Received:17 June 2020,
Published:15 September 2020
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Haocheng BAI, Jing FENG, Sanbin WANG. PT-Cy combined with ruxolitinib and tocilizumab prevents aGVHD after haploidentical HSCT[J]. Journal of Third Military Medical University, 2020, 42(17): 1712-1716.
Haocheng BAI, Jing FENG, Sanbin WANG. PT-Cy combined with ruxolitinib and tocilizumab prevents aGVHD after haploidentical HSCT[J]. Journal of Third Military Medical University, 2020, 42(17): 1712-1716. DOI: 10.16016/j.1000-5404.202006155.
Objective
2
To evaluate the efficacy of post-transplant cyclophosphamide (PT-Cy) combined with ruxolitinib and tocilizumab in the prevention of acute graft versus host disease (aGVHD) after haploidentical allogeneic peripheral blood hematopoietic stem cell transplantation (HSCT) by a single-arm prospective study.
Methods
2
A total of 56 patients undergoing haploidentical allogeneic peripheral blood HSCT in our department from January 1
2019 to March 1
2020 were recruited in this study. The GHVD prevention regiments included: cyclophosphamide 40 mg/kg×2 d (+3~+4 d)
ciclosporin 2 mg/kg (+5~+180 d) and mycophenolate sodium enteric-coated tablets 10 mg/kg (+5~+35 d)
tocilizumab 8 mg/kg×1 d (-1 d)
and ruxolitinib (-1~+180 d). The effect of transplantation and adverse effect of aGVHD were observed.
Results
2
The implantation of stem cells was completed successfully among all the 56 patients (100%)
with an implantation time of neutrophils of 13 d and of platelets of 17 d. The incidence of grade Ⅱ~Ⅳ aGVHD was 23.2%
and that of grade Ⅲ~Ⅳ was 12.5%. One patient died due to poor control of aGVHD
6 patients had pulmonary infection; 12 patients had human cytomegalovirus infection or persistent viral copy number rise; 8 patients had Epstein-Barr virus infection or persistent viral copy number rise; and 8 patients had hematopoietic suppression. During the follow-up of 2~16 months (median 8 months)
nonrelapse mortality (NRM) was 7.2%
and overall survival rate (OS) was 91.4%.
Conclusion
2
;PT-Cy combined with ruxolitinib and tocilizumab regimen can effectively prevent aGVHD for haplotype concomitant transplantation patients. No significant increases of bacterial and viral infections are observed. This program has a higher incidence of hematopoietic suppression and a good overall tolerance.
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