Wynik wyszukiwania w bazie Polska Bibliografia Lekarska GBL
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PALUSZEWSKA
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Tytuł oryginału:
G-CSF administered in time-sequenced setting during remission induction and consolidation therapy of adult acute lymphoblastic leukemia has beneficial influence on early recovery and possibly improves long-term outcome: a randomized multicenter study.
Autorzy:
Hołowiecki
Jerzy,
Giebel
Sebastian,
Krzemień
Sławomira,
Krawczyk-Kuliś
Małgorzata,
Jagoda
Krystyna,
Kopera
Małgorzata,
Hołowiecka
Beata,
Grosicki
Sebastian,
Hellmann
Andrzej,
Dmoszyńska
Anna,
Paluszewska
Monika,
Robak
Tadeusz,
Konopka
Lech,
Maj
Stanisław,
Wojnar
Jerzy,
Wojciechowska
Maria,
Skotnicki
Aleksander,
Baran
Wojciech,
Cioch
Maria
Źródło:
Leuk. Lymphoma 2002: 43 (2) s.315-325, il., tab., bibliogr. 25 poz.
Sygnatura GBL:
312,939
Hasła klasyfikacyjne GBL:
farmacja
hematologia
onkologia
Typ dokumentu:
praca kliniczna
tytuł obcojęzyczny
praca opublikowana za granicą
Wskaźnik treści:
ludzie
Streszczenie angielskie:
Sixty-four untreated adult acute lymphoblastic leukemia (ALL) patients were randomized to receive chemotherapy alone, n = 31 or chemotherapy and granulocyte colony stimulating factor (G-CSF), n = 33. During induction patients received G-CSF for 5 days between four weekly Epirubicin + Vcradministrations, starting 36 h after each application and finishing 48 h before the next one with the intention to possibly generate a cell cycle dependent protection of normal hematopoietic progenitors and to stimulate granulopoiesis. The complete remission (CR) rate equaled 94 p.c. in the G-CSF group and 87 p.c in controls. Patients who received G-CSF, if compared to the controls, had shorter granulocytopenia during induction and consolidation, displayed a lower infection rate, completed the induction-consolidation quicker and stayed shorter in hospital during induction, p 0.001 - 0.04. Follow-up at 2 years revealed a rather higher probability of survival (59 vs. 27 p.c., p = 0.04) and a lower relapse rate (32 vs. 60 p.c.) in G-CSF arm than in controls. The beneficial influence of G-CSF administered in time-sequenced fashion on survival needs further confirmation.
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