Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28429
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dc.contributor.authorRoss, P J-
dc.contributor.authorWasan, H S-
dc.contributor.authorCroagh, D-
dc.contributor.authorNikfarjam, Mehrdad-
dc.contributor.authorNguyen, N-
dc.contributor.authorAghmesheh, M-
dc.contributor.authorNagrial, A M-
dc.contributor.authorBartholomeusz, D-
dc.contributor.authorHendlisz, A-
dc.contributor.authorAjithkumar, T-
dc.contributor.authorIwuji, C-
dc.contributor.authorWilson, N E-
dc.contributor.authorTurner, D M-
dc.contributor.authorJames, D C-
dc.contributor.authorYoung, E-
dc.contributor.authorHarris, M T-
dc.date2021-12-23-
dc.date.accessioned2022-01-10T03:24:23Z-
dc.date.available2022-01-10T03:24:23Z-
dc.date.issued2022-02-
dc.identifier.citationESMO Open 2022; 7(1): 100356en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/28429-
dc.description.abstractUnresectable locally advanced pancreatic cancer (LAPC) is generally managed with chemotherapy or chemoradiotherapy, but prognosis is poor with a median survival of ∼13 months (or up to 19 months in some studies). We assessed a novel brachytherapy device, using phosphorous-32 (32P) microparticles, combined with standard-of-care chemotherapy. In this international, multicentre, single-arm, open-label pilot study, adult patients with histologically or cytologically proven unresectable LAPC received 32P microparticles, via endoscopic ultrasound-guided fine-needle implantation, planned for week 4 of 5-fluorouracil, leucovorin, irinotecan and oxaliplatin (FOLFIRINOX) or gemcitabine/nab-paclitaxel chemotherapy, per investigator's choice. The primary endpoint was safety and tolerability measured using Common Terminology Criteria for Adverse Events version 4.0. The lead efficacy endpoint was local disease control rate at 16 weeks. Fifty patients were enrolled and received chemotherapy [intention-to-treat (ITT) population]. Forty-two patients received 32P microparticle implantation [per protocol (PP) population]. A total of 1102 treatment-emergent adverse events (TEAEs) were reported in the ITT/safety population (956 PP), of which 167 (139 PP) were grade ≥3. In the PP population, 41 TEAEs in 16 (38.1%) patients were possibly or probably related to 32P microparticles or implantation procedure, including 8 grade ≥3 in 3 (7.1%) patients, compared with 609 TEAEs in 42 (100%) patients attributed to chemotherapy, including 67 grade ≥3 in 28 patients (66.7%). The local disease control rate at 16 weeks was 82.0% (95% confidence interval: 68.6% to 90.9%) (ITT) and 90.5% (95% confidence interval: 77.4% to 97.3%) (PP). Tumour volume, carbohydrate antigen 19-9 levels, and metabolic tumour response at week 12 improved significantly. Ten patients (20.0% ITT; 23.8% PP) had surgical resection and median overall survival was 15.2 and 15.5 months for ITT and PP populations, respectively. Endoscopic ultrasound-guided 32P microparticle implantation has an acceptable safety profile. This study also suggests clinically relevant benefits of combining 32P microparticles with standard-of-care systemic chemotherapy for patients with unresectable LAPC.en
dc.language.isoeng
dc.subject(32)P microparticlesen
dc.subjectbrachytherapyen
dc.subjectlocal disease control rateen
dc.subjectlocally advanced pancreatic canceren
dc.subjectsafety profileen
dc.titleResults of a single-arm pilot study of 32P microparticles in unresectable locally advanced pancreatic adenocarcinoma with gemcitabine/nab-paclitaxel or FOLFIRINOX chemotherapy.en
dc.typeJournal Articleen
dc.identifier.journaltitleESMO Openen
dc.identifier.affiliationLeicester Royal Infirmary, University Hospitals of Leicester NHS Trust, Leicester, UK..en
dc.identifier.affiliationThe Crown Princess Mary Cancer Centre, Westmead Hospital, Westmead, Australia..en
dc.identifier.affiliationGuy's & St Thomas' Hospital NHS Foundation Trust, London, UK..en
dc.identifier.affiliationImperial College Healthcare NHS Trust, London, UK..en
dc.identifier.affiliationAddenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK..en
dc.identifier.affiliationSouthern Star Research Pty Ltd, Gordon, Australia..en
dc.identifier.affiliationMonash Health, Clayton, Australia..en
dc.identifier.affiliationOncoSil Medical Limited, Sydney, Australia..en
dc.identifier.affiliationSouthern Medical Day Care Centre, Wollongong, Australia..en
dc.identifier.affiliationAustin Healthen
dc.identifier.affiliationRoyal Adelaide Hospital, Adelaide, Australia..en
dc.identifier.affiliationInstitut Jules Bordet, Brussels, Belgium..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/34953400/en
dc.identifier.doi10.1016/j.esmoop.2021.100356en
dc.type.contentTexten
dc.identifier.orcid0000-0003-4866-276Xen
dc.identifier.pubmedid34953400
local.name.researcherNikfarjam, Mehrdad
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptSurgery (University of Melbourne)-
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