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Sequential vs myeloablative vs reduced intensity conditioning for patients with myelodysplastic syndromes with an excess of blasts at time of allogeneic haematopoietic cell transplantation: a retrospective study by the chronic malignancies working party of the EBMT.
Potter, V; Gras, L; Koster, L; Kroger, N; Sockel, K; Ganser, A; Finke, J; Labussiere-Wallet, H; Peffault de Latour, R; Koc, Y; Salmenniemi, U; Smidstrup Friis, L; Jindra, P; Schroeder, T; Tischer, J; Arat, M; Pascual Cascon, M; de Wreede, L C; Hayden, P; Raj, K; Drozd-Sokolowska, J; Scheid, C; McLornan, D P; Robin, M; Yakoub-Agha, I.
Afiliação
  • Potter V; Kings College Hospital NHS Foundation Trust, London, UK. victoriapotter@nhs.net.
  • Gras L; EBMT Statistical Unit, Leiden, Netherlands.
  • Koster L; EBMT Leiden Study Unit, Leiden, Netherlands.
  • Kroger N; University Hospital Eppendorf, Hamburg, Germany.
  • Sockel K; Universitaetsklinikum Dresden, Dresden, Germany.
  • Ganser A; Hannover Medical School, Hannover, Germany.
  • Finke J; University of Freiburg, Freiburg, Germany.
  • Labussiere-Wallet H; Centre Hospitalier Lyon Sud, Lyon, France.
  • Peffault de Latour R; Saint-Louis Hospital, BMT Unit, Paris, France.
  • Koc Y; Medicana International Hospital Istanbul, Istanbul, Turkey.
  • Salmenniemi U; HUCH Comprehensive Cancer Center, Helsinki, Finland.
  • Smidstrup Friis L; Bone Marrow Transplant Unit L, 4043, Copenhagen, Denmark.
  • Jindra P; Charles University Hospital, Pilsen, Czech Republic.
  • Schroeder T; University Hospital Essen, Dusseldorf, Germany.
  • Tischer J; Klinikum Grosshadern, Munich, Germany.
  • Arat M; Demiroglu Bilim University Istanbul Florence Nightingale Hospital, Stanbul, Turkey.
  • Pascual Cascon M; Hospital Regional de Málaga, Málaga, Spain.
  • de Wreede LC; Leiden University Medical Center, Dept of Biomedical Data Sciences, Leiden, Netherlands.
  • Hayden P; Department of Haematology, Trinity College Dublin, St. James's Hospital, Dublin, Ireland.
  • Raj K; University College London Hospitals NHS Trust, London, UK.
  • Drozd-Sokolowska J; Medical University of Warsaw, Warsaw, Poland.
  • Scheid C; University of Cologne, Cologne, Germany.
  • McLornan DP; University College London Hospitals NHS Trust, London, UK.
  • Robin M; Saint-Louis Hospital, BMT Unit, Paris, France.
  • Yakoub-Agha I; CHU de Lille, Univ Lille, INSERM U1286, Infinite, 59000, Lille, France.
Bone Marrow Transplant ; 59(2): 224-231, 2024 02.
Article em En | MEDLINE | ID: mdl-37993503
ABSTRACT
The optimal conditioning for patients with higher risk MDS receiving potentially curative allogeneic haematopoietic stem cell transplant(allo-HCT) remains to be defined. This is particularly the case for patients with excess of blasts at time of allo-HCT. Sequential (Seq) conditioning, whereby chemotherapy is followed rapidly by transplant conditioning, offers an opportunity to decrease disease burden, potentially improving outcomes allo-HCT outcomes. Herein we present the only analysis comparing Seq to myeloablative (MAC) and reduced intensity conditioning (RIC) specifically focussed on MDS patients with excess of blasts at allo-HCT. 303 patients were identified in the EBMT registry, receiving RIC (n = 158), Seq (n = 105), and MAC (n = 40). Median follow-up was 67.2 months and median age at allo-HCT was 59.5 years (IQR 53.5-65.6). For the entire cohort, 3 y overall survival (OS) was 50% (95% CI 45-56%) and relapse free survival (RFS) 45% (95% CI 40-51%). No significant differences in OS (log-rank p = 0.13) and RFS (log-rank p = 0.18) were observed between conditioning protocols. On multivariable analysis, lower performance status, worse IPSS-R cytogenetics, sibling donor (compared to 8/8 MUD) and ≥20% blasts at allo-HCT were associated with worse outcomes. In conclusion, the Seq protocol did little to influence the outcome in this high-risk group of patients, with outcomes mostly determined by baseline disease risk and patient characteristics such as performance status.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Limite: Aged / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Limite: Aged / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article