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1.
Br J Haematol ; 182(2): 222-230, 2018 07.
Artigo em Inglês | MEDLINE | ID: mdl-29740809

RESUMO

We sought a regimen that incorporates optimal novel agents and balances efficacy with toxicity in transplant-ineligible multiple myeloma (MM) patients. Our study evaluated modified lenalidomide-bortezomib-dexamethasone (RVD lite) in this population and was administered over a 35-day cycle. Lenalidomide 15 mg was given orally on days 1-21; bortezomib 1·3 mg/m2 weekly subcutaneously on days 1, 8, 15 and 22; and dexamethasone 20 mg orally was given on the day of and day after bortezomib for 9 cycles followed by 6 cycles of consolidation with lenalidomide and bortezomib. The primary objective was to evaluate the overall response rate (ORR); secondary objectives included safety, progression-free survival (PFS) and overall survival (OS). Fifty-three eligible patients were screened between April 2013 and May 2015; 50 received at least one dose of therapy. Median age at study entry was 73 years (range 65-91). The ORR was 86% and 66% of patients achieved a very good partial response or better. Median PFS was 35·1 months (95% confidence interval 30·9-not reached) and median OS was not reached at a median follow-up of 30 months. Peripheral neuropathy was reported in 31 (62%) patients with only 1 patient experiencing grade 3 symptoms. RVD lite is a well-tolerated and highly effective regimen, with robust PFS and OS, in the transplant-ineligible MM population.


Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Mieloma Múltiplo/tratamento farmacológico , Administração Cutânea , Administração Oral , Idoso , Idoso de 80 Anos ou mais , Protocolos de Quimioterapia Combinada Antineoplásica/farmacocinética , Bortezomib/administração & dosagem , Bortezomib/farmacocinética , Dexametasona/administração & dosagem , Dexametasona/farmacocinética , Intervalo Livre de Doença , Esquema de Medicação , Feminino , Humanos , Estimativa de Kaplan-Meier , Lenalidomida/administração & dosagem , Lenalidomida/farmacocinética , Masculino , Medidas de Resultados Relatados pelo Paciente , Estudos Prospectivos , Resultado do Tratamento
2.
Clin J Oncol Nurs ; 12(2): 317-37, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18390467

RESUMO

Constipation is a major source of distress for patients with cancer, significantly affecting quality of life. It can be secondary to disease sequelae, side effects of treatment, or preexisting conditions. It often is unrecognized, underassessed, and ineffectively managed. Nurses play a key role in the prevention and management of constipation and need evidence-based interventions. This article summarizes the existing research evidence for constipation interventions and identifies gaps. Many of the strategies have been evaluated in nononcology populations; researchers should evaluate their effectiveness in oncology populations.


Assuntos
Constipação Intestinal/prevenção & controle , Difusão de Inovações , Medicina Baseada em Evidências/organização & administração , Neoplasias/complicações , Pesquisa em Enfermagem/organização & administração , Enfermagem Oncológica/organização & administração , Causalidade , Constipação Intestinal/diagnóstico , Constipação Intestinal/etiologia , Constipação Intestinal/enfermagem , Fibras na Dieta/administração & dosagem , Humanos , Laxantes/classificação , Laxantes/farmacologia , Laxantes/uso terapêutico , Papel do Profissional de Enfermagem , Avaliação em Enfermagem , Guias de Prática Clínica como Assunto , Qualidade de Vida/psicologia , Projetos de Pesquisa
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