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Influence of Mixed Chimerism on Outcome in Children With Anaemia After Haematopoietic Stem Cell Transplantation

Overview
Journal In Vivo
Specialty Oncology
Date 2019 Oct 31
PMID 31662537
Citations 1
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Abstract

Background/aim: In patients with non-malignant diseases, mixed chimerism is not a rare phenomenon. The clinical impacts of chimerism following allogeneic haematopoietic stem cell transplantation (allo-HSCT) in children with congenital anaemia (CA) and severe aplastic anaemia (SAA) were analysed.

Patients And Methods: We studied twenty-seven consecutive children with congenital and acquired anaemia who had undergone allogeneic haematopoietic stem cell transplantations. In the observed group of patients, the median of the follow-up was 6.12 years (2.00-14.8 years).

Results: Overall survival (OS) did not depend on the type of disease p=0.1. OS did not significantly differ in patients who received more than 5x10/kg stem cells (91%) and those who received less than 5x10/kg (85%) (p=0.61). Two patterns of stable mixed chimerism (SMC) were observed: SMC (95-97% cells of the donor), and SMC with a fluctuation between 50-90% of the cells of the donor. None of the surviving patients received immunosuppression treatments of chronic Graft-versus-Host Disease (cGvHD).

Conclusion: Our results showed that mixed chimerism did not influence the survival of children with congenital and aplastic anaemia following allo-HSCT.

Citing Articles

Acute Lymphoblastic Leukemia in Children: Better Transplant Outcomes After Total Body Irradiation-based Conditioning.

Styczynski J, Debski R, Czyzewski K, Gagola K, Marquardt E, Roszkowski K In Vivo. 2021; 35(6):3315-3320.

PMID: 34697163 PMC: 8627707. DOI: 10.21873/invivo.12627.

References
1.
Bonfim C, Ribeiro L, Nichele S, Bitencourt M, Loth G, Koliski A . Long-term Survival, Organ Function, and Malignancy after Hematopoietic Stem Cell Transplantation for Fanconi Anemia. Biol Blood Marrow Transplant. 2016; 22(7):1257-1263. DOI: 10.1016/j.bbmt.2016.03.007. View

2.
Dubovsky J, Daxberger H, Fritsch G, Printz D, Peters C, Matthes S . Kinetics of chimerism during the early post-transplant period in pediatric patients with malignant and non-malignant hematologic disorders: implications for timely detection of engraftment, graft failure and rejection. Leukemia. 1999; 13(12):2059, 2060-9. View

3.
Miano M, Dufour C . The diagnosis and treatment of aplastic anemia: a review. Int J Hematol. 2015; 101(6):527-35. DOI: 10.1007/s12185-015-1787-z. View

4.
Stikvoort A, Gertow J, Sundin M, Remberger M, Mattsson J, Uhlin M . Chimerism patterns of long-term stable mixed chimeras posthematopoietic stem cell transplantation in patients with nonmalignant diseases: follow-up of long-term stable mixed chimerism patients. Biol Blood Marrow Transplant. 2013; 19(5):838-44. DOI: 10.1016/j.bbmt.2013.02.015. View

5.
Yoshida N, Kobayashi R, Yabe H, Kosaka Y, Yagasaki H, Watanabe K . First-line treatment for severe aplastic anemia in children: bone marrow transplantation from a matched family donor versus immunosuppressive therapy. Haematologica. 2014; 99(12):1784-91. PMC: 4258757. DOI: 10.3324/haematol.2014.109355. View