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Busulfan- or Thiotepa-Based Conditioning in Myelofibrosis: A Phase II Multicenter Randomized Study from the GITMO Group
Authors:Francesca Patriarca  Arianna Masciulli  Andrea Bacigalupo  Stefania Bregante  Chiara Pavoni  Maria Chiara Finazzi  Alberto Bosi  Domenico Russo  Franco Narni  Giuseppe Messina  Emilio Paolo Alessandrino  Angelo Michele Carella  Giuseppe Milone  Benedetto Bruno  Sonia Mammoliti  Barbara Bruno  Renato Fanin  Francesca Bonifazi  Alessandro Rambaldi
Institution:1. Udine University Hospital, DAME, University of Udine, Udine, Italy;2. “Papa Giovanni XXIII” Hospital, Bergamo, Italy;3. “Fondazione A. Gemelli”, University Hospital, Rome, Italy;4. IRCSS “San Martino” Hospital, Genoa, Italy;5. Hematology, University of Florence, Florence, Italy;6. ASST Hospital of Brescia, DSCS, Brescia University, Brescia, Italy;7. University Hospital of Modena, Modena, Italy;8. “Bianchi-Melacrino-Morelli” Hospital, Reggio Calabria, Italy;9. IRCSS San Matteo Hospital, Pavia, Italy;10. IRCSS, San Giovanni Rotondo Hospital (FG), San Giovanni Rotondo, Italy;11. Ferrarotto Hospital, Catania, Italy;12. “Citta’ della Salute e della Scienza” University Hospital, DBMSS, University of Torino, Torino, Italy;13. Trial Clinical Office, Gruppo Italiano Trapianto Midollo Osseo (GITMO), Genoa, Italy;14. Institute of Hematology “Seragnoli”, University Hospital “S. Orsola Malpighi”, Bologna, Italy;15. Department of Hematology-Oncology, University of Milano, Milan, Italy
Abstract:We report a randomized study comparing fludarabine in combination with busulfan (FB) or thiotepa (FT), as conditioning regimen for hematopoietic stem cell transplantation (HSCT) in patients with myelofibrosis. The primary study endpoint was progression-free survival (PFS).Sixty patients were enrolled with a median age of 56 years and an intermediate-2 or high-risk score in 65%, according to the Dynamic International Prognostic Staging System (DIPSS). Donors were HLA-identical sibling (n = 25), matched unrelated (n = 25) or single allele mismatched unrelated (n = 10). With a median follow-up of 22 months (range, 1 to 68 months), outcomes at 2 years after HSCT in the FB arm versus the FT arm were as follows: PFS, 43% versus 55% (P = .28); overall survival (OS), 54% versus 70% (P = .17); relapse/progression, 36% versus 24% (P = .24); nonrelapse mortality (NRM), 21% in both arms (P = .99); and graft failure, 14% versus 10% (P = .96). A better PFS was observed in patients with intermediate-1 DIPSS score (P = .03). Both neutrophil engraftment and platelet engraftment were significantly influenced by previous splenectomy (hazard ratio HR], 2.28; 95% confidence interval CI], 1.16 to 4.51; P = .02) and splenomegaly at transplantation (HR, 0.51; 95% CI, 0.27 to 0.94; P = .03). In conclusion, the clinical outcome after HSCT was comparable when using either a busulfan or thiotepa based conditioning regimen.
Keywords:Gruppo Italiano Trapianti di Midollo Osseo  (GITMO)    Myelofibrosis  Allogeneic stem cell transplantation  Reduced-intensity conditioning regimen  Busulfan  Thiotepa
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