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Comparison of rabbit ATLG and ATG for GVHD prophylaxis in hematological malignancies with haploidentical hematopoietic stem cell transplantation
Rabbit anti-human T lymphocyte globulin (ATLG) and anti-thymocyte globulin (ATG) are commonly used for graft-versus-host disease (GVHD) prophylaxis in allogeneic hematopoietic stem cell transplantation (HSCT). Yet, their efficacy and safety have seldom been compared in hematological malignancies wit...
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Published in: | Annals of hematology 2024-05, Vol.103 (5), p.1729-1736 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Rabbit anti-human T lymphocyte globulin (ATLG) and anti-thymocyte globulin (ATG) are commonly used for graft-versus-host disease (GVHD) prophylaxis in allogeneic hematopoietic stem cell transplantation (HSCT). Yet, their efficacy and safety have seldom been compared in hematological malignancies with haploidentical HSCT. A retrospective analysis with 28 ATLG (total dosage, 20–30 mg/kg) and 18 ATG (total dosage, 8–10 mg/kg) patients were performed. The cumulative incidences of chronic GVHD and relapse were comparable between both groups. ATLG showed a trend towards a lower acute GVHD incidence (28.6% vs. 44.4%,
P
= 0.242) and 3-year non-relapse mortality (10.7% vs. 27.8%,
P
= 0.160), and had a significantly higher 3-year overall survival (OS, 64.3% vs. 33.3%,
P
= 0.033) and GVHD-free and relapse-free survival (GRFS, 32.1% vs. 11.1%,
P
= 0.045) compared with ATG. Multivariate Cox regression analysis demonstrated ATLG was independently associated with a favorable OS (hazard ratio [HR] = 0.37, 95% confidence interval [CI]: 0.16–0.86,
P
= 0.020) and GRFS (HR = 0.51, 95%CI: 0.26-1.00,
P
= 0.051). Furthermore, ATLG had a lower risk of fever (25.0% vs. 61.1%,
P
= 0.014) and hemorrhage cystitis (7.1% vs. 38.9%,
P
= 0.008) than ATG-T. In conclusion, ATLG confers more survival benefit and a better safety profile than ATG and can be used in hematological malignancies with haploidentical HSCT. Prospective designed trials with a larger sample size are warranted to confirm the results in the future. |
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ISSN: | 0939-5555 1432-0584 |
DOI: | 10.1007/s00277-024-05724-w |