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Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2006

Measuring therapeutic response in chronic graft-versus-host disease: National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: IV. Response Criteria Working Group report.

РекомендацииСтатьяResearch Support, N.I.H., IntramuralПоддержка правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Pavletic Steven Z, Martin Paul, Lee Stephanie J, Mitchell Sandra, Jacobsohn David, Cowen Edward W, Turner Maria L, Akpek Gorgun, Gilman Andrew, McDonald George, Schubert Mark, Berger Ann, Bross Peter, Chien Jason W, Couriel Daniel, Dunn J P, Fall-Dickson Jane, Farrell Ann, Flowers Mary E D, Greinix Hildegard, Hirschfeld Steven, Gerber Lynn, Kim Stella, Knobler Robert, Lachenbruch Peter A, Miller Frederick W, Mittleman Barbara, Papadopoulos Esperanza, Parsons Susan K, Przepiorka Donna, Robinson Michael, Ward Michael, Reeve Bryce, Rider Lisa G, Shulman Howard, Schultz Kirk R, Weisdorf Daniel, Vogelsang Georgia B, Response Criteria Working Group

Аннотация

The lack of standardized criteria for quantitative measurement of therapeutic response in clinical trials poses a major obstacle for the development of new agents in chronic graft-versus-host disease (GVHD). This consensus document was developed to address several objectives for response criteria to be used in chronic GVHD-related clinical trials. The proposed measures should be practical for use both by transplantation and nontransplantation medical providers, adaptable for use in adults and in children, and focused on the most important chronic GVHD manifestations. The measures should also give preference to quantitative, rather than semiquantitative, measures; capture information regarding signs, symptoms, and function separately from each other; and use validated scales whenever possible to demonstrate improved patient outcomes and meet requirements for regulatory approval of novel agents. Based on these criteria, we propose a set of measures to be considered for use in clinical trials, and forms for data collection are provided (). Measures should be made at 3-month intervals and whenever major changes are made in treatment. Provisional definitions of complete response, partial response, and progression are proposed for each organ and for overall outcomes. The proposed response criteria are based on current expert consensus opinion and are intended to improve consistency in the conduct and reporting of chronic GVHD trials, but their use remains to be demonstrated in practice.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты