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1.
Phlebology ; 35(8): 623-630, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32390517

RESUMO

OBJECTIVES: The aim of this study was to assess inter­ and intra­observer agreement of detection and grading of oedema measured by vascular physicians using ultrasonography. METHOD: In this observational study, three investigators read 113 videos of ultrasonography of the medial lower leg of 77 patients using a 15-18 MHz linear probe and reported whether oedema was present or not and, if present, to what extent. The videos were selected by the coordinator and sent every two months for a period of six months to the three investigators. Intra­ and interobserver agreements were calculated using the Fleiss Kappa coefficient, reported with their 95% confidence interval and interpreted using the Landis and Koch values. RESULTS: Inter-observer agreement as to whether oedema was present or not was 0.88 (0.77-0.98), 0.96 (0.89-1.0) and 0.91 (0.80-1.0) for the first, second and third readings, respectively. The concordance was considered to be "excellent." Inter-observer agreement as to the severity of oedema was 0.52 (0.38-0.65), 0.53 (0.39-0.66) and 0.61 (0.47-0.75) for the first, second and third readings, respectively. The concordance was "moderate". Intra-observer reliability for the diagnosis of oedema was only 0.89 (0.70-1.0), 0.93 (0.75-1.0) and 0.92 (0.74-1.0) for the first, second and third reader, respectively, which was "excellent". CONCLUSIONS: The inter-observer agreement interpreting ultrasound videos using standard probes was excellent. Only moderate agreement in grading the severity of the edema using our arbitrary criteria was shown.


Assuntos
Tornozelo , Médicos , Edema/diagnóstico por imagem , Humanos , Variações Dependentes do Observador , Reprodutibilidade dos Testes , Ultrassonografia
2.
Eur Respir Rev ; 24(137): 378-91, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26324799

RESUMO

Tracheal or bronchial proximal stenoses occur as complications in 20-30% of lung cancers, resulting in a dramatic alteration in quality of life and poor prognosis. Bronchoscopic management of these obstructions is based on what are known as "thermal" techniques for intraluminal stenosis and/or placement of tracheal or bronchial prostheses for extrinsic compressions, leading to rapid symptom palliation in the vast majority of patients. This invasive treatment should only be used in cases of symptomatic obstructions and in the presence of viable bronchial tree and downstream parenchyma. This review aims to clarify 1) the available methods for assessing the characteristics of stenoses before treatment, 2) the various techniques available including their preferred indications, outcomes and complications, and 3) the integration of interventional bronchoscopy in the multidisciplinary management of proximal bronchial cancers and its synergistic effects with the other specific treatments (surgery, radiotherapy or chemotherapy).


Assuntos
Obstrução das Vias Respiratórias/terapia , Broncopatias/terapia , Broncoscopia/métodos , Criocirurgia , Eletrocoagulação , Terapia a Laser , Neoplasias Pulmonares/terapia , Cuidados Paliativos , Fotoquimioterapia , Estenose Traqueal/terapia , Obstrução das Vias Respiratórias/diagnóstico , Obstrução das Vias Respiratórias/etiologia , Broncopatias/diagnóstico , Broncopatias/etiologia , Broncoscópios , Broncoscopia/efeitos adversos , Broncoscopia/instrumentação , Terapia Combinada , Procedimentos Clínicos , Criocirurgia/efeitos adversos , Criocirurgia/instrumentação , Eletrocoagulação/efeitos adversos , Eletrocoagulação/instrumentação , Humanos , Terapia a Laser/efeitos adversos , Terapia a Laser/instrumentação , Lasers , Neoplasias Pulmonares/complicações , Neoplasias Pulmonares/diagnóstico , Seleção de Pacientes , Fotoquimioterapia/efeitos adversos , Fotoquimioterapia/instrumentação , Fatores de Risco , Stents , Estenose Traqueal/diagnóstico , Estenose Traqueal/etiologia , Resultado do Tratamento
3.
J Thorac Oncol ; 10(2): 309-15, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25319181

RESUMO

BACKGROUND: Solitary fibrous tumors of the pleura (SFTP) refer as to a heterogeneous group of mesenchymal malignancies with various anatomic and histology features. Upfront surgical resection is the standard approach, but recurrences may be aggressive and difficult to treat. The most widely accepted staging system has been proposed by De Perrot et al. Because SFTPs are rare, evidence to support a role for perioperative chemotherapy is scarce. Likewise, the predictive or prognostic relevance of the De Perrot system may be questioned. METHODS: Multicenter retrospective study of patients with histologically proven SFTP with complete follow-up from surgical diagnostic to tumor recurrence and death. RESULTS: Sixty-eight patients were included. Tumor stage was 0/I for 29 (43%) patients, II for 23 (34%) patients, III for seven (10%) patients, and IV for nine (13%) patients. Postoperative chemotherapy was given to seven patients, mostly with stage III/IV SFTP, mostly consisting of doxorubicin-based regimen. Recurrence rate and median relapse-free survival after surgery were 3%, 52%, 71%, and 80% (p < 0.001), and 107, 70, 29, 11 months (p < 0.001) for stage 0/I, II, III, and IV tumors, respectively. At time of tumor recurrence, 14 patients received exclusive chemotherapy. Highest disease control rates were observed with trabectedin, and gemcitabine-dacarbazine combination. CONCLUSION: Our study confirms the prognostic value of the De Perrot staging system, as well as its possible predictive value for perioperative chemotherapy decision-making, whereas the efficacy of currently available regimens to significantly reduce the risk of tumor recurrence remains questionable. Trabectedin may be of interest for recurrent tumors.


Assuntos
Neoplasias Pleurais/terapia , Tumor Fibroso Solitário Pleural/terapia , Adulto , Idoso , Idoso de 80 Anos ou mais , Progressão da Doença , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estadiamento de Neoplasias , Neoplasias Pleurais/patologia , Neoplasias Pleurais/cirurgia , Padrões de Prática Médica , Prognóstico , Estudos Retrospectivos , Tumor Fibroso Solitário Pleural/patologia , Tumor Fibroso Solitário Pleural/cirurgia , Resultado do Tratamento
4.
J Clin Oncol ; 33(9): 992-9, 2015 Mar 20.
Artigo em Inglês | MEDLINE | ID: mdl-25667280

RESUMO

PURPOSE: Approximately 1% of lung adenocarcinomas are driven by oncogenic ROS1 rearrangement. Crizotinib is a potent inhibitor of both ROS1 and ALK kinase domains. PATIENTS AND METHODS: In the absence of a prospective clinical trial in Europe, we conducted a retrospective study in centers that tested for ROS1 rearrangement. Eligible patients had stage IV lung adenocarcinoma, had ROS1 rearrangement according to fluorescent in situ hybridization, and had received crizotinib therapy through an individual off-label use. Best response was assessed locally using RECIST (version 1.1). All other data were analyzed centrally. RESULTS: We identified 32 eligible patients. One patient was excluded because next-generation sequencing was negative for ROS1 fusion. Median age was 50.5 years, 64.5% of patients were women, and 67.7% were never-smokers. Thirty patients were evaluable for progression-free survival (PFS), and 29 patients were evaluable for best response. We observed four patients with disease progression, two patients with stable disease, and objective response in 24 patients, including five complete responses (overall response rate, 80%; disease control rate, 86.7%). Median PFS was 9.1 months, and the PFS rate at 12 months was 44%. No unexpected adverse effects were observed. Twenty-six patients received pemetrexed (either alone or in combination with platinum and either before or after crizotinib) and had a response rate of 57.7% and a median PFS of 7.2 months. CONCLUSION: Crizotinib was highly active at treating lung cancer in patients with a ROS1 rearrangement, suggesting that patients with lung adenocarcinomas should be tested for ROS1. Prospective clinical trials with crizotinib and other ROS1 inhibitors are ongoing or planned.


Assuntos
Adenocarcinoma/tratamento farmacológico , Carcinoma Pulmonar de Células não Pequenas/tratamento farmacológico , Rearranjo Gênico , Neoplasias Pulmonares/tratamento farmacológico , Proteínas Tirosina Quinases/genética , Proteínas Proto-Oncogênicas/genética , Pirazóis/uso terapêutico , Piridinas/uso terapêutico , Adenocarcinoma/genética , Adulto , Idoso , Carcinoma Pulmonar de Células não Pequenas/genética , Crizotinibe , Progressão da Doença , Intervalo Livre de Doença , Europa (Continente) , Feminino , Humanos , Imuno-Histoquímica , Hibridização in Situ Fluorescente , Neoplasias Pulmonares/genética , Masculino , Pessoa de Meia-Idade , Mutação , Uso Off-Label , Estudos Prospectivos , Inibidores de Proteínas Quinases/uso terapêutico , Estudos Retrospectivos , Translocação Genética , Resultado do Tratamento
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