Incidence, Risk Factors, and Impact on Transplant Outcomes of Cytokine Release Syndrome After Infusion of Haploidentical Stem Cells With Anti-Thymocyte Globulin.

BACKGROUND

Cytokine release syndrome (CRS) after graft infusion under anti-thymocyte globulin (ATG)-based haploidentical (haplo)-hematopoietic stem cell transplantation is unclear.

OBJECTIVE

The purpose of this study was to explore the clinical implications of CRS after graft infusion under ATG-based haplo-SCT.

STUDY

DESIGN

We retrospectively analyzed the data of 259 patients who underwent haplo-SCT, graded CRS, and evaluated transplant outcomes.

RESULTS

CRS occurred in 103/259 (39.8%) of the recipients. Severe CRS (Grades 3-5) was not observed. Fever was the most common manifestation (89.3%), and all cases occurred only after peripheral blood stem cell (PBSC) infusion. According to the multivariable analysis, being older than 55 years (OR 2.486 (1.124-5.496), p = 0.024), having higher CRP levels during conditioning (OR 3.011 (95% CI, 1.766-5.134), p < 0.001), and receiving PBSC as the sole stem cell source (OR 2.478 (95% CI, 1.077-5.700), p = 0.033) could predict the development of CRS, whereas an HCT-CI score ≥ 2 was an independent risk factor for Grade 2 CRS (OR 4.259 (95% CI, 1.515-11.969, p = 0.006)). The 3-year OS was not significantly different between the two groups, with 79% (95% CI, 61-97) for Grade 2 CRS and 85% (95% CI, 80-90) for Grade 0-1 CRS (p = 0.288). The GRFS rates in the two groups were 69% (95% CI, 49-90) and 67% (95% CI, 60-74), respectively (p = 0.644).

CONCLUSION

Our results suggest that CRS is common in patients receiving ATG-based haplo-SCT and does not affect survival.