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  • Agranulocytosis  (1)
  • Consolidation therapy  (1)
  • Key words Iliac crest bone biopsy  (1)
  • 1
    ISSN: 1432-0584
    Keywords: Non-Hodgkin's lymphomas ; Chemotherapy ; Consolidation therapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Twenty four patients with high grade malignant NHL (stage II 8, stage III 4, stage IV 12 patients respectively) were treated with a response-oriented regimen: Treatment was initiated according to the CHOP-protocol. Patients achieving at least a partial remission after 2 and a complete remission (CR) after 4 cycles were continued on CHOP to a total of 9 cycles. Patients not meeting these criteria were switched to a combination of Etoposide, Ifosfamide, Methotrexate, and Bleomycin (VIM-Bleo). With CHOP treatment, 16 patients (67%) achieved a CR. Of the remaining 8, 7 were treated with VIM-Bleo; 5 of these entered CR for a overall CR rate of 21/24 (88%). With a median follow up of 28 months 7 patients relapsed: 6 relapses occurred in patients with a rapid initial response and treated only with CHOP. We conclude, that there is a significant risk of relapse even in patients readily responding to CHOP and that consolidation therapy with a non cross-resistant regimen may improve results in these patients.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1963
    Keywords: Schlüsselwörter Knochen ; Beckenkammbiopsie ; Spongiosastruktur ; Morphometrie ; Key words Iliac crest bone biopsy ; Microcomputed tomography ; Cancellous bone ; Histomorphometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary The combined histological and microcomputed analysis of human iliac crest biopsies leads to major advances in our understanding of three-dimensional bone architecture. Microcomputed tomography avoids the time-consuming reconstruction and artifacts of serial sections. Furthermore, its high resolution allows the recording of structural differences as low as 10 mm. Thus, three-dimensional analysis in combination with histological evaluation of cellular dynamics facilitates earlier and easier recording of changes of cancellous bone.
    Notes: Zusammenfassung Es wird die kombinierte Anwendung und quantitative Auswertung 2dimensionaler histologischer Schnitte sowie 2- und 3dimensionaler Mikrotomogramme zur Analyse der Knochenstruktur in Knochenbiopsien beschrieben. Gegenüber dem sehr zeitaufwendigen Verfahren der 3dimensionalen Rekonstruktion aus histologischen Schnitten ist die Mikrotomographie (μCT) schnell genug, um für Routineuntersuchungen in Frage zu kommen. Überdies arbeitet die μCT zerstörungsfrei und vermeidet Schnittartefakte. Art und Ausmaß krankheitsbedingter Spongiosaveränderungen können anhand der 3 D-Tomogramme, dank ihrer hohen Ortsauflösung von rund 10 μm, sehr exakt dargestellt werden. Besonders in Knochenbiopsien mit einer Reduktion der Spongiosastruktur wird das Ausmaß der Strukturveränderungen 3dimensional wesentlich deutlicher als im 2dimensionalen Schnittpräparat. Das Verfahren stellt ein wichtiges Bindeglied zwischen nichtinvasiv erhobenen Strukturdaten und histologischen Veränderungen dar.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1041
    Keywords: Agranulocytosis ; OPC-8212 ; quinolinone derivative ; 3,4-dihydro-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-2(1H)- quinolinone ; bone-marrow progenitor cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary 3,4-dihydro-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-2(1H)-quinolinone (OPC-8212) is a quinolinone derivative with positive inotropic properties. In order to elucidate the effect of OPC-8212 on the haemopoietic system we studied its in vitro effect on bone-marrow progenitor cells (granulocyte/monocyte colonyforming units [CFU-GM] and erythroid burst-forming units [BFU-E]), on the proliferation and secretion of granulocyte/monocyte colony-stimulating factor (GM-CSF) and interferon-γ (IFN-γ) by peripheral lymphocytes, and on GM-CSF secretion by fibroblasts from healthy individuals. The dose-effect relations of OPC-8212 on CFU-GM proliferation and on lymphocytic GM-CSF secretion showed no effect at very low drug concentrations, with a threshold at the lower end of the therapeutic range and highly significant dose-dependent inhibition at concentrations above that threshold. BFU-E, peripheral lymphocyte proliferation and lymphocytic IFN-γ secretion were depressed, although to a lesser extent, in a linear dose-dependent fashion. OPC-8212 did not affect GM-CSF secretion by one strain of fibroblasts but reduced it at higher concentrations in assays with another strain of cells. We conclude that direct toxic effects on bone-marrow progenitor cells, in combination with the inhibition of cytokines involved in the regulation of haemopoiesis in certain susceptible individuals, may be responsible for idiosyncratic reactions to OPC-8212.
    Type of Medium: Electronic Resource
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