Yonsei Med J.  2018 Jul;59(5):643-651. 10.3349/ymj.2018.59.5.643.

Effects and Predictive Factors of Immunosuppressive Therapy Combined with Umbilical Cord Blood Infusion in Patients with Severe Aplastic Anemia

Affiliations
  • 1Department of Hematology, Taihe Hospital Affiliated to Hubei University of Medicine, Shiyan, China. chuchengwan@126.com

Abstract

PURPOSE
To investigate the efficacy and safety of umbilical cord blood (UCB) infusion (UCBI) plus immunosuppressive therapy (IST) treatment in comparison to IST treatment, as well as predictive factors for clinical responses, in severe aplastic anemia (SAA) patients.
MATERIALS AND METHODS
Totally, 93 patients with SAA were enrolled in this cohort study. In the IST group, rabbit antithymocyte globulin (r-ATG) combined with cyclosporine A (CsA) was administered, while in the IST+UBCI group, r-ATG, CsA, and UCB were used.
RESULTS
After 6 months of treatment, UCBI+IST achieved a higher complete response (CR) rate (p=0.002) and an elevated overall response rate (ORR) (p=0.004), compared to IST. Regarding hematopoietic recovery at month 6, platelet responses in the UCBI+IST group were better than those in the IST group (p=0.002), and UCBI+IST treatment facilitated increasing trends in absolute neutrophil count (ANC) response (p=0.056). Kaplan-Meier curves illuminated UCBI+IST achieved faster ANC response (p < 0.001) and platelet response (p < 0.001), compared with IST therapy. There was no difference in overall survival (OS) between the two groups (p=0.620). Furthermore, logistic regression analysis demonstrated that UCBI+IST was an independent predicting factor for both CR (p=0.001) and ORR (p < 0.001), compared to IST; meanwhile, very severe aplastic anemia (VSAA) and ANC could predict clinical responses as well. However, Cox proportional hazard regression indicated that VSAA (p=0.003), but not UCBI+IST, affected OS. Safety profiles showed that UCBI+IST therapy did not elevate adverse events, compared with IST treatment.
CONCLUSION
UCBI+IST achieved better clinical responses and hematopoietic recovery than IST, and was well tolerated in SAA patients.

Keyword

Effect; predictive factors; immunosuppressive therapy (IST); umbilical cord blood infusion (UCBI); severe aplastic anemia (SAA)

MeSH Terms

Anemia, Aplastic*
Antilymphocyte Serum
Blood Platelets
Cohort Studies
Cyclosporine
Fetal Blood*
Humans
Logistic Models
Neutrophils
Umbilical Cord*
Antilymphocyte Serum
Cyclosporine

Figure

  • Fig. 1 Comparison of treatment responses between UCBI+IST and IST treatments at 6 months. Both CR and ORR were higher in the UCBI+IST group than the IST group. Differences between groups were detected by chi-square test. p<0.05 was considered significant. IST, immunosuppressive therapy; UCBI, umbilical cord blood infusion; ORR, overall response rate; CR, complete response; PR, partial response; NR, no remission.

  • Fig. 2 K-M curves analysis for days to ANC, platelet, and hemoglobin responses in the UCBI+IST and IST groups. K-M curves revealed that patients in the UCBI+IST group achieved faster ANC (A) and platelet (B) responses, compared to the IST group. While no difference was discovered in hemoglobin response (C). Differences between groups were detected by K-M curves and log-rank test. p<0.05 was considered significant. K-M, Kaplan-Meier; ANC, absolute neutrophil count; IST, immunosuppressive therapy; UCBI, umbilical cord blood infusion.

  • Fig. 3 Accumulating OS rates of patients in UCBI+IST and IST groups. No difference in accumulating OS rates between the two groups was found. Differences between groups were detected by Kaplan-Meier curve and log-rank test. p<0.05 was considered significant. OS, overall survival; IST, immunosuppressive therapy; UCBI, umbilical cord blood infusion.

  • Fig. 4 Comparison of adverse events between IST and UCBI+IST treatments. No differences were observed in infection, fever, hemorrhage, ATG-related serum diseases, and rush between IST and UCBI+IST groups. Differences between groups were evaluated by chi-square test. p<0.05 was considered significant. IST, immunosuppressive therapy; UCBI, umbilical cord blood infusion; ATG, antithymocyte globulin.


Reference

1. Yu Z, Zhou F, Ge LF, Liu XM, Fang Y, Xie L, et al. High-dose immunosuppressive therapy combined with cord blood infusion and non-myeloablative peripheral blood stem cell transplantation for patients with severe aplastic anemia. Eur Rev Med Pharmacol Sci. 2013; 17:2613–2618. PMID: 24142608.
2. Li Y, Sheng Z, Niu S, Ge L, Ren C, Zou Y. Rapid and complete reconstitution of autologous haemopoiesis after cord blood infusion in treatment-naive patients with severe aplastic anemia receiving high-dose cyclophosphamide/ATG therapy. Eur J Haematol. 2013; 90:45–50. PMID: 23106334.
Article
3. Xie LN, Fang Y, Yu Z, Song NX, Kong FS, Liu XM, et al. Increased immunosuppressive treatment combined with unrelated umbilical cord blood infusion in children with severe aplastic anemia. Cell Immunol. 2014; 289:150–154. PMID: 24838091.
Article
4. Kurre P, Johnson FL, Deeg HJ. Diagnosis and treatment of children with aplastic anemia. Pediatr Blood Cancer. 2005; 45:770–780. PMID: 15706582.
Article
5. Young NS, Calado RT, Scheinberg P. Current concepts in the pathophysiology and treatment of aplastic anemia. Blood. 2006; 108:2509–2519. PMID: 16778145.
Article
6. Scheinberg P, Young NS. How I treat acquired aplastic anemia. Blood. 2012; 120:1185–1196. PMID: 22517900.
Article
7. Füreder W, Valent P. Treatment of refractory or relapsed acquired aplastic anemia: review of established and experimental approaches. Leuk Lymphoma. 2011; 52:1435–1445. PMID: 21635205.
Article
8. Brodsky RA, Chen AR, Dorr D, Fuchs EJ, Huff CA, Luznik L, et al. High-dose cyclophosphamide for severe aplastic anemia: long-term follow-up. Blood. 2010; 115:2136–2141. PMID: 20018919.
Article
9. Hattori M, Terasawa T, Tsushita K, Utsumi M, Kawano F, Saito H, et al. The status of antithymocyte globulin therapy for adult patients in Japan: retrospective analysis of a nationwide survey. Int J Hematol. 2008; 87:48–55. PMID: 18224413.
Article
10. Gluckman E, Broxmeyer HA, Auerbach AD, Friedman HS, Douglas GW, Devergie A, et al. Hematopoietic reconstitution in a patient with Fanconi's anemia by means of umbilical-cord blood from an HLA-identical sibling. N Engl J Med. 1989; 321:1174–1178. PMID: 2571931.
Article
11. Mao P, Wang S, Wang S, Zhu Z, Liv Q, Xuv Y, et al. Umbilical cord blood transplant for adult patients with severe aplastic anemia using anti-lymphocyte globulin and cyclophosphamide as conditioning therapy. Bone Marrow Transplant. 2004; 33:33–38. PMID: 14704655.
Article
12. Rosenthal J, Woolfrey AE, Pawlowska A, Thomas SH, Appelbaum F, Forman S. Hematopoietic cell transplantation with autologous cord blood in patients with severe aplastic anemia: an opportunity to revisit the controversy regarding cord blood banking for private use. Pediatr Blood Cancer. 2011; 56:1009–1012. PMID: 21370429.
Article
13. Auerbach AD. Umbilical cord blood transplants for genetic disease: diagnostic and ethical issues in fetal studies. Blood Cells. 1994; 20:303–309. PMID: 7749111.
14. Eapen M, Rubinstein P, Zhang MJ, Camitta BM, Stevens C, Cairo MS, et al. Comparable long-term survival after unrelated and HLA-matched sibling donor hematopoietic stem cell transplantations for acute leukemia in children younger than 18 months. J Clin Oncol. 2006; 24:145–151. PMID: 16382124.
Article
15. Camitta BM, Storb R, Thomas ED. Aplastic anemia (first of two parts): pathogenesis, diagnosis, treatment, and prognosis. N Engl J Med. 1982; 306:645–652. PMID: 7035946.
16. Bacigalupo A, Hows J, Gluckman E, Nissen C, Marsh J, Van Lint MT, et al. Bone marrow transplantation (BMT) versus immunosuppression for the treatment of severe aplastic anaemia (SAA): a report of the EBMT SAA working party. Br J Haematol. 1988; 70:177–182. PMID: 3056497.
Article
17. Camitta BM. What is the definition of cure for aplastic anemia? Acta Haematol. 2000; 103:16–18. PMID: 10705154.
Article
18. Ustun C, Giannotti F, Zhang MJ, Wang HL, Brunstein C, Labopin M, et al. Outcomes of UCB transplantation are comparable in FLT3+ AML: results of CIBMTR, EUROCORD and EBMT collaborative analysis. Leukemia. 2017; 31:1408–1414. PMID: 28119528.
Article
19. Raut S, Shah S, Shah K, Patel K, Talati S, Parikh S, et al. Improving outcome of thalassemia with hematopoetic stem cell transplantation: an experience of Gujarat Cancer Research Institute. Indian J Hematol Blood Transfus. 2016; 32:284–291. PMID: 27429520.
Article
20. MacMillan ML, DeFor TE, Young JA, Dusenbery KE, Blazar BR, Slungaard A, et al. Alternative donor hematopoietic cell transplantation for Fanconi anemia. Blood. 2015; 125:3798–3804. PMID: 25824692.
Article
21. Xu LX, Cao YB, Liu ZY, Wu YM, Wang ZH, Yan B, et al. [Transplantation of haploidentical-hematopoietic stem cells combined with two kind of third part cells for chronic aplastic anemia: one case report]. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013; 21:1522–1525. PMID: 24370041.
22. Huang X, Liu D. Related HLA-mismatched/haploidentical hematopoietic stem cell transplantation without in vitro T-cell depletion: observations of a single Chinese center. Clin Transpl. 2011; 237–245. PMID: 22755417.
23. Baron F, Nagler A. Novel strategies for improving hematopoietic reconstruction after allogeneic hematopoietic stem cell transplantation or intensive chemotherapy. Expert Opin Biol Ther. 2017; 17:163–174. PMID: 27927023.
Article
24. Azuma H, Watanabe E, Otsuka Y, Negishi Y, Ohkura S, Shinya E, et al. Induction of langerin+ Langerhans cell-like cells expressing reduced TLR3 from CD34+ cord blood cells stimulated with GM-CSF, TGF-β1, and TNF-α. Biomed Res. 2016; 37:271–281. PMID: 27784870.
25. Liu Y, Chen XH, Si YJ, Li ZJ, Gao L, Gao L, et al. Reconstruction of hematopoietic inductive microenvironment after transplantation of VCAM-1-modified human umbilical cord blood stromal cells. PLoS One. 2012; 7:e31741. PMID: 22384064.
Article
26. Liu Y, Yi L, Wang L, Chen L, Chen X, Wang Y. Ginsenoside Rg1 protects human umbilical cord blood-derived stromal cells against tert-Butyl hydroperoxide-induced apoptosis through Akt-FoxO3a-Bim signaling pathway. Mol Cell Biochem. 2016; 421:75–87. PMID: 27522666.
Article
27. Li J, Wong WH, Chan S, Chim JC, Cheung KM, Lee TL, et al. Factors affecting mesenchymal stromal cells yield from bone marrow aspiration. Chin J Cancer Res. 2011; 23:43–48. PMID: 23467386.
Article
28. Sanz J, Arango M, Carpio N, Montesinos P, Moscardó F, Martín G, et al. Autoimmune cytopenias after umbilical cord blood transplantation in adults with hematological malignancies: a single-center experience. Bone Marrow Transplant. 2014; 49:1084–1088. PMID: 24887383.
Article
29. Miano M, Dufour C. The diagnosis and treatment of aplastic anemia: a review. Int J Hematol. 2015; 101:527–535. PMID: 25837779.
Article
30. Peffault de Latour R, Rocha V, Socié G. Cord blood transplantation in aplastic anemia. Bone Marrow Transplant. 2013; 48:201–202. PMID: 23292234.
Article
31. Young NS, Scheinberg P, Calado RT. Aplastic anemia. Curr Opin Hematol. 2008; 15:162–168. PMID: 18391779.
Article
32. Scheinberg P, Cooper JN, Sloand EM, Wu CO, Calado RT, Young NS. Association of telomere length of peripheral blood leukocytes with hematopoietic relapse, malignant transformation, and survival in severe aplastic anemia. JAMA. 2010; 304:1358–1364. PMID: 20858879.
Article
33. Red Blood Cell Disease (Anemia) Group. Chinese Society of Hematology. Chinese Medical Association. Chinese expert consensus on the diagnosis and treatment of aplastic anemia (2017). Zhonghua Xue Ye Xue Za Zhi. 2017; 38:1–5. PMID: 28219216.
34. Ohga S, Ichino K, Goto K, Hattori S, Nomura A, Takada H, et al. Unrelated donor cord blood transplantation for childhood severe aplastic anemia after a modified conditioning. Pediatr Transplant. 2006; 10:497–500. PMID: 16712610.
Article
35. Ruangkanchanasetr P, Srichaikul T, Supaporn T. Triple immunosuppressive therapy can accelerate the recovery of antibody-mediated pure red cell aplasia and allow successful concurrent resumption of erythropoietin. J Med Assoc Thai. 2012; 95(Suppl 5):S92–S95.
36. Sun YQ, He GL, Chang YJ, Xu LP, Zhang XH, Han W, et al. The incidence, risk factors, and outcomes of primary poor graft function after unmanipulated haploidentical stem cell transplantation. Ann Hematol. 2015; 94:1699–1705. PMID: 26152553.
Article
37. Kong Y, Chang YJ, Wang YZ, Chen YH, Han W, Wang Y, et al. Association of an impaired bone marrow microenvironment with secondary poor graft function after allogeneic hematopoietic stem cell transplantation. Biol Blood Marrow Transplant. 2013; 19:1465–1473. PMID: 23879970.
Article
Full Text Links
  • YMJ
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr