TY - JOUR
T1 - Bone marrow versus mobilized peripheral blood stem cells in haploidentical transplants using posttransplantation cyclophosphamide
AU - Ruggeri, Annalisa
AU - Labopin, Myriam
AU - Bacigalupo, Andrea
AU - Gülbas, Zafer
AU - Koc, Yener
AU - Blaise, Didier
AU - Bruno, Benedetto
AU - Irrera, Giuseppe
AU - Tischer, Johanna
AU - Diez-Martin, Jose Luiz
AU - Castagna, Luca
AU - Ciceri, Fabio
AU - Mohty, Mohamad
AU - Nagler, Arnon
N1 - Publisher Copyright:
© 2018 American Cancer Society
PY - 2018/4/1
Y1 - 2018/4/1
N2 - BACKGROUND: Incidence of graft-versus-host disease (GVHD) in haploidentical bone marrow (BM) transplants using posttransplantion cyclophosphamide (PT-Cy) is low, whereas GVHD using mobilized peripheral blood stem cells (PBSC) ranges between 30% and 40%. METHODS: To evaluate the effect of stem cell source in haploidentical transplantation with PT-Cy, we analyzed 451 patients transplanted for acute myeloid leukemia or acute lymphoblastic leukemia reported to the European Society for Blood and Marrow Transplantation. RESULTS: BM was used in 260 patients, and PBSC were used in 191 patients. The median follow-up was 21 months. Engraftment was lower in BM (92% vs 95%, P < 0.001). BM was associated with a lower incidence of stage II-IV and stage III-IV acute GVHD (21% vs 38%, P ≤.01; and 4% vs 14%, P <.01, respectively). No difference in chronic GVHD, relapse, or nonrelapse mortality were found for PBSC or BM. The 2-year overall survival (OS) was 55% versus 56% (P =.57) and leukemia-free survival (LFS) was 49% versus 54% (P =.74) for BM and PBSC, respectively. On multivariate analysis, PBSC were associated with an increased risk of stage II-IV (hazard ratio [HR], 2.1; P <.001) and stage III-IV acute GVHD (HR, 3.8; P <.001). For LFS and OS, reduced intensity conditioning was the only factor associated with treatment failure (LFS: HR, 1.40; P =.04) and relapse (HR, 1.62; P =.02). CONCLUSION: In patients with acute leukemia in first or second remission receiving haploidentical transplantation with PT-Cy, the use of PBSC increases the risk of acute GVHD, whereas survival outcomes are comparable. Cancer 2018;124:1428-37.
AB - BACKGROUND: Incidence of graft-versus-host disease (GVHD) in haploidentical bone marrow (BM) transplants using posttransplantion cyclophosphamide (PT-Cy) is low, whereas GVHD using mobilized peripheral blood stem cells (PBSC) ranges between 30% and 40%. METHODS: To evaluate the effect of stem cell source in haploidentical transplantation with PT-Cy, we analyzed 451 patients transplanted for acute myeloid leukemia or acute lymphoblastic leukemia reported to the European Society for Blood and Marrow Transplantation. RESULTS: BM was used in 260 patients, and PBSC were used in 191 patients. The median follow-up was 21 months. Engraftment was lower in BM (92% vs 95%, P < 0.001). BM was associated with a lower incidence of stage II-IV and stage III-IV acute GVHD (21% vs 38%, P ≤.01; and 4% vs 14%, P <.01, respectively). No difference in chronic GVHD, relapse, or nonrelapse mortality were found for PBSC or BM. The 2-year overall survival (OS) was 55% versus 56% (P =.57) and leukemia-free survival (LFS) was 49% versus 54% (P =.74) for BM and PBSC, respectively. On multivariate analysis, PBSC were associated with an increased risk of stage II-IV (hazard ratio [HR], 2.1; P <.001) and stage III-IV acute GVHD (HR, 3.8; P <.001). For LFS and OS, reduced intensity conditioning was the only factor associated with treatment failure (LFS: HR, 1.40; P =.04) and relapse (HR, 1.62; P =.02). CONCLUSION: In patients with acute leukemia in first or second remission receiving haploidentical transplantation with PT-Cy, the use of PBSC increases the risk of acute GVHD, whereas survival outcomes are comparable. Cancer 2018;124:1428-37.
KW - acute graft-versus-host disease
KW - acute leukemia
KW - haploidentical transplantation
KW - posttransplantation cyclophosphamide
KW - stem cell source
UR - http://www.scopus.com/inward/record.url?scp=85040865297&partnerID=8YFLogxK
U2 - 10.1002/cncr.31228
DO - 10.1002/cncr.31228
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C2 - 29360162
AN - SCOPUS:85040865297
SN - 0008-543X
VL - 124
SP - 1428
EP - 1437
JO - Cancer
JF - Cancer
IS - 7
ER -