297 research outputs found

    El TriĂĄsico de la regiĂłn de Monterde-Alhama de AragĂłn (Provincia de Zaragoza)

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    Se estudian los materiales en facies Buntsandstein y Muschelkalk de los afloramientos triĂĄsicos situados entre Monterde y el Norte de Alhama de AragĂłn. Para ello se han levantado siete columnas estratigrĂĄficas, habiĂ©ndose obtenido dos de ellas con un mayor detalle. DespuĂ©s de establecerse seis grandes tramos (unidades litoestratigrĂĄficas informales), claramente diferenciables, se estudian las variaciones verticales dentro de cada uno de ellos, asĂ­ como las relaciones entre los mismos. En las reconstrucciones paleogeogrĂĄficas y en la evoluciĂłn sedimentaria> se resalta tanto la existencia de importantes umbrales durante la gĂ©nesis de las tres unidades inferiores, como la transiciĂłn gradual de depĂłsitos marinos a continentales, y la presencia de interrupciones sedimentarias que, a veces, originan paleosuelos bien desarrollados. [RÉSUMÉ] On a studiĂ© les materiaux en faciĂ©s Buntsandstein et Muschelkalk des afleurments triassiques compris entre Monterde et le nord d'Alhama de AragĂłn. On a levĂ© sept colonnes, dont deux en dĂ©taille. AprĂ©s avoir Ă©tabli six unitĂ©s litostratigraphiques informelles trĂ©s differentes, on a Ă©tudiĂ© les variations verticales de chaque une ainsi que ses relations mutuelles. On fait sortir des importants seuils pendant la genĂ©se des trois unitĂ©s inferieures par les reconstructions palĂ©ogĂ©ographiques et l'evolution sĂ©dimentaire, ainsi que la transition paulatine des dĂ©pots continentaux a marins et divers interruptions de la sedimentation, soulignĂ©s parfois par des paleochenaux. [AB5TRACT] The Buntsandstein and Muschelkalk facies have been surveyed in the outcrops between Monterde and the North of Alhama de AragĂłn. Seven stratigraphic sections have been studied, two in greater detail. After stablishing six informal lithostratigraphical units, very different each other, thcir vertical variations are studied as well as their mutual relations. The palaeogeogi-aphic reconstructions and the sedinĂ­entary evolution point out the existence of several shoals during tSe genesis of tSe three lower units as well as tSe transition from continental to marine deposits and several sedimentary breaks, sometimes niarked by paleosoils

    Geological factors of the Guadalajara landscapes (Central Spain) and their relevance to landscape studies

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    The landscapes of a territory are the consequence of its history; overlapped geological, vegetable and cultural histories usually exist on a landscape. At the Mediterranean domain, however, a translucent vegetation exists, and its history is closely related to the geologic and cultural histories, because low-technology agricultural uses on a different hardness rock background control vegetation. Thus, in areas like the Guadalajara province, the geologic composition and the human activities can be considered the primary conditions for landscape configuration. Both condition the typologies, distribution and relative importance of the geotic, biotic and anthropogenic components of landscapes. A complex network of interrelations among all them exists but, in the base of which lie the geology of the territory, included relief, because it has amore independent influence since man cannot modify the geologic factors; such as the colour of the rocks, the size and distribution of rock bodies, the palaeogeographic domains and the tectonic structure all which control landscape development and configuration. Moreover, geology influences conditions and even limit, the presence, typologies and development of the biotic and anthropogenic elements. These factors also have a major relevance for environmental management, educational and economic policy, and, in some cases, for environmental impact assessment.Depto. de GeodinĂĄmica, EstratigrafĂ­a y PaleontologĂ­aFac. de Ciencias GeolĂłgicasTRUEpu

    Geological factors of the Guadalajara landscapes (Central Spain) and their relevance to landscape studies

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    The landscapes of a territory are the consequence of its history; overlapped geological, vegetable and cultural histories usually exist on a landscape. At the Mediterranean domain, however, a translucent vegetation exists, and its history is closely related to the geologic and cultural histories, because low-technology agricultural uses on a different hardness rock background control vegetation. Thus, in areas like the Guadalajara province, the geologic composition and the human activities can be considered the primary conditions for landscape configuration. Both condition the typologies, distribution and relative importance of the geotic, biotic and anthropogenic components of landscapes. A complex network of interrelations among all them exists but, in the base of which lie the geology of the territory, included relief, because it has amore independent influence since man cannot modify the geologic factors; such as the colour of the rocks, the size and distribution of rock bodies, the palaeogeographic domains and the tectonic structure all which control landscape development and configuration. Moreover, geology influences conditions and even limit, the presence, typologies and development of the biotic and anthropogenic elements. These factors also have a major relevance for environmental management, educational and economic policy, and, in some cases, for environmental impact assessment

    First Latin American clinical practice guidelines for the treatment of systemic lupus erythematosus: Latin American Group for the Study of Lupus (GLADEL, Grupo Latino Americano de Estudio del Lupus)-Pan-American League of Associations of Rheumatology (PANLAR)

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    Systemic lupus erythematosus (SLE), a complex and heterogeneous autoimmune disease, represents a significant challenge for both diagnosis and treatment. Patients with SLE in Latin America face special problems that should be considered when therapeutic guidelines are developed. The objective of the study is to develop clinical practice guidelines for Latin American patients with lupus. Two independent teams (rheumatologists with experience in lupus management and methodologists) had an initial meeting in Panama City, Panama, in April 2016. They selected a list of questions for the clinical problems most commonly seen in Latin American patients with SLE. These were addressed with the best available evidence and summarised in a standardised format following the Grading of Recommendations Assessment, Development and Evaluation approach. All preliminary findings were discussed in a second face-to-face meeting in Washington, DC, in November 2016. As a result, nine organ/system sections are presented with the main findings; an 'overarching' treatment approach was added. Special emphasis was made on regional implementation issues. Best pharmacologic options were examined for musculoskeletal, mucocutaneous, kidney, cardiac, pulmonary, neuropsychiatric, haematological manifestations and the antiphospholipid syndrome. The roles of main therapeutic options (ie, glucocorticoids, antimalarials, immunosuppressant agents, therapeutic plasma exchange, belimumab, rituximab, abatacept, low-dose aspirin and anticoagulants) were summarised in each section. In all cases, benefits and harms, certainty of the evidence, values and preferences, feasibility, acceptability and equity issues were considered to produce a recommendation with special focus on ethnic and socioeconomic aspects. Guidelines for Latin American patients with lupus have been developed and could be used in similar settings.Fil: Pons Estel, Bernardo A.. Centro Regional de Enfermedades Autoinmunes y ReumĂĄticas; ArgentinaFil: Bonfa, Eloisa. Universidade de Sao Paulo; BrasilFil: Soriano, Enrique R.. Instituto Universitario Hospital Italiano de Buenos Aires. Rectorado.; ArgentinaFil: Cardiel, Mario H.. Centro de InvestigaciĂłn ClĂ­nica de Morelia; MĂ©xicoFil: Izcovich, Ariel. Hospital AlemĂĄn; ArgentinaFil: Popoff, Federico. Hospital Aleman; ArgentinaFil: Criniti, Juan M.. Hospital AlemĂĄn; ArgentinaFil: VĂĄsquez, Gloria. Universidad de Antioquia; ColombiaFil: Massardo, Loreto. Universidad San SebastiĂĄn; ChileFil: Duarte, Margarita. Hospital de ClĂ­nicas; ParaguayFil: Barile Fabris, Leonor A.. Hospital Angeles del Pedregal; MĂ©xicoFil: GarcĂ­a, Mercedes A.. Universidad de Buenos Aires. Facultad de Medicina. Hospital de ClĂ­nicas General San MartĂ­n; ArgentinaFil: Amigo, Mary Carmen. Centro MĂ©dico Abc; MĂ©xicoFil: Espada, Graciela. Gobierno de la Ciudad de Buenos Aires. Hospital General de Niños "Ricardo GutiĂ©rrez"; ArgentinaFil: Catoggio, Luis J.. Hospital Italiano. Instituto Universitario. Escuela de Medicina; ArgentinaFil: Sato, Emilia Inoue. Universidade Federal de Sao Paulo; BrasilFil: Levy, Roger A.. Universidade do Estado de Rio do Janeiro; BrasilFil: Acevedo VĂĄsquez, Eduardo M.. Universidad Nacional Mayor de San Marcos; PerĂșFil: ChacĂłn DĂ­az, Rosa. PoliclĂ­nica MĂ©ndez GimĂłn; VenezuelaFil: Galarza Maldonado, Claudio M.. CorporaciĂłn MĂ©dica Monte SinaĂ­; EcuadorFil: Iglesias Gamarra, Antonio J.. Universidad Nacional de Colombia; ColombiaFil: Molina, JosĂ© Fernando. Centro Integral de ReumatologĂ­a; ColombiaFil: Neira, Oscar. Universidad de Chile; ChileFil: Silva, ClĂłvis A.. Universidade de Sao Paulo; BrasilFil: Vargas Peña, Andrea. Hospital Pasteur Montevideo; UruguayFil: GĂłmez Puerta, JosĂ© A.. Hospital Clinic Barcelona; EspañaFil: Scolnik, Marina. Instituto Universitario Hospital Italiano de Buenos Aires. Rectorado.; ArgentinaFil: Pons Estel, Guillermo J.. Centro Regional de Enfermedades Autoinmunes y ReumĂĄticas; Argentina. Hospital Provincial de Rosario; ArgentinaFil: Ugolini Lopes, Michelle R.. Universidade de Sao Paulo; BrasilFil: Savio, VerĂłnica. Instituto Universitario Hospital Italiano de Buenos Aires. Rectorado.; ArgentinaFil: Drenkard, Cristina. University of Emory; Estados UnidosFil: Alvarellos, Alejandro J.. Hospital Privado Universitario de CĂłrdoba; ArgentinaFil: Ugarte Gil, Manuel F.. Universidad Cientifica del Sur; PerĂș. Hospital Nacional Guillermo Almenara Irigoyen; PerĂșFil: Babini, Alejandra. Instituto Universitario Hospital Italiano de Buenos Aires. Rectorado.; ArgentinaFil: Cavalcanti, AndrĂ©. Universidade Federal de Pernambuco; BrasilFil: Cardoso Linhares, Fernanda Athayde. Hospital Pasteur Montevideo; UruguayFil: Haye Salinas, Maria Jezabel. Hospital Privado Universitario de CĂłrdoba; ArgentinaFil: Fuentes Silva, Yurilis J.. Universidad de Oriente - NĂșcleo BolĂ­var; VenezuelaFil: Montandon De Oliveira E Silva, Ana Carolina. Universidade Federal de GoiĂĄs; BrasilFil: Eraso Garnica, Ruth M.. Universidad de Antioquia; ColombiaFil: Herrera Uribe, SebastiĂĄn. Hospital General de Medellin Luz Castro de GutiĂ©rrez; ColombiaFil: GĂłmez MartĂ­n, DIana. Instituto Nacional de la NutriciĂłn Salvador Zubiran; MĂ©xicoFil: Robaina Sevrini, Ricardo. Universidad de la RepĂșblica; UruguayFil: Quintana, Rosana M.. Hospital Provincial de Rosario; Argentina. Centro Regional de Enfermedades Autoinmunes y ReumĂĄticas; ArgentinaFil: Gordon, Sergio. Hospital Interzonal General de Agudos Dr Oscar Alende. Unidad de ReumatologĂ­a y Enfermedades Autoinmunes SistĂ©micas; ArgentinaFil: Fragoso Loyo, Hilda. Instituto Nacional de la NutriciĂłn Salvador Zubiran; MĂ©xicoFil: Rosario, Violeta. Hospital Docente Padre Billini; RepĂșblica DominicanaFil: Saurit, VerĂłnica. Hospital Privado Universitario de CĂłrdoba; ArgentinaFil: Appenzeller, Simone. Universidade Estadual de Campinas; BrasilFil: Dos Reis Neto, Edgard Torres. Universidade Federal de Sao Paulo; BrasilFil: Cieza, Jorge. Hospital Nacional Edgardo Rebagliati Martins; PerĂșFil: GonzĂĄlez Naranjo, Luis A.. Universidad de Antioquia; ColombiaFil: GonzĂĄlez Bello, Yelitza C.. Ceibac; MĂ©xicoFil: Collado, MarĂ­a Victoria. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones MĂ©dicas; ArgentinaFil: Sarano, Judith. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones MĂ©dicas; ArgentinaFil: Retamozo, Maria Soledad. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas. Centro CientĂ­fico TecnolĂłgico Conicet - CĂłrdoba. Instituto de Investigaciones en Ciencias de la Salud. Universidad Nacional de CĂłrdoba. Instituto de Investigaciones en Ciencias de la Salud; ArgentinaFil: Sattler, MarĂ­a E.. Provincia de Buenos Aires. Ministerio de Salud. Hospital Interzonal de Agudos "Eva PerĂłn"; ArgentinaFil: Gamboa CĂĄrdenas, Rocio V.. Hospital Nacional Guillermo Almenara Irigoyen; PerĂșFil: Cairoli, Ernesto. Universidad de la RepĂșblica; UruguayFil: Conti, Silvana M.. Hospital Provincial de Rosario; ArgentinaFil: Amezcua Guerra, Luis M.. Instituto Nacional de Cardiologia Ignacio Chavez; MĂ©xicoFil: Silveira, Luis H.. Instituto Nacional de Cardiologia Ignacio Chavez; MĂ©xicoFil: Borba, Eduardo F.. Universidade de Sao Paulo; BrasilFil: Pera, Mariana A.. Hospital Interzonal General de Agudos General San MartĂ­n; ArgentinaFil: Alba Moreyra, Paula B.. Universidad Nacional de CĂłrdoba. Facultad de Medicina; ArgentinaFil: Arturi, Valeria. Hospital Interzonal General de Agudos General San MartĂ­n; ArgentinaFil: Berbotto, Guillermo A.. Provincia de Buenos Aires. Ministerio de Salud. Hospital Interzonal de Agudos "Eva PerĂłn"; ArgentinaFil: Gerling, Cristian. Hospital Interzonal General de Agudos Dr Oscar Alende. Unidad de ReumatologĂ­a y Enfermedades Autoinmunes SistĂ©micas; ArgentinaFil: Gobbi, Carla Andrea. Universidad Nacional de CĂłrdoba. Facultad de Medicina; Argentina. Consejo Nacional de Investigaciones CientĂ­ficas y TĂ©cnicas; ArgentinaFil: Gervasoni, Viviana L.. Hospital Provincial de Rosario; ArgentinaFil: Scherbarth, Hugo R.. Hospital Interzonal General de Agudos Dr Oscar Alende. Unidad de ReumatologĂ­a y Enfermedades Autoinmunes SistĂ©micas; ArgentinaFil: Brenol, JoĂŁo C. Tavares. Hospital de Clinicas de Porto Alegre; BrasilFil: Cavalcanti, Fernando. Universidade Federal de Pernambuco; BrasilFil: Costallat, Lilian T. Lavras. Universidade Estadual de Campinas; BrasilFil: Da Silva, Nilzio A.. Universidade Federal de GoiĂĄs; BrasilFil: Monticielo, Odirlei A.. Hospital de Clinicas de Porto Alegre; BrasilFil: Seguro, Luciana Parente Costa. Universidade de Sao Paulo; BrasilFil: Xavier, Ricardo M.. Hospital de Clinicas de Porto Alegre; BrasilFil: Llanos, Carolina. Universidad CatĂłlica de Chile; ChileFil: MontĂșfar Guardado, RubĂ©n A.. Instituto Salvadoreño de la Seguridad Social; El SalvadorFil: Garcia De La Torre, Ignacio. Hospital General de Occidente; MĂ©xicoFil: Pineda, Carlos. Instituto Nacional de RehabilitaciĂłn; MĂ©xicoFil: Portela HernĂĄndez, Margarita. Umae Hospital de Especialidades Centro Medico Nacional Siglo Xxi; MĂ©xicoFil: Danza, Alvaro. Hospital Pasteur Montevideo; UruguayFil: Guibert Toledano, Marlene. Medical-surgical Research Center; CubaFil: Reyes, Gil Llerena. Medical-surgical Research Center; CubaFil: Acosta Colman, Maria Isabel. Hospital de ClĂ­nicas; ParaguayFil: Aquino, Alicia M.. Hospital de ClĂ­nicas; ParaguayFil: Mora Trujillo, Claudia S.. Hospital Nacional Edgardo Rebagliati Martins; PerĂșFil: Muñoz Louis, Roberto. Hospital Docente Padre Billini; RepĂșblica DominicanaFil: GarcĂ­a Valladares, Ignacio. Centro de Estudios de InvestigaciĂłn BĂĄsica y ClĂ­nica; MĂ©xicoFil: Orozco, MarĂ­a Celeste. Instituto de RehabilitaciĂłn PsicofĂ­sica; ArgentinaFil: Burgos, Paula I.. Pontificia Universidad CatĂłlica de Chile; ChileFil: Betancur, Graciela V.. Instituto de RehabilitaciĂłn PsicofĂ­sica; ArgentinaFil: AlarcĂłn, Graciela S.. Universidad Peruana Cayetano Heredia; PerĂș. University of Alabama at Birmingahm; Estados Unido

    Reducing the environmental impact of surgery on a global scale: systematic review and co-prioritization with healthcare workers in 132 countries

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    Abstract Background Healthcare cannot achieve net-zero carbon without addressing operating theatres. The aim of this study was to prioritize feasible interventions to reduce the environmental impact of operating theatres. Methods This study adopted a four-phase Delphi consensus co-prioritization methodology. In phase 1, a systematic review of published interventions and global consultation of perioperative healthcare professionals were used to longlist interventions. In phase 2, iterative thematic analysis consolidated comparable interventions into a shortlist. In phase 3, the shortlist was co-prioritized based on patient and clinician views on acceptability, feasibility, and safety. In phase 4, ranked lists of interventions were presented by their relevance to high-income countries and low–middle-income countries. Results In phase 1, 43 interventions were identified, which had low uptake in practice according to 3042 professionals globally. In phase 2, a shortlist of 15 intervention domains was generated. In phase 3, interventions were deemed acceptable for more than 90 per cent of patients except for reducing general anaesthesia (84 per cent) and re-sterilization of ‘single-use’ consumables (86 per cent). In phase 4, the top three shortlisted interventions for high-income countries were: introducing recycling; reducing use of anaesthetic gases; and appropriate clinical waste processing. In phase 4, the top three shortlisted interventions for low–middle-income countries were: introducing reusable surgical devices; reducing use of consumables; and reducing the use of general anaesthesia. Conclusion This is a step toward environmentally sustainable operating environments with actionable interventions applicable to both high– and low–middle–income countries

    El Triåsico de los alrededores de Nuevalos (Zona de Monasterio de Piedra, Cordillera Ibérica)

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    Depto. de GeodinĂĄmica, EstratigrafĂ­a y PaleontologĂ­aFac. de Ciencias GeolĂłgicasTRUEpu

    Effects of PM<sub>10</sub> Airborne Particles from Different Regions of a Megacity on In Vitro Secretion of Cytokines by a Monocyte Line during Different Seasons

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    Several epidemiological studies have demonstrated that particulate matter (PM) in air pollution can be involved in the genesis or aggravation of different cardiovascular, respiratory, perinatal, and cancer diseases. This study assessed the in vitro effects of PM10 on the secretion of cytokines by a human monocytic cell line (THP-1). We compared the chemotactic, pro-inflammatory, and anti-inflammatory cytokines induced by PM10 collected for two years during three different seasons in five different Mexico City locations. MIP-1α, IP-10, MCP-1, TNF-α, and VEGF were the main secretion products after stimulation with 80 Όg/mL of PM10 for 24 h. The THP-1 cells showed a differential response to PM10 obtained in the different sites of Mexico City. The PM10 from the north and the central city areas induced a higher pro-inflammatory cytokine response than those from the south. Seasonal pro-inflammatory cytokine secretion always exceeded anti-inflammatory secretion. The rainy-season-derived particles caused the lowest pro-inflammatory effects. We concluded that toxicological assessment of airborne particles provides evidence supporting their potential role in the chronic exacerbation of local or systemic inflammatory responses that may worsen the evolution of some chronic diseases

    On the tectonic origin of Iberian topography

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    The present-day topography of the Iberian peninsula can be considered as the result of the MesozoicCenozo–ic tectonic evolution of the Iberian plate (including rifting and basin formation during the Mesozoic and compression and mountain building processes at the borders and inner part of the plate, during the Tertiary, followed by Neogene rifting on the Mediterranean side) and surface processes acting during the Quaternary. The northern-central part of Iberia (corresponding to the geological units of the Duero Basin, the Iberian Chain, and the Central System) shows a mean elevation close to one thousand meters above sea level in average, some hundreds of meters higher than the southern half of the Iberian plate. This elevated area corresponds to (i) the top of sedimentation in Tertiary terrestrial endorheic sedimentary basins (Paleogene and Neogene) and (ii) planation surfaces developed on Paleozoic and Mesozoic rocks of the mountain chains surrounding the Tertiary sedimentary basins. Both types of surfaces can be found in continuity along the margins of some of the Tertiary basins. The Bouguer anomaly map of the Iberian peninsula indicates negative anomalies related to thickening of the continental crust. Correlations of elevation to crustal thickness and elevation to Bouguer anomalies indicate that the dierent landscape units within the Iberian plate can be ascribed to dierent patterns: (1) The negative Bouguer anomaly in the Iberian plate shows a rough correlation with elevation, the most important gravity anomalies being linked to the Iberian Chain. (2) Most part of the so-called Iberian Meseta is linked to intermediate-elevation areas with crustal thickening; this pattern can be applied to the two main intraplate mountain chains (Iberian Chain and Central System) (3) The main mountain chains (Pyrenees and Betics) show a direct correlation between crustal thickness and elevation, with higher elevation/crustal thickness ratio for the Central Systemvs. the Betics and the Pyrenees. Other features of the Iberian topography, namely the longitudinal pro le of the main rivers in the Iberian peninsula and the distribution of present-day endorheic areas, are consistent with the Tertiary tectonic evolution and the change from an endorheic to an exorheic regime during the Late Neogene and the Quaternary. Some of the problems involving the timing and development of the Iberian Meseta can be analysed considering the youngest reference level, constituted by the shallow marine Upper Cretaceous limestones, that indicates strong dierences induced by (i) the overall Tertiary and recent compression in the Iberian plate, responsible for dierences in elevation of the reference level of more than 6 km between the mountain chains and the endorheic basins and (ii) the eect of Neogene extension in the Mediterranean margin, responsible for lowering several thousands of meters toward the East and uplift of rift shoulders. A part of the recent uplift within the Iberian plate can be attributed o sostatic uplift in zones of crustal thickening

    Measurable Residual Disease Assessed by Flow-Cytometry Is a Stable Prognostic Factor for Pediatric T-Cell Acute Lymphoblastic Leukemia in Consecutive SEHOP Protocols Whereas the Impact of Oncogenetics Depends on Treatment.

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    Robust and applicable risk-stratifying genetic factors at diagnosis in pediatric T-cell acute lymphoblastic leukemia (T-ALL) are still lacking, and most protocols rely on measurable residual disease (MRD) assessment. In our study, we aimed to analyze the impact of NOTCH1, FBXW7, PTEN, and RAS mutations, the measurable residual disease (MRD) levels assessed by flow cytometry (FCM-MRD) and other reported risk factors in a Spanish cohort of pediatric T-ALL patients. We included 199 patients treated with SEHOP and PETHEMA consecutive protocols from 1998 to 2019. We observed a better outcome of patients included in the newest SEHOP-PETHEMA-2013 protocol compared to the previous SHOP-2005 cohort. FCM-MRD significantly predicted outcome in both protocols, but the impact at early and late time points differed between protocols. The impact of FCM-MRD at late time points was more evident in SEHOP-PETHEMA 2013, whereas in SHOP-2005 FCM-MRD was predictive of outcome at early time points. Genetics impact was different in SHOP-2005 and SEHOP-PETHEMA-2013 cohorts: NOTCH1 mutations impacted on overall survival only in the SEHOP-PETHEMA-2013 cohort, whereas homozygous deletions of CDKN2A/B had a significantly higher CIR in SHOP-2005 patients. We applied the clinical classification combining oncogenetics, WBC count and MRD levels at the end of induction as previously reported by the FRALLE group. Using this score, we identified different subgroups of patients with statistically different outcome in both Spanish cohorts. In SHOP-2005, the FRALLE classifier identified a subgroup of high-risk patients with poorer survival. In the newest protocol SEHOP-PETHEMA-2013, a very low-risk group of patients with excellent outcome and no relapses was detected, with borderline significance. Overall, FCM-MRD, WBC count and oncogenetics may refine the risk-stratification, helping to design tailored approaches for pediatric T-ALL patients
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