Zobrazeno 1 - 10
of 169
pro vyhledávání: '"F. Albertioni"'
Autor:
F. Albertioni, Xin Wang
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 29:414-418
Clofarabine, a new-generation purine nucleoside analogue, was thought to work via three mechanisms: incorporation into DNA; induction of apoptosis; and inhibition of ribonucleotide reductase, and showed significant efficacy in pediatric relapsed/refr
Publikováno v:
European Journal of Drug Metabolism and Pharmacokinetics. 20:225-232
2-Chloro-2'-deoxyadenosine (CdA), a newly developed anticancer drug, has been tested in phase II trials in the treatment of lymphoproliferative disorders. 2-Chloro-2'-arabino-fluoro-2'-deoxyadenosine (CAFdA), an acid stable derivative of CdA with pro
Autor:
K Wallman, G Tjønnfjord, C M Stolt, M Hedenus, D Heldal, E Hippe, F Albertioni, Stein A. Evensen, Gunnar Juliusson, Claes Malm
Publikováno v:
Journal of Clinical Oncology. 13:989-995
PURPOSE To evaluate the clinical efficacy and safety of 2-chlorodeoxyadenosine (CdA) when administered by subcutaneous injection to patients with symptomatic hairy cell leukemia (HCL), and to evaluate predictive factors for response. PATIENTS AND MET
Publikováno v:
Journal of Liquid Chromatography. 18:1123-1135
Plasma protein binding of 2-chloro-2′-arabino-fluoro-2′-deoxyadenosine (CAFDA), 2-chloro-2′-deoxyadenosine (CdA), 2-fluoro-1-β-D-arabinofuranosyladenine (F-araA) and structurally related analogues 2-chloro-adenosine (2-Cl-Ado), 5′-chloro-5
Publikováno v:
Journal of Clinical Oncology. 10:1514-1518
PURPOSE The antimetabolite 2-chloro-2'-deoxyadenosine (CdA) is a promising alternative to alkylating agents for the treatment of lymphoproliferative disorders. Its use, however, is hampered by the need for intravenous (IV) administration. The aim of
Publikováno v:
British journal of haematology. 114(3)
The pyrimidine analogue cytosine arabinoside (AraC) is one of the most effective drugs used in the treatment of acute leukaemia. Overexpression of the multidrug resistance (MDR-1) gene and its product, P-glycoprotein (P-gp), is associated with cellul
Autor:
K, Lotfi, E, Månsson, J, Chandra, Y, Wang, D, Xu, E, Knaust, T, Spasokoukotskaja, E, Liliemark, S, Eriksson, F, Albertioni
Publikováno v:
British journal of haematology. 113(2)
Cross-resistance between different classes of anti-neoplastic agents can jeopardize successful combination cancer chemotherapy. In this study, we observed an unexpected cross-resistance between the podophyllotoxine derivative etoposide (VP) and the n
Publikováno v:
Cancer research. 59(23)
2F-Adenine arabinoside (fludarabine, Fara-A) and 2-chloro-2'-deoxyadenosine (cladribine, CdA) are nucleoside analogues with antineoplastic activity in vitro and in vivo. Lack of clinical resistance between CdA and Fara-A has been demonstrated in pati
Autor:
K, Lotfi, E, Månsson, T, Spasokoukotskaja, B, Pettersson, J, Liliemark, C, Peterson, S, Eriksson, F, Albertioni
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 5(9)
The objective of the present study was to investigate the biochemical pharmacology of 2-chloro-2'-arabino-fluoro-2'-deoxyadenosine (CAFdA)--a fluorinated analogue of cladribine [2-chloro-2'-deoxyadenosine, Leustatin (CdA)] with improved acid and meta
Publikováno v:
Advances in experimental medicine and biology. 431
Seventeen patients with CLL were treated with oral 2-chloro-2'-deoxyadenosine (cladribine, CdA, 10 mg/m2) on 3 consecutive days and the pharmacokinetic parameters of CdA in patient plasma and its intracellular nucleotides (CdAMP, CdATP) in circulatin