need not be admitted for collection of blood as it can be done as
an outpatient procedure. But the patient has to be admitted for
administering the cultured cells for about a day or two.
6. What are all problems that are anticipated during the
administration of the cells?
In
general there are no major adverse effects. This is so because the
patients are given back the cells that were originally collected from
them. Therefore the infusion is well tolerated. But during the process of
destruction of the cancer cells by the cultured cells that are transfused,
the patient may experience fever/fatigue on the day of administration. The
risk of this is however is small. It occurred in less than 1% of patients
in a study population that included more than 1400 patients.
7. What precautions does NCRM take during
the culture?
a) The culture technique is sterile so as to ensure that
no bacterial contamination takes place. This is also objectively tested by
using ‘Endotoxin test’. If it is negative it implies that there is no
bacterial contamination and only then will the
cultured cells be administered to the patients.
b) The collected cells will be subjected to IPT
(Immunophenotyping) this is specially important for Blood cancers. After
expansion the cultured cells will once again be subjected to IPT
and only on fully satisfying ourselves that the desired cells are present
they would be administered to the patients. IPT is done through a third
party organization.
8. What is the success rate?
As in the treatment of cancers
by other methods the patients who come early do better. A study which
compared patients who have undergone the conventional treatment alone
(Group 1) with that of the patients who have undergone the Immunotherapy
in addition to the conventional treatment (Group 2) a 38% better results
with the of the patients of Group 2 has been reported.
9. What are the Dosage requirements and timing of administration?
The
dose is determined on a case to case basis. If the cancer is solid and has
been removed completely by surgery 2 transfusions may be sufficient while
4 –6 Transfusions are required if the patients is receiving chemotherapy
after surgery. 4 –6 Transfusions are required for blood malignancies.
The timing
for blood malignancies is when the patient is in remission. The
timing for solid cancer is just before the patient is to receive
chemotherapy or after 1 week of the patient receiving chemotherapy. This
is to ensure that a good amount of peripheral blood stem cells are
available for the treatment process
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