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Influence of comorbidities on outcome in 1102 patients with an allogeneic hematopoietic stem cell transplantation.
Janscak, Marie; Stelmes, Anne; van den Berg, Jana; Heim, Dominik; Halter, Joerg; Drexler, Beatrice; Arranto, Christian; Passweg, Jakob; Medinger, Michael.
Afiliación
  • Janscak M; Division of Hematology, University Hospital Basel, Basel, Switzerland.
  • Stelmes A; University of Basel, Basel, Switzerland.
  • van den Berg J; Division of Hematology, University Hospital Basel, Basel, Switzerland.
  • Heim D; University of Basel, Basel, Switzerland.
  • Halter J; Division of Hematology, University Hospital Basel, Basel, Switzerland.
  • Drexler B; University of Basel, Basel, Switzerland.
  • Arranto C; Division of Hematology, University Hospital Basel, Basel, Switzerland.
  • Passweg J; University of Basel, Basel, Switzerland.
  • Medinger M; Division of Hematology, University Hospital Basel, Basel, Switzerland.
Article en En | MEDLINE | ID: mdl-39138337
ABSTRACT
The hematopoietic comorbidity risk index (HCT-CI) is a pre-transplant risk assessment tool used to qualify comorbidities to predict non-relapse mortality (NRM) of patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT). HSCT procedures continue to improve. Therefore, the predictive value of HCT-CI needs to be re-evaluated. Our study is a retrospective analysis of pre-existing comorbidities assessing the relevance of the HCT-CI on the outcome of consecutive patients (n = 1102) undergoing allo-HSCT from 2006-2021. HCT-CI was classified as low (HCT-CI 0), intermediate (HCT-CI 1-2) and high-risk (HCT-CI ≥ 3). At 10 years, NRM for low, intermediate, and high-risk HCT-CI group was 21.0%, 26.0%, and 25.8% (p = 0.04). NRM difference was significant between low to intermediate (p < 0.001), but not between intermediate to high-risk HCT-CI (p = 0.22). Overall survival (OS) at 10 years differed significantly with 49.9%, 39.8%, and 31.1%, respectively (p < 0.001). In multivariate analysis of HCT-CI organ subgroups, cardiac disease was most strongly associated with NRM (HR = 1.73, p = 0.02) and OS (HR = 1.77, p < 0.001). All other individual organ comorbidities influenced NRM to a lesser extent. Further, donor (HR = 2.20, p < 0.001 for unrelated and HR = 2.17, p = 0.004 for mismatched related donor), disease status (HR = 1.41, p = 0.03 for advanced disease) and previous HSCT (HR = 1.55, p = 0.009) were associated with NRM. Improvement in transplant techniques and supportive care may have improved outcome with respect to comorbidities.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Bone Marrow Transplant / Bone marrow transplant / Bone marrow transplantation Asunto de la revista: TRANSPLANTE Año: 2024 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Bone Marrow Transplant / Bone marrow transplant / Bone marrow transplantation Asunto de la revista: TRANSPLANTE Año: 2024 Tipo del documento: Article País de afiliación: Suiza