Skip to main content
. 2022 Sep 29;12:941068. doi: 10.3389/fonc.2022.941068

Table 7.

Logistic analysis of adverse events for ORR during treatment in all patients.

Risk factors Univariable P value Multivariable P value
HR (95% CI) Adjusted HR (95% CI)
Leucopenia 0.461 (0.036–5.890) 0.551
Thrombocytopenia 0.677 (0.086–5.307) 0.710
Lymphopenia 0.493 (0.080–3.033) 0.445
Anemia 0.335 (0.060–2.084) 0.251
Elevated ALT 2.420 (0.398–14.734) 0.338
Elevated AST 0.162 (0.007–3.629) 0.251
Elevated GGT 3.355 (0.195–57.720) 0.404
Elevated TBIL 0.936 (0.145–6.052) 0.945
Hypothyroidism 0.236 (0.029–1.889) 0.174
Hand–foot syndrome 1.004 (0.152–6.618) 0.997
Rash 9.420 (1.213–73.189) 0.032# 4.382 (1.297–14.803) 0.017*
RCCEP 8.236 (0.186–364.788) 0.276
Urine protein 0.053 (0.004–0.645) 0.021#
Muscle soreness 0.655 (0.019–22.765) 0.815
Diarrhea 0.145 (0.013–1.611) 0.116
Poor appetite 0.259 (0.029–2.322) 0.228
Gingival bleeding 5.497 (0.311–97.185) 0.245

#p < 0.1, *p < 0.05.

ALT, alanine aminotransferase; AST, aspartic aminotransferase; GGT, γ- glutamyl transpeptidase; TBIL, total bilirubin; RCCEP, reactive cutaneous capillary endothelial proliferation.