Haploidentical Related Donor Hematopoietic Stem Cell Transplantation for Dedicator-of-Cytokinesis 8 Deficiency Using Post-Transplantation Cyclophosphamide

التفاصيل البيبلوغرافية
العنوان: Haploidentical Related Donor Hematopoietic Stem Cell Transplantation for Dedicator-of-Cytokinesis 8 Deficiency Using Post-Transplantation Cyclophosphamide
المؤلفون: Mark Parta, Thomas E. Hughes, Alexandra F. Freeman, Heidi H. Kong, Safa Baris, Helen C. Su, Elif Karakoc-Aydiner, Niki M. Moutsopoulos, Nirali N. Shah, Steve M. Holland, Dennis D. Hickstein, Kristen Cole
المساهمون: Shah, Nirali N., Freeman, Alexandra F., Su, Helen, Cole, Kristen, Parta, Mark, Moutsopoulos, Niki M., Baris, Safa, Karakoc-Aydiner, Elif, Hughes, Thomas E., Kong, Heidi H., Holland, Steve M., Hickstein, Dennis D.
المصدر: Biology of Blood and Marrow Transplantation. 23:980-990
بيانات النشر: Elsevier BV, 2017.
سنة النشر: 2017
مصطلحات موضوعية: medicine.medical_specialty, BLOOD, Cyclophosphamide, Platelet Engraftment, Haploidentical transplantation, medicine.medical_treatment, Hematopoietic stem cell transplantation, Gastroenterology, HEMATOLOGIC MALIGNANCIES, NONMALIGNANT DISORDERS, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, VERSUS-HOST-DISEASE, Medicine, Transplantation, HYPER-IGE SYNDROME, business.industry, Hematology, Immune reconstitution, Total body irradiation, COMBINED IMMUNODEFICIENCY, BONE-MARROW-TRANSPLANTATION, Fludarabine, Surgery, CHRONIC GRANULOMATOUS-DISEASE, Dedicator-of-cytokinesis-8 (DOCK8) deficiency, surgical procedures, operative, 030220 oncology & carcinogenesis, Transplantation Conditioning, business, DOCK8 Deficiency, ALPHA-BETA, DOCK8 DEFICIENCY, Busulfan, 030215 immunology, medicine.drug
الوصف: Dedicator-of-cytokinesis 8 (DOCK8) deficiency, a primary immunodeficiency disease, can be reversed by allogeneic hematopoietic stem cell transplantation (HSCT); however, there are few reports describing the use of alternative donor sources for HSCT in DOCK8 deficiency. We describe HSCT for patients with DOCK8 deficiency who lack a matched related or unrelated donor using bone marrow from haploidentical related donors and post-transplantation cyclophosphamide (PT/Cy) for graft-versus-host disease (GVHD) prophylaxis. Seven patients with DOCK8 deficiency (median age, 20 years; range, 7 to 25 years) received a haploidentical related donor HSCT. The conditioning regimen included 2 days of low-dose cyclophosphamide, 5 days of fludarabine, 3 days of busulfan, and 200 cGy total body irradiation. GVHD prophylaxis consisted of PT/Cy 50 mg/kg/day on days +3 and +4 and tacrolimus and mycophenolate mofetil starting at day +5. The median times to neutrophil and platelet engraftment were 15 and 19 days, respectively. All patients attained >90% donor engraftment by day +30. Four subjects developed acute GVHD (1 with maximum grade 3). No patient developed chronic GVHD. With a median follow-up time of 20.6 months (range, 9.5 to 31.7 months), 6 of 7 patients are alive and disease free. Haploidentical related donor HSCT with PT/Cy represents an effective therapeutic approach for patients with DOCK8 deficiency who lack a matched related or unrelated donor. Published by Elsevier Inc. on behalf of the American Society for Blood and Marrow Transplantation.
وصف الملف: application/pdf
تدمد: 1083-8791
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6dcb0f23b44a1bca52e6aa17a1336cfTest
https://doi.org/10.1016/j.bbmt.2017.03.016Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....b6dcb0f23b44a1bca52e6aa17a1336cf
قاعدة البيانات: OpenAIRE