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. 2019 Aug 14;14(3):357–367. doi: 10.5009/gnl18269

Table 3.

Efficacy and Safety in CPT A versus CPT B/C Patients According to RBV Protocol

Variable CPT A without RBV n° 56 CPT B/C without RBV n° 14 p-value
HCV RNA SVR12 50 (89.3) 11 (78.6) 0.2
Anemia 2 (3.6) 1 (7.1) 0.4
Fatigue 5 (8.9) 5 (35.7) 0.02
Headache 0 0 NS
Diarrhea 0 0 NS
SAE 0 1 (7.1) 0.2

CPT A flat RBV n° 78 CPT B/C flat RBV n° 9

HCV RNA SVR12 78 (100) 7 (77.8) 0.01
Anemia 14 (17.9) 3 (33.3) 0.2
Fatigue 17 (21.8) 2 (22.2) 0.6
Headache 5 (6.4) 0 0.5
Diarrhea 2 (2.6) 0 0.8
SAE 1 (1.3) 1 (11.1) 0.08

CPT A weight dose RBV n° 73 CPT B/C weight dose RBV n° 5

HCV RNA SVR12 71 (98) 5 (100) 0.8
Anemia 26 (35.6) 4 (80) 0.05
Fatigue 25 (34.2) 3 (60) 0.2
Headache 5 (6.8) 1 (20) 0.3
Diarrhea 2 (2.7) 0 0.8
SAE 0 0 NS

Data are presented as number (%).

CPT, Child-Pugh-Turcotte; RBV, ribavirin; HCV, hepatitis C virus; SAE, severe adverse event; NS, significant.