Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/117096
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dc.contributor.authorFasching, Peter Andreas-
dc.contributor.authorHack, Carolin Christine-
dc.contributor.authorNabieva, Naiba-
dc.contributor.authorMaass, Nicolai-
dc.contributor.authorAktaş, Bahriye-
dc.contributor.authorKümmel, Sherko-
dc.contributor.authorThomssen, Christoph-
dc.contributor.authorWolf, Christopher-
dc.contributor.authorKolberg, Hans-Christian-
dc.date.accessioned2024-11-11T08:18:12Z-
dc.date.available2024-11-11T08:18:12Z-
dc.date.issued2024-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/119056-
dc.identifier.urihttp://dx.doi.org/10.25673/117096-
dc.description.abstractBackground: The monarchE and NATALEE trials demonstrated the benefit of CDK4/6 inhibitor (CDK4/6i) therapy in adjuvant breast cancer (BC) treatment. Patient selection, based on clinical characteristics, delineated those at high (monarchE) and high/intermediate recurrence risk (NATALEE). This study employed a historical patient cohort to describe the proportion and prognosis of patients eligible for adjuvant CDK4/6i trials. Methods: Between 2009 and 2011, 3529 patients were enrolled in the adjuvant PreFace clinical trial (NCT01908556). Eligibility criteria included postmenopausal patients with hormone receptor-positive (HRpos) BC for whom a five-year upfront therapy with letrozole was indicated. Patients were categorized into prognostic groups according to monarchE and NATALEE inclusion criteria, and their invasive disease-free survival (iDFS) and overall survival (OS) were assessed. Results: Among 2891 HRpos patients, 384 (13.3 %) met the primary monarchE inclusion criteria. The majority (n = 261) qualified due to having ≥ 4 positive lymph nodes. For NATALEE, 915 out of 2886 patients (31.7 %) met the eligibility criteria, with 126 patients (13.7 %) being node-negative. Patients from monarchE with ≥ 4 positive lymph nodes and NATALEE with stage III BC exhibited the poorest prognosis (3-year iDFS rate 0.87). Patients ineligible for the trials demonstrated prognoses similar to the most favorable patient groups within the eligibility criteria. Conclusion: Patient populations eligible for monarchE and NATALEE trials differed. Nearly a third of the postmenopausal HRpos population, previously under upfront letrozole treatment, met the NATALEE prognostic eligibility criteria. As certain eligible groups had a prognosis similar to non-eligible patients, it might be interesting to explore additional patient groups for CDK4/6i therapy.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc610-
dc.titlePrognostic impact of selection criteria of current adjuvant endocrine therapy trials NATALEE and monarchE in postmenopausal HRpos/HER2neg breast cancer patients treated with upfront letrozoleeng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleEuropean journal of cancer-
local.bibliographicCitation.volume209-
local.bibliographicCitation.publishernameElsevier-
local.bibliographicCitation.publisherplaceAmsterdam [u.a.]-
local.bibliographicCitation.doi10.1016/j.ejca.2024.114239-
local.openaccesstrue-
dc.identifier.ppn1899268847-
cbs.publication.displayform2024-
local.bibliographicCitation.year2024-
cbs.sru.importDate2024-11-11T08:17:36Z-
local.bibliographicCitationEnthalten in European journal of cancer - Amsterdam [u.a.] : Elsevier, 1992-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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