PMID- 19167686 OWN - NLM STAT- MEDLINE DCOM- 20090406 LR - 20220330 IS - 1523-6536 (Electronic) IS - 1083-8791 (Linking) VI - 15 IP - 2 DP - 2009 Feb TI - Treatment of acute leukemia with unmanipulated HLA-mismatched/haploidentical blood and bone marrow transplantation. PG - 257-65 LID - 10.1016/j.bbmt.2008.11.025 [doi] AB - Allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains one of the best therapeutic options to cure acute leukemia (AL). However, many patients have no human leukocyte antigen (HLA)-matched donor. Recently, we developed a new method for HLA-mismatched/haploidentical transplantation without in vitro T cell depletion (TCD). This method combined granulocyte-colony stimulating factor (G-CSF)-primed bone marrow and peripheral blood with intensive immunosuppression. We analyzed the outcome of 250 consecutive patients with AL who underwent HLA-mismatched/haploidentical transplantation with 1-3 mismatched loci of HLA-A, B, and DR from family donors via our new transplant protocol. Two hundred forty-nine patients achieved sustained, full donor chimerism. The incidence of grade 2-4 acute graft-versus-host disease (aGVHD) was 45.8%, and that of grades 3 and 4 was 13.4%, which was not associated with the extent of HLA disparity. The cumulative incidence of total chronic GVHD (cGVHD) was 53.9% and that of extensive cGVHD was 22.6% in 217 evaluable patients. One hundred forty-one of the 250 patients survived free of disease recurrence at a median of 1092 days (range: 442-2437 days) of follow-up. Seventeen patients received DLI as a treatment for relapse after transplantation and 7 patients achieved leukemia-free survival (LFS). The 3-year probability of LFS for acute myelogenous leukemia (AML) was 70.7% and 55.9%, and for acute lymphoblastic leukemia (ALL) it was 59.7% and 24.8% in standard-risk and high-risk groups, respectively. Lower LFS were associated with diagnosis of acute leukemia in the high-risk group (P= .001, relative risk [RR], 95% confidence interval [CI]: 2.94[1.535-5.631]) and the occurrence of aGVHD of grades 3 and 4 (P= .004). HLA-mismatched/haploidentical HSCT was feasible with unmanipulated blood and bone marrow harvest. FAU - Huang, Xiao-Jun AU - Huang XJ AD - Institute of Hematology, Peking University, Beijing, People's Republic of China. xjhrm@medmail.com.cn FAU - Liu, Dai-Hong AU - Liu DH FAU - Liu, Kai-Yan AU - Liu KY FAU - Xu, Lan-Ping AU - Xu LP FAU - Chen, Huan AU - Chen H FAU - Han, Wei AU - Han W FAU - Chen, Yu-Hong AU - Chen YH FAU - Zhang, Xiao-Hui AU - Zhang XH FAU - Lu, Dao-Pei AU - Lu DP LA - eng PT - Clinical Trial PT - Journal Article PL - United States TA - Biol Blood Marrow Transplant JT - Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation JID - 9600628 RN - 0 (HLA Antigens) RN - 0 (HLA-A Antigens) RN - 0 (HLA-B Antigens) RN - 0 (HLA-DR Antigens) SB - IM MH - Acute Disease MH - Adolescent MH - Adult MH - Bone Marrow Transplantation/*methods MH - Child MH - Child, Preschool MH - Disease-Free Survival MH - Female MH - Graft vs Host Disease/immunology MH - HLA Antigens/*immunology MH - HLA-A Antigens MH - HLA-B Antigens MH - HLA-DR Antigens MH - Haplotypes/*immunology MH - Histocompatibility/*immunology MH - Humans MH - Leukemia/*therapy MH - Leukemia, Myeloid, Acute/mortality/therapy MH - Male MH - Middle Aged MH - Peripheral Blood Stem Cell Transplantation/*methods MH - Precursor Cell Lymphoblastic Leukemia-Lymphoma/mortality/therapy MH - Transplantation, Homologous/immunology MH - Treatment Outcome MH - Young Adult EDAT- 2009/01/27 09:00 MHDA- 2009/04/07 09:00 CRDT- 2009/01/27 09:00 PHST- 2008/08/25 00:00 [received] PHST- 2008/11/14 00:00 [accepted] PHST- 2009/01/27 09:00 [entrez] PHST- 2009/01/27 09:00 [pubmed] PHST- 2009/04/07 09:00 [medline] AID - S1083-8791(08)00576-4 [pii] AID - 10.1016/j.bbmt.2008.11.025 [doi] PST - ppublish SO - Biol Blood Marrow Transplant. 2009 Feb;15(2):257-65. doi: 10.1016/j.bbmt.2008.11.025.