Abstract 398P
Background
IN10018 is a highly potent and selective oral inhibitor of focal adhesion kinase (FAK). Preclinical data showed that IN10018 in combination with PLD had synergistic antitumor effect and can further enhance immunotherapeutic effect in TNBC animal model. This study was to evaluate the safety and antitumor activity of IN10018 combined with PLD +/- anti-PD-1 antibody, Toripalimab in metastatic TNBC.
Methods
All enrolled metastatic TNBCs who had failed in 1-2 lines of systemic therapy were assigned to either doublet group: IN10018+PLD or triplet group: IN10018+PLD+Toripalimab. Phase Ib-dose finding part was to identify the recommended phase II dose (RP2D) of triplet combination. Phase II-dose expansion part was to evaluate the primary endpoint of objective response rate (ORR) and secondary endpoints of disease control rate (DCR), duration of response (DOR), progression-free survival (PFS), overall survival (OS) and safety.
Results
At data cutoff of April 28, 2023, 12 pts received IN10018+PLD and 14 pts received IN10018+PLD+Toripalimab. Median follow-up duration was 7.2 mo (range: 4.9-9.7) in doublet group and 6.0 mo (range: 2.0-10.5) in triplet group. The RP2D was determined as IN10018 100mg qd + PLD 40mg/m2 q4w + Toripalimab 3 mg/kg q2w. In doublet group, ORR by investigators was 16.7% (95% CI, 2.1-48.4); DCR was 50% (95% CI, 21.1-78.9); median PFS was 3.65 mo (95% CI, 1.77-NA); and median OS was 7.52 mo (95% CI, 5.59-NA). In triplet group, ORR by investigators was 14.3% (95% CI, 3.8-42.8); DCR was 78.6% (95% CI, 49.2-95.3); median PFS was 9.26 mo (95% CI, 3.02-NA); and median OS was not reached. No drug-related death was observed. In doublet group, TEAEs grade ≥3 occurred in 58.3% pts with TEAEs in ≥2 pts being WBC and neutrophil count decreased; SAE occurred in 2 pts with 1 related to treatment. In triplet group, TEAEs grade ≥3 occurred in 64.3% pts with TEAEs in ≥2 pts being anemia, WBC and neutrophil count decreased; SAE occurred in 5 pts with 4 related to treatment.
Conclusions
The combination of IN10018 with PLD and Toripalimab showed promising antitumor activity in metastatic TNBC. The combination safety profile was comparable to each single agent with no additional safety signal.
Clinical trial identification
NCT05830539.
Editorial acknowledgement
Legal entity responsible for the study
InxMed (Shanghai) Co., Ltd, Shanghai, China.
Funding
InxMed (Shanghai) Co., Ltd, Shanghai, China.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
424P - Pyrotinib plus capecitabine for trastuzumab-resistant, HER2-positive advanced breast cancer: Updated survival results from the phase II PICTURE trial
Presenter: Xichun Hu
Session: Poster session 03
425P - Real world quality of life (QoL) in breast cancer (BC) patients treated with cyclin-dependent kinase 4/6 inhibitors (CDK4/6i)
Presenter: Blanca Tavara
Session: Poster session 03
427P - Pyrotinib plus trastuzumab versus pertuzumab plus trastuzumab in patients with HER2-positive metastatic breast cancer: A multicenter, retrospective study
Presenter: biyun Wang
Session: Poster session 03
428P - Palbociclib dose patterns in Swedish patients with metastatic breast cancer: 5-year update from the SIRI study
Presenter: Antonis Valachis
Session: Poster session 03
429P - The impact of HER2 status on the efficacy of CDK 4/6 inhibitors: A multicenter study
Presenter: Hasan Yildirim
Session: Poster session 03
430P - Real-world patient characteristics and treatment patterns in HR+/HER2+ metastatic breast cancer patients in 5 European countries
Presenter: Carmen Criscitiello
Session: Poster session 03
431P - Distribution and prognostic role of HER2 status of circulating tumor cells (CTCs) and tumor-derived extracellular vesicles (tdEVs) in HER2- metastatic breast cancer (MBC) patients (pts)
Presenter: Eleonora Nicolo
Session: Poster session 03
432P - Ki67 and progesterone receptor status could be predict sensitivity to cyclin-dependent kinase inhibitor
Presenter: Lucia Navarro Berlanga
Session: Poster session 03
433P - Effectiveness and safety of vinorelbine + inetetamab + pyrotinib in ≥second-line treatment of HER2-positive metastatic breast cancer
Presenter: Wu Fan
Session: Poster session 03