scholarly journals Lower Graft-versus-Host Disease and Relapse Risk in Post-Transplant Cyclophosphamide–Based Haploidentical versus Matched Sibling Donor Reduced-Intensity Conditioning Transplant for Hodgkin Lymphoma

2019 ◽  
Vol 25 (9) ◽  
pp. 1859-1868 ◽  
Author(s):  
Sairah Ahmed ◽  
Jennifer A. Kanakry ◽  
Kwang W. Ahn ◽  
Carlos Litovich ◽  
Hisham Abdel-Azim ◽  
...  
Keyword(s):  
Hodgkin Lymphoma ◽  
Graft Versus Host Disease ◽  
Reduced Intensity Conditioning ◽  
Host Disease ◽  
Relapse Risk ◽  
Graft Versus Host ◽  
Post Transplant ◽  
Sibling Donor ◽  
Matched Sibling ◽  
Reduced Intensity

scholarly journals Impact of Cyclosporine Levels on the Development of Acute Graft versus Host Disease after Reduced Intensity Conditioning Allogeneic Stem Cell Transplantation

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Irene García Cadenas ◽  
David Valcarcel ◽  
Rodrigo Martino ◽  
J. L. Piñana ◽  
Pere Barba ◽  
...  
Keyword(s):  
Graft Versus Host Disease ◽  
Disease Status ◽  
Blood Levels ◽  
Close Monitoring ◽  
Reduced Intensity Conditioning ◽  
Host Disease ◽  
Graft Versus Host ◽  
The Impact ◽  
Reduced Intensity ◽  
Acute Graft

We analyze the impact of cyclosporine (CsA) levels in the development of acute graft-versus-host disease (aGVHD) after reduced intensity conditioning allogeneic hematopoietic transplantation (allo-RIC). We retrospectively evaluated 156 consecutive patients who underwent HLA-identical sibling allo-RIC at our institution. CsA median blood levels in the 1st, 2nd, 3rd and 4th weeks after allo-RIC were 134 (range: 10–444), 219 (54–656), 253 (53–910) and 224 (30–699) ng/mL; 60%, 16%, 11% and 17% of the patients had median CsA blood levels below 150 ng/mL during these weeks. 53 patients developed grade 2–4 aGVHD for a cumulative incidence of 45% (95% CI 34–50%) at a median of 42 days. Low CsA levels on the 3rd week and sex-mismatch were associated with the development of GVHD. Risk factors for 1-year NRM and OS were advanced disease status (HR: 2.2,P=0.02) and development of grade 2–4 aGVHD (HR: 2.5,P<0.01), while there was a trend for higher NRM in patients with a low median CsA concentration on the 3rd week (P=0.06). These results emphasize the relevance of sustaining adequate levels of blood CsA by close monitoring and dose adjustments, particularly when engraftment becomes evident. CsA adequate management will impact on long-term outcomes in the allo-RIC setting.

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