作者
Alexandros Spyridonidis,Myriam Labopin,Bipin N. Savani,Riitta Niittyvuopio,Didier Blaise,Charles Craddock,Gèrard Socié,Uwe Platzbecker,Dietrich W. Beelen,Noël Milpied,Jan J. Cornelissen,Arnold Ganser,Anne Huynh,Laimonas Griškevičius,Sebastian Giebel,Mahmoud Aljurf,Éolia Brissot,Florent Malard,Jordi Esteve,Zinaida Perić,Frédéric Baron,Annalisa Ruggeri,Christoph Schmid,Maria Gilleece,Norbert Claude Gorin,Francesco Lanza,Roni Shouval,Jurjen Versluis,Gesine Bug,Yngvar Fløisand,Fabio Ciceri,Jaime Sanz,Ali Bazarbachi,Arnon Nagler,Mohamad Mohty
摘要
To address limitations of the currently used reduced-intensity/myeloablative conditioning (RIC/MAC) classification scheme we aimed to develop a tool that can capture more standardized the conditioning intensity of allogeneic hematopoietic cell transplantation (HCT). We assigned intensity weight scores for frequently used conditioning regimen components and used their sum to generate the transplant conditioning intensity (TCI) score. We retrospectively tested the impact of TCI on 8255 adult (45–65 years) acute myeloid leukemia patients who underwent HCT in first complete remission. A Cox model for early nonrelapse mortality (NRM) yielded a 3-group TCI risk scheme (low, intermediate, high) with respective TCI scores of [1–2], [2.5–3.5] and [4–6]. On multivariate modeling, TCI grouping was highly and better predictive for early (day 100 and 180) NRM, 2-year NRM and relapse (REL) as compared with the RIC/MAC classification. Validation was done on 200 bootstrap samples. Moreover, TCI scoring enabled the identification of a distinct subgroup of RIC and MAC conditioning regimens with an intermediate TCI [2.5–3.5] score that had identical outcomes and which are frequently referred as “reduced toxicity conditioning”. TCI scheme provides an improvement of the RIC/MAC classification. We propose TCI as a new tool to define and measure the conditioning regimen intensity.