4 TRATAMIENTOS SCLC-ES EN 1.ª LINE EN EUROPA : ATEZOLIZUMAB, DURVALUMAB ,SERPLULIMAB Y TISLELIZUMAB.
LURBINECTEDIN CON IMFORTE TODO EL MUNDO SABE QUE DE APROBARSE NO SERÍA PARA TRATAMIENTO DE PRIMERA LÍNEA .... SINO QUE SERÍA PARA EL MANTENIMIENTO EN EL ENTORNO DE PRIMERA LÍNEA ... O SEA SERÍA UN TRATAMIENTO TRAS LA PRIMERA LÍNEA DE INDUCCIÓN ... PARA QUE LOS PACIENTES NO SE VAYAN A SEGUNDA LÍNEA .
04 marzo 2019
Leiomyosarcoma . A patient-derived orthotopic xenograft (PDOX) nude-mouse model precisely identifies effective and ineffective therapies for recurrent leiomyosarcoma
Science Direct , en su edición de Abril 2019 , publica un Extenso Articulo en el que se Presentan los Resultados de un Ensayo Inicial para el Tratamiento de Leiomyosarcomas Modelo PDOX con varios de los actuales Farmacos : Yondelis , Gemcitabine combinado con Docetaxel , Temozolomide , Doxorubicin , Pazopanib y Olaratumab .
Resultaron Altamente Efectivos : Yondelis , Gemcitabine combinado con Docetaxel y Temozolomide .
El resto de Fármacos ( Pazopànib , Olaratumab y Doxorubin ) resultaron Ineficazes . A tener en cuenta que Doxorubicina resulta ser el Tratamiento Actual en Primera línea .
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Pharmacological Research , Volume 142, April 2019, Pages 169-175.
A patient-derived orthotopic xenograft (PDOX) nude-mouse model precisely identifies effective and ineffective therapies for recurrent Leiomyosarcoma .
Authors
Zhang Z1, Hu K2, Kiyuna T3, Miyake K3, Kawaguchi K3, Igarashi K3, Nelson SD4, Li Y4, Singh SR5, Hoffman RM6.
Author information
1
AntiCancer, Inc., 7917 Ostrow Street, San Diego, CA 92111, USA; Department of Surgery, University of California San Diego, CA 92103, USA; Department of Oncology, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, China.
2
Department of Oncology, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, China.
3
AntiCancer, Inc., 7917 Ostrow Street, San Diego, CA 92111, USA; Department of Surgery, University of California San Diego, CA 92103, USA.
4
Department of Pathology, University of California, Los Angeles, CA 90095, USA.
5
Basic Research Laboratory, National Cancer Institute, Frederick, MD 21702, USA.
6
AntiCancer, Inc., 7917 Ostrow Street, San Diego, CA 92111, USA; Department of Surgery, University of California San Diego, CA 92103, USA.
Abstract
Leiomyosarcoma is a rare and recalcitrant disease. Doxorubicin (DOX) is usually considered first-line treatment for this disease, but frequently is ineffective. In order to individualize therapy for this and other cancers, we have developed the patient-derived orthotopic xenograft (PDOX) mouse model. In the present study, we implanted a recurrent leiomyosarcoma from a resected tumor from the patient's thigh into the femoral muscle of nude mice.
The Following Drugs Were Tested on the Leiomyosarcoma PDOX Model: DOX, The Combination of Gemcitabine (GEM) and Docetaxel (DOC), Trabectedin (TRA), Temozolomide (TEM), Pazopanib (PAZ) and Olaratumab (OLA).
Of These Agents GEM/DOC, TRA and TEM Were Highly Effective in the Leiomyosarcoma PDOX model, The Other Agents, Including First-Line Therapy DOX,Were Ineffective.
Thus the leiomyosarcoma PDOX model could precisely distinguish effective and ineffective drugs, demonstrating the potential of the PDOX model for leiomyosarcoma.
Copyright © 2019. Published by Elsevier Ltd.
El resto de Fármacos ( Pazopànib , Olaratumab y Doxorubin ) resultaron Ineficazes . A tener en cuenta que Doxorubicina resulta ser el Tratamiento Actual en Primera línea .
***************************
Pharmacological Research , Volume 142, April 2019, Pages 169-175.
A patient-derived orthotopic xenograft (PDOX) nude-mouse model precisely identifies effective and ineffective therapies for recurrent Leiomyosarcoma .
Authors
Zhang Z1, Hu K2, Kiyuna T3, Miyake K3, Kawaguchi K3, Igarashi K3, Nelson SD4, Li Y4, Singh SR5, Hoffman RM6.
Author information
1
AntiCancer, Inc., 7917 Ostrow Street, San Diego, CA 92111, USA; Department of Surgery, University of California San Diego, CA 92103, USA; Department of Oncology, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, China.
2
Department of Oncology, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, China.
3
AntiCancer, Inc., 7917 Ostrow Street, San Diego, CA 92111, USA; Department of Surgery, University of California San Diego, CA 92103, USA.
4
Department of Pathology, University of California, Los Angeles, CA 90095, USA.
5
Basic Research Laboratory, National Cancer Institute, Frederick, MD 21702, USA.
6
AntiCancer, Inc., 7917 Ostrow Street, San Diego, CA 92111, USA; Department of Surgery, University of California San Diego, CA 92103, USA.
Abstract
Leiomyosarcoma is a rare and recalcitrant disease. Doxorubicin (DOX) is usually considered first-line treatment for this disease, but frequently is ineffective. In order to individualize therapy for this and other cancers, we have developed the patient-derived orthotopic xenograft (PDOX) mouse model. In the present study, we implanted a recurrent leiomyosarcoma from a resected tumor from the patient's thigh into the femoral muscle of nude mice.
The Following Drugs Were Tested on the Leiomyosarcoma PDOX Model: DOX, The Combination of Gemcitabine (GEM) and Docetaxel (DOC), Trabectedin (TRA), Temozolomide (TEM), Pazopanib (PAZ) and Olaratumab (OLA).
Of These Agents GEM/DOC, TRA and TEM Were Highly Effective in the Leiomyosarcoma PDOX model, The Other Agents, Including First-Line Therapy DOX,Were Ineffective.
Thus the leiomyosarcoma PDOX model could precisely distinguish effective and ineffective drugs, demonstrating the potential of the PDOX model for leiomyosarcoma.
Copyright © 2019. Published by Elsevier Ltd.
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