Abstract 38P
Background
Patients who reach pathological complete remission (PCR) after neoadjuvant therapy for triple-negative breast cancer (TNBC) have a better overall prognosis and do not require additional adjuvant therapy postoperatively according to current guidelines; however, some patients still have a lower survival rate.
Methods
We identified TNBC patients who completed neoadjuvant therapy and achieved PCR registered in the Surveillance, Epidemiology, and End Results (SEER) database between 2010 and 2015. We analyzed the relationship between clinicopathological characteristics and overall survival, seeking to explore the high-risk factors for poor prognosis in patients who achieved PCR after neoadjuvant therapy for TNBC.
Results
A total of 1237 TNBC patients without distant metastases completed neoadjuvant therapy and achieved PCR, and their 5-year overall survival rate was 90.78%. We incorporated age, TNM stage (AJCC 7th edition), and presence of lymph node metastasis as variables to construct a multifactorial COX proportional risk model. The results found no statistically significant effect on survival time in stage II patients compared to stage I patients (HR=1.057, 95%CI 0.540-2.069, P=0.872), but statistically significant compared to stage III patients (HR=2.441, 95%CI 1.159-5.144, P=0.019). There was a statistically significant effect on survival time in patients with lymph node metastases compared to those without lymph node metastases (HR=1.913, 95%CI 1.253-2.921, P=0.003); and no statistically significant effect on survival time in patients younger than 40 years compared to those older than 40 years (HR=1.190, 95%CI 0.615-2.302, P= 0.605).
Conclusions
Younger age is not a factor influencing the prognosis of TNBC patients with PCR. For patients with stage III or lymph node metastases, even if PCR is achieved, further adjuvant therapy may be needed to improve prognosis. The type of adjuvant therapy to be used may need to be further confirmed by future prospective clinical trials.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The author.
Funding
Has not received any funding.
Disclosure
The author has declared no conflicts of interest.
Resources from the same session
415P - Initial experience in a real-world Asian cohort with a circulating tumor DNA (ctDNA) mutation-based multi-cancer early detection (MCED) assay
Presenter: Steven Tucker
Session: Poster Display
Resources:
Abstract
416P - Three-dimensional bioprinting model of ovarian cancer for identification of patient-specific therapy response
Presenter: Jiangang Zhang
Session: Poster Display
Resources:
Abstract
417P - Early experience in using plasma-only multi-omic minimal residual disease testing in early-stage colorectal cancer patients from Asia and the Middle East
Presenter: Shaheenah Dawood
Session: Poster Display
Resources:
Abstract
418P - Decoding the intricate cellular makeup of immune-related adverse events using single-cell and spatial analysis
Presenter: Dmitrii Shek
Session: Poster Display
Resources:
Abstract
420P - Combinatory genomic and transcriptomic sequencing of Chinese KRAS mutant non-small cell lung cancer revealed molecular and inflammatory heterogeneity in tumor microenvironment
Presenter: Xuchao Zhang
Session: Poster Display
Resources:
Abstract
421P - Comprehensive genomic profiling (CGP) unravels somatic BRCA (sBRCA) and homologous recombinant repair (HRR) gene alterations across multi-cancer spectrum
Presenter: Ramya Kodandapani
Session: Poster Display
Resources:
Abstract
422P - CD8Teff distinguished tumor immunotyping heterogeneity and enables precision immunotherapy
Presenter: luhui Mao
Session: Poster Display
Resources:
Abstract
423P - Insights into clinically actionable biomarkers in an Indian cancer cohort of 1000 patients using comprehensive genomic profiling (CGP)
Presenter: Mithua Ghosh
Session: Poster Display
Resources:
Abstract
424P - MD Anderson Cancer Center global precision oncology decision support (Glo-PODS) clinical trial genomic support: Pilot program at the Prince of Wales Hospital (Chinese University of Hong Kong - CUHK)
Presenter: Brigette Ma
Session: Poster Display
Resources:
Abstract
425P - Engineered <italic>Lactococcus lactis</italic> as a personalized cancer vaccine platform induces antitumour immunity via membrane-inserted peptide for neoantigens
Presenter: Meng Zhu
Session: Poster Display
Resources:
Abstract