Abstract 430P
Background
The prognosis of patients with breast cancer brain metastasis (BCBM) remains significantly poor. Accurate prediction of the prognosis of BCBM patients is very important for formulating treatment strategies.
Methods
We retrospectively collected clinicopathological data and MR images per patient diagnosed with BCBM at our center from 2001 to 2021, and validated the updated breast graded prognostic assessment (uB-GPA) in our cohort. Then cox regression analysis was used to identify prognostic clinical factors. Preprocessed MR images and prognostic clinical factors were used together to develop an end-to-end deep learning network based on the transformer encoder in the training set. After feature encoding by the encoder, output sequences were passed to a multi-task logistic regression model to obtain the patients' risk scores. The prognostic performance of the model was evaluated in the test set.
Results
A total of 700 patients with BCBM were enrolled, with a median OS of 11 months (95%CI: 9.8-12.2m). The concordance index (C-index) of uB-GPA was 0.563 (0.551-0.575). Nine clinical factors were shown to be associated with poorer prognosis of patients with BCBM: Age greater than 48 years at BC diagnosis (P=0.003), KPS less than 80 at BCBM diagnosis (P=0.001), triple-negative subtype (P<0.001), initial metastasis site other than the brain (P<0.001), number of brain metastases ≥3 (P<0.001), concurrent leptomeningeal metastasis (P=0.008), not receiving radiotherapy after diagnosis (P=0.003), liver metastasis (P=0.006), and lung metastasis (P=0.049). A deep learning model based on both MR images and clinical factors was developed in the training set (n=166), yielded the C-index of 0.664 and areas under the receiver operative characteristic curve of 0.705, 0.723 and 0.790 respectively for predicting 3-m, 6-m and 12-m OS in the test set (n=36). The median OS of patients in high and low-risk group were 5m (95%CI: 4-9m) and 14m (95%CI: 13m-?), respectively.
Conclusions
This study developed a novel tool to predict survival of patients with BCBM and achieve good performance. It helps in identifying patients' risk of death and in formulating personalized management strategies.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
383P - Clinical experience with TTX-MC138: A first-in-class therapy against metastatic cancer
Presenter: Andreas Varkaris
Session: Poster session 15
385P - A phase II study of nivolumab, ipilimumab plus bicalutamide in metastatic breast cancer
Presenter: David Page
Session: Poster session 15
388P - Anlotinib or bevacizumab combined with chemotherapy for the second-line HER-2 negative metastatic breast cancer: A retrospective cohort study
Presenter: jin xiang
Session: Poster session 15
390P - SARELIFE: An Italian, multicentric real-world study of sacituzumab govitecan (SG) in pretreated metastatic triple-negative breast cancer (mTNBC)
Presenter: Maria Cona
Session: Poster session 15
391P - Real-world activity of sacituzumab govitecan for metastatic breast cancer
Presenter: Stefania Morganti
Session: Poster session 15
392P - Quality-adjusted time without symptoms of disease progression or toxicity of treatment (Q-TWiST) analysis to assess benefit-risk of sacituzumab govitecan (SG) in previously treated patients (pts) with metastatic triple-negative breast cancer (mTNBC)
Presenter: Adam Brufsky
Session: Poster session 15