Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38972
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dc.contributor.authorCollins G.en
dc.contributor.authorTatarczuch M.en
dc.contributor.authorHildyard C.en
dc.contributor.authorSubesinghe M.en
dc.contributor.authorEyre T.A.en
dc.date.accessioned2021-05-14T13:18:34Zen
dc.date.available2021-05-14T13:18:34Zen
dc.date.copyright2017en
dc.date.created20180128en
dc.date.issued2018-01-29en
dc.identifier.citationBlood. Conference: 59th Annual Meeting of the American Society of Hematology, ASH 2017. Atlanta, GA United States. 130 (Supplement 1) (no pagination), 2017. Date of Publication: December 2017.en
dc.identifier.issn1528-0020en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/38972en
dc.description.abstractBackground: Approximately 25% of patients with cHL have relapsed or refractory (r/r) disease. Although salvage chemo-radiotherapy followed by autologous stem cell transplant (ASCT) offers the best chance of freedom from treatment failure (FFTF) (~50%), a portion patients have a poor prognosis despite this approach. Traditional prognostic scores are less well validated than in de novo disease, and hence F-FDG PET-CT, the gold-standard imaging modality in cHL, has an increasing role as a powerful prognostic indicator in this context. Our aims were a) to compare response rates to salvage therapy using F-FDG PET-CT (reported according to Lugano 2014 criteria) with trialreported outcomes; and b) to assess the prognostic value of F-FDG PET-CT in this context. Method(s): Retrospective data were collected on r/r cHL patients treated across 3 UK hospital sites (2011-2017). PET-CT scans were retrospectively reviewed according to Lugano 2014 response criteria i.e. complete metabolic response (CMR), partial metabolic response (PMR), no metabolic response (NMR) and progressive metabolic disease (PMD). Prognostic scores were calculated as described by Jostings et al. 2000. Result(s): 34 patients were identified: 21 with refractory cHL (<90 days) and 13 with relapsed disease. Median age was 43 years (range 14-77). Median time to relapse was 94 weeks (193-687). 100% patients had a prognostic score of <2, with 90% <1 (score unable to be calculated: n=2). 88% patients achieved an overall response (ORR) after 1 line salvage therapy, with 33% achieving CMR and 55% PMR ( F-FDG PET not performed: n=1). Patients were treated with 1-4 lines of salvage therapy (median= 1), with 33% receiving brentuximab vedotin. Of the 82% patients that proceeded to ASCT, 46% were in CMR, 50% were in PMR and 4% had mixed disease response. 47% of patients achieved CMR post-ASCT, with FFTF in 37% (Post-ASCT FFDG PET unavailable: n=3). As shown in the table below, there was a 55% rate of FFTF in patients with CMR post 1 line salvage therapy, compared with a 23% rate of FFTF in patients with PMR post 1 line salvage. 38% of patients with an overall CMR pre-ASCT had FFTF, compared with 43% with overall PMR. Conclusion(s): There is a wide discrepancy in FFTF, comparable with previous trial data, between patients achieving CMR and those achieving a PMR on F-FDG PET-CT post 1 line salvage chemotherapy. However, patients who received multiple lines of salvage therapy achieved similar rates of FF2F, irrespective of their metabolic response on their pre-ASCT F-FDG PET-CT. This suggests that F-FDG PET-CT may have limited prognostic value in this setting (Table presented).en
dc.languageenen
dc.languageEnglishen
dc.publisherAmerican Society of Hematologyen
dc.subjectclinical articleen
dc.subjectcontrolled clinical trialen
dc.subjectcontrolled studyen
dc.subjectdrug therapyen
dc.subjectfemaleen
dc.subjecthumanen
dc.subjecthuman cellen
dc.subjectmaleen
dc.subjectmetabolic disorderen
dc.subjectoutcome assessmenten
dc.subject*positron emission tomography-computed tomographyen
dc.subjectrecurrent diseaseen
dc.subjectrelapseen
dc.subjectretrospective studyen
dc.subject*salvage therapyen
dc.subject*stem cellen
dc.subjecttreatment failureen
dc.subjectbrentuximab vedotinen
dc.subjectconference abstracten
dc.subjectcancer chemotherapyen
dc.subjectadulten
dc.subjectcancer prognosisen
dc.subject*cancer recurrenceen
dc.subject*classical Hodgkin lymphomaen
dc.title18f-FDG PET-CT assessment of responses to salvage therapy and autologous stem cell transplant (ASCT) in relapsed/refractory classical hodgkin lymphoma (cHL).en
dc.typeConference Abstracten
dc.identifier.affiliationHaematologyen
local.date.conferencestart2017-12-09en
dc.identifier.source620334011en
dc.identifier.institution(Tatarczuch) Department of Haematology, Monash Health, Clayton, Australia (Tatarczuch) Churchill Hospital, Haematology Department, Oxford University Hospital, Oxford, United Kingdom (Hildyard, Eyre) Department of Haematology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom (Subesinghe) Radiology, Oxford University Hospital, Oxford, United Kingdom (Collins) Oxford Cancer and Haematology Centre, Churchill Hospital, Oxford, United Kingdomen
dc.description.addressM. Tatarczuch, Department of Haematology, Monash Health, Clayton, Australiaen
dc.subject.keywordmetabolic disorderen
dc.subject.keywordoutcome assessmenten
dc.subject.keyword*positron emission tomography-computed tomographyen
dc.subject.keywordrecurrent diseaseen
dc.subject.keywordrelapseen
dc.subject.keywordretrospective studyen
dc.subject.keyword*salvage therapyen
dc.subject.keyword*stem cellen
dc.subject.keywordtreatment failureen
dc.subject.keywordcontrolled studyen
dc.subject.keyworddrug therapyen
dc.subject.keywordclinical articleen
dc.subject.keyword*classical Hodgkin lymphomaen
dc.subject.keyword*cancer recurrenceen
dc.subject.keywordcancer prognosisen
dc.subject.keywordcancer chemotherapyen
dc.subject.keywordadulten
dc.subject.keywordcontrolled clinical trialen
dc.subject.keywordfemaleen
dc.subject.keywordhumanen
dc.subject.keywordhuman cellen
dc.subject.keywordmaleen
dc.relation.libraryurlLibKey Linken
dc.description.publicationstatusCONFERENCE ABSTRACTen
local.date.conferenceend2017-12-12en
dc.rights.statementCopyright 2018 Elsevier B.V., All rights reserved.en
dc.identifier.affiliationext(Tatarczuch) Churchill Hospital, Haematology Department, Oxford University Hospital, Oxford, United Kingdom-
dc.identifier.affiliationext(Hildyard, Eyre) Department of Haematology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom-
dc.identifier.affiliationext(Subesinghe) Radiology, Oxford University Hospital, Oxford, United Kingdom-
dc.identifier.affiliationext(Collins) Oxford Cancer and Haematology Centre, Churchill Hospital, Oxford, United Kingdom-
dc.identifier.affiliationmh(Tatarczuch) Department of Haematology, Monash Health, Clayton, Australia-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeConference Abstract-
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