Tocilizumab, tacrolimus and methotrexate for the prevention of acute graft- <i>versus</i> -host disease: low incidence of lower gastrointestinal tract disease

William R. Drobyski(Medical College of Wisconsin), Anikó Szabó(Medical College of Wisconsin), Fenlu Zhu(Medical College of Wisconsin), Carolyn A. Keever-Taylor(Medical College of Wisconsin), Kyle Hebert(Medical College of Wisconsin), Renee Dunn(Medical College of Wisconsin), Sharon Yim(Medical College of Wisconsin), Bryon D. Johnson(Medical College of Wisconsin), Anita D’Souza(Medical College of Wisconsin), Mary Eapen(Medical College of Wisconsin), Timothy S. Fenske(Medical College of Wisconsin), Parameswaran Hari(Medical College of Wisconsin), Mehdi Hamadani(Medical College of Wisconsin), Mary M. Horowitz(Medical College of Wisconsin), J. Douglas Rizzo(Medical College of Wisconsin), Wael Saber(Medical College of Wisconsin), Nirav N. Shah(Medical College of Wisconsin), Bronwen E. Shaw(Medical College of Wisconsin), Marcelo C. Pasquini(Medical College of Wisconsin)
Haematologica
January 19, 2018
Cited by 51Open Access
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Abstract

We conducted a phase 2 study in which patients undergoing allogeneic hematopoietic stem cell transplantation received tocilizumab in addition to standard immune suppression with tacrolimus and methotrexate for graft-versus-host disease prophylaxis. Thirty-five patients were enrolled between January 2015 and June 2016. The median age of the cohort was 66 (range: 22-76). All patients received busulfan-based conditioning, and were transplanted with human leukocyte antigen-matched related or matched unrelated bone marrow or peripheral stem cell grafts. The cumulative incidences of grades II-IV and III-IV acute graft-versus-host disease were 14% (95% CI 5-30) and 3% (95% CI 0-11) at day 100, and 17% (95% CI 7-31) and 6% (95% CI 1-16) at day 180, respectively. Notably, there were no cases of graft-versus-host disease of the lower gastrointestinal tract within the first 100 days. A comparison to 130 matched controls who only received tacrolimus and methotrexate demonstrated a lower cumulative incidence of grades II-IV acute graft-versus-host disease (17% versus 45%, P=0.003) and a significant increase in grades II-IV acute graft-versus-host disease-free survival at six months (69% versus 42%, P=0.001) with tocilizumab, tacrolimus and methotrexate, which was the primary endpoint of the study. Immune reconstitution was preserved in patients treated with tocilizumab, tacrolimus and methotrexate, as T-cell and B-cell subsets recovered to near normal levels by 6-12 months post-transplantation. We conclude that tocilizumab has promising activity in preventing acute graft-versus-host disease, particularly in the lower gastrointestinal tract, and warrants examination in a randomized setting.


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