PharmaMar Recibe el Ok de la FDA Para Iniciar Fase I con PM54 en Combi con Inmuno Para Posible Tratamiento . PARA EI RELEVO DE LURBINECTEDIN ESTABAN PM184 Y PM14 AMBOS RETIRADOS POR LA CIA. AHORA HAY OTROS DOS FÁRMACOS EN FASE I EN EL INTENTO DE RELEVAR A LURBINECTEDIN : PM54 Y PM534 ... EL PROBLEMA ES QUE AMBOS AÚN ESTAN EN FASE I CON TODO LO QUE ESTO IMPLICA EN CUESTIÓN DE PLAZOS ... YA QUE PARA REALUZAR 3 FASES CLÍNICAS HACEN FALTA DE 12 A 15 AÑOS ... NOS IRÍAMOS AL 2040.
13 febrero 2020
Lurbinectedin Confers Clinical Benefit in Malignant Pleural Mesothelioma .
Mewire News , 12-02-2020 | Mesothelioma | News .
Lurbinectedin has clinical activity and acceptable toxicity in the second- and third-line treatment of malignant pleural mesothelioma, say phase 2 trial investigators.
The study met its primary endpoint, with just over half of the participants remaining progression-free at 12 weeks, without any new safety signals being observed, they add.
The researchers therefore note: “Lurbinectedin emerges as a new treatment option and evaluation in a larger, randomized trial is warranted.”
Indeed, 54% of the 42 patients given lurbinectedin were progression-free at 12 weeks, and the median progression-free survival (PFS) was 4.1 months. In all, 58.4%, 30.5%, and 12.7% of patients remained free from progression at 3, 6, and 9 months, respectively.
The median overall survival (OS) was 11.1 months, with a respective 73.8% and 44.9% of patients alive at 6 and 12 months. The researchers note that the median OS “came close to the upper limits of any published OS so far.”
One patient each had a complete and partial response to treatment, while 47.6% had stable disease for at least 12 weeks, giving a disease control rate of 52.4%. The median duration of disease control was 6.6 months, with 27.3% of patients displaying disease control for at least 8 months. ...
Lurbinectedin has clinical activity and acceptable toxicity in the second- and third-line treatment of malignant pleural mesothelioma, say phase 2 trial investigators.
The study met its primary endpoint, with just over half of the participants remaining progression-free at 12 weeks, without any new safety signals being observed, they add.
The researchers therefore note: “Lurbinectedin emerges as a new treatment option and evaluation in a larger, randomized trial is warranted.”
Indeed, 54% of the 42 patients given lurbinectedin were progression-free at 12 weeks, and the median progression-free survival (PFS) was 4.1 months. In all, 58.4%, 30.5%, and 12.7% of patients remained free from progression at 3, 6, and 9 months, respectively.
The median overall survival (OS) was 11.1 months, with a respective 73.8% and 44.9% of patients alive at 6 and 12 months. The researchers note that the median OS “came close to the upper limits of any published OS so far.”
One patient each had a complete and partial response to treatment, while 47.6% had stable disease for at least 12 weeks, giving a disease control rate of 52.4%. The median duration of disease control was 6.6 months, with 27.3% of patients displaying disease control for at least 8 months. ...
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