Antithymocyte globulin plus post-transplant cyclophosphamide combination as graft-versus-host disease prophylaxis in haploidentical peripheral blood stem cell transplantation for hematological malignancies
Background Post-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT) increase the risk of acute/chronic graft-versus-host disease (GVHD). Whether ATG/PT-Cy is feasible for Asian patients undergoing haploSCT is un...
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| Published in | International journal of hematology Vol. 115; no. 4; pp. 525 - 533 |
|---|---|
| Main Authors | , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Singapore
Springer Singapore
01.04.2022
Springer Nature B.V |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0925-5710 1865-3774 1865-3774 |
| DOI | 10.1007/s12185-021-03280-x |
Cover
| Abstract | Background
Post-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT) increase the risk of acute/chronic graft-versus-host disease (GVHD). Whether ATG/PT-Cy is feasible for Asian patients undergoing haploSCT is unclear, and an optimal strategy for GVHD prophylaxis is needed.
Materials and methods
We retrospectively analyzed 61 hematologic malignancy patients who underwent peripheral blood haploSCT using ATG/PT-Cy from January 2013 to December 2018. We also compared the effects of ATG/PT-Cy (ATG group;
n
= 61) with historical data from patients who underwent haploSCT using sirolimus/PT-Cy (non-ATG group;
n
= 22).
Results
Cumulative incidences of grades II–IV acute GVHD and moderate to severe chronic GVHD did not differ significantly. The ATG group had higher incidence of Epstein–Barr virus (EBV) reactivation, but neither group had post-transplant lymphoproliferative disorders. The ATG group also had a higher OS rate (2-year OS in ATG group vs. non-ATG group: 43.4% vs. 27.3%, respectively;
P
= 0.071).
Conclusion
ATG/PT-Cy is an acceptable strategy for GVHD prophylaxis in Asian patients undergoing haploSCT. |
|---|---|
| AbstractList | Post-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT) increase the risk of acute/chronic graft-versus-host disease (GVHD). Whether ATG/PT-Cy is feasible for Asian patients undergoing haploSCT is unclear, and an optimal strategy for GVHD prophylaxis is needed.BACKGROUNDPost-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT) increase the risk of acute/chronic graft-versus-host disease (GVHD). Whether ATG/PT-Cy is feasible for Asian patients undergoing haploSCT is unclear, and an optimal strategy for GVHD prophylaxis is needed.We retrospectively analyzed 61 hematologic malignancy patients who underwent peripheral blood haploSCT using ATG/PT-Cy from January 2013 to December 2018. We also compared the effects of ATG/PT-Cy (ATG group; n = 61) with historical data from patients who underwent haploSCT using sirolimus/PT-Cy (non-ATG group; n = 22).MATERIALS AND METHODSWe retrospectively analyzed 61 hematologic malignancy patients who underwent peripheral blood haploSCT using ATG/PT-Cy from January 2013 to December 2018. We also compared the effects of ATG/PT-Cy (ATG group; n = 61) with historical data from patients who underwent haploSCT using sirolimus/PT-Cy (non-ATG group; n = 22).Cumulative incidences of grades II-IV acute GVHD and moderate to severe chronic GVHD did not differ significantly. The ATG group had higher incidence of Epstein-Barr virus (EBV) reactivation, but neither group had post-transplant lymphoproliferative disorders. The ATG group also had a higher OS rate (2-year OS in ATG group vs. non-ATG group: 43.4% vs. 27.3%, respectively; P = 0.071).RESULTSCumulative incidences of grades II-IV acute GVHD and moderate to severe chronic GVHD did not differ significantly. The ATG group had higher incidence of Epstein-Barr virus (EBV) reactivation, but neither group had post-transplant lymphoproliferative disorders. The ATG group also had a higher OS rate (2-year OS in ATG group vs. non-ATG group: 43.4% vs. 27.3%, respectively; P = 0.071).ATG/PT-Cy is an acceptable strategy for GVHD prophylaxis in Asian patients undergoing haploSCT.CONCLUSIONATG/PT-Cy is an acceptable strategy for GVHD prophylaxis in Asian patients undergoing haploSCT. Background Post-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT) increase the risk of acute/chronic graft-versus-host disease (GVHD). Whether ATG/PT-Cy is feasible for Asian patients undergoing haploSCT is unclear, and an optimal strategy for GVHD prophylaxis is needed. Materials and methods We retrospectively analyzed 61 hematologic malignancy patients who underwent peripheral blood haploSCT using ATG/PT-Cy from January 2013 to December 2018. We also compared the effects of ATG/PT-Cy (ATG group; n = 61) with historical data from patients who underwent haploSCT using sirolimus/PT-Cy (non-ATG group; n = 22). Results Cumulative incidences of grades II–IV acute GVHD and moderate to severe chronic GVHD did not differ significantly. The ATG group had higher incidence of Epstein–Barr virus (EBV) reactivation, but neither group had post-transplant lymphoproliferative disorders. The ATG group also had a higher OS rate (2-year OS in ATG group vs. non-ATG group: 43.4% vs. 27.3%, respectively; P = 0.071). Conclusion ATG/PT-Cy is an acceptable strategy for GVHD prophylaxis in Asian patients undergoing haploSCT. BackgroundPost-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT) increase the risk of acute/chronic graft-versus-host disease (GVHD). Whether ATG/PT-Cy is feasible for Asian patients undergoing haploSCT is unclear, and an optimal strategy for GVHD prophylaxis is needed.Materials and methodsWe retrospectively analyzed 61 hematologic malignancy patients who underwent peripheral blood haploSCT using ATG/PT-Cy from January 2013 to December 2018. We also compared the effects of ATG/PT-Cy (ATG group; n = 61) with historical data from patients who underwent haploSCT using sirolimus/PT-Cy (non-ATG group; n = 22).ResultsCumulative incidences of grades II–IV acute GVHD and moderate to severe chronic GVHD did not differ significantly. The ATG group had higher incidence of Epstein–Barr virus (EBV) reactivation, but neither group had post-transplant lymphoproliferative disorders. The ATG group also had a higher OS rate (2-year OS in ATG group vs. non-ATG group: 43.4% vs. 27.3%, respectively; P = 0.071).ConclusionATG/PT-Cy is an acceptable strategy for GVHD prophylaxis in Asian patients undergoing haploSCT. Post-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT) increase the risk of acute/chronic graft-versus-host disease (GVHD). Whether ATG/PT-Cy is feasible for Asian patients undergoing haploSCT is unclear, and an optimal strategy for GVHD prophylaxis is needed. We retrospectively analyzed 61 hematologic malignancy patients who underwent peripheral blood haploSCT using ATG/PT-Cy from January 2013 to December 2018. We also compared the effects of ATG/PT-Cy (ATG group; n = 61) with historical data from patients who underwent haploSCT using sirolimus/PT-Cy (non-ATG group; n = 22). Cumulative incidences of grades II-IV acute GVHD and moderate to severe chronic GVHD did not differ significantly. The ATG group had higher incidence of Epstein-Barr virus (EBV) reactivation, but neither group had post-transplant lymphoproliferative disorders. The ATG group also had a higher OS rate (2-year OS in ATG group vs. non-ATG group: 43.4% vs. 27.3%, respectively; P = 0.071). ATG/PT-Cy is an acceptable strategy for GVHD prophylaxis in Asian patients undergoing haploSCT. |
| Author | Lien, Ming-Yu Lin, Ching-Chan Lo, Wen-Jyi Lin, Che-Hung Lin, Chen-Yuan Chen, Tzu-Ting Bai, Li-Yuan Hsieh, Ching-Yun Chiu, Chang-Fang Yeh, Su-Peng |
| Author_xml | – sequence: 1 givenname: Tzu-Ting surname: Chen fullname: Chen, Tzu-Ting organization: Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, China Medical University – sequence: 2 givenname: Ching-Chan surname: Lin fullname: Lin, Ching-Chan organization: Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, China Medical University, College of Medicine, China Medical University – sequence: 3 givenname: Wen-Jyi surname: Lo fullname: Lo, Wen-Jyi organization: Stem Cell Research Laboratory, Department of Medical Research, China Medical University Hospital – sequence: 4 givenname: Ching-Yun surname: Hsieh fullname: Hsieh, Ching-Yun organization: Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, China Medical University, College of Medicine, China Medical University – sequence: 5 givenname: Ming-Yu surname: Lien fullname: Lien, Ming-Yu organization: Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, China Medical University – sequence: 6 givenname: Che-Hung surname: Lin fullname: Lin, Che-Hung organization: Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, China Medical University – sequence: 7 givenname: Chen-Yuan surname: Lin fullname: Lin, Chen-Yuan organization: Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, China Medical University – sequence: 8 givenname: Li-Yuan surname: Bai fullname: Bai, Li-Yuan organization: Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, China Medical University, College of Medicine, China Medical University – sequence: 9 givenname: Chang-Fang surname: Chiu fullname: Chiu, Chang-Fang organization: Cancer Center, China Medical University Hospital, China Medical University – sequence: 10 givenname: Su-Peng orcidid: 0000-0001-6981-8677 surname: Yeh fullname: Yeh, Su-Peng email: supengyeh@gmail.com organization: Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, China Medical University |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35226308$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_jtct_2024_07_017 crossref_primary_10_1038_s41375_024_02225_7 crossref_primary_10_1016_j_blre_2023_101078 crossref_primary_10_3390_curroncol31050211 crossref_primary_10_1038_s41408_024_01032_8 |
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| Keywords | ATG Sirolimus Haploidentical PBSCT |
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Post-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT)... Post-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT) increase the... BackgroundPost-transplant cyclophosphamide (PT-Cy) and calcineurin inhibitors used in peripheral blood haplo-identical stem cell transplantation (haploSCT)... |
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| Title | Antithymocyte globulin plus post-transplant cyclophosphamide combination as graft-versus-host disease prophylaxis in haploidentical peripheral blood stem cell transplantation for hematological malignancies |
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