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1.
Science ; 382(6669): 362, 2023 Oct 27.
Artigo em Inglês | MEDLINE | ID: mdl-37883563

RESUMO

Attacks have left many research laboratories without staff or in ruins.

2.
Science ; 381(6659): 723, 2023 08 18.
Artigo em Inglês | MEDLINE | ID: mdl-37590343

RESUMO

Many fear erosion of academic freedom and loss of talent.

3.
Science ; 381(6653): 17, 2023 Jul 07.
Artigo em Inglês | MEDLINE | ID: mdl-37410826

RESUMO

Researchers criticize approval of new funding for religious schools without requirements for broader curriculum.

5.
Am J Hematol ; 89(11): 1024-9, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25052698

RESUMO

Treatment of primary central nervous system lymphoma (PCNSL) in elderly patients remains unsatisfactory. To develop a new high-dose methotrexate (HD-MTX)-based regimen including idarubicin, a phase 1 multicenter dose escalation study was conducted to determine the maximum-tolerated dose (MTD) of idarubicin. Thirty-five immunocompetent patients with PCNSL were enrolled. The median age was 65 years (range, 60-70 years). MTX and vindesine (VDS) were given at the fixed dose of 3 g/m(2) (6-hr intravenous [IV]) and 3 mg/m(2) IV on day 1, respectively. Prednisolone (PRED) was given at the fixed dose of 60 mg/m(2) (IV or orally) on days 1-5. Idarubicin was escalated in increments of 2 mg/m(2) with doses ranging from 12-18 mg/m(2) IV on day 1. Treatment was repeated three times every 3 weeks. Dose-limiting toxicity (DLT) was defined as grade 4 neutropenia for more than 7 days, thrombocytopenia grade 4 or nonhaematological toxicity more than grade 2. The MTD of idarubicin was reached at 16 mg/m(2) . At this level, the main haematological toxicities were thrombocytopenia grade 4: 5% and neutropenia grade 3 or 4 (52%); the main nonhaematological toxicities were grade 3 or 4 infectious disease (5%) and grade 2 renal failure (9%). For the study population, median overall and progression-free survival were 19 and 13 months, respectively. Our study suggests that the MTD of idarubicin in combination with HD-MTX, VDS, and PRED, should be 16 mg/m(2) . Further studies will be necessary to challenge a standard treatment in elderly patients with PCNSL.


Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Neoplasias do Sistema Nervoso Central/tratamento farmacológico , Linfoma Difuso de Grandes Células B/tratamento farmacológico , Linfoma não Hodgkin/tratamento farmacológico , Idoso , Protocolos de Quimioterapia Combinada Antineoplásica/administração & dosagem , Protocolos de Quimioterapia Combinada Antineoplásica/efeitos adversos , Neoplasias do Sistema Nervoso Central/terapia , Quimiorradioterapia , Intervalo Livre de Doença , Relação Dose-Resposta a Droga , Feminino , Humanos , Idarubicina/administração & dosagem , Idarubicina/efeitos adversos , Imunocompetência , Infecções/etiologia , Estimativa de Kaplan-Meier , Linfoma Difuso de Grandes Células B/terapia , Linfoma não Hodgkin/terapia , Masculino , Metotrexato/administração & dosagem , Metotrexato/efeitos adversos , Pessoa de Meia-Idade , Neutropenia/induzido quimicamente , Cuidados Paliativos , Prednisolona/administração & dosagem , Prednisolona/efeitos adversos , Recidiva , Indução de Remissão , Insuficiência Renal/induzido quimicamente , Trombocitopenia/induzido quimicamente , Resultado do Tratamento , Vindesina/administração & dosagem , Vindesina/efeitos adversos
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