Source:http://linkedlifedata.com/resource/pubmed/id/10975387
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2000-12-4
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pubmed:abstractText |
The purpose of the study was to evaluate the safety and long-term efficacy of an intensive chemotherapy regimen associated with G-CSF in HIV-associated non-Hodgkin's lymphoma (NHL). Fifty two consecutive patients with HIV infection, aggressive NHL and CD4+ cells > or = 100 x 10(6)/l were included. The median CD4 cell count was 276 x 10(6)/l. Nineteen tumors were of the Burkitt's type, 23 were large cells, 7 immunoblastic, and 3 anaplastic. Twenty-five patients had stage IV disease (bone marrow involvement in 7, and central nervous system in 9). Three cycles of ACVBP (doxorubicine, cyclophosphamide, vindesine, bleomycin, prednisolone) were given. A fourth cycle was delivered to patients in partial remission or with initial bulky disease. The induction was followed by three cycles of CVM (cyclophosphamide, etoposide, methotrexate). G-CSF 5 microg/kg was used at each cycle. Results showed that 37 patients (71%) achieved a complete remission. With a median follow-up of 74 months, 8 of them have relapsed. The median survival was 15 months and 34 patients have died (21 with NHL). The 4-year estimate survival was 33.9% (95% CI, 19.8%-47.4%). The Relative Dose-Intensity of the chemotherapy was 85% for doxorubicine and 87% for cyclophosphamide. In a multivariate analysis, homosexual men and patients with ECOG < 2 had a lower risk for death: RR = 0.32 (95% CI, 0.15-0.65) and RR = 0.36 (95% CI, 0.18-0.74), respectively. Achievement of complete remission was strongly associated with survival. In conclusion, it seems that in HIV-infected patients with NHL and a CD4 cell count above 100 x 10(6)/l, high complete remission rate and prolonged survival can be achieved with the intensive LNHIV-91 regimen.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Bleomycin,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclophosphamide,
http://linkedlifedata.com/resource/pubmed/chemical/Doxorubicin,
http://linkedlifedata.com/resource/pubmed/chemical/Etoposide,
http://linkedlifedata.com/resource/pubmed/chemical/Granulocyte Colony-Stimulating...,
http://linkedlifedata.com/resource/pubmed/chemical/Methotrexate,
http://linkedlifedata.com/resource/pubmed/chemical/Prednisone,
http://linkedlifedata.com/resource/pubmed/chemical/Vindesine
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1042-8194
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
39
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
87-95
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pubmed:dateRevised |
2006-4-24
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pubmed:meshHeading |
pubmed-meshheading:10975387-Actuarial Analysis,
pubmed-meshheading:10975387-Adult,
pubmed-meshheading:10975387-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:10975387-Bleomycin,
pubmed-meshheading:10975387-CD4 Lymphocyte Count,
pubmed-meshheading:10975387-Cyclophosphamide,
pubmed-meshheading:10975387-Disease-Free Survival,
pubmed-meshheading:10975387-Doxorubicin,
pubmed-meshheading:10975387-Drug Evaluation,
pubmed-meshheading:10975387-Etoposide,
pubmed-meshheading:10975387-Female,
pubmed-meshheading:10975387-Follow-Up Studies,
pubmed-meshheading:10975387-Granulocyte Colony-Stimulating Factor,
pubmed-meshheading:10975387-Hospitalization,
pubmed-meshheading:10975387-Humans,
pubmed-meshheading:10975387-Lymphoma, AIDS-Related,
pubmed-meshheading:10975387-Lymphoma, Non-Hodgkin,
pubmed-meshheading:10975387-Male,
pubmed-meshheading:10975387-Methotrexate,
pubmed-meshheading:10975387-Middle Aged,
pubmed-meshheading:10975387-Prednisone,
pubmed-meshheading:10975387-Recurrence,
pubmed-meshheading:10975387-Survival Rate,
pubmed-meshheading:10975387-Treatment Outcome,
pubmed-meshheading:10975387-Vindesine
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pubmed:year |
2000
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pubmed:articleTitle |
Intensive chemotherapy (LNHIV-91 regimen) and G-CSF for HIV associated non-Hodgkin's lymphoma.
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pubmed:affiliation |
Department of Immunology and Hematology, Hôpital St Louis, Paris, France.
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pubmed:publicationType |
Journal Article
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