Abstract 6P
Background
Neoadjuvant chemotherapy (NAC) results in a pathologic complete response (pCR) and is associated with disease-free survival and overall survival. The apparent diffusion coefficient (ADC) indicates the stability of water molecules and is used to predict the response of solid tumors to chemotherapy. Therefore, we evaluated the changes in ADC using diffusion-weighted breast magnetic resonance imaging (MRI) to predict pCR in patients with breast cancer treated with NAC.
Methods
From August 2013 to April 2019, 50 patients (mean age, 55 years; age range, 31–75 years) were treated with nanoparticle albumin-bound paclitaxel (nab-PTX) (260 mg/m2) every 3 weeks for four cycles ± concurrent trastuzumab (8 mg, 6 mg/kg) every 3 weeks for four cycles in human epidermal growth factor receptor 2 (HER2)-positive patients followed by FEC (5-fluorouracil/epirubicin/cyclophosphamide, 500/100/500 mg/m2) every 3 weeks for four cycles. pCR was defined as the absence of any residual invasive cancer or ductal carcinoma in situ in the breast. Changes in ADC (Δnab-PTX: post nab-PTX – pre nab-PTX, ΔFEC: post FEC – pre nab-PTX) were also calculated.
Results
The tumor phenotypes were triple negative (TN) (n = 25) and HER2 positive (n = 25). pCR was achieved in 27 patients [54%] (11 with TN disease and 16 with HER2-positive disease). The mean pre nab-PTX ADC and ΔFEC ADC in pCR patients were 0.718±0.157 × 10-3 mm2 and 0.621±0.357 × 10-3 mm2, respectively, and they were not associated with pCR (p = 0.06 and p = 0.248, respectively). However, the mean post nab-PTX ADC and Δnab-PTX ADC were 1.117±0.303 × 10-3 mm2 and 0.400±0.311 × 10-3 mm2, respectively, and they were associated with pCR (p < 0.01 and p = 0.01, respectively). Using receiver operating characteristic (ROC) analysis with Δnab-PTX ADC, the area under the curve was 0.691 [95% confidence interval: 0.54–0.841] in all patients. Δnab-PTX ADC and pCR were significantly correlated (p = 0.00463).
Conclusions
High Δnab-PTX ADCs in diffusion-weighted breast MRI may be promising findings for the successful prediction of pCR in patients treated with NAC using nab-PTX followed by FEC.
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
65P - Updated efficacy and safety of entrectinib in patients with NTRK fusion-positive tumours: Integrated analysis of STARTRK-2, STARTRK-1 and ALKA-372-001
Presenter: Christian Rolfo
Session: Poster display session
Resources:
Abstract
66P - Brain metastases, treatment patterns and outcomes in ROS1-positive NSCLC patients from US oncology community centers
Presenter: Matthew Krebs
Session: Poster display session
Resources:
Abstract
67P - Pooled safety analysis of tepotinib in Asian patients with advanced solid tumours
Presenter: Kentaro Yamazaki
Session: Poster display session
Resources:
Abstract
68P - A novel anti-EGFR antibody HLX07 for potential treatment of squamous cell carcinoma of the head and neck
Presenter: Ming Mo Hou
Session: Poster display session
Resources:
Abstract
69P - Irinotecan and cisplatin therapy-induced neutropenia as a prognostic factor in patients with extensive-disease small cell lung cancer
Presenter: Hiroshi Ishikawa
Session: Poster display session
Resources:
Abstract
70P - Is safe and efficient by intraoperative endoscopic nasobiliary drainage over primary closure of the common bile duct for cholecystolithiasis combined with common bile duct stones: A meta-analysis
Presenter: Jiasheng Cao
Session: Poster display session
Resources:
Abstract
71P - Irreversible electroporation versus radiotherapy after induction chemotherapy on survival in patients with locally advanced pancreatic cancer: A propensity score analysis
Presenter: Chaobin He
Session: Poster display session
Resources:
Abstract
72P - Novel technique of near-focus mode for accurate operation during endoscopic submucosal tunneling procedure: A two-center comparative study
Presenter: Wei Peng
Session: Poster display session
Resources:
Abstract
73P - Cabozantinib in combination with anti-PD1 immune checkpoint inhibitor in syngeneic tumour mouse models
Presenter: Rachel Sparks
Session: Poster display session
Resources:
Abstract
74TiP - Phase I study of BI 836880, a VEGF/Ang2-blocking nanobody®, as monotherapy and in combination with BI 754091, an anti-PD-1 antibody, in Japanese patients (pts) with advanced solid tumours
Presenter: Kentaro Yamazaki
Session: Poster display session
Resources:
Abstract