107 results match your criteria: "Helios Medical Center[Affiliation]"

The potential role of modern US in the follow-up of patients with retroperitoneal fibrosis.

Diagn Interv Radiol

April 2015

From the Departments of Diagnostic and Interventional Radiology (L.K. e-mail: H.E., P.H., W.P.), and Urology (A.S.B., S.R.), HELIOS Medical Center Wuppertal, University Hospital Witten/Herdecke, Wuppertal, Germany; the Dean`s Office (M.H.), Department of Medical Education, Heinrich-Heine University Medical Faculty, Duesseldorf, Germany.

Purpose: We aimed to evaluate a standardized ultrasonography (US) algorithm for the visualization of pathologic para-aortic tissue in retroperitoneal fibrosis (RPF).

Materials And Methods: Thirty-five patients with lumbar RPF of typical extent, as determined by abdominal magnetic resonance imaging, were included. Examinations were conducted using standardized abdominal US with axial sections obtained at the levels of the renal arteries, aortic bifurcation, and both common iliac arteries.

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Post-imatinib surgery in advanced/metastatic GIST: is it worthwhile in all patients?

Ann Oncol

February 2010

Melanoma and Sarcoma Unit, Department of Surgery, Istituto Nazionale Tumori, Milan, Italy. Electronic address:

Background: Surgical indication for metastatic gastrointestinal stromal tumor (GIST) treated with imatinib is not yet established.

Materials And Methods: We analyzed 80 patients who underwent surgery for metastatic GIST after imatinib therapy from July 2002 to October 2007. Patients were divided into those with surgery at best clinical response (group A, n = 49) and those with surgery at focal progression (group B, n = 31).

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Adenoviral (ADV) gene therapy with the thymidine kinase gene (TK) under control of the Rous sarcoma virus (RSV) promotor followed by the administration of acyclovir leads to replication errors in transcription and to cell death. This concept of ADV-RSV-TK has been established for the treatment of ovarian cancer cells. The purpose of this investigation was to clarify whether cell death after ADV-RSV-TK gene therapy and acyclovir administration is indeed due to apoptosis induction, whether the synergistic effect of ADV-RSV-TK gene therapy with chemotherapy was limited to the primary mechanism of action or whether the vector transduction itself exerted any pro-apoptotic effect was examined using the epithelial cell lines OVCAR-3 and MDAH-2774, established from human poorly differentiated serous ovarian cancer.

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Article Synopsis
  • CAR expression is crucial for adenovirus entry into cells, but it is uncertain if gene therapy with the ADV-RSV-TK construct affects CAR levels.
  • Research using various techniques found that CAR is present on cell membranes and undergoes some intracellular movement, depending on how the cells grow.
  • The study showed that TK expression increases with the viral dose and that different cancer cell lines respond differently to the therapy, indicating that the sensitivity to treatment is likely due to internal cellular processes rather than changes in CAR expression.
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Adenovirus (ADV)-mediated gene therapy with the thymidine kinase (TK) gene under control of the Rous sarcoma virus (RSV) promotor followed by the administration of acyclovir has been established in vitro for the treatment of ovarian cancer cells and has been used as the basis for intraperitoneal phase I clinical trials. It is unclear how long a significant degree of transgene translation can be expected after adenovirus-mediated TK transduction, where the transcriptional complex is localized in the nucleus in an episomal fashion and thus without stable integration. The possible interaction of acyclovir pretreatment with subsequent ADV-RSV-TK transduction also remains to be elucidated.

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A total of 60 clinical fungal isolates from patients without prior amphotericin B treatment and three control strains were evaluated for their intrinsic susceptibility to amphotericin B (AmB) using microdilution, Etest and disc diffusion assays, on three media each, Roswell Park Memorial Institute (RPMI) 1640, Antibiotic Medium 3 (AM3) and High Resolution Medium. The fungal strains included isolates of Aspergillus fumigatus (n = 10), Aspergillus terreus (n = 12), Aspergillus nidulans (n = 9), Candida albicans (n = 6) and Candida lusitaniae (n = 23). The A.

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The in vitro susceptibility of 15 strains of six genera of zygomycetes including Rhizopus oryzae (Rhizopus arrhizus), Rhizopus stolonifer, Mucor circinelloides (three), Absidia corymbifera (three), Rhizomucor pusillus (three), Cunninghamella bertholletiae (two), and Syncephalastrum racemosum (two) to nine antifungal agents were determined by the NCCLS M38-A broth microdilution method. Geometric means of the minimal inhibitory concentrations (MIC) were: amphotericin B 0.07 mg l(-1) (range 0.

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