Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26628
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dc.contributor.authorMartinez-Calle, Nicolas-
dc.contributor.authorKirkwood, Amy A-
dc.contributor.authorLamb, Maxine-
dc.contributor.authorSmith, Alex-
dc.contributor.authorKhwaja, Jahanzaib-
dc.contributor.authorManos, Kate-
dc.contributor.authorShrubsole, Caroline-
dc.contributor.authorGray, Nicola-
dc.contributor.authorLewis, Katharine-
dc.contributor.authorTivey, Ann-
dc.contributor.authorBishton, Mark J-
dc.contributor.authorHawkes, Eliza A-
dc.contributor.authorAhearne, Matthew J-
dc.contributor.authorOsborne, Wendy-
dc.contributor.authorCollins, Graham P-
dc.contributor.authorIllidge, Timothy-
dc.contributor.authorLinton, Kim M-
dc.contributor.authorCwynarski, Kate-
dc.contributor.authorBurton, Cathy-
dc.contributor.authorFox, Christopher P-
dc.date2021-05-26-
dc.date.accessioned2021-05-31T22:59:12Z-
dc.date.available2021-05-31T22:59:12Z-
dc.date.issued2021-07-
dc.identifier.citationAdvances in Therapy 2021; 38(7): 3789-3802en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26628-
dc.description.abstractBrentuximab vedotin (BV)-CHP is the new standard regimen for first-line treatment of systemic anaplastic large cell lymphoma (sALCL). We undertook a retrospective analysis of consecutive patients diagnosed with sALCL, treated in routine practice, to serve as a benchmark analysis for comparison BV-CHP efficacy in routine practice. Patients aged 16 years or older with sALCL treated in seven UK and Australian centres and from 14 additional centres from the UK Haematological Malignancy Research Network database (n = 214). Treatment allocation was clinician choice and included best supportive care (BSC). Main outcomes were time to treatment failure (TTF) and overall survival (OS). Multivariable analysis for predictors of both TTF and OS was also undertaken. The median age 52 years (range 16-93), 18% ECOG ≥ 3 and 40% of cases were ALK positive. CHOP (cyclophosphamide, adriamycin, vincristine, prednisolone) was employed in 152 (71%) of patients and CHOEP (CHOP + etoposide) in 4% of patients. For CHOP-treated patients overall response rate (ORR) was 65% and complete response (CR) 47%. Only 9% of patients underwent autologous stem cell transplant (ASCT). With 57 months median follow-up, 4-year TTF and OS were 41.2% (95% CI 33.1-49.1) and 58.9% (95% CI 50.3-66.5) respectively. Multivariable analysis showed ALK+ status was independently associated with superior TTF (HR 0.36, 95% CI 0.21-0.63) but not OS (0.44, 95% CI 0.18-1.07). We present a retrospective analysis with mature follow-up of one of the largest multicentre populations of sALCL available, comparable to similar large retrospective studies. ALK status remains a strong predictor of outcomes. These data serve as a robust benchmark for BV-CHP as the new standard of care for sALCL. Similar real-world evidence with BV-CHP will be desirable to confirm the findings of ECHELON-2.en
dc.language.isoeng-
dc.subjectAdcetrisen
dc.subjectAutologous stem cell transplantationen
dc.subjectBrentuximab vedotinen
dc.subjectCHOEPen
dc.subjectCHOPen
dc.titleSystemic ALCL Treated in Routine Clinical Practice: Outcomes Following First-Line Chemotherapy from a Multicentre Cohort.en
dc.typeJournal Articleen
dc.identifier.journaltitleAdvances in Therapyen
dc.identifier.affiliationOxford University Hospitals NHS Foundation Trust, Oxford, UKen
dc.identifier.affiliationOlivia Newton-John Cancer Research Instituteen
dc.identifier.affiliationRussell Centre for Clinical Haematology, Nottingham University Hospitals NHS Trust, City Hospital Campus, Hucknall Road, Nottingham, NG5 1PB, UKen
dc.identifier.affiliationAustin Healthen
dc.identifier.affiliationSir Charles Gairdner Hospital, Perth, Australiaen
dc.identifier.affiliationCRUK and UCL Cancer Trials Centre, UCL Cancer Institute, London, UKen
dc.identifier.affiliationHaematological Malignancy Research Network, University of York, York, UKen
dc.identifier.affiliationUniversity College of London Hospitals, NHS Foundation Trust, London, UKen
dc.identifier.affiliationNewcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle, UKen
dc.identifier.affiliationOxford University Hospitals NHS Foundation Trust, Oxford, UKen
dc.identifier.affiliationCancer Sciences, University of Manchester and the Christie, NHS Foundation Trust, Manchester, UKen
dc.identifier.affiliationRussell Centre for Clinical Haematology, Nottingham University Hospitals NHS Trust, City Hospital Campus, Hucknall Road, Nottingham, NG5 1PB, UKen
dc.identifier.affiliationUniversity Hospitals of Leicester NHS Trust, Leicester, UKen
dc.identifier.affiliationNewcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle, UKen
dc.identifier.affiliationCancer Sciences, University of Manchester and the Christie, NHS Foundation Trust, Manchester, UKen
dc.identifier.affiliationUniversity College of London Hospitals, NHS Foundation Trust, London, UKen
dc.identifier.affiliationLeeds Teaching Hospitals NHS Trust, Leeds, UKen
dc.identifier.affiliationRussell Centre for Clinical Haematology, Nottingham University Hospitals NHS Trust, City Hospital Campus, Hucknall Road, Nottingham, NG5 1PB, UKen
dc.identifier.doi10.1007/s12325-021-01764-0en
dc.type.contentTexten
dc.identifier.orcid0000-0002-5184-9464en
dc.identifier.pubmedid34037958-
local.name.researcherHawkes, Eliza A
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptClinical Haematology-
crisitem.author.deptClinical Haematology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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