Your browser doesn't support javascript.
loading
Centralized patient-reported outcome data collection in transplantation is feasible and clinically meaningful.
Shaw, Bronwen E; Brazauskas, Ruta; Millard, Heather R; Fonstad, Rachel; Flynn, Kathryn E; Abernethy, Amy; Vogel, Jenny; Petroske, Charney; Mattila, Deborah; Drexler, Rebecca; Lee, Stephanie J; Horowitz, Mary M; Rizzo, J Douglas.
Afiliação
  • Shaw BE; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Brazauskas R; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Millard HR; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Fonstad R; Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.
  • Flynn KE; Center for Patient Care and Outcomes Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Abernethy A; Flatiron Health, New York, New York.
  • Vogel J; Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.
  • Petroske C; Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.
  • Mattila D; Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.
  • Drexler R; Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.
  • Lee SJ; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Horowitz MM; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Rizzo JD; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Cancer ; 123(23): 4687-4700, 2017 Dec 01.
Article em En | MEDLINE | ID: mdl-28817182
BACKGROUND: Allogeneic hematopoietic cell transplantation (HCT) cures many patients, but often with the risk of late effects and impaired quality of life. The value of quantifying patient-reported outcomes (PROs) is increasingly being recognized, but the routine collection of PROs is uncommon. This study evaluated the feasibility of prospective PRO collection by an outcome registry at multiple time points from unselected HCT patients undergoing transplantation at centers contributing clinical data to the Center for International Blood and Marrow Transplant Research (CIBMTR), and then it correlated the PRO data with clinical and demographic data. METHODS: The Functional Assessment of Cancer Therapy-Bone Marrow Transplant (FACT-BMT), 36-Item Short Form Health Survey (SF-36), and Pediatric Quality of Life Inventory measures were administered before HCT, on day 100, and at 6 and 12 months. Patients were recruited by the transplant center, but posttransplant PRO collection was managed centrally by the CIBMTR. RESULTS: There were 580 eligible patients, and 390 (67%) enrolled. Feasibility was shown by high time-specific retention rates (176 of 238 at 1 year or 74%) and participant satisfaction. Factors associated with higher response rates were an age > 50 years (odds ratio [OR], 1.58; 95% confidence interval [CI], 1.03-2.41; P = .0355), white race (OR, 4.61; 95% CI, 2.66-7.99; P < .0001), and being married (OR, 2.28; 95% CI, 1.42-3.65; P = .0006) for adults and a higher family income for children (OR, 4.99; 95% CI, 2.12-11.75; P = .0002). Importantly, pre-HCT PRO scores independently predicted survival after adjustments for patient-, disease-, and transplant-related factors. The adjusted probabilities of 1-year survival were 56%, 67%, 75%, and 76% by increasing quartiles of the pre-HCT FACT-BMT score and 58%, 72%, 62%, and 82% by increasing quartiles of the pre-HCT SF-36 physical component score. CONCLUSIONS: A hybrid model of local consent for centralized PRO collection is feasible, and pretransplant PROs provide critical prognostic information for HCT outcomes. Cancer 2017;123:4687-4700. © 2017 American Cancer Society.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Coleta de Dados / Transplante de Células-Tronco Hematopoéticas / Neoplasias Hematológicas / Medidas de Resultados Relatados pelo Paciente Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Coleta de Dados / Transplante de Células-Tronco Hematopoéticas / Neoplasias Hematológicas / Medidas de Resultados Relatados pelo Paciente Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Ano de publicação: 2017 Tipo de documento: Article