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. 2023 Jun 16;13:1105474. doi: 10.3389/fonc.2023.1105474

Table 3.

Cox multivariate regression analyses of factors associated with PFS of patients.

Variables HR (95% CI) p- Value
Number of brain metastases (≥3 vs. 1–2) 1.405 (0.389–5.078) 0.604
Number of visceral metastases (including brain, ≥3 vs. 1–2) 6.255 (0.767–51.000) 0.087
Location of brain metastases (subtentorial vs. supratentorial) 6.222 (1.264–30.638) 0.025
Location of brain metastases (supratentorial and subtentorial vs. supratentorial) 5.863 (1.051–32.717) 0.044
Previous brain radiotherapy (yes vs. no) 3.268 (1.018–10.493) 0.047
Prior treatment by TKIs (yes vs. no) 1.316 (0.308–5.616) 0.711
Treatment lines for pyrotinib in metastatic setting (≥3 vs. 1–2) 4.949 (1.071–22.880) 0.041
Combined with trastuzumab (yes vs. no) 0.380 (0.129–1.117) 0.079

Model was adjusted by hormone receptors, prior exposure to endocrine therapy, lung metastasis, and liver metastases. Visceral metastases referred to lung, liver, brain, pleural, and peritoneal involvement.

CI, confidence interval; HR, hazard ratio; PFS, progression-free survival; TKIs, tyrosine kinase inhibitors.