Wynik wyszukiwania w bazie Polska Bibliografia Lekarska GBL
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Tytuł oryginału:
Production of proangiogenic cytokines during thalidomide treatment of multiple myeloma.
Autorzy:
Dmoszyńska
Anna,
Bojarska-Junak
Agnieszka,
Domański
Damian,
Roliński
Jacek,
Hus
Marek,
Soroka-Wojtaszko
Maria
Źródło:
Leuk. Lymphoma 2002: 43 (2) s.401-406, il., tab., bibliogr. 26 poz.
Sygnatura GBL:
312,939
Hasła klasyfikacyjne GBL:
farmacja
hematologia
onkologia
Typ dokumentu:
praca kliniczna
praca opublikowana za granicą
tytuł obcojęzyczny
Wskaźnik treści:
ludzie
dorośli 19-44 r.ż.
dorośli 45-64 r.ż.
dorośli = 65 r.ż.
płeć męska
płeć żeńska
Streszczenie angielskie:
Recently a growing number of studies have suggested the efficacy of thalidomide (THAL) in the treatment of relapsed or resistant multiple myeloma. Some of these studies indicate that the thalidomide antimyeloma effect is associated with decreased vessel density. Here we first present our experience with THAL treatment and then focus on the determination of the role of proangiogenic cytokines during THAL therapy. Thirty relapsing or resistant multiple myeloma (MM) patients were treated with THAL at a median dose of 400 mg/daily. Eighteen responded to THAL therapy and 12 were resistant or intolerant to THAL. We determined the plasma level of basic fibroblast growth factor (bFGF) and vascular endothelial growth factor (VEGF) as the main biological parameters associated with tumour angiogenesis. In addition I1-6 and TNFŕ levels were also assayed. Assessment of peripheral blood (PB) and bone marrow (BM) cytokine levels were done before and during THAL treatment at weeks 4 and 8 of therapy. In the responder group VEGF, bFGF I1-6 and TNFŕ concentrations were significantly decreased after four weeks of therapy both in PB and BM. In the non-responder group no significant changes in bFGF and VEGF levels were observed. However, a significant increase in IL-6 and TNF concentrations was evident. We conclude that the significant decrease of VEGF, bFGF, I1-6 and TNFŕ concentrations reflected response to THAL therapy. Also it seems that VEGF is a better marker of response to treatment than bFGF.
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