This once-a-day pill will be available on the NHS for adults with locally advanced or metastatic NSCLC, who have tested positive for the epidermal growth factor receptor (EGFR) mutation.
This is a change from the committee’s initial decision which found dacomitinib to not be a cost-effective use of NHS resources.
Clinical trial results showed that people who took dacomitinib had longer overall survival rates than those who took gefitinib (34.1 months compared with 26.8 months), a drug already recommended by NICE. Dacomitinib also increased the length of time before the disease worsened (14.7 months for dacomitinib compared with 9.2 months for gefitinib). It was however noted that dacomitinib had a higher incidence of side effects than gefitinib, so a lower dose may be needed.
Meindert Boysen, director of the Centre for Health Technology Evaluation at NICE, said: “Our committee acknowledged that dacomitinib had the potential to extend life for people with this type of lung cancer more than existing treatments currently available on the NHS.
"Responsible pricing by the company has allowed our committee to reconsider their initial decision. This has led to the positive recommendation announced today, allowing patients to benefit from this innovative treatment on the NHS.”
According to company estimates around 1,477 people will be eligible for this treatment annually.
Separately, NICE has also today published guidance that does not recommend another lung cancer drug, osimertinib, for the same patient population because the cost effectiveness estimates were above what NICE normally considers to be an acceptable use of NHS resources.