Survival benefit and biomarker analysis of pyrotinib or pyrotinib plus capecitabine for patients with HER2-positive metastatic breast cancer: a pooled analysis of two phase I studies

• Published in: Biomarker research 2023-02, Vol.11 (1), p.21-21, Article 21
• Main Authors: Guan, Xiuwen, Ma, Fei, Li, Qiao, Chen, Shanshan, Lan, Bo, Fan, Ying, Wang, Jiayu, Luo, Yang, Cai, Ruigang, Zhang, Pin, Li, Qing, Xu, Binghe
• Format: Article
• Language: English
• Subjects: 1-Phosphatidylinositol 3-kinase; AKT protein; Analysis; Antimitotic agents; Antineoplastic agents; Antitumor activity; Biomarkers; Breast cancer; Cancer; Cancer therapies; Care and treatment; Chemotherapy; Clinical trials; Concomitant mutations; Enrollments; Epidermal growth factor; ErbB-2 protein; Gene amplification; HER2-positive; Kinases; Medical prognosis; Metastases; Metastasis; Metastatic breast cancer; Mutation; Next-generation sequencing; Oncology, Experimental; p53 Protein; Patient outcomes; Patients; Protein-tyrosine kinase; Pyrotinib; Signal transduction; Software; Survival; TOR protein; Tumor proteins; Tyrosine
• ISSN: 2050-7771; 2050-7771
• DOI: 10.1186/s40364-023-00453-0

Pyrotinib, a novel irreversible tyrosine kinase inhibitor (TKI), has demonstrated promising antitumor activity to improve the overall response rate and progression-free survival (PFS) in patients with HER2-positive metastatic breast cancer (MBC). However, the survival data of pyrotinib or pyrotinib plus capecitabine in HER2-positive MBC remains scarce. Thus, we summarized the updated individual patient data from the phase I trials of pyrotinib or pyrotinib plus capecitabine, to provide a cumulative assessment on long-term outcomes and associated biomarker analysis of irreversible TKIs in HER2-positive MBC patients. We performed a pooled analysis of the phase I trials for pyrotinib or pyrotinib plus capecitabine based on the updated survival data from individual patients. Next-generation sequencing was performed on circulating tumor DNA for predictive biomarkers. A total of 66 patients were enrolled, including 38 patients from the phase Ib trial for pyrotinib and 28 patients from the phase Ic trial for pyrotinib plus capecitabine. The median follow-up duration was 84.2 months (95% CI: 74.7-93.7 months). The estimated median PFS in the entire cohort was 9.2 months (95% CI: 5.4-12.9 months) and median OS was 31.0 months (95% CI: 16.5-45.5 months). The median PFS was 8.2 months in the pyrotinib monotherapy cohort and 22.1 months in the pyrotinib plus capecitabine group, while the median OS was 27.1 months in the pyrotinib monotherapy group and 37.4 months in the pyrotinib plus capecitabine group. Biomarker analysis suggested that the patients harbored concomitant mutations from multiple pathways in HER2-related signaling network (HER2 bypass signaling pathways, PI3K/Akt/mTOR pathway and TP53) were observed with significantly poorer PFS and OS when compared to those with none or one genetic alteration (median PFS, 7.3 vs. 26.1 months, P = 0.003; median OS, 25.1 vs. 48.0 months, P = 0.013). The updated survival results based on individual patient data from the phase I trials of pyrotinib-based regimen revealed promising PFS and OS in HER2-positive MBC. Concomitant mutations from multiple pathways in HER2-related signaling network may be a potential efficacy and prognosis biomarker for pyrotinib in HER2-positive MBC. ClinicalTrials.gov. (NCT01937689, NCT02361112).