2012
DOI: 10.1002/14651858.cd009159.pub2
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Polyclonal anti-thymocyte globulins for the prophylaxis of graft-versus-host disease after allogeneic stem cell or bone marrow transplantation in adults

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Cited by 45 publications
(41 citation statements)
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“…An important role has been suggested for antithymocyte globulin (ATG) in reducing the incidence and severity of acute and chronic GVHD with a positive rebound on all aspects of QoL. 38 Our results also seem to indicate that patients who undergo HSCT at a younger age (,15 years) are more likely to achieve better longterm HRQoL outcomes (Figure 3). Indeed, these patients basically show a physical and mental health profile that is very similar to that of their peers in the general population.…”
Section: Discussionmentioning
confidence: 50%
“…An important role has been suggested for antithymocyte globulin (ATG) in reducing the incidence and severity of acute and chronic GVHD with a positive rebound on all aspects of QoL. 38 Our results also seem to indicate that patients who undergo HSCT at a younger age (,15 years) are more likely to achieve better longterm HRQoL outcomes (Figure 3). Indeed, these patients basically show a physical and mental health profile that is very similar to that of their peers in the general population.…”
Section: Discussionmentioning
confidence: 50%
“…35 In the current study, the use of ATG led to a lower incidence of grade 3-4 acute GVHD, which is in line with previous studies. 6,[36][37][38] However, no correlation was found between the use of ATG and grade 2-4 GVHD, extensive chronic GVHD, and graft failure, which in previous studies were related to ATG exposure before transplantation. The absence of a correlation may be due to the relatively low incidence of chronic GVHD and graft failure in this cohort (5% and 11% for extensive chronic GVHD and graft failure, respectively).…”
Section: Discussionmentioning
confidence: 87%
“…Patients who received ex-vivo T cell-depleted grafts were specifically excluded, given their historically low rates of grade II-IV acute GVHD of approximately 15%; notably in this setting patients do not receive any post-transplant GVHD prophylaxis [13, 14]. In comparison, in-vivo T cell depletion with ATG administration is less effective at reducing the incidence of GVHD in recipients of conventional grafts, estimated at 28% in a recent large meta-analysis, with most patients still receiving GVHD prophylaxis with calcineurin inhibitors [15]. Thus in this study we allowed inclusion of patients receiving ATG given their continued substantial risk of developing acute GVHD.…”
Section: Methodsmentioning
confidence: 99%