In
a recent report in The New England Journal of Medicine, the authors explain how two
child patients were treated with a new technique. In both, their leukaemia was
cleared and one of them remains in remission. The technique has previously had some
success on a small group of adults.
News
of medical research does not usually cover successes in just one or two
patients - so why did the researchers go public on this?
In
solid cancers you can never be sure that there are no cancer cells left in the
body but in leukaemia you can be much more certain. It is no longer a case of
looking at slides through a microscope - the latest techniques and equipment
can scrutinise large numbers of blood cells and detect the presence - or absence - of
cancerous cells.
There
are many different kinds of leukaemia, each relating to a particular kind of
blood cell. The nursery for blood cells is the red bone marrow and it is here
that leukaemia cells are produced before they are released into the circulation.
This red bone marrow is essential to life. It not only replaces red blood cells
but all the white blood cells that make up the immune system. Without it, fatal anaemia and infection are inevitable.
Doctors
can categorise the various leukaemias very accurately these days. For some
patients the prognosis is good. For others, the only hope is a stem cell (bone
marrow) transplant. These two young patients were suffering from relapsed Acute
Lymphoblastic Leukaemia (ALL).
A
stem cell transplant is usually the treatment of last resort. It uses brutal
chemotherapy to kill all the red bone marrow, diseased and healthy. Then there
is an infusion of blood stem cells, gathered from a closely matched donor. These
then set up home in the bone marrow cavities and rebuild the blood producing
tissue. It is a risky and arduous process. For some it fails to work and for
others the treatment itself proves fatal.
Medical
researchers sometimes use what they call translational research, which they also
refer to as "bench to bedside research". Scientific advances in the
lab are tried out on small groups of volunteers. These are patients who have
little to lose - maybe a stem cell transplant has already failed - and they are
willing to take the risk of acting as guinea pigs.
Translational
research is quite different to a controlled trial - it is, literally, trying
out something that they think should work to see what happens. This paper is an
example of translational research - hence the tiny numbers. The progress of
research like this is slow. Suitable patients are rare. By publishing this
early success, researchers can share knowledge and perhaps find other patients
who would benefit.
We have long had the tantalising knowledge that immune cells known as T cells (or T lymphocytes) can destroy cancer cells in the lab - but often fail to do so in the body. One of the reasons for this failure is that the immune cells cannot recognise the cancer cells as something alien to the body. Store detectives deal with a similar problem: shoplifters tend to look like honest shoppers.
In
the experimental treatment two child patients were treated with a kind of
gene therapy in which T cells were genetically altered in the lab and put into the
patient's body. The technique teaches the T cells the exact molecular pattern
they need to attack and harnesses their killing power. It's like giving store
detectives a photograph of a professional shoplifter.
There was a serious
reaction to the treatment - the children's immune systems reacted violently to
the rapid dying-off of cancer cells (tumour lysis syndrome). But both went into
remission with no trace of the ALL cells. One of them subsequently started
producing a slightly different kind of leukaemia cell but the other seemed to
be remaining clear.
Such
new forms of treatment may in time prove to be less dangerous and more
effective than the current approach, which involves strong chemotherapy drugs. For sick children and their parents in particular, a shorter and less arduous course of treatment would be a great step forward.
Chimeric Antigen Receptor-Modified T Cells for Acute
Lymphoid Leukemia," New England Journal of Medicine, Online March
25, 2013. To appear in print April 18, 2013.
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