Hematopoietic cell transplantation and cell therapy activity landscape survey in the Kingdom of Saudi Arabia; a report from the Saudi Society of Blood and Marrow Transplantation (SSBMT) - Scorecard - MDSpire

Hematopoietic cell transplantation and cell therapy activity landscape survey in the Kingdom of Saudi Arabia; a report from the Saudi Society of Blood and Marrow Transplantation (SSBMT)

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  • On behalf of Saudi Society of Blood & Marrow Transplantation (SSBMT)

  • March 8, 2024

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Clinical Scorecard: Survey of Hematopoietic Cell Transplantation and Cell Therapy Practices in Saudi Arabia: Insights from the Saudi Society of Blood and Marrow Transplantation (SSBMT)

At a Glance

CategoryDetail
ConditionHematologic malignancies and non-malignant hematologic disorders including Non-Hodgkin Lymphoma, Leukemia, Hodgkin Lymphoma, Multiple Myeloma, and Sickle Cell Disease
Key MechanismsHematopoietic Cell Transplantation (HCT) as a curative therapy involving autologous and allogeneic stem cell transplants
Target PopulationAdult and pediatric patients with malignant and non-malignant hematologic diseases in Saudi Arabia
Care SettingSpecialized hematology and transplant centers across Central, Western, and Eastern regions of Saudi Arabia

Key Highlights

  • Total of 15,031 first HCT procedures performed in Saudi Arabia since 1984, with 70% allogeneic and 30% autologous transplants.
  • Eight HCT centers distributed regionally with majority activity in the Central region; increasing transplant rates especially between 2016 and 2022.
  • High reporting participation to international registries including EBMT (75%) and CIBMTR (37%), with ongoing efforts for accreditation of centers.

Guideline-Based Recommendations

Diagnosis

  • Diagnosis of hematologic malignancies and non-malignant disorders should be confirmed prior to HCT consideration.
  • HLA typing is essential for donor selection, with full HLA match preferred for allogeneic transplants.

Management

  • Selection of autologous versus allogeneic HCT based on disease type, patient age, and donor availability.
  • Utilization of updated conditioning regimens and transplant techniques to improve outcomes.
  • Centers should pursue accreditation (FACT or JACIE) to ensure quality standards.

Monitoring & Follow-up

  • Participation in national and international registries (EBMT, CIBMTR, SBMTR) for outcome tracking and quality improvement.
  • Regular follow-up of transplant recipients for complications and long-term outcomes.

Risks

  • Risks associated with allogeneic HCT include graft-versus-host disease and transplant-related mortality.
  • Monitoring for infectious complications and relapse post-transplant is critical.

Patient & Prescribing Data

Patients with hematologic malignancies and non-malignant hematologic diseases undergoing first HCT in Saudi Arabia

Majority of transplants are allogeneic (70%) with full HLA-matched donors (85%), and increasing transplant rates observed over recent years.

Clinical Best Practices

  • Ensure multidisciplinary team involvement including adult and pediatric hematology consultants.
  • Maintain comprehensive clinical databases and contribute data to international registries for benchmarking.
  • Expand HCT capacity regionally to improve access, with focus on accreditation and quality assurance.
  • Adopt advances in conditioning regimens and supportive care to optimize transplant outcomes.

References

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