Talimogene laherparepvec, sold under the brand name Imlygic, is a biopharmaceutical medication used to treat melanoma that cannot be operated on; it is injected directly into a subset of lesions which generates a systemic immune response against the recipient's cancer. The final four year analysis from the pivotal phase 3 study upon which TVEC was approved by the FDA showed a 31.5% response rate with a 16.9% complete response (CR) rate. There was also a substantial and statistically significant survival benefit in patients with earlier metastatic disease (stages IIIb-IVM1a) and in patients who hadn't received prior systemic treatment for melanoma. The earlier stage group had a reduction in the risk of death of approximately 50% with one in four patients appearing to have met, or be close to be reaching, the medical definition of cure. Real world use of talimogene laherparepvec have shown response rates of up to 88.5% with CR rates of up to 61.5%.
Around half of people treated with talimogene laherparepvec in clinical trials experienced fatigue and chills; around 40% had fever, around 35% had nausea, and around 30% had flu-like symptoms as well as pain at the injection site. The reactions were mild to moderate in severity; 2% of people had severe reactions and these were generally cellulitis.
Talimogene laherparepvec is a genetically engineered herpes virus (an oncolytic herpes virus). Two genes were removed – one that shuts down an individual cell's defenses, and another that helps the virus evade the immune system – and a gene for human GM-CSF was added. The drug works by replicating in cancer cells, causing them to burst; it was also designed to stimulate an immune response against the patient's cancer, which has been demonstrated by multiple pieces of data, including regression of tumors which have not been injected with talimogene laherparepvec.
The drug was created and initially developed by BioVex, Inc. and was continued by Amgen, which acquired BioVex in 2011.
Cette page est générée automatiquement et peut contenir des informations qui ne sont pas correctes, complètes, à jour ou pertinentes par rapport à votre recherche. Il en va de même pour toutes les autres pages de ce site. Veillez à vérifier les informations auprès des sources officielles de l'EPFL.
vignette|340px|Illustration d'un exemple de virothérapie (thérapie génique dans ce cas, utilisant un adénovirus comme vecteur)Un nouveau gène est inséré dans un vecteur qui est un adénovirus modifié, lequel est utilisé pour introduire l'ADN modifié dans une cellule humaine. Si le transfert se déroule correctement, le nouveau gène élaborera une protéine fonctionnelle qui pourra alors exprimer son potentiel thérapeutique.
Un virus oncolytique est un virus qui peut tuer préférentiellement les cellules cancéreuses. Après l'oncolyse des cellules, d'autres particules virales ou virions sont produites, susceptibles de détruire le reste de la tumeur. Le premier cas de virus oncolytique a été décrit dès 1904 : celui d'une patiente atteinte de leucémie myéloïde en rémission après avoir vraisemblablement contracté une grippe. Une étude clinique de 2022 utilise ce type de virus dans les glioblastomes du pont de l'enfant avec des résultats prometteurs.
droite|vignette|340px|Thérapie génique à base d'un vecteur adénovirus (virothérapie). Un nouveau gène est inséré dans un vecteur dérivé d'un adénovirus, lequel est utilisé pour introduire l'ADN modifié dans une cellule humaine. Si le transfert se déroule correctement, le nouveau gène élaborera une protéine fonctionnelle qui pourra alors exprimer son potentiel thérapeutique. vignette|upright=1.5 La thérapie génique ou génothérapie est une stratégie thérapeutique qui consiste à faire pénétrer des gènes dans les cellules ou les tissus d'un individu pour traiter une maladie.
Melanoma causes the vast majority of skin cancer deaths, and there is currently no conventional treatment available that is able to cure metastatic melanoma patients. However, a novel treatment modality has recently emerged: cancer immunotherapy. Cancer im ...
Mutations in nuclear-encoded mitochondrial genes are responsible for a broad spectrum of disorders among which Leigh syndrome is the most common in infancy. No effective therapies are available for this severe disease mainly because of the limited capabili ...
2020
, , , , , ,
In near infrared fluorescence-guided surgical oncology, it is challenging to distinguish healthy from cancerous tissue. One promising research avenue consists in the analysis of the exogenous fluorophores' lifetime, which are however in the (sub-)nanosecon ...