TY - JOUR
T1 - GVHD occurrence does not reduce AML relapse following PTCy-based haploidentical transplantation: a study from the ALWP of the EBMT
AU - Baron, Frédéric
AU - Labopin, Myriam
AU - Tischer, Johanna
AU - Raiola, Anna Maria
AU - Vydra, Jan
AU - Blaise, Didier
AU - Chiusolo, Patrizia
AU - Stölzel, Friedrich
AU - Fanin, Renato
AU - Chevallier, Patrice
AU - Nagler, Arnon
AU - Ciceri, Fabio
AU - Mohty, Mohamad
PY - 2023
Y1 - 2023
N2 - The association between graft-versus-host disease (GVHD) occurrence and acute myeloid leukemia (AML) relapse in patients treated with HLA-haploidentical allogeneic hematopoietic stem cell transplantation (Haplo-HCT) with post-transplant cyclophosphamide (PTCy)-based GVHD prophylaxis has remained debated. Here, we addressed this issue in patients with active AML at transplantation. 2-year cumulative incidences of relapse and leukemia-free survival (LFS) were 49% and 32.3%, respectively. There were no associations between acute nor chronic GVHD of any grade and lower relapse incidence. However, grade I acute GVHD was associated with better LFS (HR = 0.71, 95% CI 0.51–0.99, P = 0.04). In contrast, grade III–IV acute (HR = 3.09, 95% CI 1.87–5.12, P < 0.0001) as well as extensive chronic (HR = 3.3, 95% CI 1.81–6.04, P = 0.0001) GVHD correlated with higher nonrelapse mortality leading to lower LFS (HR = 1.36, 95% CI 0.99–1.86, P = 0.056 and HR = 1.97, 95% CI 1.35–2.89, P = 0.0004, respectively). In conclusion, these data suggest a dissociation of graft-versus-leukemia effects from GVHD in patients with active AML treated with PTCy-based Haplo-HCT.
AB - The association between graft-versus-host disease (GVHD) occurrence and acute myeloid leukemia (AML) relapse in patients treated with HLA-haploidentical allogeneic hematopoietic stem cell transplantation (Haplo-HCT) with post-transplant cyclophosphamide (PTCy)-based GVHD prophylaxis has remained debated. Here, we addressed this issue in patients with active AML at transplantation. 2-year cumulative incidences of relapse and leukemia-free survival (LFS) were 49% and 32.3%, respectively. There were no associations between acute nor chronic GVHD of any grade and lower relapse incidence. However, grade I acute GVHD was associated with better LFS (HR = 0.71, 95% CI 0.51–0.99, P = 0.04). In contrast, grade III–IV acute (HR = 3.09, 95% CI 1.87–5.12, P < 0.0001) as well as extensive chronic (HR = 3.3, 95% CI 1.81–6.04, P = 0.0001) GVHD correlated with higher nonrelapse mortality leading to lower LFS (HR = 1.36, 95% CI 0.99–1.86, P = 0.056 and HR = 1.97, 95% CI 1.35–2.89, P = 0.0004, respectively). In conclusion, these data suggest a dissociation of graft-versus-leukemia effects from GVHD in patients with active AML treated with PTCy-based Haplo-HCT.
KW - AML
KW - Acute myeloid leukemia
KW - HLA-haploidentical
KW - Mismatched unrelated donor
KW - PTCy
KW - Post-transplant cyclophosphamide
KW - AML
KW - Acute myeloid leukemia
KW - HLA-haploidentical
KW - Mismatched unrelated donor
KW - PTCy
KW - Post-transplant cyclophosphamide
UR - http://hdl.handle.net/10807/274581
U2 - 10.1186/s13045-023-01403-x
DO - 10.1186/s13045-023-01403-x
M3 - Article
SN - 1756-8722
VL - 16
SP - N/A-N/A
JO - JOURNAL OF HEMATOLOGY & ONCOLOGY
JF - JOURNAL OF HEMATOLOGY & ONCOLOGY
ER -