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dc.contributor.authorDas-Gupta, E
dc.contributor.authorThomson, KJ
dc.contributor.authorBloor, Adrian
dc.contributor.authorClark, AD
dc.contributor.authorMackinnon, S
dc.contributor.authorKayani, I
dc.contributor.authorClifton-Hadley, L
dc.contributor.authorPatrick, P
dc.contributor.authorEl-Mehidi, N
dc.contributor.authorLawrie, A
dc.contributor.authorKirkwood, AA
dc.contributor.authorRussell, NH
dc.contributor.authorLinch, DC
dc.contributor.authorPeggs, KS
dc.date.accessioned2020-01-29T15:17:59Z
dc.date.available2020-01-29T15:17:59Z
dc.date.issued2019en
dc.identifier.citationDas-Gupta E, Thomson KJ, Bloor AJC, Clark AD, Mackinnon S, Kayani I, et al. Allo-HSCT in transplant-naive patients with Hodgkin lymphoma: a single-arm, multicenter study. Blood Adv. 2019;3(24):4264-70.en
dc.identifier.pmid31869413en
dc.identifier.doi10.1182/bloodadvances.2019001016en
dc.identifier.urihttp://hdl.handle.net/10541/622723
dc.description.abstractWe evaluated the role of allogeneic hematopoietic stem cell transplantation (allo-HSCT) in transplant-na•ve patients with relapsed/refractory Hodgkin lymphoma (HL) who failed to attain metabolic complete response (mCR) to 1 to 2 lines of salvage chemotherapyThose with residual but nonprogressive disease assessed by positron emission tomography/computed tomography scanning were eligible. An additional 1 to 2 cycles of salvage therapy were permissible in those with progressive disease or when required to bridge to allo-HSCT, with additional imaging at baseline before transplantation. Conditioning consisted of carmustine, etoposide, cytarabine, melphalan, and alemtuzumab. Donor lymphocyte infusions (DLI) were administered for mixed chimerism or residual or relapsed disease. Eleven patients had sibling donors, 13 had HLA-matched unrelated donors, and 7 had HLA-mismatched unrelated donors. There were no graft failures, and no episodes of grade 4 acute graft-versus-host disease (GVHD); only 19.4% of patients had grade 2 to 3 GVHD, and 22.2% had extensive chronic GVHD. The non-relapse mortality rate was 16.1% (95% confidence interval [CI], 7.1%-34.5%). Relapse incidence was 18.7% (95% CI, 8.2%-39.2%). The study met its primary objective, with a 3-year progression-free survival of 67.7% (95% CI, 48.4%-81.2%). Survival outcomes were equivalent in those with residual metabolically active disease immediately before transplantation (n = 24 [70.8%; 95% CI, 17.2%-83.7%]). Two of the 5 patients who relapsed received DLI and remained in mCR at latest follow-up, with a 3-year overall survival of 80.7% (95% CI, 61.9%-90.8%). We demonstrate encouraging results that establish a potential role for allo-HSCT in selected high-risk patients with HL. This trial was registered at www.clinicaltrials.gov as #NCT00908180.en
dc.language.isoenen
dc.relation.urlhttps://dx.doi.org/10.1182/bloodadvances.2019001016en
dc.titleAllo-HSCT in transplant-naive patients with Hodgkin lymphoma: a single-arm, multicenter studyen
dc.typeArticleen
dc.contributor.departmentNottingham University Hospital, Nottingham, United Kingdomen
dc.identifier.journalBlood Advancesen
dc.description.noteen]
refterms.dateFOA2020-02-03T16:08:25Z


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