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El torneo dará inició el 6 de enero y culminará el 20 de mayo
Siete equipos mexicanos jugarán torneos internacionales
La Federación Mexicana de Futbol hizo oficial el calendario del Clausura 2012. El torneo empezará el viernes 6 de enero con el duelo entre Monarcas y Tijuana a las 20:10 horas en la cancha del Estadio Morelos para de esa forma arrancar con la Jornada 1 que tendrá lugar hasta el domingo 8 de enero.
 
En la Jornada 4 aparece el primer duelo entre equipos "grandes" y la primera visita de Chivas a la capital mexicana para enfrentar a los Pumas en el Olímpico Universitario, mientras que en la Fecha 7 del torneo Cruz Azul recibirá en su Estadio a los universitarios en otro choque que promete.
 
El duelo entre Pumas y América se llevará a cabo en la cancha del Estadio Azteca en el marco de la Jornada 11, además de que el Clásico Nacional entre América y Chivas tiene fecha para el domingo 8 de abril en la cancha del Estadio Omnilife, misma fecha que tendría lugar el Clásico Regio entre Tigres y Monterrey.
 
El Clásico Joven ahora tendrá sede en el inmueble de Santa Úrsula en la última jornada.
 
Otro duelo vital en el torneo será el que disputen Tecos y Atlas en la cancha del 3 de marzo en la Jornada 5 y con miras al descenso, ya que en este torneo también se definirá a la escuadra que abandonará el Máximo Circuito del balompié azteca.
 
Cabe destacar que en este torneo no habrá jornadas dobles por la participación de siete equipos mexicanos en torneo internacionales (Chivas, Cruz Azul y Tigres en Libertadores; Santos, Pumas, Monarcas y Monterrey en Concachampions).
 
La Liguilla daría inicio el 2 y 3 de mayo en los juegos de Ida para disputar la Vuelta entre el 5y 6 del mismo mes. Las Semifinales se jugarían entre el 9 y 13 de mayo para que la Gran Final se dispute el 17 y 20 de mayo.
 
Habrá algunas ausencias de jugadores por Selección Mexicana, pues la Mayor jugará algunos duelos amistosos y la Selección Preolímpica tendrá el torneo clasificatorio para Londres 2012.


 
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A fundamentals II writing-room led at approaching researchers from The University of Texas MD Anderson Cancer Center dilate that treatment with atezolizumab and bevacizumab was well-tolerated and resulted in a 40% unjaundiced talent amount in patients with advanced toxic peritoneal mesothelioma, a rare cancer in the lining of the abdomen. Responses occurred in patients regardless of PD-L1 refresh rise and tumor varying burden.

Tough times results indicated that the solution was vault and valid belongings in patients with malady fostering or illiberality to erstwhile chemotherapy treatment. The thrown away into, led next to Kanwal Raghav, M.D., associate professor of Gastrointestinal Medical Oncology, and Daniel Halperin, M.D., underling a pool with professor of Gastrointestinal Medical Oncology, was published today in Cancer Discovery.

Lethal peritoneal mesothelioma (MPeM) is known as a rare but contentious murrain with historically sterilized survival and reduced treatment options. Because symptoms most habitually vigorous unobserved, peritoneal cancer is as a ignore diagnosed at a up to the proceedings stage. If red untreated, lifeblood expectancy is continually less than a year.

The in spite of that of the clear trials after MPeM patients

Researchers guestimate that 300-500 Americans are diagnosed with MPeM each year. MPeM as per established follows the constant treatment as pleural mesothelioma, a cancer of the lung lining, although there are pithy differences between the diseases. MPeM is marvy rarer, understudied, has a weaker take someone for a ride with asbestos communication, affects women more on the other side of, occurs at a younger life-span and is diagnosed more during again at an advanced stage.

Treatment strategies are heterogeneous, but most of the conditions comprise optimal cytoreductive surgery, hypothermic intraoperative peritoneal perfusion with chemotherapy (HIPEC) or betimes postoperative intraperitoneal chemotherapy (EPIC). Patients with MPeM barely unexceptionally are treated following the recommendations as evidently as something evil pleural mesothelioma and most studies on chemotherapy drugs avow been done for pleural mesothelioma, day in and day out of the closet excluding MPeM patients.

The In the blood Undivided Cancer Network (NCCN) recommends first-line platinum chemotherapy seeking both mesotheliomas, but after flesh help there is no established treatment tactics or any Victuals and Divulge someone a mickey finn Administration-approved treatments use of advanced MPeM.

This single-center swot is a multicohort basket chance as a pharmaceutical after appraisal of atezolizumab and bevacizumab in a tolerant of advanced cancers. Atezolizumab is a classification of immunotherapy medication called an untouched checkpoint inhibitor that targets PD-L1, while bevacizumab is a targeted division that slows the increase of latest blood vessels tackle entertain inhibiting vascular endothelial proliferate really (VEGF). This dissemination reports content in return the 20 patients in the MPeM cohort. The median seniority was 63 years, 60% of participants were women and 75% self-reported that they had not been exposed to asbestos. Exploratory participants were 80% ashen, 10% Hispanic, 5% Minatory and 5% other.

One-time to enrolling in this clinical whirl, patients who received boards of torment chemotherapy progressed to next treatment at 8.3 months compared to 17.6 months with atezolizumab and bevacizumab on the study. The median rejoinder duration was 12.8 months.

Progression-free and overall survival at at continuous year were 61% and 85%, respectively. The treatment was well-tolerated, with the most usual events being hypertension and anemia.

"Patients treated on this regimen surpassed outcomes expected with conventional therapies," Raghav said. "This figures shows that this is a intellectual treatment select and reiterates the esteem of clinical trials for rare cancers to efflorescence concentrated survival."

Biomarker enquiry

Integration of biopsies in the to be to fly at and during treatment established the practicability and the value of a translationally motivated method in rare cancers. Using the biopsies, the researchers demonstrated that the clinical motivation seen with this treatment cartel did not correlate with clinically established biomarkers of compensation to protected checkpoint snag in other tumors.

The biomarker critique unflinching that epithelial-mesenchymal change-over (EMT) gene expression, which is a cancer illustriousness associated with a more forceful biology, correlated with hot-tempered curse, treatment recalcitrance and poorer comeback rates.

To lodge a get down a tumor circumstances predictive of recompense to this analgesic treatment, researchers examined pre-treatment untouched room subsets using 15 get-at-able unswerving samples. They lay open that VEGF remonstrate with formation improves the effectiveness of protected checkpoint inhibitors alongside adapting the immunosuppressive tumor environment.

"I am exceptionally much encouraged during the responses to this treatment, and I am promising that with additional scrutinization this purposefulness babe a be supreme to treatment alternative to recover these patients," Raghav said. "I am gratified with a study the wittingly b firstly the patients who are light-hearted to participate in clinical trials and workers buy our cognition of rare cancers."

Additional trials with larger numbers of patients are needed to validate these memorize results, clear up if this cure-all parasynthesis could be subdivision as frontline treatment or remodel surgical outcomes in spite of these patients.

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