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Tapering and Discontinuation of Thrombopoietin Receptor Agonist Therapy in Patients with Immune Thrombocytopenia: Results from a Modified Delphi Panel.
Cooper, Nichola; Hill, Quentin A; Grainger, John; Westwood, John-Paul; Bradbury, Charlotte; Provan, Drew; Thachil, Jecko; Ramscar, Nicholas; Roy, Anuja.
Afiliación
  • Cooper N; Department of Haematology, Hammersmith Hospital, London, United Kingdom.
  • Hill QA; Department of Haematology, The Leeds Teaching Hospital, Leeds, United Kingdom.
  • Grainger J; Department of Pediatric Haematology, Royal Manchester Children's Hospital, Manchester, United Kingdom.
  • Westwood JP; Department of Haematology, University College London Hospital, London, United Kingdom.
  • Bradbury C; Bristol Haematology and Oncology Centre, University of Bristol, Bristol, United Kingdom.
  • Provan D; Department of Haematology, Barts and the London School of Medicine, London, United Kingdom.
  • Thachil J; Department of Haematology, Central Manchester University Hospital, Manchester, United Kingdom.
  • Ramscar N; Novartis UK, London, United Kingdom.
  • Roy A; Novartis Pharmaceuticals, East Hanover, New Jersey, USA.
Acta Haematol ; 144(4): 418-426, 2021.
Article en En | MEDLINE | ID: mdl-33789275
BACKGROUND: Recent evidence suggests that in patients with immune thrombocytopenia (ITP) with a stable response on thrombopoietin receptor agonists, treatment may be tapered and/or discontinued. OBJECTIVES: The objective of this study was to provide a guide for tapering and discontinuation of TPO-RA therapy in patients with ITP, based on hematologist survey results, existing evidence, and expert consensus. PATIENTS/METHODS: UK hematologists completed a survey to characterize self-reported practice patterns related to TPO-RA tapering and discontinuation in patients with ITP. Using a modified Delphi panel approach, ITP experts developed consensus statements regarding the use of TPO-RA tapering and discontinuation. RESULTS: Survey respondents estimated that 30-34% of their patients were suitable for tapering or discontinuation and that 29-35% of these patients required treatment re-initiation after an average treatment-free interval of 86-106 days. No clear predictors of patient suitability or response to tapering or discontinuation were identified. The ITP expert consensus was that approximately 30% of patients are eligible for tapering and discontinuation, which may be considered after 6-12 months for patients demonstrating an adequate treatment response (platelet count >50,000/µL at ≥75% of assessments in the preceding 6 months). Treatment re-initiation may be considered if the platelet count decreases or if the patient becomes symptomatic. Individual differences need to be taken into account when considering TPO-RA tapering or discontinuation. CONCLUSIONS: Tapering and discontinuation of TPO-RA therapy may be considered for certain patients with ITP. Further study is needed to better predict patients likely to achieve sustained off-treatment responses after tapering and discontinuation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Púrpura Trombocitopénica Idiopática / Receptores de Trombopoyetina Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Acta Haematol Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Púrpura Trombocitopénica Idiopática / Receptores de Trombopoyetina Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Acta Haematol Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Suiza