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Sitravatinib plus tislelizumab in locally recurrent or metastatic triple-negative breast cancer: a multi-cohort, single-arm, phase II clinical trial (SPARK Trial).

Molecular cancer 2025 Vol.25(1) p. 15

Liu XY, Sui XY, Xu Y, Yang F, Wu SY, Zhu XZ, Zuo K, Cao SW, Jin X, Chen L, Ma LX, Zhang WJ, Ye FG, Qu FL, Ma D, Xiao Y, Di GH, Liu GY, Yu KD, Wu J, Hu X, Jiang YZ, Wang ZH, Shao ZM, Fan L

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[BACKGROUND] While immunotherapy-chemotherapy combinations are approved for programmed death-ligand 1 (PD-L1)-positive advanced triple-negative breast cancer (TNBC), the therapeutic potential of sitra

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APA Liu XY, Sui XY, et al. (2025). Sitravatinib plus tislelizumab in locally recurrent or metastatic triple-negative breast cancer: a multi-cohort, single-arm, phase II clinical trial (SPARK Trial).. Molecular cancer, 25(1), 15. https://doi.org/10.1186/s12943-025-02505-5
MLA Liu XY, et al.. "Sitravatinib plus tislelizumab in locally recurrent or metastatic triple-negative breast cancer: a multi-cohort, single-arm, phase II clinical trial (SPARK Trial).." Molecular cancer, vol. 25, no. 1, 2025, pp. 15.
PMID 41420248

Abstract

[BACKGROUND] While immunotherapy-chemotherapy combinations are approved for programmed death-ligand 1 (PD-L1)-positive advanced triple-negative breast cancer (TNBC), the therapeutic potential of sitravatinib-enhanced immunotherapy remains unexplored.

[METHODS] This multi-cohort, single-arm study enrolled 67 patients with locally recurrent/metastatic TNBC. Cohorts A ( = 21) and B ( = 40) received sitravatinib 70 mg or 100 mg once daily plus tislelizumab, with 38/67 participants having ≥ 1 prior systemic therapy. The primary endpoint was confirmed objective response rate (ORR); secondary endpoints included median progression-free survival (PFS) and safety. Multi-omics analyses including single-cell sequencing and genomic profiling were performed on tumor samples to identify biomarkers linked to treatment response.

[RESULTS] Confirmed ORR was 38.1% (8/21) in Cohort A and 50.0% (20/40) in Cohort B. Median PFS was 8.2 months (Cohort A) and 5.4 months (Cohort B). Notably, 95.3% (41/43) of previously treated patients had PD-L1 combined positive score (CPS) < 10. No grade 4/5 treatment-related adverse events occurred. Biomarker analysis revealed Th17 cell infiltration and TYRO3/AXL/MERTK (TAM) pathway activation correlated with response, while mutations and LSM1 cancer-associated fibroblasts were enriched in non-responders. Post-treatment mutation clearance and increased CD8 T cell proportions predicted improved outcomes.

[CONCLUSIONS] Sitravatinib plus tislelizumab demonstrates promising efficacy and safety as a chemo-free regimen for metastatic TNBC, including PD-L1-negative tumors. Biomarkers such as Th17 cell infiltration, TAM signaling, and mutation dynamics may guide patient selection. These findings support further validation of this combination in PD-L1-negative TNBC and highlight the role of multi-omics in optimizing immunotherapy strategies.

[TRIAL REGISTRATION] ClinicalTrials.gov, NCT04734262.

[SUPPLEMENTARY INFORMATION] The online version contains supplementary material available at 10.1186/s12943-025-02505-5.

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