An existing cancer treatment could be used for a common form of lung cancer for which there is currently no specific treatment available, new research suggests.
Scientists found the treatment blocked cell growth in a subtype of lung cancer.
The new findings, led by the University of Glasgow, have raised hopes a large number of patients could benefit from the treatment if used in combination with additional therapies.
The scientists hope it could be deployed for use in patients in the near future, given it is already approved for the treatment of other cancers.
Cancers of the lung kill more than 1.5 million people a year around the world.
In the latest study, researchers studied adenocarcinoma, the largest subtype of lung cancer.
One third of adenocarcinoma cancers carry a mutant gene called KRAS, which the researchers show requires the activity of any of four “EGFR/ERBB growth factor receptors” to drive cell proliferation.
There are presently no KRAS-inhibiting drugs available for treatment of these cancers and first generation EGFR drugs have failed to show any benefit to this form of cancer, researchers said.
However the scientists found that, unlike first-generation EGFR inhibitors, one particular second-generation EGFR inhibitor – a multi-ERBB inhibitor – blocked the proliferation of KRAS-mutant lung cancer cells in lab studies and actually prevented the formation of KRAS-driven lung cancers in mice.
Lead author Dr Daniel Murphy, senior lecturer at the University’s Institute of Cancer Sciences, said the development was a "step on the road" for finding a cure to these lung cancers.
"This type of cancer has up until now been resistant to everything that we've thrown at it," he told ITV News.
"We've been working on these cancers for 30 or 40 years as a community, and we have had no drug that has been specifically effective.
"This is the first chink in the armour for these specific cancers, whereby by using these drugs, drugs that are already available, we can start to undermine the fitness of these cancers."
Unwanted side-effects of these drugs on normal tissues remains a concern, however new strategies to limit delivery of these drugs to the tumour site could reduce such side-effects and greatly improve the utility of this class of therapeutics.
Dr Catherine Pickworth of Cancer Research UK said: “These findings in the lab have revealed a new role for four related molecules in a particular type of lung cancer. Furthermore, by targeting these molecules in mice the researchers found this increased the effectiveness of an existing lung cancer drug.
“We now need further studies to work out if this holds true in people and what the side effects might be. We urgently need new and better ways to treat lung cancer, a disease where survival has remained stubbornly low.”
The paper, The ERBB network facilitates KRAS-driven lung tumorigenesis, is published in Science Translational Medicine.
The work was funded by a MINT Collaborative grant from Merck Sharpe & Dohme; a Deutsche Krebshilfe grant; and grants from the European Commission Marie Curie Actions and the British Lung Foundation in collaboration with the Scottish Government Chief Scientist Office.