Association of pre-existing comorbidities with outcome of allogeneic hematopoietic cell transplantation. A retrospective analysis from the EBMT - Scorecard - MDSpire

Association of pre-existing comorbidities with outcome of allogeneic hematopoietic cell transplantation. A retrospective analysis from the EBMT

  • By

  • Olaf Penack

  • Christophe Peczynski

  • Mohamad Mohty

  • Ibrahim Yakoub-Agha

  • Rafael de la Camara

  • Bertram Glass

  • Rafael F. Duarte

  • Nicolaus Kröger

  • Hélène Schoemans

  • Christian Koenecke

  • Zinaida Peric

  • Grzegorz W. Basak

  • October 30, 2021

  • 0 min

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Clinical Scorecard: Impact of Pre-existing Comorbid Conditions on Outcomes Following Allogeneic Hematopoietic Cell Transplantation: A Retrospective Study from the EBMT

At a Glance

CategoryDetail
ConditionAllogeneic hematopoietic cell transplantation (allo-HCT) for hematologic malignancies
Key MechanismsPre-existing comorbidities influence non-relapse mortality (NRM) post-allo-HCT; graft-versus-host disease, infections, and conditioning toxicities drive mortality
Target PopulationAdult patients (>18 years) with hematologic malignancies undergoing first allo-HCT from matched sibling or unrelated donors
Care SettingMulticenter transplant centers reporting to the European Society for Blood and Marrow Transplantation (EBMT)

Key Highlights

  • The Hematopoietic Cell Transplantation Comorbidity Index (HCT-CI) is adapted from Charlson index to predict NRM in allo-HCT patients.
  • EBMT registry data from 2010-2018 was used to analyze the impact of pre-existing comorbidities on transplant outcomes.
  • Comorbidities assessed include solid tumors, inflammatory bowel disease, diabetes, renal, hepatic, pulmonary, cardiac, cerebrovascular diseases, obesity, psychiatric disturbances, and others.

Guideline-Based Recommendations

Diagnosis

  • Assess pre-existing comorbidities comprehensively using EBMT Med-A form prior to allo-HCT.
  • Evaluate pulmonary function (DLCO, FEV1) to determine severity of pulmonary comorbidity.
  • Use standardized criteria for grading acute and chronic GVHD post-transplant.

Management

  • Incorporate comorbidity assessment into transplant risk stratification using HCT-CI.
  • Optimize donor selection and conditioning regimens considering patient comorbidities.
  • Apply in vivo T-cell depletion (e.g., anti-thymocyte globulin or alemtuzumab) as appropriate to reduce GVHD risk.

Monitoring & Follow-up

  • Regular follow-up reporting to EBMT registry including comorbidity status and transplant outcomes.
  • Monitor for infectious complications and GVHD severity post-transplant.
  • Track non-relapse mortality and relapse incidence using competing risk analysis.

Risks

  • Higher comorbidity burden is associated with increased non-relapse mortality.
  • Pulmonary, hepatic, cardiac, and renal comorbidities significantly impact transplant outcomes.
  • Infections requiring ongoing antimicrobial therapy post-transplant increase mortality risk.

Patient & Prescribing Data

Adults with hematologic malignancies undergoing first allo-HCT with available full comorbidity data

Improved donor selection and supportive care over time may reduce the impact of comorbidities on NRM; ongoing evaluation of HCT-CI predictive value is necessary.

Clinical Best Practices

  • Ensure complete and accurate documentation of pre-existing comorbidities prior to allo-HCT.
  • Use the HCT-CI score to guide individualized risk assessment and transplant decision-making.
  • Maintain multidisciplinary care including transplant physicians, infectious disease specialists, and supportive care teams.
  • Regularly update transplant protocols to reflect evolving evidence on comorbidity impact and management.

References

Original Source(s)

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