Haploidentical hematopoietic cell transplantation using in vitro T cell depleted grafts as salvage therapy in patients with disease relapse after prior allogeneic transplantation

2017 ◽  
Vol 96 (5) ◽  
pp. 817-827 ◽  
Author(s):  
Sebastian P. Haen ◽  
Christiane Groh ◽  
Michael Schumm ◽  
Linus Backert ◽  
Markus W. Löffler ◽  
...  
Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 4582-4582
Author(s):  
Shogo Kobayashi ◽  
Atsushi Kikuta ◽  
Masaki Ito ◽  
Hideki Sano ◽  
Kazuhiro Mochizuki ◽  
...  

Abstract Abstract 4582 Refractory acute leukemia who do not achieve second or subsequent complete remission (CR) have an extremely poor prognosis. Non-T-cell depleted (TCD) HLA-haploidentical hematopoietic cell transplantation (haplo-HCT) is a form of adoptive cellular therapy that has a high degree of efficacy in hematologic malignancies. The major problems of non-TCD haplo-HCT are severe graft-versus-host disease (GVHD), graft failure (GF) and high-risk of early death. We conducted non-TCD haplo-HCT for children with acute leukemia in non-remission as a novel therapeutic strategy. Five consecutive children under 15 (0-13) years old with hematological malignancies underwent non-TCD haplo-HCT from family donors between November 2002 and July 2010 at Fukushima Medical University Hospital. All patients were in non-remission at transplantation. One donor was mother and the other 4 donors were fathers of the patients. One patient was in 3 loci, and 4 patients were mismatched 4 loci of the allele level for HLA-A, -B, -C and -DRB1. The blast count in the marrow before transplantation was 80%, 75%, 34%, 10% and 96%, respectively. There were two acute myelogenous leukemia and three acute lymphoblastic leukemia. There were two refractory diseases to chemotherapy and three relapses after HSCT. All of them received myeloablative conditioning (2 Busulfan based, 3 TBI based). Type of graft were bone marrow in one and peripheral blood stem cell in 4. Total of 9.9 ×108/kg of nucleated bone marrow cells were infused in the patient received BMT. The median number of TNC and CD34+ cell doses were 11 (8-21.4)×108/kg and 7.9 (6.5-8.8)×106/kg in PBSCT, respectively. GVHD prophylaxis were combination of tacrolimus, methotrexate was given in one patient, combination of tacrolimus, methotrexate and prednisolone in one, combination of tacrolimus, methotrexate, prednisolone, and antihuman thymocyte immunoglobulin (ATG) in 3. All patients achieved primary engraftment at median of 13 days (11 -15) and achieved complete remission. Five patients developed acute GVHD, with grade 1 in two patients, grade 2 in two patients, grade 3 in one patient. Chronic GVHD occurred in 2 of 4 evaluable patients. Infectious complications including 2 CMV reactivation, 1 CMV-IP, 1 invasive aspergillosis, 1 candida sepsis were observed. One patient died from CMV-IP in remission, remaining 4 patients survived disease-free + 4, + 9, + 10 and + 94 months after non-TCD haplo-HCT, respectively. These preliminary results suggested that non-TCD haplo-HCT is effective strategy in children with refractory leukemia. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 4676-4676 ◽  
Author(s):  
Sara Lozano Cerrada ◽  
David Marin ◽  
Gabriela Rondon ◽  
Celina Ledesma ◽  
Uday R. Popat ◽  
...  

Abstract Introduction: The number of available salvage agents for patients with relapsed ALL has significantly increased in the last 5 years. Furthermore, these recent therapies, such as antibody and T-cell therapy, have a distinct mechanism of action and toxicity profile compared to conventional multi-drug chemotherapy combinations which have been the mainstay of ALL treatment. We sought to investigate the potential efficacy and toxicity of these agents when used prior to allogeneic hematopoietic cell transplantation (HCT), and to compare overall transplant outcomes with these different types of therapies. Methods: 126 consecutive patients with ALL in second complete remission (CR2) underwent HCT at MD Anderson Cancer Center between January 2004 and December 2015. The patient and transplant characteristics are described in Table 1. The probabilities of outcomes were calculated with the Kaplan-Meyer method. Variables found to be significant at the p<0.1 level were included in a Cox regression multivariate model. All p values are two sided. Results: With a median follow-up of 38.4 months (range 6-125), the 3-year overall survival(OS), progression-free survival (PFS) and transplant-related mortality (TRM) rates were 34.6%, 29.5% and 33.2%, respectively, for the entire group. Patients receiving well-matched transplant donors fared better than those receiving mismatched donors (Figure 1). Second CR was attained in 104 patients with the first line of salvage therapy. Salvage therapy consisted of HyperCVAD-based chemotherapy alone in 57 patients, chemotherapy plus tyrosine kinase inhibitors (TKI) in 18, chemotherapy plus rituximab in 11, chemotherapy plus inotuzumab in 5, inotuzumab monotherapy in 12, and blinatumomab monotherapy in one patient. We found no statistical difference in OS, PFS or TRM following transplant based on these prior therapies. Furthermore, we found no difference in the expected probabilities of acute or chronic GVHD. In the 8 patients treated with blinatumomab monotherapy for first or subsequent salvage, all 8 progressed following transplant at a median of 4.5 months. Eight out of 126 (6.3%) patients developed VOD; 3 out of 26 (11.5%) patients treated with inotuzumab developed VOD, but this did not impact TRM post HCT compared with other treatment groups. Conclusions: Transplant outcomes were not different following antibody or T-cell salvage therapy as compared to conventional chemotherapy in this single center, retrospective study. Larger numbers of patients will need to be studied as we continue to incorporate these newer therapies into our treatment regimens. Disclosures Ciurea: Cyto-Sen Therapeutics: Equity Ownership; Spectrum Pharmaceuticals: Other: Advisory Board. Jabbour:BMS: Consultancy; ARIAD: Consultancy; Pfizer: Research Funding; Pfizer: Consultancy; Novartis: Research Funding; ARIAD: Research Funding. Kantarjian:ARIAD: Research Funding; Bristol-Myers Squibb: Research Funding; Amgen: Research Funding; Pfizer Inc: Research Funding; Delta-Fly Pharma: Research Funding; Novartis: Research Funding. Champlin:Ziopharm Oncology: Equity Ownership, Patents & Royalties; Intrexon: Equity Ownership, Patents & Royalties.


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