Abstract 483P
Background
Androgen receptor (AR) is expressed in around 30% of triple-negative breast cancer (TNBC) tumors, and presents with different clinical evolution and resistance to standard chemotherapy. Sacituzumab govitecan (SG) is an antibody-drug conjugate recently approved in TNBC advanced tumors.
Methods
We conducted a retrospective study in 8 French University Hospitals and cancer centers. All patients with TNBC MBC treated with SG were included. The primary endpoint was progression-free survival (PFS) as per AR expression (cut-off 10%). Secondary endpoints included overall survival (OS). Univariable and multivariable analyses were performed.
Results
A total of 127 patients were included, of which 88 (69%) were AR-. The median age was 51yo (range 25 - 77), with younger patients in AR- (47yo) vs. AR+ (55.5yo; p=0.02). AR- tumors were mostly ductal subtype (95.5% vs. 82.1%; p=0.005) and higher grade III (79.8% vs. 58.3%; p=0.021). No differences were observed between AR- and AR+ in the median number of prior treatments at SG start: 2 (0 - 11) and the median number of SG cycles: 6 (1 - 28) with 27 patients (21.3%) still on SG at the time of analyses. With a median FU of 10.4m [95%CI 8.3-11.2], median PFS was 4.1m [3.7-4.7] with no differences based on AR expression (4.1m vs. 4.3 m, AR- vs. AR+, respectively; HR 0.83 [95%CI: 0.53-1.32], p=0.432). In univariable analysis, age at SG treatment (HR 0.98 [0.97-1.00]; p=0.028), adjuvant capecitabine (HR 1.65 [1.06-2.56]; p=0.025), and metastasis-free interval (MFI) (HR 2.39 [1.38-4.14] and 1.09 [0.63-1.91] for 6-24m and > 24m respectively vs. < 6m) were associated with PFS. Short MFI remained significant for worse prognosis in a multivariable analysis (HR (6-24m vs. <6m) 2.0 [1.04-3.88]; p=0.039). The mOS was 9.7m [7.1-12.2] with 67 (52.8%) patients still alive. AR was not associated with OS in the univariable (HR 0.66 [0.37-1.19]; p=0.165] or multivariable analyses (HR=0.69 [0.34-1.38]; p=0.290].
Conclusions
Despite AR+ tumors being described as lesser chemo-sensitive, in this large retrospective cohort, AR expression was not associated with benefit in terms of PFS and OS from SG in patients with advanced TNBC.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Institut Bergonie.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
478P - Germline BRCA1/2 pathogenetic variants (gBRCA1/2 PV) affect outcome of hormone (HR)-positive HER2-negative metastatic breast cancer (MBC) patients (pts) treated with cyclin-dependent kinase 4/6 inhibitor (CDK 4/6i) plus endocrine therapy (ET): The BREAK study
Presenter: Antonella Palazzo
Session: Poster session 04
479P - Radiomics to predict HER2 status in breast cancer brain metastases
Presenter: Gaia Griguolo
Session: Poster session 04
480P - Prognostic significance of somatic DNA gene rearrangement and structural atypia in metastatic breast cancer
Presenter: Hiroshi Tada
Session: Poster session 04
481P - Second generation oral selective estrogen receptor degraders (SERDs) in breast cancer: A systematic review and meta-analysis of clinical trials
Presenter: Maysa Silveira Vilbert
Session: Poster session 04
482P - Precision imaging with human epidermal growth factor receptor 2-positron emission tomography (HER2-PET) for refined treatment selection in patients with HER2-low breast cancer
Presenter: Siri af Burén
Session: Poster session 04
484P - Multi-platform characterization of HER2 expression in triple-negative breast cancer
Presenter: Ana C Garrido-Castro
Session: Poster session 04
485P - A novel approach to identify subpopulation of CTCs with metastatic potential using sc-RNA-seq
Presenter: Evgeniya Grigoryeva
Session: Poster session 04
486P - The influence of NF1 germline and somatic mutations on breast cancer patient survival
Presenter: Roope Kallionpää
Session: Poster session 04
487P - Induction of an inflammatory tumor microenvironment with oncolytic virus CF33-hNIS-antiPD-L1 intratumoral injection in patients with metastatic triple-negative breast cancer (mTNBC)
Presenter: Jamie Rand
Session: Poster session 04
488P - Comprehensive genomic profiling to identify actionable alterations for breast cancer brain metastases in the Chinese population
Presenter: Qianyi Lu
Session: Poster session 04