A. Urbanoispizua et al., HIGH-INCIDENCE OF CHRONIC GRAFT-VERSUS-HOST DISEASE AFTER ALLOGENEIC PERIPHERAL-BLOOD PROGENITOR-CELL TRANSPLANTATION, Haematologica, 82(6), 1997, pp. 683-689
Background and Objective. The incidence of acute GVHD (aGVHD) in allog
eneic peripheral blood progenitor cell transplantation (allo-PBPCT) se
ems to be similar to that seen in allogeneic bone marrow transplantati
on (allo-BMT). In contrast, some preliminary results suggest that the
incidence of chronic GVHD (cGVHD) might be higher. The aim of the pres
ent study was to analyze the actuarial probability of developing cGVHD
In allo-PBPCT, its clinical manifestations and response to treatment.
Methods. We have retrospectively analyzed clinical results from 21 al
lo-PBPCT recipients that had been transplanted at least 18 months befo
re this study and that fulfilled the following criteria: HLA identical
sibling donor, non T-cell depleted apheresis and more than 90 days of
survival with sustained engraftment. The median follow-up was 12 mont
hs (range 4.5-22). Results. Twelve out of the 21 (57%) patients presen
ted cGVHD, 1 limited and 11 extensive. The actuarial probability of cG
VHD was 72.7% (95% CI, 49-96%). The median interval from transplant to
onset was 180 days (range 95-270). Nine of the 12 cases (75%) present
ed combined skin and liver involvement. Of the other three, the liver
was involved in one case; skin, mouth, and nail cGVHD was observed in
another case; and skin and mouth involvement together with an obstruct
ive pulmonary disease was observed in the remaining case. Under therap
y, a complete resolution of cGVHD manifestations was achieved in five
cases, and a partial improvement was attained in three other cases. In
two responsive patients, cGVHD reappeared after stopping treatment. F
our patients were refractory to the treatment. Interpretation and Conc
lusions. It would appear from this retrospective and multicenter study
that, after a median follow-up of 12 months, cGVHD after allo-PBPCT c
ould be more frequent than after allo-BMT. A randomized trial with a l
arge number of patients and a sufficient follow-up will be necessary t
o answer this question definitively. (C) 1997, Ferrata Storti Foundati
on.