Myeloablative conditioning for allo-HSCT in pediatric ALL: FTBI or chemotherapy?-A multicenter EBMT-PDWP study.
Andre Manfred WillaschChristina PetersPetr SedláčekJean-Hugues DalleVassiliki Kitra-RoussouAkif YesilipekJacek WachowiakArjan LankesterArcangelo PreteAmir Ali HamidiehMarianne IfversenJochen BuechnerGergely KrivánRose-Marie HamladjiChristina Diaz de HerediaElena SkorobogatovaGérard MichelFranco LocatelliAlice BertainaPaul VeysSophie DupontReuven OrTayfun GüngörOlga AleinikovaSabina SufliarskaMikael SundinJelena RasconAin KaareDamir NemetFranca FagioliThomas Erich KlingebielJan StyczyńskiMarc BieringsKálmán NagyManuel AbecasisBoris AfanasyevMarc AnsariKim VettenrantaAmal AlseraihyAlicja ChybickaStephen RobinsonYves BertrandAlphan KupesizArdeshir GhavamzadehAntonio CamposHerbert PichlerArnaud DalissierMyriam LabopinSelim CorbaciogluAdriana Cristina BalduzziJacques-Emmanuel GalimardPeter Badernull nullPublished in: Bone marrow transplantation (2020)
Although most children with acute lymphoblastic leukemia (ALL) receive fractionated total body irradiation (FTBI) as myeloablative conditioning (MAC) for allogeneic hematopoietic stem cell transplantation (allo-HSCT), it is an important matter of debate if chemotherapy can effectively replace FTBI. To compare outcomes after FTBI versus chemotherapy-based conditioning (CC), we performed a retrospective EBMT registry study. Children aged 2-18 years after MAC for first allo-HSCT of bone marrow (BM) or peripheral blood stem cells (PBSC) from matched-related (MRD) or unrelated donors (UD) in first (CR1) or second remission (CR2) between 2000 and 2012 were included. Propensity score weighting was used to control pretreatment imbalances of the observed variables. 3.054 patients were analyzed. CR1 (1.498): median follow-up (FU) after FTBI (1.285) and CC (213) was 6.8 and 6.1 years. Survivals were not significantly different. CR2 (1.556): median FU after FTBI (1.345) and CC (211) was 6.2 years. Outcomes after FTBI were superior as compared with CC with regard to overall survival (OS), leukemia-free survival (LFS), relapse incidence (RI), and nonrelapse mortality (NRM). However, we must emphasize the preliminary character of the results of this retrospective "real-world-practice" study. These findings will be prospectively assessed in the ALL SCTped 2012 FORUM trial.
Keyphrases
- allogeneic hematopoietic stem cell transplantation
- acute lymphoblastic leukemia
- bone marrow
- stem cells
- free survival
- acute myeloid leukemia
- peripheral blood
- clinical trial
- end stage renal disease
- locally advanced
- healthcare
- type diabetes
- stem cell transplantation
- young adults
- chronic kidney disease
- randomized controlled trial
- mesenchymal stem cells
- cardiovascular events
- squamous cell carcinoma
- small cell lung cancer
- study protocol
- cross sectional
- coronary artery disease
- quality improvement
- phase ii
- cell therapy
- disease activity