Reduced-intensity Bu/Cy+ATG as conditioning regimen for allogeneic hematopoietic stem cell transplantation in the patients with hematopoietic malignant disease
Yun Cai
Abstract
Yun Cai
Abstract
Objective To study the efficacy of allogeneic hematopoietic stem cell transplantation(Allo-hsct) treating hematopoietic malignant disease patients prepared with dose-reduced Bu/Cy+ATG conditioning regimen.Methods Eighteen patients who treated with dose-reduced Bu/Cy+ATG as conditioning regimen(mephalan:4 mg/(kg·d)×3,60 mg/(kg·d)×2,Me-CCNU 450 mg/(m2·d)×1,ATG 3 mg/(kg·d)×2,and graft-versus-host disease(GVHD) prophylaxis included cyclosporin A,MMF and MTX.Results All patients achieved full donor chimerism without graft failure.After a median follow-up period of 22 months(range,3-40 months),10 patients survived event-free,in the patients who treated with HSCT,the survival rate was 66.7%.Conclusion The reduced-intensity conditioning regimen using Bu/Cy+ATG is safe,effective and with less complications in HSCT for patients with hematological malignancies.
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Objective To study the efficacy of allogeneic hematopoietic stem cell transplantation(Allo-hsct) treating hematopoietic malignant disease patients prepared with dose-reduced Bu/Cy+ATG conditioning regimen.Methods Eighteen patients who treated with dose-reduced Bu/Cy+ATG as conditioning regimen(mephalan:4 mg/(kg·d)×3,60 mg/(kg·d)×2,Me-CCNU 450 mg/(m2·d)×1,ATG 3 mg/(kg·d)×2,and graft-versus-host disease(GVHD) prophylaxis included cyclosporin A,MMF and MTX.Results All patients achieved full donor chimerism without graft failure.After a median follow-up period of 22 months(range,3-40 months),10 patients survived event-free,in the patients who treated with HSCT,the survival rate was 66.7%.Conclusion The reduced-intensity conditioning regimen using Bu/Cy+ATG is safe,effective and with less complications in HSCT for patients with hematological malignancies.
Key concepts: Medicine, Conditioning regimen, Hematopoietic stem cell transplantation, Regimen, Internal medicine, Transplantation, Gastroenterology, Haematopoiesis