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  • 1
    ISSN: 1432-1335
    Keywords: Key words Mobilization ; Chemotherapy ; Correlating CFU-GM and CD34+ cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We examined the efficiency of disease-specific “standard” chemotherapies epirubicin, cyclophosphamide (EC); cyclophosphamide, vincristine, doxorubicin, etoposide, prednisolone (CHOEP); epirubicin, ifosfamide (EPI/IFOS) for peripheral blood progenitor cell (PBPC) mobilization in comparison to well-characterized mobilization protocols, i.e. etoposide, ifosfamide, cisplatin, epirubicin (VIPE) and dexamethasone, carmustine, etoposide, cytarabine, melphalan (DexaBEAM). Twenty-seven patients with various malignancies underwent 75 apheresis procedures for PBPC collection. Median cell yields from all 75 aphereses were 1.18 × 105 mononuclear cells/kg [range (0.28–3.7) × 108], 1.4 × 105 granulocyte/macrophage-colony-forming units (CFU-GM)/kg [range (0.2–11) × 105] and 3.3 × 106 CD34+cells/kg [range (0.35–17.7) × 106. CD34+/CD90+ cells could be mobilized by all mobilization regimens used. The difference observed in the mobilization of CD34+ cells was only of low significance when the mobilization regimens were compared, whereas the mobilizations of MNC and CFU-GM were significantly different between the groups. Breast cancer patients treated with the VIPE regimen (including pretreated women) had a significantly higher CFU-GM rate than patients treated with EC (P = 0.0005). Mobilized CD34+ PBPC were correlated with CFU-GM in all apheresis products. The linear correlation coefficients differed for the various mobilization groups: DexaBEAM (r=0.9, P 〈 0.0001), VIPE (r = 0.68, P = 0.0024), CHOEP (r = 0.52, P = 0.022), EPI/IFOS (r=0.34, P=0.11) and EC (r=0.23, P=0.2). We conclude that clonogenic assays can provide additional information about the autotransplant quality, particularly when alternative or new mobilization regimens are being investigated.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1433-0415
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Etwa 1/3 aller Metastasen manifestiert sich im Skelettsystem. Solitäre Knochenmetastasen sind erheblich seltener als multiple Läsionen. Die Abgrenzung einer ossären Metastase von einem primären Knochentumor wird erleichtert durch die überdurchschnittlich häufige Lokalisation sekundärer Knochentumoren im Becken und in den Wirbelkörpern. Bei 30–35% aller Patienten mit Knochenmetastasen ist zum Zeitpunkt der Diagnose der Primärtumor unbekannt [1, 2]. Knochenmetastasen sind, zusammen mit lymphonodulären und pulmonalen Metastasen, bei unbekanntem Primärtumor in ca. 2/3 aller Fälle nachweisbar [3]. Das vordringliche Ziel der Diagnostik und Therapie von ossären Metastasen mit unbekanntem Primärtumor ist die Symptomlinderung und Komplikationsvermeidung. Einerseits ist die Lebenserwartung von Patienten mit ossären Metastasen – also die Prognose quoad vitam – in Relation zu anderen metastatischen Lokalisationen vergleichsweise gut. Andererseits muß bei Nachweis einer ossären Metastasierung die Prognose quoad curationem in der Regel als infaust eingestuft werden. Lediglich bei ossären Metastasen von Hodentumoren, Lymphomen und Schilddrüsenkarzinomen ist eine kurative Behandlungsmöglichkeit gegeben.
    Type of Medium: Electronic Resource
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