Survival following allogeneic transplant in patients with myelofibrosis

dc.contributor.authorGowin, Krisstina
dc.contributor.authorBallen, Karen
dc.contributor.authorAhn, Kwang Woo
dc.contributor.authorHu, Zhen-Huan
dc.contributor.authorAli, Haris
dc.contributor.authorArcasoy, Murat O.
dc.contributor.authorDevlin, Rebecca
dc.contributor.authorCoakley, Maria
dc.contributor.authorGerds, Aaron T.
dc.contributor.authorGreen, Michael
dc.contributor.authorGupta, Vikas
dc.contributor.authorHobbs, Gabriela
dc.contributor.authorJain, Tania
dc.contributor.authorKandarpa, Malathi
dc.contributor.authorKomrokji, Rami
dc.contributor.authorKuykendall, Andrew T.
dc.contributor.authorLuber, Kierstin
dc.contributor.authorMasarova, Lucia
dc.contributor.authorMichaelis, Laura C.
dc.contributor.authorPatches, Sarah
dc.contributor.authorPariser, Ashley C.
dc.contributor.authorRampal, Raajit
dc.contributor.authorStein, Brady
dc.contributor.authorTalpaz, Moshe
dc.contributor.authorVerstovsek, Srdan
dc.contributor.authorWadleigh, Martha
dc.contributor.authorAgrawal, Vaibhav
dc.contributor.authorAljurf, Mahmoud
dc.contributor.authorDiaz, Miguel Angel
dc.contributor.authorAvalos, Belinda R.
dc.contributor.authorBacher, Ulrike
dc.contributor.authorBashey, Asad
dc.contributor.authorBeitinjaneh, Amer M.
dc.contributor.authorCerny, Jan
dc.contributor.authorChhabra, Saurabh
dc.contributor.authorCopelan, Edward
dc.contributor.authorCutler, Corey S.
dc.contributor.authorDeFilipp, Zachariah
dc.contributor.authorGadalla, Shahinaz M.
dc.contributor.authorGanguly, Siddhartha
dc.contributor.authorGrunwald, Michael R.
dc.contributor.authorHashmi, Shahrukh K.
dc.contributor.authorKharfan-Dabaja, Mohamed A.
dc.contributor.authorKindwall-Keller, Tamila
dc.contributor.authorKröger, Nicolaus
dc.contributor.authorLazarus, Hillard M.
dc.contributor.authorLiesveld, Jane L.
dc.contributor.authorLitzow, Mark R.
dc.contributor.authorMarks, David I.
dc.contributor.authorNathan, Sunita
dc.contributor.authorNishihori, Taiga
dc.contributor.authorOlsson, Richard F.
dc.contributor.authorPawarod, Attaphol
dc.contributor.authorRowe, Jacob M.
dc.contributor.authorSavani, Bipin N.
dc.contributor.authorSavoie, Mary Lynn
dc.contributor.authorSeo, Sachiko
dc.contributor.authorSolh, Melhem
dc.contributor.authorTamari, Roni
dc.contributor.authorVerdonck, Leo F.
dc.contributor.authorYared, Jean A.
dc.contributor.authorAlyea, Edwin
dc.contributor.authorPopat, Uday
dc.contributor.authorSobecks, Ronald
dc.contributor.authorScott, Bart L.
dc.contributor.authorNakamura, Ryotaro
dc.contributor.authorMesa, Ruben
dc.contributor.authorSaber, Wael
dc.contributor.departmentMedicine, School of Medicineen_US
dc.date.accessioned2020-07-30T18:55:02Z
dc.date.available2020-07-30T18:55:02Z
dc.date.issued2020-05-08
dc.description.abstractAllogeneic hematopoietic cell transplantation (HCT) is the only curative therapy for myelofibrosis (MF). In this large multicenter retrospective study, overall survival (OS) in MF patients treated with allogeneic HCT (551 patients) and without HCT (non-HCT) (1377 patients) was analyzed with Cox proportional hazards model. Survival analysis stratified by the Dynamic International Prognostic Scoring System (DIPSS) revealed that the first year of treatment arm assignment, due to upfront risk of transplant-related mortality (TRM), HCT was associated with inferior OS compared with non-HCT (non-HCT vs HCT: DIPSS intermediate 1 [Int-1]: hazard ratio [HR] = 0.26, P < .0001; DIPSS-Int-2 and higher: HR, 0.39, P < .0001). Similarly, in the DIPSS low-risk MF group, due to upfront TRM risk, OS was superior with non-HCT therapies compared with HCT in the first-year post treatment arm assignment (HR, 0.16, P = .006). However, after 1 year, OS was not significantly different (HR, 1.38, P = .451). Beyond 1 year of treatment arm assignment, an OS advantage with HCT therapy in Int-1 and higher DIPSS score patients was observed (non-HCT vs HCT: DIPSS-Int-1: HR, 2.64, P < .0001; DIPSS-Int-2 and higher: HR, 2.55, P < .0001). In conclusion, long-term OS advantage with HCT was observed for patients with Int-1 or higher risk MF, but at the cost of early TRM. The magnitude of OS benefit with HCT increased as DIPSS risk score increased and became apparent with longer follow-up.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationGowin, K., Ballen, K., Ahn, K. W., Hu, Z. H., Ali, H., Arcasoy, M. O., Devlin, R., Coakley, M., Gerds, A. T., Green, M., Gupta, V., Hobbs, G., Jain, T., Kandarpa, M., Komrokji, R., Kuykendall, A. T., Luber, K., Masarova, L., Michaelis, L. C., Patches, S., … Saber, W. (2020). Survival following allogeneic transplant in patients with myelofibrosis. Blood advances, 4(9), 1965–1973. https://doi.org/10.1182/bloodadvances.2019001084en_US
dc.identifier.urihttps://hdl.handle.net/1805/23450
dc.language.isoen_USen_US
dc.publisherAmerican Society of Hematologyen_US
dc.relation.isversionof10.1182/bloodadvances.2019001084en_US
dc.relation.journalBlood Advancesen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectClinical trials and observationsen_US
dc.subjectMyeloid neoplasiaen_US
dc.subjectTransplantationen_US
dc.subjectMyelofibrosisen_US
dc.subjectFollow-upen_US
dc.titleSurvival following allogeneic transplant in patients with myelofibrosisen_US
dc.typeArticleen_US
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