NICE has approved Lynparza (olaparib) for NHS use in England and Wales for adults with HER2-negative, locally advanced or metastatic breast cancer who have germline BRCA1 or BRCA2 mutations, following chemotherapy.
Germline BRCA1/2 mutations account for 5–10% of breast cancers, making genetic testing essential for optimal treatment. The OlympiAD phase 3 trial demonstrated that olaparib significantly delays disease progression or death compared to standard chemotherapy, reducing the risk by 42%. Its safety profile remains consistent with known effects.
Olaparib, a precision PARP inhibitor, disrupts cancer cells’ DNA-repair mechanisms, leading to tumour cell death. Professor Andrew Tutt highlighted its impact in improving outcomes for patients with inherited BRCA mutations. AstraZeneca UK President Tom Keith-Roach welcomed NICE’s recommendation, marking the company’s 26th cancer medicine approval by NICE and SMC since 2021.
BRCA mutation testing is available and reimbursed via the NHS National Genomic Test Directory. NICE’s decision underscores the role of genetic testing in ensuring targeted therapies reach eligible patients, advancing precision medicine in oncology.