Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 33
Filter
1.
Neumol. pediátr. (En línea) ; 18(1): 14-15, 2023.
Article in Spanish | LILACS | ID: biblio-1442721

ABSTRACT

El uso de moduladores de CFTR en pacientes con fibrosis quística post trasplante pulmonar es un tema todavía controversial. Varias publicaciones reportan los beneficios del modulador elexacaftor/tezacaftor/ivacaftor en los síntomas extrapulmonares de la fibrosis quística, especialmente enfermedad sinusal, síntomas gastrointestinales y diabetes. Un número alto de pacientes debe discontinuar el tratamiento por mala tolerancia, sin embargo, no se describen interacciones de importancia con el tratamiento inmunosupresor. Se debe considerar para su uso los riesgos versus beneficios en forma individual en cada paciente.


The use of CFTR modulators in patients with cystic fibrosis after lung transplantation is still a controversial issue. Several publications report the benefits of the use of the modulator elexacaftor/tezacaftor/ivacaftor on extrapulmonary symptoms of cystic fibrosis, especially sinus disease, gastrointestinal symptoms and diabetes. A high number of patients must discontinue treatment due to poor tolerance; however, no significant interactions with immunosuppressive treatment have been described. The individual risk-benefit of each patient should be considered for its use.


Subject(s)
Humans , Cystic Fibrosis/drug therapy , Pyrazoles/therapeutic use , Pyridines/therapeutic use , Quinolines/therapeutic use , Lung Transplantation , Cystic Fibrosis Transmembrane Conductance Regulator , Cystic Fibrosis/surgery , Drug Combinations , Benzodioxoles/therapeutic use , Aminophenols/therapeutic use , Indoles/therapeutic use
2.
Brasília; CONITEC; set. 2021. 12 p. (Relatório para sociedade: informações sobre recomendações de incorporação de medicamentos e outras tecnologias no SUS, 282).
Monography in Portuguese | ColecionaSUS, LILACS | ID: biblio-1362845

ABSTRACT

Este documento é uma versão resumida do relatório técnico da Comissão Nacional de Incorporação de Tecnologias no Sistema Único de Saúde ­ Conitec e foi elaborado numa linguagem simples, de fácil compreensão, para estimular a participação da sociedade no processo de Avaliação de Tecnologias em Saúde (ATS) que antecede a incorporação, exclusão ou alteração de medicamentos, produtos e procedimentos utilizados no SUS. As recomendações da Comissão são submetidas à consulta pública pelo prazo de 20 dias. Após analisar as contribuições recebidas na consulta pública, a Conitec emite a recomendação final, que pode ser a favor ou contra a incorporação, exclusão ou alteração da tecnologia analisada. A recomendação final é, então, encaminhada ao Secretário de Ciência, Tecnologia, Inovação e Insumos Estratégicos em Saúde do Ministério da Saúde -SCTIE/MS, que decide sobre quais tecnologias em saúde serão disponibilizadas no SUS


Subject(s)
Humans , Pyridines/therapeutic use , Carcinoma, Renal Cell/drug therapy , Antineoplastic Agents, Immunological/therapeutic use , Nivolumab/therapeutic use , Kidney Neoplasms/drug therapy , Anilides/therapeutic use , Technology Assessment, Biomedical , Cost-Benefit Analysis , Neoplasm Metastasis
3.
Brasília; MS; jun. 2021. 681 p. ilus, tab.(Relatório de recomendação: medicamento, 661).
Monography in Portuguese | BRISA, LILACS, ColecionaSUS | ID: biblio-1362749

ABSTRACT

Relatório técnico com Leis que estabelece que a incorporação, a exclusão ou a alteração de novos medicamentos, produtos e procedimentos, bem como a constituição ou alteração de protocolo clínico ou de diretriz terapêutica são atribuições do Ministério da Saúde (MS). A estrutura de funcionamento da Conitec é composta por Plenário e Secretaria-Executiva. A gestão e a coordenação das atividades da Conitec, bem como a emissão do relatório de recomendação sobre as tecnologias analisadas são de responsabilidade da Secretaria-Executiva ­ exercida pelo Departamento de Gestão e Incorporação de Tecnologias e Inovação em Saúde (DGITIS/SCTIE/MS).


Subject(s)
Humans , Pyridines/therapeutic use , Carcinoma, Renal Cell/drug therapy , Antineoplastic Agents, Immunological/therapeutic use , Nivolumab/therapeutic use , Kidney Neoplasms/drug therapy , Anilides/therapeutic use , Technology Assessment, Biomedical , Cost-Benefit Analysis , Neoplasm Metastasis
5.
Medicina (B.Aires) ; 78(1): 29-32, feb. 2018. tab
Article in English | LILACS | ID: biblio-894543

ABSTRACT

Hepatocellular carcinoma (HCC) is the second cause of cancer-related death in the world and is the main cause of death in cirrhotic patients. Unfortunately, the incidence of HCC has grown significantly in the last decade. Curative treatments such as surgery, liver transplantation or percutaneous ablation can only be applied in less than 30% of cases. The multikinase inhibitor sorafenib is the first line therapy for advanced HCC. Regorafenib is the standard of care for second-line patients. However, novel and more specific potent therapeutic approaches for advanced HCC are still needed. The liver constitutes a unique immunological microenvironment, although anti-tumor immunity seems to be feasible with the use of checkpoint inhibitors such as nivolumab. Efficacy may be further increased by combining checkpoint inhibitors or by applying loco-regional treatments. The success of immune checkpoint blockade has renewed interest in immunotherapy in HCC.


El hepatocarcinoma (HCC) es la segunda causa de muerte relacionada con el cáncer en el mundo y es la principal causa de muerte en pacientes cirróticos. Desafortunadamente, la incidencia de HCC ha crecido significativamente en la última década. Los tratamientos curativos como la cirugía, el trasplante de hígado o la ablación solo pueden aplicarse en menos del 30% de los casos. El sorafenib es el tratamiento de primera línea para el HCC avanzado, mientras que el regorafenib se reserva como segunda línea. Sin embargo, todavía son necesarios nuevos enfoques terapéuticos potentes y más específicos para el HCC avanzado. El hígado constituye un microambiente inmunológico único, aunque la inmunidad antitumoral parece ser factible mediante el uso de inhibidores de punto de control como nivolumab. La eficacia puede aumentarse adicionalmente combinando inhibidores de puntos de control inmunitario o aplicando tratamientos loco-regionales. En este sentido, el éxito del uso de anticuerpos monoclonales, que bloquean el control inmunitario, ha renovado el interés en la inmunoterapia para el HCC.


Subject(s)
Humans , Carcinoma, Hepatocellular/drug therapy , Antineoplastic Agents, Immunological/therapeutic use , Immunotherapy/methods , Liver Neoplasms/drug therapy , Antibodies, Monoclonal/therapeutic use , Phenylurea Compounds/therapeutic use , Pyridines/therapeutic use , Clinical Trials as Topic , Sorafenib/therapeutic use , Nivolumab/therapeutic use
6.
Arch. endocrinol. metab. (Online) ; 61(4): 398-402, July-Aug. 2017. tab
Article in English | LILACS | ID: biblio-887574

ABSTRACT

ABSTRACT Medullary thyroid carcinoma (MTC) is a rare neuroendocrine tumor originating from parafollicular C cells of the thyroid and associated with mutations in the proto-oncogene REarranged during Transfection (RET). The prognosis of MTC depends on clinical stage, with a 95.6% 10-year survival rate among patients with localized disease and 40% among patients with advanced disease. Standard chemotherapy and radiotherapy have no significant impact on the overall survival of these patients and two tyrosine kinase receptor inhibitors (TKIs), vandetanib and cabozantinib, have been recently approved for the systemic treatment of locally advanced or metastatic MTC. However, since patients with MTC and residual or recurrent disease may have an indolent course with no need for systemic treatment, and since these drugs are highly toxic, it is extremely important to select the patients who will receive these drugs in a correct manner. It is also essential to carefully monitor patients using TKI regarding possible adverse effects, which should be properly managed when occurring.


Subject(s)
Humans , Piperidines/therapeutic use , Pyridines/therapeutic use , Quinazolines/therapeutic use , Carcinoma, Neuroendocrine/drug therapy , Protein Kinase Inhibitors/therapeutic use , Anilides/therapeutic use , Piperidines/adverse effects , Pyridines/adverse effects , Quinazolines/adverse effects , Thyroid Neoplasms/metabolism , Thyroid Neoplasms/drug therapy , Carcinoma, Neuroendocrine/metabolism , Risk Assessment , Protein Kinase Inhibitors/adverse effects , Anilides/adverse effects
7.
Pakistan Journal of Pharmaceutical Sciences. 2017; 30 (3 [Special]): 1103-1106
in English | IMEMR | ID: emr-189318

ABSTRACT

The paper is intended to analyze and evaluate the specific curative effect and safety of 2% liranaftate ointment in treating patients with tinea pedis and tinea cruris. 1,100 cases of patients with tinea pedis and tinea corporis and cruris were selected as research objects and were divided into two groups according to the random number table method. They were treated with different methods: 550 cases of patients were treated with 2% liranaftate ointment for external use in the observation group and the rest 550 cases of patients were treated with 1% bifonazole cream in the control group. The treatment time was two weeks for patients with tinea corporis and cruris and four weeks for those with tinea pedis respectively. Meanwhile, the one-month follow-up visit was conducted among the patients to compare the curative effects of two groups. After the medication, the curative effectiveness rate was 87.65% [482/550] in the observation group, while that was 84.91% [467/550] in the control group. After the average follow-up visits of [15.5 +/- 2.4], the curative effectiveness rate 96.55% [531/550] in the observation group, while that was 91.45% [503/550] in the control group. Two groups of patients recovered well with a low incidence of adverse reactions in the treatment, and the overall curative effect was good with the inter-group difference at P>0.05, so it was without statistical significance. The curative effect of 2% liranaftate ointment is safe and obvious in treating tinea pedis and tinea corporis and cruris, so it is valuable for clinical popularization and application


Subject(s)
Humans , Male , Female , Child , Adolescent , Adult , Middle Aged , Tinea Pedis/drug therapy , Naphthalenes/therapeutic use , Pyridines/therapeutic use , Thiocarbamates/therapeutic use , Ointments , Safety
8.
J. bras. pneumol ; 42(2): 146-154, Mar.-Apr. 2016. tab, graf
Article in English | LILACS | ID: lil-780891

ABSTRACT

Worldwide, venous thromboembolism (VTE) is among the leading causes of death from cardiovascular disease, surpassed only by acute myocardial infarction and stroke. The spectrum of VTE presentations ranges, by degree of severity, from deep vein thrombosis to acute pulmonary thromboembolism. Treatment is based on full anticoagulation of the patients. For many decades, it has been known that anticoagulation directly affects the mortality associated with VTE. Until the beginning of this century, anticoagulant therapy was based on the use of unfractionated or low-molecular-weight heparin and vitamin K antagonists, warfarin in particular. Over the past decades, new classes of anticoagulants have been developed, such as factor Xa inhibitors and direct thrombin inhibitors, which significantly changed the therapeutic arsenal against VTE, due to their efficacy and safety when compared with the conventional treatment. The focus of this review was on evaluating the role of these new anticoagulants in this clinical context.


O tromboembolismo venoso (TEV) está entre as principais causas de morte por doenças cardiovasculares no mundo, atrás apenas do infarto agudo do miocárdio e do acidente vascular cerebral. O TEV possui espectro de apresentação que vai desde a trombose venosa profunda até o tromboembolismo pulmonar agudo, de acordo com gravidade crescente de acometimento, sendo seu tratamento baseado na anticoagulação plena dos pacientes. Há muitas décadas, sabe-se que a anticoagulação interfere diretamente na mortalidade associada ao TEV. Até o início deste século a terapia anticoagulante se baseava no uso de heparina, em suas formas não fracionada ou de baixo peso molecular, e de antagonistas da vitamina K, principalmente a varfarina. Ao longo das últimas décadas, foram desenvolvidos novas classes de medicamentos anticoagulantes, inibidores do fator Xa e inibidores diretos da trombina, que mudaram significativamente o arsenal terapêutico do TEV, em função de suas características de eficácia e segurança em relação ao tratamento convencional, sendo o foco principal de esta revisão avaliar seu papel neste contexto clínico.


Subject(s)
Humans , Anticoagulants/therapeutic use , Venous Thromboembolism/drug therapy , Dabigatran/therapeutic use , Pyrazoles/therapeutic use , Pyridines/therapeutic use , Pyridones/therapeutic use , Rivaroxaban/therapeutic use , Thiazoles/therapeutic use , Time Factors , Warfarin/therapeutic use
9.
Braz. j. phys. ther. (Impr.) ; 19(3): 194-200, May-Jun/2015. tab, graf
Article in English | LILACS | ID: lil-751384

ABSTRACT

Objective: To investigate the relationship between self-perceived fatigue with different physical functioning tests and functional performance scales used for evaluating mobility-related disability among community-dwelling older persons. Method: This is a cross-sectional, population-based study. The sample was composed of older persons with 65 years of age or more living in Cuiabá, MT, and Barueri, SP, Brazil. The data for this study is from the FIBRA Network Study. The presence of self-perceived fatigue was assessed using self-reports based on the Center for Epidemiologic Studies-Depression Scale. The Lawton instrumental activities of daily living scale (IADL) and the advanced activities of daily living scale (AADL) were used to assess performance and participation restriction. The following physical functioning tests were used: five-step test (FST), the Short Physical Performance Battery (SPPB), and usual gait speed (UGS). Three models of logistic regression analysis were conducted, and a significance level of α<0.05 was adopted. Results: The sample was composed of 776 older adults with a mean age (SD) of 71.9 (5.9) years, of whom the majority were women (74%). The prevalence of self-perceived fatigue within the participants was 20%. After adjusting for covariates, SPPB, UGS, IADL, and AADL remained associated with self-perceived fatigue in the final multivariate regression model. Conclusion: Our results suggest that there is an association between self-perceived fatigue and lower extremity function, usual gait speed and activity limitation and participation restriction in older adults. Further cohort studies are needed to investigate which physical performance measure may be able to predict the negative impact of fatigue in older adults. .


Subject(s)
Adult , Humans , Male , Adenocarcinoma/genetics , Carcinoma, Non-Small-Cell Lung/genetics , Gene Rearrangement , Lung Neoplasms/genetics , Protein Kinase Inhibitors/therapeutic use , Pyrazoles/therapeutic use , Pyridines/therapeutic use , Receptor Protein-Tyrosine Kinases/genetics , Adenocarcinoma/metabolism , Adenocarcinoma/secondary , Carcinoma, Non-Small-Cell Lung/metabolism , Carcinoma, Non-Small-Cell Lung/secondary , Immunoenzyme Techniques , In Situ Hybridization, Fluorescence , Lung Neoplasms/metabolism , Lung Neoplasms/pathology , Prognosis , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , RNA, Messenger/genetics , Receptor Protein-Tyrosine Kinases/metabolism
10.
Yonsei Medical Journal ; : 772-777, 2015.
Article in English | WPRIM | ID: wpr-77287

ABSTRACT

PURPOSE: The aim of this study was to evaluate the effects and safety of a sleep aid for postoperative analgesia in patients undergoing arthroscopic rotator cuff repair. MATERIALS AND METHODS: Seventy-eight patients were prospectively assigned to either the zolpidem group (multimodal analgesia+zolpidem; 39 patients) or the control group (multimodal analgesia; 39 patients). Self-rated pain levels were assessed twice a day using a visual analog scale (VAS). The need for additional rescue analgesic, duration of functional recovery, and adverse effects were assessed for the first 5 days after surgery. RESULTS: The mean number of times that additional rescue analgesic was required during 5 days after surgery was 2.1+/-2.0 in the zolpidem group and 3.3+/-2.8 in the control group, a significant difference. There were no significant differences between the two groups in mean VAS pain scores during the first 5 days after surgery, although the zolpidem group had lower VAS pain scores than the control group. Additionally, there were no significant differences in duration of functional recovery and adverse effects between the two groups. CONCLUSION: The use of zolpidem for analgesia after arthroscopic rotator cuff repair provided a significant reduction in the need for rescue analgesic without increasing adverse effects. Nevertheless, mean VAS pain scores during the first 5 days after surgery did not differ between the zolpidem group and the control group.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Analgesia/methods , Analgesics/therapeutic use , Arthroscopy/adverse effects , Hypnotics and Sedatives/therapeutic use , Pain Management , Pain Measurement , Pain, Postoperative/drug therapy , Postoperative Period , Prospective Studies , Pyridines/therapeutic use , Rotator Cuff/injuries , Sleep/drug effects , Treatment Outcome , Visual Analog Scale
11.
Braz. j. infect. dis ; 17(6): 657-660, Nov.-Dec. 2013. tab
Article in English | LILACS | ID: lil-696966

ABSTRACT

OBJECTIVE: To evaluate the factors associated with plasma concentrations of atazanavir (ATV) in a cohort of well-controlled HIV infected subjects (undetectable viremia). Design: Cross-sectional study where 69 subjects were consecutively enrolled between April and November, 2011. METHODS: Patients had to be on atazanavir for at least six months, undetectable viral load for a period equal to or longer than 12 months, T CD4+ lymphocyte count higher than 200 cells/mm³, and aged between 18 years and 70 years old. Exclusion criteria were pregnancy, any neurologic disease, active opportunistic disease, hepatitis or cancer. Atazanavir plasma levels were measured by ultra-performance liquid chromatography. RESULTS AND DISCUSSION: Overall, 54 patients (mean age of 47 years and 50% women) were included in the analysis. Those without ritonavir (unboosted atazanavir) had statistically lower plasma concentrations than those with ritonavir boosted atazanavir (p = 0.001) and total and indirect bilirubin were statistically associated with plasma concentration of atazanavir (r = 0.32 and r = 0.33 respectively; p < 0.05 in both cases). no statistical association was found among gender, ethnicity, age, weight, body mass index (BMI), lipid profile, and the plasma concentration of atazanavir. CONCLUSION: in summary, as expected, concomitant ritonavir use was the only factor associated with atazanavir plasma levels. prospective studies with a larger sample size might help to observe an association of atazanavir concentrations to other characteristics such as body weight, since the p-value showed to be close to significance (p = 0.068).


Subject(s)
Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Anti-HIV Agents/blood , HIV Infections/blood , Oligopeptides/blood , Pyridines/blood , Anti-HIV Agents/pharmacokinetics , Anti-HIV Agents/therapeutic use , Chromatography, Liquid , Cohort Studies , Cross-Sectional Studies , HIV Infections/drug therapy , HIV Infections/virology , Oligopeptides/pharmacokinetics , Oligopeptides/therapeutic use , Prospective Studies , Pyridines/pharmacokinetics , Pyridines/therapeutic use , Viral Load
15.
Arq. bras. endocrinol. metab ; 53(9): 1061-1073, dez. 2009. ilus, tab
Article in English | LILACS | ID: lil-537057

ABSTRACT

Thyroid cancer incidence has significantly increased in the last three decades and many patients seek medical attention for its treatment every year. Among follicular cell-derived tumors, the majority are differentiated thyroid carcinomas (DTC), whose prognosis is very good with only 15 percent of the cases presenting disease persistence or recurrence after initial treatment. Medullary thyroid carcinoma has a worse prognosis, especially in patients with diffused cancers at the time of initial surgery. Traditional treatment options for persistent or recurrent disease include additional surgery, radioiodine treatment and TSH-suppression in DTC patients; external beam radiotherapy, and cytotoxic chemotherapy, often have low efficacy and many patients with advanced disease ultimately die. In the last two decades many of the molecular events involved in cancer formation have been uncovered. This knowledge has prompted the development of novel therapeutic strategies mainly based on the inhibition of key molecular mediators of the tumorigenic process. In particular the class of small-molecule tyrosine kinase inhibitors was enriched by many compounds that have reached clinical trials and in some cases have had approval for clinical use in specific cancers. Many of these compounds entered clinical trials also for locally advanced or metastatic thyroid carcinomas showing very promising results.


O câncer de tireoide tem aumentado significativamente nas últimas três décadas e muitos pacientes têm buscado cuidados médicos para o tratamento a cada ano. Entre os tumores derivados de células foliculares, a maioria é carcinoma diferenciado de tireoide (CDT), cujo prognóstico é muito bom, em que somente em 15 por cento dos casos a doença é persistente ou recorrente após o tratamento inicial. O carcinoma medular de tireoide tem um prognóstico pior, especialmente em pacientes com câncer difuso no momento da cirurgia inicial. As opções no tratamento tradicional para a doença persistente ou recorrente incluem cirurgia adicional, radioiodoterapia e supressão de TSH em pacientes CDT; a radioterapia externa e a quimioterapia citotóxica apresentam com frequência uma baixa eficácia e muitos pacientes com doença avançada não sobrevivem. Nas últimas duas décadas, muitos dos eventos envolvidos na formação do câncer tornaram-se conhecidos. Esse conhecimento possibilitou o desenvolvimento de novas estratégias terapêuticas, baseadas principalmente na inibição de mediador molecularchave no processo tumorigênico. Em particular, a classe das pequenas moléculas inibidoras de tirosina-quinase foi enriquecida por muitos compostos investigados em estudos clínicos e alguns casos foram aprovados para uso clínico em tipos específicos de câncer. Muitos desses compostos foram aplicados em estudos clínicos de câncer de tireoide com extensa invasão local ou metástase, mostrando resultados muito promissores.


Subject(s)
Humans , Antineoplastic Agents/therapeutic use , Carcinoma, Medullary/drug therapy , Carcinoma, Papillary/drug therapy , Protein Kinase Inhibitors/therapeutic use , Thyroid Neoplasms/drug therapy , Benzenesulfonates/therapeutic use , Carcinoma, Medullary/genetics , Carcinoma, Papillary/genetics , Imidazoles/therapeutic use , Indazoles/therapeutic use , Indoles/therapeutic use , Niacinamide/analogs & derivatives , Niacinamide/therapeutic use , Piperidines/therapeutic use , Protein Kinase Inhibitors/classification , Pyridines/therapeutic use , Pyrroles/therapeutic use , Quinazolines/therapeutic use , Thyroid Neoplasms/genetics
16.
Journal of Korean Medical Science ; : 782-788, 2009.
Article in English | WPRIM | ID: wpr-153147

ABSTRACT

The myocardial protective effects of endothelin antagonist in ischemic cardiomyopathy (ICMP), doxorubicin-induced cardiomyopathy (DOX) and pressure-overload hypertrophy by transverse aortic constriction (TAC) models have been predicted to be different. The objective of this experiment, therefore, is to evaluate the myocardial protective effect of tezosentan, an endothelin receptor antagonist, in various experimental heart failure models. Sprague-Dawley rats (6-8 weeks old, 200-300 g) were randomized to three experimental groups (n=30 each): ICMP; DOX; and TAC group. Each of these groups was randomly assigned further to the following subgroups (n=10 each): sham-operated ischemia-reperfusion subgroup (SHAM); tezosentan treated ischemia-reperfusion subgroup (Tezo); and tezosentan non-treated ischemia-reperfusion subgroup (N-Tezo). Total circulatory arrest was induced for 1 hr, followed by 2 hr of reperfusion. The left ventricular developed pressure, peak positive and negative first derivatives, and coronary blood flow were significantly different (P<0.05) among the SHAM, Tezo, and N-Tezo subgroups of the ICMP group at 30 min of reperfusion, but there were no statistically significant differences among the subgroups of the DOX and TAC groups. In conclusion, tezosentan, an endothelin receptor antagonist, showed myocardial protection effects only on the ischemic cardiomyopathy rat model, but not in the non-ischemic heart failure rat models.


Subject(s)
Animals , Male , Rats , Cardiomyopathies/chemically induced , Coronary Vessels/physiology , Disease Models, Animal , Doxorubicin/toxicity , Heart Failure/drug therapy , Hypertrophy/drug therapy , Pressure , Pyridines/therapeutic use , Rats, Sprague-Dawley , Receptors, Endothelin/antagonists & inhibitors , Reperfusion Injury/drug therapy , Tetrazoles/therapeutic use , Vasodilator Agents/therapeutic use , Ventricular Function, Left/physiology
17.
The Korean Journal of Hepatology ; : 299-308, 2009.
Article in English | WPRIM | ID: wpr-181188

ABSTRACT

Hepatocellular carcinoma (HCC) is a major global health problem, which has a grave morbidity and mortality. Over the past few decades, no effective systemic therapeutic modalities have been established for patients with the unresectable HCC in advanced stage. Sorafenib is a small molecule that blocks cancer cell proliferation by targeting the intracellular signaling pathway at the level of Raf-1 and B-Raf serine-threonine kinases, and exerts an anti-angiogenic effect by targeting the vascular endothelial growth factor receptor-1, 2 and 3, and platelet-derived growth factor receptor-beta tyrosine kinases. Recently, two clinical successful applications, SHARP and Asia-Pacific trial, of multikinase inhibitor sorafenib represent a significant advance in the treatment of advanced HCC patients without a curative chance. However, because the results of clinical trials show diverse responses in a subset of HCC patients, a molecular classification of HCC through the excavation of specific biomarkers related to its biological behavior is necessary for sorting HCC patients to each group with a biological homogeneity, ultimately leading to the most suitable individualization of molecular targeted therapy in HCC.


Subject(s)
Humans , Antineoplastic Agents/therapeutic use , Benzenesulfonates/therapeutic use , Carcinoma, Hepatocellular/pathology , Liver Neoplasms/blood supply , Neovascularization, Pathologic , Proto-Oncogene Proteins B-raf/antagonists & inhibitors , Proto-Oncogene Proteins c-raf/antagonists & inhibitors , Pyridines/therapeutic use , Receptors, Platelet-Derived Growth Factor/antagonists & inhibitors , Receptors, Vascular Endothelial Growth Factor/antagonists & inhibitors , Signal Transduction
18.
Rev. chil. urol ; 73(3): 184-190, 2008. ilus
Article in Spanish | LILACS | ID: lil-549124

ABSTRACT

Con la aparición de la terapia anti-angiogénica hace algunos años y dado a sus promisorios resultados en el manejo del cáncer renal metastático, nuestra intención es presentar una puesta al día sobre este tema, realizando para tal efecto una revisión bibliográfica completa de los trabajos mas relevantes usando como fuente la base de datos PUBMED (1996-2007) sobre la terapia antiangiogenica en el manejo del cáncer renal metastásico. El siguiente artículo hace hincapié sobre la fisiopatología de la génesis del cáncer renal y de la acción de los agentes anti-angiogénicos, los resultados de las series clínicas publicadas, las características de los agentes anti-angiogénicos y algunos enfoques terapéuticos en los cuales podrían tener un rol en el futuro.


We present an update of the molecular targeted therapy in advanced renal cell carcinoma due to their promising results. We make a complete revision in PUBMED database (1996-2007) of the most relevant studies in molecular targeted therapy for the management of metastasis renal cell carcinoma. The emphasis was done in the physiopathology of renal cell carcinoma and molecular targeted therapy, the results of clinical trials, the characteristics of these drugs and their role in future directions.


Subject(s)
Humans , Benzenesulfonates/therapeutic use , Carcinoma, Renal Cell/drug therapy , Angiogenesis Inhibitors/therapeutic use , Kidney Neoplasms/drug therapy , Pyrroles/therapeutic use , Carcinoma, Renal Cell/physiopathology , Carcinoma, Renal Cell/secondary , Indoles/therapeutic use , Kidney Neoplasms/physiopathology , Kidney Neoplasms/secondary , Pyridines/therapeutic use , Chemotherapy, Adjuvant
19.
J Indian Med Assoc ; 2007 May; 105(5): 260-2
Article in English | IMSEAR | ID: sea-103064

ABSTRACT

Diclofenac sodium, a non-selective cyclo-oxygenase inhibitor and etoricoxib, a selective cyclo-oxygenase-2 inhibitor have been widely used in treatment of patients with osteo-arthritis. Five hundred and eighty-five patients with uncomplicated knee osteo-arthritis were randomly allocated into 3 equal groups and received either diclofenac sodium, etoricoxib or placebo in a double-blind manner. The response in both the drug groups was comparable and much more than placebo group. The study shows that etoricoxib provides better clinical efficacy and gastro-intestinal tolerability in osteo-arthritis in comparison to diclofenac sodium presumably due to the selective inhibition of cyclo-oxygenase-2 by etoricoxib.


Subject(s)
Adult , Cyclooxygenase Inhibitors/therapeutic use , Diclofenac/therapeutic use , Double-Blind Method , Female , Humans , Male , Middle Aged , Osteoarthritis, Knee/drug therapy , Pyridines/therapeutic use , Sulfones/therapeutic use , Treatment Outcome
20.
Braz. j. med. biol. res ; 40(1): 117-125, Jan. 2007. ilus, graf
Article in English | LILACS | ID: lil-439676

ABSTRACT

We investigated the effect of etoricoxib, a selective cyclooxygenase-2 inhibitor, and indomethacin, a non-selective cyclooxygenase inhibitor, on experimental periodontitis, and compared their gastrointestinal side effects. A ligature was placed around the second upper left molars of female Wistar rats (160 to 200 g). Animals (6 per group) were treated daily with oral doses of 3 or 9 mg/kg etoricoxib, 5 mg/kg indomethacin, or 0.2 mL saline, starting 5 days after the induction of periodontitis, when bone resorption was detected, until the sacrifice on the 11th day. The weight and survival rate were monitored. Alveolar bone loss (ABL) was measured as the sum of distances between the cusp tips and the alveolar bone. The gastric mucosa was examined macroscopically and the periodontium and gastric and intestinal mucosa were examined by histopathology. The ongoing ABL was significantly inhibited (P < 0.05) by 3 and 9 mg/kg etoricoxib and by indomethacin: control = 4.08 ± 0.47 mm; etoricoxib (3 mg/kg) = 1.89 ± 0.26 mm; etoricoxib (9 mg/kg) = 1.02 ± 0.14 mm; indomethacin = 0.64 ± 0.15 mm. Histopathology of periodontium showed that etoricoxib and indomethacin reduced inflammatory cell infiltration, ABL, and cementum and collagen fiber destruction. Macroscopic and histopathological analysis of gastric and intestinal mucosa demonstrated that etoricoxib induces less damage than indomethacin. Animals that received indomethacin presented weight loss starting on the 7th day, and higher mortality rate (58.3 percent) compared to etoricoxib (0 percent). Treatment with etoricoxib, even starting when ABL is detected, reduces inflammation and cementum and bone resorption, with fewer gastrointestinal side effects.


Subject(s)
Animals , Female , Rats , Cyclooxygenase Inhibitors/therapeutic use , Gastric Mucosa/drug effects , Indomethacin/therapeutic use , Intestinal Mucosa/drug effects , Periodontitis/drug therapy , Pyridines/therapeutic use , Sulfones/therapeutic use , Alveolar Bone Loss/drug therapy , Rats, Wistar
SELECTION OF CITATIONS
SEARCH DETAIL