scholarly journals Autologous hematopoietic stem cell transplantation in Systemic Lupus Erythematosus and antiphospholipid syndrome: A systematic review

2017 ◽  
Vol 16 (5) ◽  
pp. 469-477 ◽  
Author(s):  
Alessia Leone ◽  
Massimo Radin ◽  
Ahlam M. Almarzooqi ◽  
Jamal Al-Saleh ◽  
Dario Roccatello ◽  
...  
Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 156-156
Author(s):  
Laisvyde Statkute ◽  
Yu Oyama ◽  
Ann Traynor ◽  
Larissa Verda ◽  
Walter G. Barr ◽  
...  

Abstract Manifestations of systemic lupus erythematosus (SLE) may in most patients be ameliorated with medications that suppress the immune system. Nevertheless, there remains a subset of SLE patients for whom current strategies are insufficient to control disease. Here we report results of autologous non-myeloablative hematopoietic stem cell transplantation single arm trial performed at Northwestern University Feinberg School of Medicine between February 1997 and January 2005 involving 50 patients with SLE refractory to standard immune suppressive therapies and either organ- or life-threatening visceral involvement. Peripheral blood stem cells were mobilized with cyclophosphamide (2.0 g/m2) and G-CSF (5 ug/kg/day), enriched ex vivo by CD34+ immunoselection, cryopreserved, and reinfused after treatment with cyclophosphamide (200 mg/kg) and equine anti-thymocyte globulin (90 mg/kg). The primary endpoint was survival, both overall survival and disease free survival. Secondary endpoints include systemic lupus erythematosus disease activity index (SLEDAI), serology (ANA and antids DNA), complement (C3 and C4), and changes in renal and pulmonary organ function assessed pre-treatment and 6 months, 12 months and then yearly for 5 years. Fifty patients were enrolled and underwent stem cell mobilization. Two patients died after mobilization, one from disseminated mucormycosis and another from active lupus after postponing the transplant for 4 months. Forty-eight patients underwent lupus non-myeloablative hematopoietic stem cell transplantation with no treatment related mortality. By intention to treat, treatment related mortality was 2% (1/50). With a mean follow-up of 29 months (range 6 month to 7.5 years ), overall survival was 84%, and probability of disease free survival at 5 years post transplant was 50%. Secondary analysis demonstrated stabilization of renal function and statistically significant improvement (p ≤ .05) in SLEDAI, ANA, anti-ds DNA, complement, and DLCO adjusted for hemoglobin (DLCOadj). In treatment refractory SLE, autologous non-myeloablative hematopoietic stem cell transplantation results in marked amelioration of disease activity, long term disease remission, improvement in serologic markers, and either stabilization or reversal of organ dysfunction.


2016 ◽  
Vol 31 (suppl_1) ◽  
pp. i134-i134
Author(s):  
Saltanat Tuganbekova ◽  
Natalya Krivoruchko ◽  
Lina Zaripova ◽  
Manarbek Askarov ◽  
Gulnar Rakhimbekova ◽  
...  

Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 150-150 ◽  
Author(s):  
Richard K. Burt ◽  
Yu Oyama ◽  
Laisvyde Statkute ◽  
Nela Krosnjar ◽  
Larissa Verda ◽  
...  

Abstract Unlike leukemia in which the goal of hematopoietic stem cell transplantation (HSCT) is myeloablation and immune suppression is an unwanted side effect, for autoimmune diseases the goal of autologous HSCT is immune ablation and myeloablation is an unwanted side effect. We, therefore, have performed autologous non-myeloablative hematopoietic stem cell transplantation (NST) in treatment refractory systemic lupus erythematosus (SLE) using an intense immune suppressive (“ablative”) regimen followed by autologous stem cell support to shorten the post NST cytopenic interval. Autologous NST has been performed in 45 patients with severe SLE treated over the last 7 years at Northwestern University (Chicago). Candidates were less than 60 years old with either renal (WHO class III or IV nephritis), CNS (cerebritis, transverse myelitis), or pulmonary (alveolar hemorrhage, interstitial pneumonitis, shrinking lung syndrome) involvement or vasculitis despite pulse cyclophosphamide, autoimmune transfusion dependent cytopenias despite steroids, danazol, and alkylating agents, or anti-phospholipid syndrome defined by Sapporo criteria with recurrent thrombi despite anti-coagulation. Peripheral blood stem cells were mobilized with 2.0 g.m2 cyclophosphamide and granulocyte colony-stimulating factor and CD34+ enriched (Isolex, Baxter). The immune ablative conditioning regimen consisted of 200mg/kg cyclophosphamide, and 90mg/kg equine antithymocyte globulin. One patient died from mucormycosis after HSC mobilization (treatment-related mortality-TRM). Four patients died of causes unrelated to NST at 11, 15, 18, and 30 months after NST. Three died of relapsed SLE, one patient with a history of Libman-Sacks died of MRSA endocarditis at 18 months after NST while in remission. Complete remission defined as a prednisone ≤ 10 mg/day with no evidence of active disease and no other immune suppressive drugs except hydroxychloroquine was achieved in 66% of patients. In these 45 patients, autologous NST for SLE had a 2% TRM and 66% long term disease free remission. If patients maintain remission for 2 years, relapse is unlikely. Figure Figure


Blood ◽  
2005 ◽  
Vol 106 (8) ◽  
pp. 2700-2709 ◽  
Author(s):  
Laisvyde Statkute ◽  
Ann Traynor ◽  
Yu Oyama ◽  
Kim Yaung ◽  
Larissa Verda ◽  
...  

AbstractSystemic lupus erythematosus (SLE) is the most common disease associated with antiphospholipid syndrome (APS). We, therefore, evaluated 46 patients with refractory SLE treated by autologous hematopoietic stem cell transplantation (HSCT) for a history of APS prior to transplantation. The prevalence of SLE-related APS in our patient population was 61% (28 of 46 patients with refractory SLE). Nineteen of 28 patients with APS had lupus anticoagulant (LA) or high titers of anticardiolipin antibodies (ACLAs), either immunoglobulin (Ig)G or IgM, when evaluated at study entry. Six of 8 evaluable LA+ patients became and remained LA–; 5 of 7 initially ACLA IgG+ patients and 9 of 11 ACLA IgM+ patients demonstrated normalization of ACLA titers when followed after HSCT. Eighteen of 22 patients refractory to chronic anticoagulation discontinued anticoagulation therapy a median of 4 months after transplantation; 78% of them remained free of thrombotic events and in complete SLE remission for up to 78 months (median, 15 months) after HSCT. There was no treatment-related mortality. Autologous HSCT may be performed safely in patients with APS and appears to be effective therapy for eliminating ALPAs and preventing thrombotic complications in patients with SLE.


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