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2.
Ugeskr Laeger ; 176(8A): V08130525, 2014 Feb 17.
Artigo em Dinamarquês | MEDLINE | ID: mdl-25350304

RESUMO

This article is based on a systematic literature search and meta-analyses of clinical data regarding effects of bisphosphonates (BP) and denosumab (DS) on preventing skeletal related events (SRE) in patients with bone metastases from solid tumours. Although there are pharmacological differences between the different types of BP no major differences were observed between BP in preventing SRE or in adverse events. Treatment with DS has in three randomised trials showed a greater effect than BP in preventing SRE. The optimal choice of bone-anti-resorptive agent should depend on the patient's general condition, renal function and treatment logistics.


Assuntos
Neoplasias Ósseas , Conservadores da Densidade Óssea/uso terapêutico , Neoplasias Ósseas/complicações , Neoplasias Ósseas/diagnóstico por imagem , Neoplasias Ósseas/tratamento farmacológico , Neoplasias Ósseas/secundário , Neoplasias da Mama/patologia , Denosumab/uso terapêutico , Difosfonatos/uso terapêutico , Feminino , Humanos , Neoplasias Pulmonares/patologia , Masculino , Metanálise como Assunto , Neoplasias da Próstata/patologia , Radiografia
3.
Ugeskr Laeger ; 169(44): 3768-71, 2007 Oct 29.
Artigo em Dinamarquês | MEDLINE | ID: mdl-18028847

RESUMO

It is important for dying patients that their doctors are trained to diagnose that death is near. Typical clinical signs of impending death are described: the patient is bedbound, semicomatose, only able to take sips of fluid and no longer able to take oral drugs. Care of the dying is exclusively focused on palliation. A limited number of drugs are needed to ensure alleviation of symptoms during the last days of life. The drugs can all be administered by subcutaneous route. Clinical guidelines promote structuring optimal care for the dying. Home death is desired by many patients but so far only achieved by a minority.


Assuntos
Procedimentos Clínicos , Cuidados Paliativos , Assistência Terminal , Serviços de Assistência Domiciliar , Humanos , Cuidados Paliativos/métodos , Assistência Terminal/métodos
4.
Cancer Immunol Immunother ; 56(9): 1485-99, 2007 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17285289

RESUMO

p53 Mutations are found in up to 30% of breast cancers and peptides derived from over-expressed p53 protein are presented by class I HLA molecules and may act as tumor-associated epitopes in cancer vaccines. A dendritic cell (DC) based p53 targeting vaccine was analyzed in HLA-A2+ patients with progressive advanced breast cancer. DCs were loaded with 3 wild-type and 3 P2 anchor modified HLA-A2 binding p53 peptides. Patients received up to 10 sc vaccinations with 5 x 10(6) p53-peptide loaded DC with 1-2 weeks interval. Concomitantly, 6 MIU/m(2) interleukine-2 was administered sc. Results from a phase II trial including 26 patients with verified progressive breast cancer are presented. Seven patients discontinued treatment after only 2-3 vaccination weeks due to rapid disease progression or death. Nineteen patients were available for first evaluation after 6 vaccinations; 8/19 evaluable patients attained stable disease (SD) or minor regression while 11/19 patients had progressive disease (PD), indicating an effect of p53-specific immune therapy. This was supported by: (1) a positive correlation between p53 expression of tumor and observed SD, (2) therapy induced p53 specific T cells in 4/7 patients with SD but only in 2/9 patients with PD, and (3) significant response associated changes in serum YKL-40 and IL-6 levels identifying these biomarkers as possible candidates for monitoring of response in connection with DC based cancer immunotherapy. In conclusion, a significant fraction of breast cancer patients obtained SD during p53-targeting DC therapy. Data encourage initiation of a randomized trial in p53 positive patients evaluating the impact on progression free survival.


Assuntos
Neoplasias da Mama/terapia , Vacinas Anticâncer/uso terapêutico , Células Dendríticas/imunologia , Glicoproteínas/sangue , Interleucina-6/sangue , Fragmentos de Peptídeos/imunologia , Proteína Supressora de Tumor p53/imunologia , Adipocinas , Adulto , Idoso , Biomarcadores Tumorais/sangue , Neoplasias da Mama/imunologia , Proteína 1 Semelhante à Quitinase-3 , Células Dendríticas/transplante , Feminino , Humanos , Lectinas , Pessoa de Meia-Idade , Vacinação
5.
Carcinogenesis ; 25(6): 923-9, 2004 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-14976127

RESUMO

The incidence rate of testicular cancer has increased during the last 50 years. An interplay between changing environmental factors and individual susceptibility, e.g. in foreign compound metabolizing enzymes, may have important influences on the risk of testicular cancer. The cytochrome P4501A2 (CYP1A2) enzyme and the bimodally expressed enzyme N-acetyltransferase2 (NAT2) metabolize many procarcinogens/carcinogens. The aim of this population-based case-control study was to investigate if CYP1A2 or NAT2 activity measured as a ratio of urinary metabolites of dietary caffeine is a risk factor in testicular cancer. 378 men participated (80 seminomas, 104 non-seminomas and 194 controls). The CYP1A2 activity was lower in the cases than in the controls [median and 30-70% percentiles: 4.7 (3.9-5.7) and 5.2 (4.4-6.4), respectively]. The subjects were classified in tertiles with low, medium or high CYP1A2 activity. A low CYP1A2 activity was associated with the highest risk of testicular cancer. Including all participants except men using drugs suspected to influence CYP1A2 activity (n = 15), medium and low activity conferred odds ratios (ORs) of 1.54 [confidence intervals of 95% (CI(95%)) 0.93-2.55] and 2.11; CI(95%) (1.23-3.62), respectively, of having testicular cancer. Excluding smokers (n = 157) the ORs of medium and low activity were 3.63; CI(95%) (1.53-8.60) and 4.70; CI(95%) (2.03-10.89), respectively. After further exclusion of cases that had received chemotherapy or radiation (n = 47), similar significant results were achieved. In the groups with the lowest CYP1A2 activity the ORs for seminoma and non-seminoma were 2.12; CI(95%) (0.93-4.81) and 2.10; CI(95%) (1.02-4.32). The phenotype of NAT2 was not associated with testicular cancer. In conclusion, we found no association of NAT2 phenotype to testicular cancer, whereas significant associations between CYP1A2 activity and testicular cancer were shown.


Assuntos
Citocromo P-450 CYP1A2/metabolismo , Neoplasias Testiculares/enzimologia , Adulto , Estudos de Casos e Controles , Humanos , Masculino , Pessoa de Meia-Idade
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