FDA разрешило испанской компании PharmaMar, подразделению Grupo Zeltia, начать производство препарата PM1183, предназначенного для лечения рака груди и других видов опухолей.
В сообщении PharmaMar говорится, что процесс создания препарата завершен и компания готова к его производству.
Главным из линейки продуктов PharmaMar является онкологический препарат Yondelis, продажи которого в 2013 году составили 73 млн евро, на 10% больше, чем в предыдущем году. В стадии разработки находится серия других противораковых препаратов.
Zeltia SA – испанская группа биофармацевтических компаний, основанная в 1939 году и специализирующаяся в химико-фармацевтической отрасли. В 2013 году компания заняла первое место в биотехнологическом секторе Испании в рейтинге корпоративной репутации MERCO. В 2013 году выручка Zeltia составила 142 млн евро. Прибыль в 2013 году выросла на 72% и составила 16,1 млн евро.
09 abril 2014
Aplidin Hoy en la AACR . Aplidin® se Confirma como un “ First In Class Drug” Destacando por Primera vez su Mecanismo de Acción que Muestra que su Diana Terapéutica en las Células Tumorales es la Proteína eEF1a .
Aporta nuevos datos sobre su mecanismo de acción, destacando la Diana Terapéutica y confirmando su estatus como “ First in Class Drug ”.
Un estudio de Alejandro Losada y cols. (“Role of the eukaryotic elongation factor eEF1A in the mechanism of action of Aplidin”) destaca el importante papel que desempeña el factor de elongación 1A (eEF1A) en la actividad biológica que ejerce el fármaco en las células tumorales. Este trabajo demuestra que células tumorales resistentes a Aplidin® expresan bajos niveles de eEF1A comparadas a células tumorales sensibles al fármaco.
La re-introducción de dicha proteína en las células resistentes hace que estas se vuelvan sensibles al tratamiento.
Se presenta también un modelo molecular demostrando la interacción de Aplidin® con eEF1A.
En definitiva, estos resultados indican que eEF1A es la diana celular de Aplidin®.
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Role of the eukaryotic elongation factor eEF1A in the mechanism of action of Aplidin .
Presentation Time: Wednesday, Apr 09, 2014, 8:00 AM -12:00 PM
Author Block: Alejandro Losada1, Juan F. Martínez-Leal1, Federico Gago2, Carmen Cuevas1, Luis F. Garcia-Fernández1, Carlos M. Galmarini1. 1PharmaMar, S.A., Madrid, Spain; 2Universidad de Alcalá (UAH), Madrid, Spain
Abstract Body: Aplidin is a cyclic depsipeptide of the family of didemnins, originally isolated from the colonial tunicate Aplidium albicans. Aplidin is being evaluated in a phase III clinical trial in patients with relapse or refractory multiple myeloma. As part of its antitumor activity, Aplidin induces rapid oxidative stress, activation of Rac1 and phosphorylation of p38 and JNK1 stress kinases, which together trigger the apoptotic death of tumor cells.
Didemnin B (DB), a molecule closely related to Aplidin, has been previously shown to interact with the GTP-bound conformation of the eukaryotic elongation factor eEF1A, an interaction that was related to the didemnin’s B ability to inhibit protein synthesis (J. Biol. Chem. 1994, 269:15411-14). A structural model for this interaction has been proposed (J. Med. Chem. 2004, 47:4439-52). We wanted to investigate whether eEF1A had any role in the mechanism of action of Aplidin.
Using the DARTS technique, we observed that Aplidin treatment of tumor cells and subsequent digestion of the cellular extracts with different proteases, resulted in a significant increase in the stabililty of eEF1A against protease digestion, suggesting a direct effect of Aplidin on this protein.
We previously generated, by continuous exposure to increasing concentrations of the drug, a HeLa derivative cell line (HeLa-APL-R) that showed specific resistance to Aplidin as well as to other related didemnins and tamandarins (Br. J. Cancer 2004, 91:1405-13). We investigated whether there was any difference in the expression levels of eEF1A between HeLa-wt and HeLa-APL-R cell lines.
Since two isoforms of the elongation factor are expressed in tumor cells, eEF1A1 and eEF1A2, we checked the relative amount of both proteins at the mRNA and protein levels using DNA microarrays and iTRAQ, respectively. Remarkably, we observed that the mRNA and protein levels of eEF1A2 isoform were lower in HeLa-APL-R resistant cells as compared to their parental cell line.
No significant changes were seen in the levels of eEF1A1. The reduced levels of eEF1A2 protein in HeLa-APL-R cells were further confirmed by western blotting using isoform-specific antibodies. To explore the effect of the restoration of the eEF1A2 levels in the HeLa resistant clone, we generated two cell lines stably overexpressing eEF1A1 or eEF1A2 and checked their sensitivity to Aplidin in dose-response cytotoxicity experiments.
Both cell lines partially recovered the sensitivity to Aplidin, with the eEF1A2-overexpressing cell line having an even slightly higher sensitivity to the compound. In eEF1A overexpressing cells, Aplidin induced a robust cytostatic effect. At the molecular level, Aplidin induced the phosphorylation of p38 as well as ERK MAPKs, but not JNK phosphorylation or PARP cleavage, two key events in the cytotoxic signaling of the drug.
These results could indicate a role of eEF1A in the biological activity of Aplidin in tumor cells.
Un estudio de Alejandro Losada y cols. (“Role of the eukaryotic elongation factor eEF1A in the mechanism of action of Aplidin”) destaca el importante papel que desempeña el factor de elongación 1A (eEF1A) en la actividad biológica que ejerce el fármaco en las células tumorales. Este trabajo demuestra que células tumorales resistentes a Aplidin® expresan bajos niveles de eEF1A comparadas a células tumorales sensibles al fármaco.
La re-introducción de dicha proteína en las células resistentes hace que estas se vuelvan sensibles al tratamiento.
Se presenta también un modelo molecular demostrando la interacción de Aplidin® con eEF1A.
En definitiva, estos resultados indican que eEF1A es la diana celular de Aplidin®.
**************************************
Role of the eukaryotic elongation factor eEF1A in the mechanism of action of Aplidin .
Presentation Time: Wednesday, Apr 09, 2014, 8:00 AM -12:00 PM
Author Block: Alejandro Losada1, Juan F. Martínez-Leal1, Federico Gago2, Carmen Cuevas1, Luis F. Garcia-Fernández1, Carlos M. Galmarini1. 1PharmaMar, S.A., Madrid, Spain; 2Universidad de Alcalá (UAH), Madrid, Spain
Abstract Body: Aplidin is a cyclic depsipeptide of the family of didemnins, originally isolated from the colonial tunicate Aplidium albicans. Aplidin is being evaluated in a phase III clinical trial in patients with relapse or refractory multiple myeloma. As part of its antitumor activity, Aplidin induces rapid oxidative stress, activation of Rac1 and phosphorylation of p38 and JNK1 stress kinases, which together trigger the apoptotic death of tumor cells.
Didemnin B (DB), a molecule closely related to Aplidin, has been previously shown to interact with the GTP-bound conformation of the eukaryotic elongation factor eEF1A, an interaction that was related to the didemnin’s B ability to inhibit protein synthesis (J. Biol. Chem. 1994, 269:15411-14). A structural model for this interaction has been proposed (J. Med. Chem. 2004, 47:4439-52). We wanted to investigate whether eEF1A had any role in the mechanism of action of Aplidin.
Using the DARTS technique, we observed that Aplidin treatment of tumor cells and subsequent digestion of the cellular extracts with different proteases, resulted in a significant increase in the stabililty of eEF1A against protease digestion, suggesting a direct effect of Aplidin on this protein.
We previously generated, by continuous exposure to increasing concentrations of the drug, a HeLa derivative cell line (HeLa-APL-R) that showed specific resistance to Aplidin as well as to other related didemnins and tamandarins (Br. J. Cancer 2004, 91:1405-13). We investigated whether there was any difference in the expression levels of eEF1A between HeLa-wt and HeLa-APL-R cell lines.
Since two isoforms of the elongation factor are expressed in tumor cells, eEF1A1 and eEF1A2, we checked the relative amount of both proteins at the mRNA and protein levels using DNA microarrays and iTRAQ, respectively. Remarkably, we observed that the mRNA and protein levels of eEF1A2 isoform were lower in HeLa-APL-R resistant cells as compared to their parental cell line.
No significant changes were seen in the levels of eEF1A1. The reduced levels of eEF1A2 protein in HeLa-APL-R cells were further confirmed by western blotting using isoform-specific antibodies. To explore the effect of the restoration of the eEF1A2 levels in the HeLa resistant clone, we generated two cell lines stably overexpressing eEF1A1 or eEF1A2 and checked their sensitivity to Aplidin in dose-response cytotoxicity experiments.
Both cell lines partially recovered the sensitivity to Aplidin, with the eEF1A2-overexpressing cell line having an even slightly higher sensitivity to the compound. In eEF1A overexpressing cells, Aplidin induced a robust cytostatic effect. At the molecular level, Aplidin induced the phosphorylation of p38 as well as ERK MAPKs, but not JNK phosphorylation or PARP cleavage, two key events in the cytotoxic signaling of the drug.
These results could indicate a role of eEF1A in the biological activity of Aplidin in tumor cells.
PM01183 hoy en la AACR : Potential Use of Pharmacogenomic Modeling for Patient Stratification in the Phase II trial of PM01183 in Pancreatic Cancer .
Un estudio retrospectivo de Manuel Hidalgo y cols. (“Potencial use of pharmacogenomic modelling for patients stratification in the Phase II trial of PM01183 in pancreatic cancer”) destaca la utilidad de los tests genómicos para lograr una mejor estratificación de los pacientes con cáncer de páncreas que son candidatos a tratamiento con el antitumoral PM01183.
En concreto, se han empleado estos tests para evaluar perfiles de quimiosensibilidad, con el objetivo de predecir qué pacientes son susceptibles de ser incluidos en un estudio fase II con PM01183 e, incluso, para predecir la tasa de respuesta.
En este estudio retrospectivo sobre 32 pacientes, los autores concluyeron que 3 pacientes tuvieron un perfil de quimiosensibilidad positivo a PM01183, 2 de los cuales podían presentar una respuesta clínica al PM01183, que fue demostrada finalmente en uno de ellos.
De esta forma, se reafirma la hipótesis de que estas técnicas de evaluación de la quimiosensibilidad podrían ser útiles, en el futuro, para mejorar la selección de los pacientes que pudieran participar en los ensayos clínicos de este fármaco.
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Presentation Time: Wednesday, Apr 09, 2014, 8:00 AM -12:00 PM
Author Block:
Manuel Hidalgo, Mark Ricigliano, Brandon Cooper, Miguel Aracil Avilla, Carlos Galmarini.Spanish National Cancer Ctr. (CNIO), Madrid, Spain; CellPath Therapeutics, Inc, Rockville, MD; PharmaMar, Madrid, Spain
Abstract Body:
Background:
Pharmacogenomic assays (PGx) can be effectively used to enrich a patient population for a clinical trial. Only those patients predicted to respond a priori to a chemotherapeutic either as a single-agent or in combination should be enrolled. Critical data obtained from patient stratification based on chemosensitivity profiles can be used to further develop companion diagnostics and inform future drug development strategy.
The objective of this retrospective study was to evaluate if chemosensitivity profiles could have been used to predict the enrollment status and overall response rate of 32 study participants in the Phase II trial of PM01183 in pancreatic cancer. Methods.
Patients with pancreatic adenocarcinoma who progressed following 1st line gemcitabine treatment were enrolled and venous blood was collected in a standard 10 ml sodium heparin Vacutainer tube. Circulating tumor and invasive cells (CTIC) were isolated using a modified cell invasion assay (Vitatex, Stony Brook, NY), and RNA from the isolated CTICs was extracted for microarray gene-expression analysis (Affymetrix, Santa Clara CA). Tumor growth inhibition data from 24 cancer cell lines was obtained and was used to construct the PGx model of PM01183.
Chemosensitivity profiles for each patient based on 10 chemotherapeutics was determined using proprietary software (CellPath Therapeutics, Inc. Baltimore, MD). Non-parametric rank correlation was then used to obtain an R-value of the patient sensitivity profile compared to the PM01183 template to determine enrollment status. Only patients with a positive correlated chemosensitivity profile (R+) to the PM01183 template should have been enrolled in the study.
Results:
Three patients (9%) presented a sensitivity profile that was R+ to the PM01183 template and would have been enrolled if the chemosensitivity profile assay were used prospectively. Of the three patients selected, only two patients presented an R-value > 0.20 which would have indicated a potential clinical response to PM01183. Of the two patients selected as potential responders, one patient clinically demonstrated a PR.
Conclusion :
The chemosensitivity profile assay for PM01183 correctly identified the one PR in the 32 patients cohort. These data warrant further efforts to confirm the potential of the chemosensitivity profile in a larger series of patients and disease types. If confirmed, this technique could be useful to guide patient recruitment in clinical trials.
En concreto, se han empleado estos tests para evaluar perfiles de quimiosensibilidad, con el objetivo de predecir qué pacientes son susceptibles de ser incluidos en un estudio fase II con PM01183 e, incluso, para predecir la tasa de respuesta.
En este estudio retrospectivo sobre 32 pacientes, los autores concluyeron que 3 pacientes tuvieron un perfil de quimiosensibilidad positivo a PM01183, 2 de los cuales podían presentar una respuesta clínica al PM01183, que fue demostrada finalmente en uno de ellos.
De esta forma, se reafirma la hipótesis de que estas técnicas de evaluación de la quimiosensibilidad podrían ser útiles, en el futuro, para mejorar la selección de los pacientes que pudieran participar en los ensayos clínicos de este fármaco.
*********************************************
Presentation Time: Wednesday, Apr 09, 2014, 8:00 AM -12:00 PM
Author Block:
Manuel Hidalgo, Mark Ricigliano, Brandon Cooper, Miguel Aracil Avilla, Carlos Galmarini.Spanish National Cancer Ctr. (CNIO), Madrid, Spain; CellPath Therapeutics, Inc, Rockville, MD; PharmaMar, Madrid, Spain
Abstract Body:
Background:
Pharmacogenomic assays (PGx) can be effectively used to enrich a patient population for a clinical trial. Only those patients predicted to respond a priori to a chemotherapeutic either as a single-agent or in combination should be enrolled. Critical data obtained from patient stratification based on chemosensitivity profiles can be used to further develop companion diagnostics and inform future drug development strategy.
The objective of this retrospective study was to evaluate if chemosensitivity profiles could have been used to predict the enrollment status and overall response rate of 32 study participants in the Phase II trial of PM01183 in pancreatic cancer. Methods.
Patients with pancreatic adenocarcinoma who progressed following 1st line gemcitabine treatment were enrolled and venous blood was collected in a standard 10 ml sodium heparin Vacutainer tube. Circulating tumor and invasive cells (CTIC) were isolated using a modified cell invasion assay (Vitatex, Stony Brook, NY), and RNA from the isolated CTICs was extracted for microarray gene-expression analysis (Affymetrix, Santa Clara CA). Tumor growth inhibition data from 24 cancer cell lines was obtained and was used to construct the PGx model of PM01183.
Chemosensitivity profiles for each patient based on 10 chemotherapeutics was determined using proprietary software (CellPath Therapeutics, Inc. Baltimore, MD). Non-parametric rank correlation was then used to obtain an R-value of the patient sensitivity profile compared to the PM01183 template to determine enrollment status. Only patients with a positive correlated chemosensitivity profile (R+) to the PM01183 template should have been enrolled in the study.
Results:
Three patients (9%) presented a sensitivity profile that was R+ to the PM01183 template and would have been enrolled if the chemosensitivity profile assay were used prospectively. Of the three patients selected, only two patients presented an R-value > 0.20 which would have indicated a potential clinical response to PM01183. Of the two patients selected as potential responders, one patient clinically demonstrated a PR.
Conclusion :
The chemosensitivity profile assay for PM01183 correctly identified the one PR in the 32 patients cohort. These data warrant further efforts to confirm the potential of the chemosensitivity profile in a larger series of patients and disease types. If confirmed, this technique could be useful to guide patient recruitment in clinical trials.
Eli Lilly y Takeda reciben Multa de 3.000 y 6.000 Millones $ respectivamente ... por Ocultar los riesgos de cáncer de su medicamento para la diabetes Actos.
El jurado de la ciudad de Lafayette, en Luisiana, ordenó que la empresa japonesa Takeda, con sede en Osaka, pague 6.000 millones de dólares, en tanto que a su socia Eli Lilly, con sede en Indianápolis (Indiana) le impuso otra de 3.000 millones.
“Yo espero que los ejecutivos de Takeda en Japón escuchen claramente lo que este jurado ha dicho”, declaró Mark Lanier, abogado de Terrence Allen, afectado por tomar el medicamento contra la diabetes Actos, que según las autoridades sanitarias puede aumentar el riesgo de contraer cáncer de vejiga.
El jurado ya había otorgado 1.500 millones de dólares en daños compensatorios a Terrence Allen, que culpa al medicamento de haber desarrollado cáncer de vejiga.
La adjudicación de 9.000 millones de dólares por parte del jurado es una de las más grandes en la historia de Estados Unidos, pero es probable que se reduzca porque el Tribunal Supremo de Justicia ha dictaminado que los daños punitivos, impuestos por mala práctica, deben ser proporcionales a las compensaciones por daños.
...
“Yo espero que los ejecutivos de Takeda en Japón escuchen claramente lo que este jurado ha dicho”, declaró Mark Lanier, abogado de Terrence Allen, afectado por tomar el medicamento contra la diabetes Actos, que según las autoridades sanitarias puede aumentar el riesgo de contraer cáncer de vejiga.
El jurado ya había otorgado 1.500 millones de dólares en daños compensatorios a Terrence Allen, que culpa al medicamento de haber desarrollado cáncer de vejiga.
La adjudicación de 9.000 millones de dólares por parte del jurado es una de las más grandes en la historia de Estados Unidos, pero es probable que se reduzca porque el Tribunal Supremo de Justicia ha dictaminado que los daños punitivos, impuestos por mala práctica, deben ser proporcionales a las compensaciones por daños.
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Café . Efectos de la cafeína contra el Alzheimer, según estudio francés .
(Alemania, 8 abril. DPA). - ¿Cafeína contra el olvido? El café ayuda a la concentración y a mantenerse despierto. Sin embargo, parece que sus efectos no se quedan ahí. De acuerdo a un estudio publicado hoy por la Universidad de Bonn y Lille (Francia) la cafeína ayudaría también a largo plazo contra el Alzheimer.
El equipo de investigación de las dos universidades descubrió en sus ensayos de laboratorio con ratones que una sustancia activa parecida a la cafeína impide el almacenamiento de la proteína Tau en el cerebro. El depósito de esas proteínas Tau es uno de los dos indicadores principales de la enfermedad de Alzheimer.
El efecto positivo de la cafeína en otros indicadores como la proteína Beta-amiloide, uno de los principales responsables del Alzheimer, ya se ha probado con anterioridad en ratones. En esos estudios la cafeína redujo de forma significativa los niveles anormales de proteína Beta-amiloide.
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El equipo de investigación de las dos universidades descubrió en sus ensayos de laboratorio con ratones que una sustancia activa parecida a la cafeína impide el almacenamiento de la proteína Tau en el cerebro. El depósito de esas proteínas Tau es uno de los dos indicadores principales de la enfermedad de Alzheimer.
El efecto positivo de la cafeína en otros indicadores como la proteína Beta-amiloide, uno de los principales responsables del Alzheimer, ya se ha probado con anterioridad en ratones. En esos estudios la cafeína redujo de forma significativa los niveles anormales de proteína Beta-amiloide.
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