Keiju Sasaki , Shin Takahashi , Kota Ouchi , Hidekazu Shirota , Nobuaki Sato , Kouji Kaneko , Norikazu Masuda , Fumiyoshi Fujishima , Satoko Sato , Chikashi Ishioka
{"title":"Dynamic predictive power of TP53 signatures in breast cancer prognosis: Pre- and post-neoadjuvant chemotherapy insights","authors":"Keiju Sasaki , Shin Takahashi , Kota Ouchi , Hidekazu Shirota , Nobuaki Sato , Kouji Kaneko , Norikazu Masuda , Fumiyoshi Fujishima , Satoko Sato , Chikashi Ishioka","doi":"10.1016/j.tranon.2025.102398","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>The <em>TP53</em> signature determined using a biopsy specimen before neoadjuvant chemotherapy (pre-NAC biopsy specimens) predicts NAC response and prognosis in breast cancer. We aimed to compare the clinical utility of the <em>TP53</em> signature determined using pre-NAC biopsy specimens and surgical specimens after NAC (post-NAC surgical specimens).</div></div><div><h3>Methods</h3><div>This observational cohort study included patients with paired pre-NAC biopsy and post-NAC surgical specimens, analyzing the association between the <em>TP53</em> signature from each specimen and prognosis (UMIN000042055).</div></div><div><h3>Results</h3><div>Pre-NAC biopsy specimens classified 71 patients into those having a <em>TP53</em> mutant signature (pre-mt, <em>n</em> = 47) and wild-type signature (pre-wt, <em>n</em> = 24), with the same for post-NAC surgical specimens (post-mt, <em>n</em> = 16 and post-wt, <em>n</em> = 55). Among the 47 pre-mt patients, 31 became post-wt (pre-mt/post-wt), whereas 16 remained post-mt (pre-mt/post-mt). All pre-wt patients remained post-wt (pre-wt/post-wt). Recurrence-free survival (RFS) was significantly shorter in the pre-mt group than in the pre-wt group, although no significant difference was observed between the post-mt and post-wt groups. Change in the <em>TP53</em> signature following NAC did not affect predictive ability of the <em>TP53</em> signature determined using pre-NAC biopsy specimens.</div></div><div><h3>Conclusions</h3><div>The <em>TP53</em> signature status should be determined using pre-NAC biopsy specimens.</div></div>","PeriodicalId":48975,"journal":{"name":"Translational Oncology","volume":"56 ","pages":"Article 102398"},"PeriodicalIF":5.0000,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Oncology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1936523325001299","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Background
The TP53 signature determined using a biopsy specimen before neoadjuvant chemotherapy (pre-NAC biopsy specimens) predicts NAC response and prognosis in breast cancer. We aimed to compare the clinical utility of the TP53 signature determined using pre-NAC biopsy specimens and surgical specimens after NAC (post-NAC surgical specimens).
Methods
This observational cohort study included patients with paired pre-NAC biopsy and post-NAC surgical specimens, analyzing the association between the TP53 signature from each specimen and prognosis (UMIN000042055).
Results
Pre-NAC biopsy specimens classified 71 patients into those having a TP53 mutant signature (pre-mt, n = 47) and wild-type signature (pre-wt, n = 24), with the same for post-NAC surgical specimens (post-mt, n = 16 and post-wt, n = 55). Among the 47 pre-mt patients, 31 became post-wt (pre-mt/post-wt), whereas 16 remained post-mt (pre-mt/post-mt). All pre-wt patients remained post-wt (pre-wt/post-wt). Recurrence-free survival (RFS) was significantly shorter in the pre-mt group than in the pre-wt group, although no significant difference was observed between the post-mt and post-wt groups. Change in the TP53 signature following NAC did not affect predictive ability of the TP53 signature determined using pre-NAC biopsy specimens.
Conclusions
The TP53 signature status should be determined using pre-NAC biopsy specimens.
期刊介绍:
Translational Oncology publishes the results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of oncology patients. Translational Oncology will publish laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer. Peer reviewed manuscript types include Original Reports, Reviews and Editorials.