Table 5.
Pooled incidence of grade ≥3 treatment-related adverse events in the two groups.
| Events | Study numbers | A + T group, % (95% CI) | TKI group, % (95% CI) | RR (95% CI) | P value |
|---|---|---|---|---|---|
| Hypertension | 6 | 26.5 (23.1-29.9) | 2.8 (1.5-4.1) | 4.98 (3.54-6.99) | <0.01 |
| Proteinuria | 6 | 4.8 (3.1-6.4) | 0.9 (0-2.6) | 13.50 (4.19-43.46) | <0.01 |
| Hemorrhage | 4 | 2.4 (0.9-3.9) | 1.5 (0.2-2.8) | 1.65 (0.62-4.34) | 0.313 |
| Thrombosis | 3 | 1.4 (0.2-2.5) | 1.7 (0.4-2.9) | 0.79 (0.30-2.11) | 0.644 |
| Dermatitis acneiform | 3 | 14.9 (10.6-19.2) | 9.6 (6.2-13.1) | 1.51 (0.97-2.37) | 0.069 |
| Diarrhea | 6 | 3.5 (2.1-5.0) | 1.6 (0.4-2.7) | 2.58 (1.35-4.91) | 0.004 |
| Paronychia | 3 | 2.8 (1.2-4.5) | 3.1 (1.4-4.7) | 1.02 (0.48-2.17) | 0.960 |
| Pruritus | 2 | 1.0 (0-2.1) | 0.9 (0-2.1) | 1.42 (0.28-7.13) | 0.670 |
| Rash | 6 | 2.3 (1.4-3.7) | 3.9 (2.4-5.3)- | 1.12 (0.81-1.55) | 0.494 |
| Stomatitis | 3 | 1.3 (0.3-2.5) | 1.3 (0.2-2.3) | 1.02 (0.33-3.14) | 0.972 |
| Dry skin | 3 | 0.6 (0-1.5) | 2.2 (0.3-4.1) | 0.65 (0.17-2.46) | 0.526 |
| Fatigue | 3 | 1.5 (0.2-2.8) | 0.5 (0-1.3) | 3.09 (0.75-12.75) | 0.119 |
| Decreased appetite | 4 | 2.0 (0.7-3.4) | 1.3 (0.3-2.4) | 1.53 (0.55-4.25) | 0.416 |
| Anemia | 4 | 1.8 (0.6-3.0) | 0.6 (0-1.4) | 2.33 (0.78-6.95) | 0.129 |
| Bilirubin | 3 | 1.4 (0-2.9) | 1.0 (0-2.0) | 0.78 (0.19-3.11) | 0.725 |
| AST | 3 | 4.4 (2.3-6.4) | 5.2 (3-7.4) | 0.96 (0.558-1.66) | 0.893 |
| ALT | 3 | 3.0 (1.3-4.7) | 4.1 (2.1-6.1) | 0.83 (0.42-1.64) | 0.589 |
| Interstitial lung disease | 2 | 0.9 (0-2.1) | 0.9 (0-2.1) | 0.51 (0.05-5.57) | 0.580 |
ALT: alanine aminotransferase; AST: aspartate aminotransferase; TKI: tyrosine kinase inhibitor; A + T: angiogenic inhibitors combined with TKI.