Statins enhance trastuzumab deruxtecan efficacy: preclinical synergy in HER2-negative models and clinical benefit in HER2-positive metastatic breast cancer

LetterAçık Erişim

Özet

Trastuzumab deruxtecan (T-DXd) has demonstrated significant efficacy in metastatic breast cancer (mBC) with varying HER2 expression. Statins have been shown to increase HER2 membrane localization and stability, potentially enhancing responses to HER2-targeted therapies. We investigated whether statins enhance T-DXd activity through a translational approach combining a preclinical HER2-negative model and a real-world HER2-positive mBC cohort. In the preclinical arm, 60 female Wistar albino rats were induced with mammary tumors using N-methyl-N-nitrosourea (MNU). Animals were randomized into five groups: Control, MNU-only, MNU + T-DXd, MNU+statin, and MNU + T-DXd+statin. In the clinical arm, 109 patients with HER2-positive mBC who received T-DXd were retrospectively analyzed. The combination of T-DXd and statin significantly reduced tumor volume compared to either monotherapy (p < 0.0001) in a preclinical rat model. HER2 protein levels were found to be elevated in the statin and combination groups, as demonstrated by both IHC and Western blot analyses. In a real-world cohort of 109 heavily pretreated patients with HER2-positive mBC receiving T-DXd, concomitant statin use was associated with significantly improved median progression-free survival (mPFS) and median overall survival (mOS). Our findings revealed that statin use significantly enhanced the efficacy of T-DXd in both a preclinical HER2-negative rat model and patients with HER2-positive mBC. Prospective clinical trials are warranted to validate these observations. © The Author(s) 2026.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/10100Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1186/s40164-026-00787-zYayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorSahin, Taha Koray
dc.contributor.authorOrhan, Cemal
dc.contributor.authorOzercan, Ibrahim Hanifi
dc.contributor.authorMuglu, Harun
dc.contributor.authorEr, Besir
dc.contributor.authorAkyildiz, Arif
dc.contributor.authorTunbekici, Salih
dc.contributor.authorOruc, Ahmet
dc.contributor.authorAykan, Musa Baris
dc.contributor.authorKoylu, Bahadir
dc.contributor.authorAkdogan, Orhun
dc.contributor.authorOnur, Ilknur Deliktas
dc.contributor.authorAtes, Ozturk
dc.contributor.authorYazici, Ozan
dc.contributor.authorSelcukbiricik, Fatih
dc.contributor.authorKaradurmus, Nuri
dc.contributor.authorAraz, Murat
dc.contributor.authorErdem, Dilek
dc.contributor.authorGoker, Erdem
dc.contributor.authorBilici, Ahmet
dc.contributor.authorAksoy, Sercan
dc.contributor.authorGuven, Deniz Can
dc.date.accessioned2026-10-18T20:25:21.295669495Z
dc.date.available2026-10-18T20:25:21.295669495Z
dc.date.issued2026
dc.description.abstractTrastuzumab deruxtecan (T-DXd) has demonstrated significant efficacy in metastatic breast cancer (mBC) with varying HER2 expression. Statins have been shown to increase HER2 membrane localization and stability, potentially enhancing responses to HER2-targeted therapies. We investigated whether statins enhance T-DXd activity through a translational approach combining a preclinical HER2-negative model and a real-world HER2-positive mBC cohort. In the preclinical arm, 60 female Wistar albino rats were induced with mammary tumors using N-methyl-N-nitrosourea (MNU). Animals were randomized into five groups: Control, MNU-only, MNU + T-DXd, MNU+statin, and MNU + T-DXd+statin. In the clinical arm, 109 patients with HER2-positive mBC who received T-DXd were retrospectively analyzed. The combination of T-DXd and statin significantly reduced tumor volume compared to either monotherapy (p < 0.0001) in a preclinical rat model. HER2 protein levels were found to be elevated in the statin and combination groups, as demonstrated by both IHC and Western blot analyses. In a real-world cohort of 109 heavily pretreated patients with HER2-positive mBC receiving T-DXd, concomitant statin use was associated with significantly improved median progression-free survival (mPFS) and median overall survival (mOS). Our findings revealed that statin use significantly enhanced the efficacy of T-DXd in both a preclinical HER2-negative rat model and patients with HER2-positive mBC. Prospective clinical trials are warranted to validate these observations. © The Author(s) 2026.
dc.identifier.doi10.1186/s40164-026-00787-z
dc.identifier.issn2162-3619
dc.identifier.issue1
dc.identifier.pmcidPMC13244906
dc.identifier.pmid42260640
dc.identifier.scopus2-s2.0-105041218832
dc.identifier.startpage49
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/10100
dc.identifier.volume15
dc.language.isoen
dc.publisherBioMed Central Ltd
dc.relation.ispartofExperimental Hematology and Oncology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectApoptosis
dc.subjectBreast cancer
dc.subjectHER2-low
dc.subjectStatin
dc.subjectSynergistic effect
dc.subjectTrastuzumab deruxtecan
dc.subjectcaspase 3
dc.subjectcaspase 9
dc.subjectepidermal growth factor receptor 2
dc.subjecthydroxymethylglutaryl coenzyme A reductase inhibitor
dc.subjectprotein Bax
dc.subjectprotein bcl 2
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectcontrolled study
dc.subjectdrug efficacy
dc.subjectdrug potentiation
dc.subjectfemale
dc.subjecthuman epidermal growth factor receptor 2 negative breast cancer
dc.subjecthuman epidermal growth factor receptor 2 positive breast cancer
dc.subjectimmunohistochemistry
dc.subjectLetter
dc.subjectMAPK signaling
dc.subjectmetastatic breast cancer
dc.subjectMNU-induced mammary carcinogenesis
dc.subjectmonotherapy
dc.subjectnonhuman
dc.subjectoverall survival
dc.subjectPi3K/Akt signaling
dc.titleStatins enhance trastuzumab deruxtecan efficacy: preclinical synergy in HER2-negative models and clinical benefit in HER2-positive metastatic breast cancer
dc.typeLetter
dspace.entity.typePublication
rdl.citation.scopus0
rdl.departmentDepartment of Medical Oncology, Erzincan Binali Yildirim University Medical School, Erzincan, 24000, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexPUBMED