According to Talktokemi findings, Olaparib has been used for advanced cancers according to study the dubbed the OlympiA trial has now demonstrated its effectives at the early or “curative” stage, researchers say.
According to Scientists
say they have made a breakthrough in the treatment of breast cancer by using
the targeted cancer drug olaparib after chemotherapy.
A major trial
in the use of olaparib at an early stage has shown that giving women the drug
following chemotherapy significantly reduces the risk of inherited breast
cancer returning or spreading.
The trial
showed that after a median 2.5 years of follow-up, 85.9% of patients were free
of their cancer, compared with 77.1% who had received a placebo. This
represented a 42% overall drop in the risk of cancer returning.
Similarly,
87.5% of olaparib patients were alive and free of disease which had spread to
other parts of their body, compared with 80.4% who were given a placebo, a 43%
drop in the risk of cancer spreading via distant metastases.
The trial was
conducted by a series of international partners, including London’s Institute
of Cancer Research (ICR), with the results released on Thursday at the American
Society of Clinical Oncology (ASCO) annual meeting and published in The New
England Journal of Medicine.
The ICR said
the trial suggested olaparib, which exploits a genetic weakness in cancer
cells, “could become a new treatment option to reduce the risk of recurrence or
metastasis in women with inherited forms of high-risk early breast cancer – and
could lead to more patients being cured”.
OlympiA
steering committee chair Professor Andrew Tutt, professor of oncology at the
ICR, said in a statement: “We are thrilled that our global academic and
industry partnership in OlympiA has been able to help identify a possible new
treatment option for women with early-stage breast cancer who have inherited
mutations in their BRCA1 or BRCA2 genes.
“Women with
early-stage breast cancer who have inherited BRCA1 or BRCA2 mutations are
typically diagnosed at a younger age. Up to now, there has been no treatment
that specifically targets the unique biology of these cancers to reduce the
rate of recurrence, beyond initial treatment such as surgery, hormone
treatment, radiotherapy and chemotherapy.
“This major
international study coordinated by the Breast International Group shows that
giving olaparib for a year to patients with inherited BRCA mutations after they
have completed initial treatment increases the chances that they will remain
free of invasive or metastatic breast cancer.”
Prof Tutt
said olaparib had the potential to be used “as a follow-on to all the standard
initial breast cancer treatments to reduce the rate of life-threatening
recurrence and cancer spread for many patients identified through genetic
testing to have mutations in these genes”.
He added the
frequency of significant side effects from the drug in the study was relatively
low.
The ICR’s
chief executive, Professor Paul Workman, said: “Olaparib was the first cancer
drug in the world to target inherited genetic faults. It is also now the first
targeted drug to have been shown to effectively treat patients with inherited
mutations and early-stage breast cancer, potentially curing some women of their
disease. This is a major breakthrough.
“It’s
fantastic that decades of ICR science into identifying cancer’s weaknesses –
alongside academic, charity and industry partners in the UK and worldwide – has
led to global trials which are now changing the outlook for patients. I am now
keen to see this new treatment be approved and made available to patients in
the UK and worldwide as fast as possible.
www.talktokemi.blogspot.co.uk
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