Abstract 444P
Background
Antiangiogenic drugs have demonstrated synergistic effect with anti-PD-1 antibody in advanced triple-negative breast cancer (TNBC). Anlotinib is an oral multi-target tyrosine kinase inhibitor (TKI) that strongly inhibits VEGFR, PDGFR, FGFR, and c-kit. Preclinical studies showed that metronomic chemotherapy inhibited angiogenesis and enhanced the efficacy of immunotherapy in TNBC via modulation of the tumor immune microenvironment. We hereby conducted a trial to investigate the efficacy and safety of sintilimab (anti-PD-1 antibody) plus anlotinib and metronomic chemotherapy as a potential novel therapeutic strategy in advanced TNBC and explore potential biomarkers.
Methods
43 cases were planning to be included in this trial. The eligible patients who had received no more than two lines of chemotherapy for metastatic disease were enrolled and received sintilimab (200 mg iv q3w) and anlotinib (12 mg po d1-14 q3w) plus capecitabine (500 mg po, tid) or vinorelbine (40 mg po, tiw) until disease progression or intolerable toxicity. The primary endpoint is objective response rate (ORR).
Results
As of April 2023, a total of 38 patients were enrolled, and 36 patients were evaluable for efficacy. 3 patients (8.3%) achieved complete response (CR). 6 patients (16.7%) achieved partial response (PR). 21 patients (58.3%) achieved stable disease (SD). The ORR is 25.0% (95%CI 0.12-0.42) and DCR is 83.3% (95%CI 0.67-0.94). The median PFS was 6.6 months (95%CI 2.12-11.08). The most common grade 1 or 2 adverse events (AEs) include elevated thyroid stimulating hormone (58.33%, 21/36), elevated bilirubin (27.78%, 10/36) , hand-foot syndrome (22.22%, 8/36), leukopenia (19.44%,7/36) and nausea (16.67%, 6/36) . Grade 3 AEs include elevated bilirubin (2.78%, 1/36), hypertension (2.78%, 1/36) and herpes zoster (2.78%, 1/36). No grade 4 or 5 AEs occurred.
Conclusions
Our date showed that sintilimab in combination with anlotinib plus metronomic chemotherapy have shown favorable efficacy and acceptable safety profile in patients with advanced TNBC.
Clinical trial identification
ChiCTR2100044725.
Editorial acknowledgement
Legal entity responsible for the study
H. Li.
Funding
The Start-up fund of Shandong Cancer Hospital (Grant No.2020- PYB10) Beijing Science and Technology Innovation Fund (Grant No.KC2021-ZZ-0010-1) Natural Science Foundation of Shandong Province (No. ZR2022LZL004).
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
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
393P - Real-world (RW) use patterns, effectiveness, and tolerability of sacituzumab govitecan (SG) for second-line (2L) and later treatment of metastatic triple-negative breast cancer (mTNBC)
Presenter: Kevin Kalinsky
Session: Poster session 03
394P - CDK4/6 inhibitors in metastatic breast cancer: An Italian real-world experience
Presenter: Francesco Pantano
Session: Poster session 03
395P - Interim analysis (IA) of the giredestrant (G) + ipatasertib (IPAT) arm in MORPHEUS Breast Cancer (BC): A phase I/II study of G treatment (tx) combinations in patients (pts) with oestrogen receptor-positive (ER+), HER2-negative, locally advanced/metastatic BC (LA/mBC)
Presenter: Kyung Jung
Session: Poster session 03
396P - Real-world treatment and survival outcomes in previously untreated patients with metastatic triple-negative breast cancer (mTNBC) in the United States (US)
Presenter: Kevin Punie
Session: Poster session 03
398P - A phase Ib/II study of IN10018/FAKi in combination with pegylated liposomal doxorubicin (PLD) and toripalimab in metastatic triple-negative breast cancer (TNBC): IN10018-010
Presenter: Xichun Hu
Session: Poster session 03
399P - Results from a first-in-human phase Ia/b study of LX-039, an oral selective estrogen receptor (ER) degrader (SERD), in postmenopausal patients with ER+, HER2- advanced breast cancer (ABC)
Presenter: weina shen
Session: Poster session 03
400P - The impact of CDK4/6 inhibitors on bone health: An Italian real-world experience
Presenter: Roberta Scafetta
Session: Poster session 03
401P - Utidelone in combination with etoposide and bevacizumab in HER2-negative breast cancer with brain metastasis (UTOBIA-BM): A prospective, single-arm, phase II trial
Presenter: Yehui Shi
Session: Poster session 03