A new precision medicine targeting cancer’s ability to repair its DNA has shown promising results in the first clinical trial of the drug class.
The new study, designed to test the drug’s safety, found that half of patients given the new drug either alone or with platinum chemotherapy saw their cancer stop growing, and two patients saw their tumours shrink or disappear completely.
Damage to the DNA in cells is the root cause of cancer – but it is also a fundamental weakness in tumours, and cancer cells can be killed by further damaging their DNA or attacking their ability to repair it.
The new phase I trial tested the first in a new family of drugs blocking a key DNA repair protein called ATR. Phase I trials are designed to assess the safety of new treatments, and it’s unusual to see a clinical response at this stage.
A team at The Institute of Cancer Research, London, and The Royal Marsden NHS Foundation Trust, led a trial of the benefit of an ATR inhibitor called berzosertib either on its own or with chemotherapy in 40 patients with very advanced tumours, treated in hospitals around the world.
The researchers established the doses at which the drug was safe for use in further clinical trials, and found berzosertib on its own caused only mild side effects.
Surprisingly for a phase I trial, the researchers also found that berzosertib stopped tumours growing in over half of patients given the drug either on its own or with chemotherapy – 20 out of 38 patients whose treatment response could be measured.
The drug’s benefit in blocking DNA repair was even more marked in patients also given chemotherapy, which works by causing DNA damage. In these patients, 15 of 21, or 71 per cent saw their disease stabilise – suggesting that chemotherapy boosted sensitivity to berzosertib.
The drug is now moving forward in further trials, and the hope is that it could be developed into a new targeted treatment for patients, and help overcome resistance to other precision medicines such as PARP inhibitors that target DNA repair.
The new results are published in the Journal of Clinical Oncology and the trial was funded by Merck, the manufacturer of the drug.