Scientists report
"unprecedented" success using T-cells to treat cancer
An
international team of researchers has seen "extraordinary" results using patients' own immune
cells to fight cancer. In one trial, 94 percent of patients with acute lymphoblastic
leukaemia saw their symptoms disappear entirely.
For patients with other
types of blood cancer, response rates have been above 80 percent, and more than
half have experienced complete remission, cancer
researchers reported at
the American Association for the Advancement for Science conference over the
weekend.
The new T-cell treatment is a type of immunotherapy, and it involves taking a patient's own immune cells - specifically, white blood cells called T-cells - and reprogramming them to attack tumours. It's sort of like creating a tailor-made vaccine response against cancer.
The new T-cell treatment is a type of immunotherapy, and it involves taking a patient's own immune cells - specifically, white blood cells called T-cells - and reprogramming them to attack tumours. It's sort of like creating a tailor-made vaccine response against cancer.
Scientists have been
working on immunotherapy for decades, but have only recently started testing
this new T-cell therapy in humans. Due to the experimental nature of the
research, for now, the trials have been limited to patients who are no longer
responding to other treatments, and only have a few months to live.
But results are finally
beginning to emerge, and, if the conference presentation is anything to go by,
the treatment has incredible potential for patients with unresponsive tumours.
"This is unprecedented
in medicine, to be honest, to get response rates in this range in these very
advanced patients," Stanley Riddell, an immunotherapy researcher at Fred
Hutchinson Cancer Research Centre in Seattle, explained at the conference, as The Guardian reports.
"In the laboratory and
in clinical trials, we are seeing dramatic responses in patients with tumours
that are resistant to conventional high-dose chemotherapy," he added in
a press statement. "The merging of gene therapy, synthetic
biology and cell biology is providing new treatment options for patients with
refractory malignancies and represents a novel class of therapeutics with the
potential to transform cancer care."
T-cells are white blood
cells that are responsible for detecting foreign or abnormal cells - including
cancerous ones - and then latching onto them to tell the rest of the immune
system that they need to be attacked.
Unfortunately, this immune
response is often not quick or aggressive enough to get rid of fast-growing
tumours. Over time, T-cells become exhausted, and some tumour types learn to
evade them, allowing them to dodge the immune system altogether.
This is where immunotherapy
comes in - to put the system into overdrive, scientists perform what's known as
adoptive T-cell transfer. This means they first extract patients' T-cells from
their blood, and, using gene transfer, introduce receptors that will
aggressively target a specific cancer cell. Once back inside the body, these
newly engineered T-cells regenerate to create an army of immune cells prepped
to take down tumours.
Using this technique,
Riddell reports that he and his colleagues have seen"sustained
regression" in
previously terminal cases of acute lymphoblastic leukaemia, Non-Hodgkin
lymphoma, and chronic lymphocytic leukaemia.
The results have been
submitted for publication, and are now undergoing peer-review, which means we
can't get too excited about them just yet, and there aren't huge amount of
details to go off - but we do know that the aforementioned trial with the 94
percent success rate involved 35 patients, and the blood cancer study that
achieved greater than 80 percent response rates involved 40 participants.
To be clear, as promising
as these results are, this therapy is never likely to be a potential 'cure' for
cancer, and will most likely be reserved for the most extreme cases. This is
mainly because the potential side effects are severe - during the trials, 20 patients
suffered symptoms of
fever, hypotension, and neurotoxicity due to something called cytokine release
syndrome, and two patients died.
"Much like chemotherapy
and radiotherapy, it’s not going to be a save-all," said
Riddell. "These are in patients that have failed everything.
Most of the patients in our trial would be projected to have two to five months
to live ... [But] I think immunotherapy has finally made it to a pillar of
cancer therapy."
Italian cancer researcher
Chiara Bonini also spoke at the conference, and was more hopeful about the
therapy, as The Guardian reports.
"This is really a
revolution," she said.
"T-cells are a living drug, and in particular they have the potential to
persist in our body for our whole lives ... Imagine translating this to cancer
immunotherapy, to have memory T-cells that remember the cancer and are ready
for it when it comes back."
Riddell's lab is now
working on applying the T-cell therapy to a wider range of cancers - not just
blood cancers - and is trying to make engineered T-cells safer and easier to
design. The team also wants to track how long patients remain in remission
following the treatment before progressing with broader trials.
We'll need to wait for
peer-reviewed results before we know exactly how excited we should get about
T-cell therapy, so watch this space.
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