Genotype, oxidase status, and preceding infection or autoinflammation do not affect allogeneic HCT outcomes for CGD

Jennifer W Leiding1,2, Danielle E Arnold3, Suhag Parikh4

  • 1Division of Allergy and Immunology, Department of Pediatrics, Johns Hopkins University, Baltimore, MD.

Blood
|August 10, 2023
PubMed

Insights

Hematopoietic cell transplantation (HCT) offers a definitive cure for chronic granulomatous disease (CGD), leading to improved health and reduced disease burden. Early HCT is recommended, even with active infections or inflammation, to prevent complications.

Area of Science:

  • Immunology
  • Hematology
  • Pediatric Medicine

Background:

  • Chronic granulomatous disease (CGD) is a primary immunodeficiency causing severe infections and inflammation.
  • Hematopoietic cell transplantation (HCT) is the definitive treatment, but optimal patient selection and the impact of active disease require clarification.

Purpose of the Study:

  • To evaluate the outcomes of HCT for CGD.
  • To identify factors influencing survival and complications after HCT.
  • To compare HCT outcomes with conventional non-HCT management.

Main Methods:

  • Multi-institutional retrospective and prospective study of 391 CGD patients (non-HCT and HCT groups).
  • Data collected from 1996 to 2018, with a median follow-up of 3.7 years post-HCT.
  • Multivariate analysis to assess survival predictors.

Main Results:

  • 3-year overall survival was 82% and event-free survival was 69% post-HCT.
  • Lower Lansky/Karnofsky score and HLA-mismatched donors negatively impacted survival.
  • HCT resolved infections, improved growth/nutrition, and reduced medication use, even in patients with active disease pre-transplant.

Conclusions:

  • HCT provides durable resolution of CGD symptoms and reduces disease burden.
  • Patients with active infections or inflammation are suitable candidates for HCT.
  • HCT should be considered early to avoid comorbidities impacting performance status.