Efficacy of adjuvant capecitabine in residual triple negative breast cancer: a multicenter observational Turkish Oncology Group (TOG) study

dc.contributor.authorTasci, Elif Senocak
dc.contributor.authorKutlu, Yasin
dc.contributor.authorOlmez, Omer Fatih
dc.contributor.authorMutlu, Arda Ulas
dc.contributor.authorGundogdu, Yasemin
dc.contributor.authorSeyyar, Mustafa
dc.contributor.authorYildiz, Ibrahim
dc.date.accessioned2026-08-12T17:38:49Z
dc.date.issued2024
dc.departmentFırat Üniversitesi
dc.description.abstractBackgroundTriple negative breast cancer (TNBC) is characterized by high rates of recurrence, especially in patients with residual disease after neoadjuvant chemotherapy (NAC). Capecitabine is being used as standard adjuvant treatment in residual TNBC. We aimed to investigate the real-life data regarding the efficacy of capecitabine in residual TNBC.Design and methodsIn this retrospective multicenter study, TNBC patients with residual disease were evaluated. Patients, who received standard anthracycline and taxane-based NAC and adjuvant capecitabine were eligible. Overall survival (OS), disease free survival (DFS) and toxicity were analyzed.Results170 TNBC patients with residual disease were included. Of these, 62.9% were premenopausal. At the time of analysis, the recurrence rate was 30% and death rate was 18%. The 3-year DFS and OS were 66% and 74%, respectively. In patients treated with adjuvant capecitabine, residual node positive disease stood out as an independent predictor of DFS (p = 0.024) and OS (p = 0.032). Undergoing mastectomy and the presence of T2 residual tumor was independent predictors of DFS (p = 0.016) and OS (p = 0.006), respectively.ConclusionThe efficacy of capecitabine was found lower compared to previous studies. Selected patients may have further benefit from addition of capecitabine. The toxicity associated with capecitabine was found lower than anticipated.
dc.identifier.doi10.1080/14656566.2024.2337261
dc.identifier.endpage484
dc.identifier.issn1465-6566
dc.identifier.issn1744-7666
dc.identifier.issue4
dc.identifier.orcid0000-0002-7433-3591
dc.identifier.orcid0000-0001-7499-7155
dc.identifier.orcid0000-0002-2575-5819
dc.identifier.orcid0000-0001-5885-3047
dc.identifier.orcid0000-0002-1976-3951
dc.identifier.pmid38568074
dc.identifier.scopus2-s2.0-85189873288
dc.identifier.scopusqualityQ2
dc.identifier.startpage477
dc.identifier.urihttps://doi.org/10.1080/14656566.2024.2337261
dc.identifier.urihttps://hdl.handle.net/11508/58585
dc.identifier.volume25
dc.identifier.wosWOS:001196635300001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofExpert Opinion on Pharmacotherapy
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectCapecitabine
dc.subjectbreast cancer
dc.subjectresidual tumor
dc.subjecttriple negative
dc.subjecttoxicity
dc.titleEfficacy of adjuvant capecitabine in residual triple negative breast cancer: a multicenter observational Turkish Oncology Group (TOG) study
dc.typeArticle

Dosyalar