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dc.contributor.authorBundred, Nigel
dc.contributor.authorPorta, Nuria
dc.contributor.authorBrunt, Adrian Murray
dc.contributor.authorCramer, Angela
dc.contributor.authorHanby, Andrew
dc.contributor.authorShaaban, Abeer M
dc.contributor.authorRakha, Emad A
dc.contributor.authorArmstrong, Anne
dc.contributor.authorCutress, Ramsey I
dc.contributor.authorDodwell, David
dc.contributor.authorEmson, Marie A
dc.contributor.authorEvans, Abigail
dc.contributor.authorHartup, Sue M
dc.contributor.authorHorgan, Kieran
dc.contributor.authorMiller, Sarah E
dc.contributor.authorMcIntosh, Stuart A
dc.contributor.authorMorden, James P
dc.contributor.authorNaik, Jay
dc.contributor.authorNarayanan, Sankaran
dc.contributor.authorOoi, Jane
dc.contributor.authorSkene, Anthony I
dc.contributor.authorCameron, David A
dc.contributor.authorBliss, Judith M
dc.date.accessioned2024-07-15T14:00:08Z
dc.date.available2024-07-15T14:00:08Z
dc.date.issued2022-04-01
dc.identifier.citationBundred N, Porta N, Brunt AM, Cramer A, Hanby A, Shaaban AM, Rakha EA, Armstrong A, Cutress RI, Dodwell D, Emson MA, Evans A, Hartup SM, Horgan K, Miller SE, McIntosh SA, Morden JP, Naik J, Narayanan S, Ooi J, Skene AI, Cameron DA, Bliss JM. Combined Perioperative Lapatinib and Trastuzumab in Early HER2-Positive Breast Cancer Identifies Early Responders: Randomized UK EPHOS-B Trial Long-Term Results. Clin Cancer Res. 2022 Apr 1;28(7):1323-1334. doi: 10.1158/1078-0432.CCR-21-3177en_US
dc.identifier.issn1078-0432
dc.identifier.eissn1557-3265
dc.identifier.doi10.1158/1078-0432.CCR-21-3177
dc.identifier.pmid35165099
dc.identifier.urihttp://hdl.handle.net/20.500.14200/5141
dc.description.abstractPurpose: EPHOS-B aimed to determine whether perioperative anti-HER2 therapy inhibited proliferation and/or increased apoptosis in HER2-positive breast cancer. Patients and methods: This randomized phase II, two-part, multicenter trial included newly diagnosed women with HER2-positive invasive breast cancer due to undergo surgery. Patients were randomized to: part 1 (1:2:2), no treatment (control), trastuzumab or lapatinib; part 2 (1:1:2) control, trastuzumab, or lapatinib and trastuzumab combination. Treatment was given for 11 days presurgery. Coprimary endpoints were change in Ki67 and apoptosis between baseline and surgery tumor samples (biologic response: ≥30% change). Central pathology review scored residual cancer burden (RCB). Relapse-free survival (RFS) explored long-term effects. Results: Between November 2010 and September 2015, 257 patients were randomized (part 1: control 22, trastuzumab 57, lapatinib 51; part 2: control 29, trastuzumab 32, combination 66). Ki67 response was evaluable for 223 patients: in part 1 Ki67 response occurred in 29/44 (66%) lapatinib versus 18/49 (37%) trastuzumab (P = 0.007) and 1/22 (5%) control (P < 0.0001); in part 2 in 36/49 (74%) combination versus 14/31 (45%) trastuzumab (P = 0.02) and 2/28 (7%) control (P < 0.0001). No significant increase in apoptosis after 11 days was seen in treatment groups. Six patients achieved complete pathologic response (pCR, RCB0) and 13 RCB1, all but two in the combination group. After 6 years median follow-up, 28 (11%) had recurrence and 19 (7%) died. No recurrences or deaths were observed among patients who achieved a pCR. Ki67% falls ≥50% associated with fewer recurrences (P = 0.002). Conclusions: Early response after short duration anti-HER2 dual therapy identifies cancers dependent on the HER2 pathway providing a strategy for exploring risk-adapted individualized treatment de-escalation.en_US
dc.language.isoenen_US
dc.publisherAmerican Association for Cancer Researchen_US
dc.relation.urlhttps://aacrjournals.org/clincancerresen_US
dc.rights©2022 The Authors; Published by the American Association for Cancer Research.
dc.subjectClinical pathologyen_US
dc.subjectPublic health. Health statistics. Occupational health. Health educationen_US
dc.titleCombined perioperative lapatinib and trastuzumab in rarly HER2-positive breast cancer identifies early responders: randomized UK EPHOS-B trial long-term resultsen_US
dc.typeArticleen_US
dc.source.journaltitleClinical Cancer Researchen_US
rioxxterms.versionNAen_US
dc.contributor.trustauthorShaaban, Abeer M
dc.contributor.departmentHistopathologyen_US
dc.contributor.roleMedical and Dentalen_US
oa.grant.openaccessnaen_US


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