Abstract
Acute graft-versus-host-disease (aGVHD) is a frequent and often lethal complication of allogeneic hematopoeitic stem cell transplant (allo HSCT) despite current prophylactic regimen. It is fueled by the release of pro-inflammatory cytokines such as interleukin-6 (IL-6), leading to damage of host tissues. Front-line treatment with glucocorticoids provide 30-40% complete response. Tocilizumab is a humanized anti-IL-6 receptor (IL-6R) monoclonal antibody that binds to both soluble and membrane-expressed IL-6R, inhibiting IL-6–mediated proinflammatory activity. A case report and a recent small series (8 patients) with steroid refractory GVHD(SR GVHD) showed encouraging single agent activity of tocilizumab(Gergis et al, 2010; Drobyski et al, 2011). We report our experience on 9 patients who had SR aGVHD and received tocilizumab therapy.
Tocilizumabwas administered intravenously at a dose of 8 mg/kg every 2 to 3 weeks. aGVHD grading and responses were based on consensus criteria (Przepiorka et al, 1995). Patients were monitored for toxicities and infections.
The median age at transplant was 48 years (range 25-61). Four patients had double cord allo HSCT, 2 had matched related, 2 unrelated (with one 9/10 matched) and 1 haploidentical after a failed cord HSCT. Six patients had received myeloablative and 3 reduced intensity allo HSCT. All but one patient received tacrolimus and methotrexate for aGVHD prophylaxis, and all were in complete remission of their underlying disease at time of aGVHD. Table 1 includes responses and outcomes to tocilizumab therapy. All patients had GI involvement and 6 patients had two organs involved. Median aGVHD grade was 3 (range 3-4). The median time from first aGVHD onset to tocilizumab administration was 44 days (range 14-176). The median number of infusions was 2(1-6). There were no allergic or infusion-related events. Two patients (22%) had a complete response (CR), and two had mixed responses with CR in one organ, but no response in another. Only one of nine patients survived. Six patients (67%) died from aGVHD and its complications, one from CMV and one from septic shock. The median survival from start of tocilizumab was 26 days (range 13-759).
Patient . | Day of aGVHD Onset . | Overall Grade of GVHD Prior . | Organ Involvement (stage) . | GVHD Treatments Prior . | Day to Tocilizumab Administration from Transplant . | # of Doses . | Overall Response to Tocilizumab . | Current Status . | Days Surviving since Tocilizumab Initiation . | Primary Cause of Death . |
---|---|---|---|---|---|---|---|---|---|---|
1 | + 26 | 3 | GI (2) Liver ( 2) | Steroids Basiliximab | + 70 | 6 | CR | Dead | 308 | Infection- CMV |
2 | +30 | 4 | GI (3) Liver (4) | Steroids Budesonide | + 176 | 2 | NR | Dead | 25 | aGVHD |
3 | +18 | 3 | GI (4) Liver (1) | MMF Budesonide Steroids | + 39 | 1 | GI : NR Liver: CR | Dead | 20 | aGVHD |
4 | +60 | 3 | GI (2) | Steroids Tacrolimus MMF | + 74 | 6 | CR | Alive and disease free | 759 | NA |
5 | + 25 | 3 | Skin (2) GI (4) | Steroids Sirolimus Budesonide | +86 | 1 | NR | Dead | 13 | Alveolar hemorrhage aGVHD |
6 | + 90 | 3 | GI (1) Liver(2) | Budesonide Steroids Tacrolimus | +266 | 2 | GI: CR Liver: NR | Dead | 26 | Klebsiella pneumonia, septic shock |
7 | +28 | 3 | GI (4) | Sirolimus Budesonide Steroids | +97 | 2 | NR | Dead | 33 | aGVHD |
8 | +43 | 3 | Liver (3) GI(3) | MMF Budesonide Steroids | +85 | 2 | NR | Dead | 16 | aGVHD |
9 | +29 | 4 | GI (4) Liver (4) | Steroids MMF budesonide | +43 | 2 | NR | Dead | 107 | aGVHD |
Patient . | Day of aGVHD Onset . | Overall Grade of GVHD Prior . | Organ Involvement (stage) . | GVHD Treatments Prior . | Day to Tocilizumab Administration from Transplant . | # of Doses . | Overall Response to Tocilizumab . | Current Status . | Days Surviving since Tocilizumab Initiation . | Primary Cause of Death . |
---|---|---|---|---|---|---|---|---|---|---|
1 | + 26 | 3 | GI (2) Liver ( 2) | Steroids Basiliximab | + 70 | 6 | CR | Dead | 308 | Infection- CMV |
2 | +30 | 4 | GI (3) Liver (4) | Steroids Budesonide | + 176 | 2 | NR | Dead | 25 | aGVHD |
3 | +18 | 3 | GI (4) Liver (1) | MMF Budesonide Steroids | + 39 | 1 | GI : NR Liver: CR | Dead | 20 | aGVHD |
4 | +60 | 3 | GI (2) | Steroids Tacrolimus MMF | + 74 | 6 | CR | Alive and disease free | 759 | NA |
5 | + 25 | 3 | Skin (2) GI (4) | Steroids Sirolimus Budesonide | +86 | 1 | NR | Dead | 13 | Alveolar hemorrhage aGVHD |
6 | + 90 | 3 | GI (1) Liver(2) | Budesonide Steroids Tacrolimus | +266 | 2 | GI: CR Liver: NR | Dead | 26 | Klebsiella pneumonia, septic shock |
7 | +28 | 3 | GI (4) | Sirolimus Budesonide Steroids | +97 | 2 | NR | Dead | 33 | aGVHD |
8 | +43 | 3 | Liver (3) GI(3) | MMF Budesonide Steroids | +85 | 2 | NR | Dead | 16 | aGVHD |
9 | +29 | 4 | GI (4) Liver (4) | Steroids MMF budesonide | +43 | 2 | NR | Dead | 107 | aGVHD |
While the few tocilizumab treated patients with SR aGVHD reported in the literature have experienced a high response rate of 67%(CR and PR), our limited experience showed a less impressive 22% CR. Although tocilizumab has some activity in the treatment of SR aGVHD, it may not be significantly better than other available agents.
Off Label Use: There is currently no standard of practice of steroid-refractory GVHD, every treatment option besides steroids are considered off-label. However, there is evidence to support its use. Tocilizumab Tocilizumab is a humanized anti–IL-6 receptor (anti–IL-6R) monoclonal antibody that binds both soluble and membrane-expressed IL-6R, inhibiting IL-6–mediated proinflammatory activity. In this study, we report our experience with the administration of tocilizumab, an anti-interleukin 6 receptor antibody, in the treatment of steroid refractory GVHD.
Author notes
Asterisk with author names denotes non-ASH members.
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