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  • 3 years ago
(Adnkronos) - I pazienti adulti affetti da carcinoma polmonare non a piccole cellule (NSCLC) avanzato, con alterazioni genetiche che causano lo skipping dell’esone 14 del fattore di transizione mesenchimale epiteliale (METex14), hanno una nuova opzione terapeutica. L’Agenzia italiana del farmaco ha infatti ammesso alla rimborsabilità tepotinib, un nuovo farmaco sviluppato da Merck per trattare questo tipo di tumore. 

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00:00 The Italian Pharmaceutical Agency has admitted to the remuneration of tepotinib, the drug
00:09 developed by Merck for the treatment of lung carcinoma not in small cells, advanced with
00:15 genetic alterations that cause the skipping of zone 14 of the mesenchymal-epithelial
00:21 transition factor in adult patients.
00:23 The lung tumor has 40,000 new cases in Italy every year and more than half of these are
00:30 in the advanced stage.
00:31 Of these, about 70% are lung tumors not in small cells and therefore fall into the category
00:41 in which we can apply precision medicine in which we have to identify the predictive biomarkers
00:47 among which MET, this Exon Skipping Mutation of the Met zone, which concerns about 2 to
00:54 4% of patients affected by lung tumor not in small cells in the advanced stage.
01:00 Tepotinib is an inhibitor of the tyrosinkinase of the MET gene, able to block the mechanism
01:06 that the gene implements to grow the tumor.
01:09 Tepotinib acts on a mutation of the zone 14 of the MET gene, has made a very complex
01:16 corporeal study, which is important in its complexity, only the part that concerned
01:23 patients already pre-treated with chemotherapy has been accepted and this was the indication
01:27 that it had then at the European and Italian level.
01:31 So we are talking about patients who have adenocarcinoma diagnosis, receive a first-line
01:36 chemotherapy treatment, when this treatment of first-line chemotherapy ends up working
01:41 the disease increases, the presence of the MET gene, which would have been better to identify
01:45 at the beginning, will allow to use tepotinib and oral Bervia, a daily compress, which has
01:51 the possibility to block this disease for a year, to reduce the dimensions by about
01:59 45% and double the survival of these patients.
02:03 For more than 40 years, Merck has been committed to meet the needs of patients who are not
02:07 satisfied.
02:08 With the launch of tepotinib we are going to satisfy this aspect.
02:14 They are patients who would not have therapeutic alternatives in a pathology such as lung cancer,
02:21 which we know is the first cause of tumors in men and the second in women and above all
02:28 be the first cause of death in men.
02:32 Oncology is now an area of primary interest for Merck.
02:36 Oncology is now an area of absolute interest for Merck and we have, let's say, in assessment
02:44 about 9 compounds out of the 15 components of the Merck Italia pharmaceutical division,
02:49 so you can imagine how important is the commitment on the part of our company within oncology.
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