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2.
Dermatology ; 221(4): 303-5, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20798484

RESUMO

We report a case of drug rash with eosinophilia and systemic symptoms (DRESS) due to telaprevir (VX-950), a specific inhibitor of the hepatitis C virus (HCV) serine protease. A 57-year-old woman with chronic hepatitis C was included in a phase 2 rollover study of VX-950. She received VX-950 in combination with pegylated interferon alfa-2a and ribavirin. Six weeks later, she developed a generalized pruritic maculopapular exanthema with malaise, fever, dyspnoea and lymph node swelling. She had an eosinophilia (up to 2.7 × 109 cells/l), large activated lymphocytes and increased concentrations of aminotransferases. Histological examination of a cutaneous biopsy was consistent with a drug rash reaction. The HCV treatment was stopped, and she was treated with topical and oral steroids. Cutaneous and systemic symptoms disappeared within 1 month. Telaprevir was considered the culprit drug. We report to our knowledge the first case of DRESS syndrome due to telaprevir. The safety data of telaprevir is derived mainly from the PROVE1, PROVE2 and PROVE3 studies. They showed a high frequency of cutaneous side effects reported under the imprecise terms of pruritus and rash, leading to an increased rate of treatment discontinuation. Telaprevir, due to its efficacy, is probably on the way to obtaining regulatory approval in the near future. It is therefore important to be aware of the high incidence of cutaneous side effects and better describe them. Our observation suggests that potentially severe hypersensitivity reactions may belong to the spectrum of rashes induced by this drug.


Assuntos
Toxidermias/etiologia , Eosinofilia/induzido quimicamente , Exantema/induzido quimicamente , Oligopeptídeos/efeitos adversos , Corticosteroides/uso terapêutico , Anti-Inflamatórios/uso terapêutico , Antivirais/efeitos adversos , Antivirais/uso terapêutico , Ensaios Clínicos Fase II como Assunto , Toxidermias/tratamento farmacológico , Toxidermias/virologia , Quimioterapia Combinada/efeitos adversos , Dispneia/induzido quimicamente , Eosinofilia/patologia , Exantema/patologia , Feminino , Febre/induzido quimicamente , Hepacivirus/efeitos dos fármacos , Hepatite C Crônica/tratamento farmacológico , Hepatite C Crônica/virologia , Humanos , Interferon alfa-2 , Interferon-alfa/efeitos adversos , Interferon-alfa/uso terapêutico , Pessoa de Meia-Idade , Oligopeptídeos/uso terapêutico , Polietilenoglicóis/efeitos adversos , Polietilenoglicóis/uso terapêutico , Proteínas Recombinantes , Ribavirina/efeitos adversos , Ribavirina/uso terapêutico , Transaminases/sangue , Resultado do Tratamento
4.
Bull Cancer ; 96(12): 1163-71, 2009 Dec.
Artigo em Francês | MEDLINE | ID: mdl-19948451

RESUMO

Despite technical advances in many areas of diagnostic radiology, the detection and imaging of advanced-stage ovarian carcinoma remains a challenge. The metabolic imaging using positron-emission tomography (PET), more recently integrated PET/CT can provide a different perspective and contribute to a best understanding of the disease. After to describe the advantages and the limits of this technology, this review reports the performances of FDG-PET in recent studies, in different settings: initial staging, restaging, detection of recurrences and predicting response to chemotherapy. PET imaging appears, like in others cancers, to be specially useful for the diagnosis of recurrence, when clinical or radiological recurrence is suspected or when CA125 levels are rising. Moreover, it influence significantly the patient management. But this imaging can also improve the detection of lesions in others settings, and we considers this potential impact treatment, particularly when a optimal surgery is indicated. At the end, PET with FDG or others tracers could be using to predict the early response to systemic therapy and to stop quickly an inefficient treatment.


Assuntos
Fluordesoxiglucose F18 , Recidiva Local de Neoplasia/diagnóstico por imagem , Neoplasias Ovarianas/diagnóstico por imagem , Tomografia por Emissão de Pósitrons/métodos , Compostos Radiofarmacêuticos , Antígeno Ca-125/sangue , Feminino , Fluordesoxiglucose F18/farmacocinética , Humanos , Recidiva Local de Neoplasia/sangue , Recidiva Local de Neoplasia/tratamento farmacológico , Recidiva Local de Neoplasia/cirurgia , Estadiamento de Neoplasias/métodos , Neoplasias Ovarianas/sangue , Neoplasias Ovarianas/tratamento farmacológico , Neoplasias Ovarianas/cirurgia , Compostos Radiofarmacêuticos/farmacocinética
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