Abstract 368P
Background
Neoadjuvant chemotherapy (NACT) is a frequently used treatment method in breast cancer. Achieving pathological complete response (pCR) is one of the surrogate marker for long-term survival. Sarcopenia is considered a poor prognostic factor in breast cancer. The association between pCR and sarcopenia has not been fully elucidated in neoadjuvant setting in breast cancer. It was aimed to evaluate the effect of sarcopenia on pCR and overall survival (OS) in breast cancer patients with NACT.
Methods
Patients with NACT between 2014 and 2021 were included in the study. SMI (skeletal muscle index), VFA (visceral fat tissue area), sarcopenic obesity (VFA/SMI) were determined at the level of the third lumbar vertebra on PET-CT images before and after NACT. Patients were categorized according to pCR. The relationship between pCR and clinicopathological features and PET-CT parameters were evaluated by logistic regression analysis. Kaplan-Meier method was used for survival analysis.
Results
The medical records of 56 patients who received NACT were reviewed and twenty-three patients who met the inclusion criteria were included in the study. They were classified as sarcopenic according to the previously determined cutoff value for sarcopenia (SMI: 38.9 cm2/m2). Sarcopenia was present in 50% of patients. Post-NACT sarcopeni was found in 20% of the patients. The rate of post -NACT sarcopenic obesity was %27.3. pCR was achieved in 28.3% of patients. Sarcopenia was not associated with clinicopathologic features, pCR and OS. There was no association between clinicopathologic factors and pCR. Recurrence, post treatment high VFA, and post treatment sarcopenic obesity were significantly associated with survival. In multivariate analysis post treatment high VFA level was significantly associated with increased mortality (HR: 3.278 CI: 95% (1.143-9.401), p= 0.027).
Conclusions
Dynamic follow-up for sarcopenic obesity and visceral adipose tissue increase may improve the survival in breast cancer with NACT. Further prospective studies will be elucidated the relationship between breast cancer and sarcopenia.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
G. Tahtacı.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
371P - Adherence to standardized and structured electronic symptom reporting (ePRO) via mobile app in HER2-positive breast cancer treated with HER2 biosimilar trastuzumab
Presenter: Andreas Trojan
Session: Poster session 03
372P - Prevalence of BRCA1 and BRCA2 mutation among Indian breast cancer patients: A multicentre cross-sectional study
Presenter: Shona Nag
Session: Poster session 03
374P - Evaluation of symptom severity, tolerability, and physical function in the I-SPY2 trial
Presenter: Amrita Basu
Session: Poster session 03
375TiP - A phase I, 2-part, multicenter, first-in-human dose-escalation and dose-expansion study of DS-1103a with trastuzumab deruxtecan (T-DXd) in patients with advanced solid tumors
Presenter: Ludimila Cavalcante
Session: Poster session 03
388P - Subgroup analysis of patients (pts) with HER2-low metastatic breast cancer (mBC) with brain metastases (BMs) at baseline from DESTINY-Breast04, a randomized phase III study of trastuzumab deruxtecan (T-DXd) vs treatment of physician’s choice (TPC)
Presenter: Junji Tsurutani
Session: Poster session 03
391P - Detrimental effect on overall survival of CDK4/6 inhibitor dose reduction if immortal time bias is considered
Presenter: Andreas Bjerrum
Session: Poster session 03
392P - The prognostic impact of BMI in patients with HR+/HER2- advanced breast cancer on first-line endocrine therapy with or without a CDK 4/6 inhibitor
Presenter: Senna Lammers
Session: Poster session 03