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Sickle cell disease management: Senegal welcomes a new treatment

Auteur: Yandé Diop

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Prise en charge de la drépanocytose : Le Sénégal accueille un nouveau traitement

Senegal has taken a major step forward in the management of sickle cell disease with the arrival of a hydroxyurea formulation (DREPAF). This is a historic turning point for the thousands of patients living with this genetic disease, which is particularly common in West Africa.

The announcement was made during a postgraduate teaching (PGT) course dedicated to sickle cell disease, in the presence of experts from several African and European countries.

Until now, hydroxyurea, despite being considered a standard treatment in OECD countries, remained difficult to access in Senegal: rare, expensive, and, above all, not always available in pharmacies. DREPAF changes the game, enabling continuous and long-term treatment for patients, particularly children, for the first time. "This is a revolution in patient care," stated Professor Bérengère Koehl, emphasizing that this availability "can transform the lives of sickle cell patients in Africa."

Invited from Mali, Professor Nathalie Ayot recalled the long history of delays in the treatment of sickle cell disease on the continent. "The arrival of an effective and accessible molecule is a tremendous joy. It's a thorn removed from the side of African doctors," she declared.

Professor Jacques-Emmanuel from Senegal announced that the country will become the headquarters for regional training programs for healthcare professionals. The goal: to rapidly disseminate the correct use of the medication throughout sub-Saharan Africa. Senegal was chosen as the first country to have the program available, but the ambition is continental: to extend the DREPAF (Regional Training and Development Program for Healthcare Professionals) to the entire region in a short timeframe.

A molecule proven for 75 years

Unlike a new drug, hydroxyurea benefits from decades of scientific experience. Used since the 1950s for other hematological diseases, it has demonstrated its effectiveness in reducing vaso-occlusive crises, hospitalizations, serious complications, and mortality associated with sickle cell disease. It acts on blood cell production, improves circulation, decreases red blood cell adhesion, and increases fetal hemoglobin, thus protecting patients from painful crises.

With the arrival of DREPAF, Senegal is entering a new era in the fight against sickle cell disease. For specialists, this represents a concrete and immediate change: treatments that are available, affordable, and can be administered daily.

"We hope for a clear improvement in the quality of life and survival of patients," concluded Professor Jacques-Emmanuel.

Auteur: Yandé Diop
Publié le: Mercredi 19 Novembre 2025

Commentaires (2)

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    Quantbusiness il y a 10 heures

    Ce traitement que vous decrivez existe ici aux US depuis tres longtemps. Peut etre qu'il a ete homologue en Europe par l'organe de regulation EMA europeen medecice agency je 16 fevrier 2022. Avant il fallait une greffe de moelle osseuse c'etait le soc ou standard of care ou traitement debase ou de reference. Il faut preciser qu'il est destine aux enfants de 12 ans au moins et plus. Il permet de reduire l'anemie hemolytique et la frequence des crises. Cela dit, il existe des cures fonctionelles qui adresse le probleme au niveau genetique. Cette cure vise a corriger le gene defectueux reponsable de ce probleme. Casgevy et Lyfgenia sont des traitements qui sont consideres comme des cures pour cette maladie. Je pense que bientot Lyfgenia sera autorise pour les enfants de moins de 12 ans car il est en test ou phase finale de validation. Lyfgenia a deja ete teste sur cette population avec une efficacite similaire mais le nombre de malades n'etait pas assez suffisant pour valider les statistiques. Vertex et Blurbird sont les cies qui ont developpe ces traitement revolutionaires qui sont l'equivalent d'une cure a cette maladie.

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    Quantbusiness il y a 9 heures

    Ohhhhh j'ai oublie de mentionner que Casgevy et Lyfgenia sont des cure donc un seul traitement suffit pour le reste de la vie du malade. Le suivi des malades qui ont recus ce traitement est documente.

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