Post-Transplant Complications
Bone Marrow Transplantation (2003) 32, 205–211. doi:10.1038/sj.bmt.1704085
A revised day +7 predictive score for transplant-related mortality: serum cholinesterase, total protein, blood urea nitrogen,
glutamyl transferase, donor type and cell dose
M P Sormani2, R Oneto1, B Bruno1, M Fiorone1, T Lamparelli1, F Gualandi1, A M Raiola1, A Dominietto1, M T Van Lint1, F Frassoni1, P Bruzzi2 and A Bacigalupo1
- 1Divisione Ematologia II Ospedale San Martino, Genova, Italy
- 2Unita' Epidemiologia Clinica, Istituto Scientifio Tumori, Genova
Correspondence: Dr A Bacigalupo, Divisione Ematologia 2 (PAD 5/II), Ospedale San Martino, Largo Rosanna Benzi 10, 16132 Genova, Italy
Received 27 June 2002; Accepted 22 January 2003.
Abstract
We have previously described a scoring system for patients undergoing hemopoietic stem cell transplantation (HSCT) based on day +7 blood urea nitrogen (BUN) and serum bilirubin levels. We have revised that scoring system using a formal multivariate approach based on a training phase (305 patients) and a validation phase (217 patients). Day +7 BUN, serum cholinesterase (CHE), total proteins (TP), gamma glutamyl transferase (
GT), donor type and cell dose at transplant were included in the new score. The score distribution identified three groups of patients in the training set (<25, 25-75, >75 percentile of the score) which were classified as low, intermediate and high risk. Their actuarial risk of transplant-related mortality (TRM) at 6 years was, respectively, 12, 38 and 60%. In the validation set the 6 year actuarial TRM was, respectively, 15, 40 and 69%. High risk patients had more graft-versus-host disease (GvHD) (P<0.0001) and lower platelet counts (P<0.0001). This study confirms that GvHD and TRM can be predicted on day +7 after HSCT: pre-emptive GvHD therapy may be one option for high-risk patients and is being tested in a prospective randomized trial. The score for single patients can be calculated on the web site http://213.26.110.20/lrm/day_seven_score.html.
Keywords:
leukemia, GvHD

