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Tipos de Cancer / Leucemia / Leucemia de Célula Pilosa / Recursos de NCI
National Cancer Institute®
Ultima Vez Modificado: 1 de octubre del 2002
1
UI - 1381218
AU - Glaspy JA; Souza L; Scates S; Narachi M; Blatt L; Ambersley J; Golde DW
TI -
Treatment of hairy cell leukemia with granulocyte colony-stimulating
factor and recombinant consensus interferon or recombinant
interferon-alpha-2b.
SO - J Immunother 1992 Apr;11(3):198-208
AD - Department of Medicine, UCLA School of Medicine.
Patients with hairy cell leukemia and neutropenia (absolute neutrophil
count less than 1.5 x 10(9)/L) were treated with recombinant granulocyte
colony-stimulating factor (G-CSF) at doses of 3.6 and 7.2 micrograms/kg
by daily subcutaneous injection, until normalization of neutrophil
counts occurred. Patients then received either recombinant
interferon-alpha-2b (r-IFN-alpha-2b) or a unique IFN, recombinant
consensus IFN (rIFN-con-1), each given at doses of 10 micrograms/m2
subcutaneously three times a week, coupled with continued daily G-CSF
therapy, for 3 months. After 3 months the G-CSF was discontinued;
patients continued to take IFN for 1 year. All 10 patients responded to
G-CSF with normalization of neutrophil counts within 2 weeks; the
increase in neutrophil counts was greater in previously splenectomized
patients. Four patients were treated with r-IFN-alpha-2b, and six were
treated with rIFN-con-1. No patients developed recurrent neutropenia
with the initiation of IFN therapy. Nine patients are evaluable for
response to IFN. Five of six patients demonstrated hematologic
improvement with rIFN-con-1, with two patients obtaining complete
responses. All three patients receiving r-IFN-alpha-2b demonstrated
hematologic improvement; one complete response was observed. Toxicities
of both IFNs included influenza-like symptoms. We conclude that G-CSF
can abrogate the myelosuppressive effects of IFN, and may be a useful
adjunct to this therapy in neutropenic patients. We conclude that
rIFN-con-1, the product of a synthetic gene, has activity in the
treatment of hairy cell leukemia, and merits clinical investigation in
other settings.
2
UI - 8096405
AU - Reiter Z; Tomson S; Ozes ON; Taylor MW
TI -
Combination treatment of 2-chlorodeoxyadenosine and type I interferon on
hairy cell leukemia-like cells: cytotoxic effect and MHC-unrestricted
killer cell regulation.
SO - Blood 1993 Apr 1;81(7):1699-708
AD - Division of Morphological Sciences, Faculty of Medicine, Technion,
Haifa, Israel.
Hairy cell leukemia (HCL) is a lymphoproliferative disorder of B
lymphocytes. Interferons (IFNs), especially of the alpha (alpha)
subtype, have shown a significant antitumor effect in HCL patients.
However, the therapeutic effect of IFN-alpha is still rather limited.
The purine analogue 2-chlorodeoxy-adenosine (2-CdA) was reported
recently to be an effective agent in the treatment of HCL. In the
present study, we find that the HCL cell lines HS-1 and HS-2 as well as
Eskol and its IFN-resistant clone (IREs-4) are sensitive to the
cytotoxic activity of 2-CdA. Combination treatment of IFN-Con1 and 2-CdA
results in a synergistic effect at low doses but an additive inhibitory
effect at higher concentrations. IREs-4 cells responded only to 2-CdA
treatment. All the HCL cell lines are resistant to natural killer (NK)
cell-mediated cytotoxicity (CMC) but are relatively sensitive to
IFN-Con1-primed or interleukin-2 (IL-2)-primed NK-CMC activities. No
inhibition in killing ability was measured when only the effector cells
(NK) were treated with 2-CdA. Pretreatment of the HCL target cells with
2-CdA increases their susceptibility to NK-CMC. Pretreatment with
IFN-Con1 can reduce the susceptibility of target cells to NK-CMC in
HS-1, HS-2, and Eskol cells but not in the IFN-resistant clone IREs-4.
2-CdA abolished this IFN-induced protection against NK-CMC. Normal
fibroblasts only responded to treatment with relatively high doses of
2-CdA, and only a moderate additive cell growth inhibitory effect was
seen in combination of 2-CdA with IFN-Con1. Only high doses of 2-CdA
increased the susceptibility of fibroblast culture to NK-CMC. Thus,
combination of IFN-Con1 and 2-CdA results in an in vitro enhancement of
the direct antiproliferative/cytotoxic activity of each treatment alone
and increases the efficacy of the NK activity against the HCL cell
lines.
3
UI - 3144411
AU - Flandrin G; Coiffier B
TI -
[Perspectives for an epidemiological study of hairy cell leukemia]
SO - C R Acad Sci III 1988;307(3):105-7
AD - Laboratoire central d'Hematologie, Hopital Saint-Louis, Paris.
A strong male predominance (4/1) has been noticed in all series of hairy
cell leukemia (HCL) and we wonder whether there could be a link between
male predominance and occupation. From a series of 161 patients observed
by two different groups, the repartition of profession suggest an
aetiological link between HCL and occupational exposure, particularly
radiation, benzene and other solvents, since it appears that the
proportion of medical workers (6%), mechanic divers (22%), printers and
painters (10%) and farmers (11%) represent a high proportion of
patients. Aware of the relative rarity of the disease we suggested to
set up a national registry of the cases of HCL, the precise incidence of
which remains unknown, and to start a classical case-referent study.
The above citations and abstracts reflect those newly added to CANCERLIT for the month and topic listed in the title. The citations have been retrieved from CANCERLIT using a predefined search strategy of indexed subject terms. Although the search strategy has been refined as best as possible, citations may appear that are not directly related to the topic, and occasionally relevant references may be omitted.
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Calcium Leucovorin, Citrovorum Factor, Folinic Acid
Cladribine (2-CDA, Leustatin®)
Cyclophosphamide (Cytoxan®, Neosar®, Endoxan®)
Cyclosporine (Neoral®, Sandimmune®, Restasis®, Gengraf®)
Cytarabine (Cytosar-U®, Ara-C)
Irinotecan (Camptosar®, CPT-11)
Leucovorin (Calcium Leucovorin, Citrovorum Factor, Folinic Acid)
Calcium Leucovorin, Citrovorum Factor, Folinic Acid
Leucovorin (Calcium Leucovorin, Citrovorum Factor, Folinic Acid)
Leuprolide Acetate (Lupron®, Lupron Depot®, Eligard®, Prostap®, Viadur®) - For Men
Leuprolide Acetate (Lupron®, Lupron Depot®, Eligard®, Prostap®, Viadur®) - For Women
Lupron®, Lupron Depot®, Eligard®, Prostap®, Viadur®
Lupron®, Lupron Depot®, Eligard®, Prostap®, Viadur®
Busulfan (Myleran®, Busulfex®)
Intravesicular Mitomycin (Mutamycin®, Mitomycin-C, given into the bladder)
Mechlorethamine (Mustargen®, Nitrogen Mustard)
mechlorethamine, mustine, Mustargen®
Megestrol (Megace®, Megace-ES®)
Mercaptopurine (Purinethol®, 6-MP)
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Mexate®, Folex®, Rheumatrex®, Amethopterin, MTX
Mitomycin (Mutamycin®, Mitomycin-C)
Morphine Sulfate (Given by IV)
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MS Contin®, Avinza®, Kadian®, Oramorph SR®
Mutamycin®, Mitomycin-C, given into the bladder
Nitrogen mustard (mechlorethamine, mustine, Mustargen®)
Bendamustine Hydrochloride (Treanda®)
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Toposar®, VePesid®, Etopophos®,VP-16
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Tretinoin (Vesanoid®, All-Trans-Retinoic Acid, ATRA)
Triptorelin (Trelstar LA® and Trelstar Depot®)

