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dc.contributor.authorWardley, Andrew M
dc.contributor.authorKilburn, L
dc.contributor.authorKernaghan, S
dc.contributor.authorMacpherson, I
dc.contributor.authorBaird, RD
dc.contributor.authorRoylance, R
dc.contributor.authorStephens, P
dc.contributor.authorOikonomidou, O
dc.contributor.authorBraybrooke, JP
dc.contributor.authorTuthill, M
dc.contributor.authorAbraham, J
dc.contributor.authorWinter, MC
dc.contributor.authorKingston, B
dc.contributor.authorWilkinson, K
dc.contributor.authorBliss, JM
dc.contributor.authorRing, A
dc.contributor.authorTurner, N
dc.contributor.authorPlasma, MTMG
dc.date.accessioned2020-08-10T08:09:23Z
dc.date.available2020-08-10T08:09:23Z
dc.date.issued2020en
dc.identifier.citationWardley AM, Kilburn L, Kernaghan S, Macpherson I, Baird RD, Roylance R, et al. Abstract P1-19-07: Results from plasmaMATCH trial treatment cohort B: A phase II trial of neratinib plus fulvestrant in ER positive breast cancer or neratinib alone in ER negative breast cancer in patients with aHER2mutation identified via ctDNA screening (CRUK/15/010). Cancer Research. 2020;80(4):P1-19-07-P1-19-07.en
dc.identifier.pmidNo PMIDen
dc.identifier.doi10.1158/1538-7445.sabcs19-p1-19-07en
dc.identifier.urihttp://hdl.handle.net/10541/623115
dc.description.abstractBackground: HER2 mutations occur in approximately 3% of HER2 non-amplified cancers and include missense substitutions and indels within the tyrosine kinase domain resulting in oncogenic HER2 activation. Neratinib, an irreversible EGFR, HER2 and ERBB4 tyrosine kinase inhibitor, has demonstrated activity in pre-clinical HER2 mutant models, and in a prior phase I trial with HER2 mutations identified through tumour testing. The plasmaMATCH trial Cohort B assessed the efficacy of neratinib in BC patients with a HER2 mutation identified in ctDNA testing. Methods: The plasmaMATCH trial was an open-label, multi-centre, multi-cohort platform trial, consisting of ctDNA testing in ~1000 patients with advanced BC. Patients with a HER2 mutation identified via ctDNA testing were registered to Cohort B. Patients were treated with 240mg neratinib once daily. Patients with ER positive BC were also treated with fulvestrant 500mg intramuscularly on Cycle 1 Days 1 and 15, and Cycle 2 onwards every 28 days. The primary endpoint for Cohort B was confirmed objective response rate as defined by RECIST v1.1. Using a single stage A'Hern design with a target response rate of 25%, unacceptable response rate of 5%, alpha=5% and power=80%, at least 3 responses out of 16 evaluable patients were required to infer efficacy. Results: Following ctDNA testing, 21 patients enrolled in Cohort B (58% of patients with HER2 mutations identified in ctDNA testing). Eighteen (86%) were ER positive, 2 (10%) were HER2 amplified, and 18 (86%) had visceral metastases. The most common HER2 mutations detected in baseline plasma were L755S (47.6%), V777L (19%), and S310F (14.3%). In the 20 evaluable patients, confirmed response rate was 25.0% (95%CI 8.7-49.1%, 5/20) (first 16 evaluable patients: 4/16, 25.0% (95%CI 7.3-52.4)). One patient had a complete response, ongoing at 29 months duration, and three additional patients had unconfirmed partial responses. Median progression free survival was 5.4 months (IQR 3.4-9.1) and median duration of response was 5.7 months (IQR 3.7-9.7 months) with 3 patients continuing on treatment. The most common clinically significant grade 3 or 4 adverse events were diarrhoea (20%) and hypertension (15%). Conclusions: Neratinib, with or without fulvestrant, was active in advanced BC patients with HER2 mutations identified in ctDNA testing, meeting the pre-specified threshold for efficacy.en
dc.language.isoenen
dc.relation.urlhttps://dx.doi.org/10.1158/1538-7445.sabcs19-p1-19-07en
dc.titleResults from plasmaMATCH trial treatment cohort B: A phase II trial of neratinib plus fulvestrant in ER positive breast cancer or neratinib alone in ER negative breast cancer in patients with a HER2 mutation identified via ctDNA screening (CRUK/15/010)en
dc.typeMeetings and Proceedingsen
dc.contributor.departmentThe NIHR Manchester Clinical Research Facility at The Christie NHS FT and Division of Cancer Sciences Manchesteren
dc.identifier.journalCancer Researchen
dc.description.noteen]


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