Post-transplant cyclophosphamide versus anti-thymocyte globulin for graft-versus-host disease prevention in haploidentical transplantation for adult acute lymphoblastic leukemia

Arnon Nagler(Tel Aviv University), Abraham S. Kanate(West Virginia University), Myriam Labopin(Hôpital Saint-Antoine), Fabio Ciceri(IRCCS Ospedale San Raffaele), Emanuele Angelucci(Ospedale Policlinico San Martino), Yener Koç(Antalya IVF), Zafer Gülbaş, William Arcese(University of Rome Tor Vergata), Johanna Tischer(LMU Klinikum), Pietro Pioltelli(Azienda Ospedaliera San Gerardo), Hakan Özdoğu(Başkent University), Boris V. Afanasyev(First Pavlov State Medical University of St. Petersburg), Depei Wu(Soochow University), Mutlu Arat(Istanbul Florence Nightingale Hospital), Zinaida Perić(University Hospital Centre Zagreb), Sebastian Giebel(The Maria Sklodowska-Curie National Research Institute of Oncology), Bipin N. Savani(Vanderbilt University Medical Center), Mohamad Mohty(Sorbonne Université)
Haematologica
April 30, 2020
Cited by 55Open Access
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Abstract

Graft-versus-host disease (GVHD) prophylaxis for unmanipulated haploidentical hematopoietic cell transplantation (haplo-HCT) include post-transplant cyclophosphamide (PTCy) and anti-thymocyte globulin (ATG). Utilizing EBMT registry, we compared ATG versus PTCy based GVHD prophylaxis in adult acute lymphoblastic leukemia (ALL) patients undergoing haplo-HCT. Included were 434 patients; ATG (n=98) and PTCy (n=336). Median follow-up was ~2 years. Baseline characteristics were similar between the groups except that the ATG-group was more likely to have relapsed/refractory ALL (P=0.008), non-TBI conditioning (P<0.001), peripheral blood graft source (P=<0.001) and transplanted at an earlier time-period (median year of HCT 2011 vs. 2015). The 100-day grade II-IV and III-IV acute-GVHD was similar between ATG and PTCy, as was 2-year chronic-GVHD. On multivariate analysis (MVA), leukemia-free survival (LFS) and overall survival (OS) was better with PTCy compared to ATG prophylaxis. Relapse incidence (RI) was lower in the PTCy group (P=0.03), while non-relapse mortality (NRM) was not different. Advanced disease and lower performance score were associated with poorer LFS and OS and advanced disease with inferior GVHD-free/relapse-free survival (GRFS). Peripheral grafts were associated with higher GVHD compared to bone marrow grafts. In ALL patients undergoing unmanipulated haplo-HCT, PTCy for GVHD prevention resulted in lower RI and improved LFS and OS compared to ATG.


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