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Paris (AFP)
While it is commonly believed that breast cancer can be treated well now, this is not the case with so-called “triple negative” cancer, which affects about 15% of patients, or 9,000 new cases per year.
Its characteristic: it does not present any marker (hormone receptors or HER2 protein) on the surface of cancer cells, likely to respond to an existing targeted therapy.
The risk of recurrence is high: 30% within three years of diagnosis.
In the event of recurrence with metastases, the prognosis of this cancer has not improved over the past 20 years for lack of effective therapies: a five-year survival rate of 11.3%.
Affected women are often younger than average (40% are under 40).
Aude Le Roux, 35, is in this case. His “triple negative” cancer, detected in March 2020, has metastasized. Mother of a three-year-old boy, whom she “would like to see grow”, she knows that the months are now numbered for her. The only concrete hope for the moment: the next access in France to a new treatment, the Trodelvy: “it is not the miracle treatment but it will allow to gain months of life”, she says.
This new therapy is an antibody treatment combined with chemotherapy, manufactured by the American laboratory Gilead, which is aimed at women “in treatment failure” after having already received two other treatments.
Study results showed that the median progression-free survival of these tumors was increased by four months and that the median overall survival was doubled (12.1 months, compared to 6.7 months with chemotherapy).
“This is real progress, we have never had such good results in this situation for metastatic triple negative breast cancer,” Delphine Loirat, a medical oncologist at the Curie Institute and principal investigator, told AFP. of the ASCENT study, which evaluated this therapy.
“Urgent need”
The Minister of Health Olivier Véran, recently announced to the National Assembly: the Trodelvy will be available in France with early access from November 1.
Until now, pending the marketing authorization (AMM) by the European Medicines Agency – which has just been given -, nominative temporary authorizations for use (ATU) had been granted in France , benefiting only a few dozen women.
But the country then ran into a supply problem.