Pill that slashes risk of breast cancer recurring to be available on NHS
Ribociclib (known by the brand name Kisqali) targets specific proteins that contribute to cancer cell growth
A new pill has been approved for NHS use, offering a significant reduction in the risk of certain breast cancers recurring.
The decision by the National Institute for Health and Care Excellence (Nice) is expected to benefit about 4,000 people.
Ribociclib (known by the brand name Kisqali), manufactured by Novartis, operates by targeting specific proteins that contribute to cancer cell growth.
It will be administered in conjunction with an aromatase inhibitor, a medication that blocks oestrogen production, a hormone known to fuel some breast cancers.
While this approval marks a significant step forward, concerns have been raised about access for patients with other types of breast cancer.
The treatment will be an option for patients with hormone receptor-positive, HER2-negative early breast cancer which has responded to initial treatments, including surgery, but has a higher risk of returning.

It has been made available on the NHS with interim funding from the Cancer Drugs Fund.
However, Claire Rowney, chief executive at Breast Cancer Now, said on Thursday that the charity is ādeeply concernedā that āthousandsā of other patients with early breast cancer could miss out.
āDespite the promising potential for adjuvant ribociclib to cut the risk of cancer coming back by almost a third (28.5 per cent), todayās decision means only certain people with high-risk node positive disease, and none with high-risk node negative disease, would receive it,ā she added.
āWhile drug approvals are always welcome, itās disappointing that so many people could be denied access to this vital treatment and the chance to alleviate some anxiety about their cancer returning.ā
According to Nice, its committee found cost-effectiveness estimates āwere not suitable for decision making in the context of a recommendation for routine useā because the āclinical and economic evidence was too uncertainā.
It has asked Novartis for further evidence for the wider eligible population and a further committee meeting will be held in June.
Breast Cancer Now urged Nice and Novartis to āwork together to resolve the uncertainties around cost-effectivenessā in a bid to āensure a swift change to guidance so that everyone who could benefit can receive adjuvant ribociclibā.
It also called for the Scottish Medicines Consortium to consider the treatment āat paceā so it is made available across the UK.
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