Roche immunotherapy Tecentriq gains European approval for breast cancer

By Reuters Staff

ZURICH(Reuters) - 29/8/2019

Roche's Tecentriq (atezolizumab) has won European approval for use against a tough-to-treat breast cancer, helping the Swiss drugmaker to widen use of an immunotherapy that has so far been eclipsed in revenue terms by more-established rival medicines.

The European Commission approved Tecentriq with Abraxane (paclitaxel protein-bound) for people with metastatic triple-negative breast cancer that tests positive for a protein believed to help tumours to evade attack by the body's immune system, Roche said on Thursday.

Tecentriq trailed rival immunotherapies Keytruda (pembrolizumab) and Opdivo (nivolumab) - produced by Merck and Bristol-Myers Squibb respectively - to market but has been racking up approvals.

These include approvals for niche indications such as metastatic triple-negative breast cancer. Some 15-20% of breast cancer is triple-negative, meaning tumours lack three characteristics for which there are more treatment options.

"The European approval of this Tecentriq combination represents a significant step forward in the treatment of this aggressive breast cancer, where the unmet medical need is great," Roche Chief Medical Officer Sandra Horning said in a statement.

Tecentriq, having steadily added approvals in new cancer indications and new geographies, is on track to surpass $1.5 billion in annual sales in 2019, its third full year on the market.

Opdivo and Keytruda, which had a two-year head start on Tecentriq, achieved sales of $6.7 billion and $7.2 billion respectively in 2018.

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