Response data for patients who donated serial samples
Patient no. . | Treatment group . | Day-29 response* . | EVR at wk 12† . | ETR at wk 48‡ . | SVR at wk 72 or beyond§ . | Summary . |
---|---|---|---|---|---|---|
1 | B | + | + | + | + | SVR |
2 | A | + | + | - | - | Breakthrough |
3∥ | A | + | + | + | + | SVR |
4 | A | - | + | + | - | Relapse |
5∥ | A | + | + | + | + | SVR |
6¶ | A | - | - | - | - | Nonresponder |
7 | A | + | + | + | + | SVR |
8 | A | - | - | - | - | Nonresponder |
9 | A | - | - | - | - | Nonresponder |
10 | C | - | + | + | - | Relapse |
11 | C | + | + | + | + | SVR |
12 | C | - | - | - | - | Nonresponder |
13 | C | - | + | + | + | SVR |
14 | C | - | + | + | - | Relapse |
15 | C | - | - | - | - | Nonresponder |
16 | B | + | + | + | + | SVR |
17 | B | - | - | - | - | Nonresponder |
18 | B | + | + | + | - | Relapse |
19 | B | + | + | - | - | Breakthrough |
20 | B | - | - | - | - | Nonresponder |
21 | B | - | + | - | - | Breakthrough |
22 | B | + | + | + | + | SVR |
23 | B | - | - | - | - | Nonresponder |
24 | B | - | - | - | - | Nonresponder |
25 | B | - | - | + | - | Relapse |
26 | B | + | + | + | + | SVR |
27 | B | - | - | - | - | Nonresponder |
28 | B | + | + | + | + | SVR |
29 | B | + | + | + | + | SVR |
Patient no. . | Treatment group . | Day-29 response* . | EVR at wk 12† . | ETR at wk 48‡ . | SVR at wk 72 or beyond§ . | Summary . |
---|---|---|---|---|---|---|
1 | B | + | + | + | + | SVR |
2 | A | + | + | - | - | Breakthrough |
3∥ | A | + | + | + | + | SVR |
4 | A | - | + | + | - | Relapse |
5∥ | A | + | + | + | + | SVR |
6¶ | A | - | - | - | - | Nonresponder |
7 | A | + | + | + | + | SVR |
8 | A | - | - | - | - | Nonresponder |
9 | A | - | - | - | - | Nonresponder |
10 | C | - | + | + | - | Relapse |
11 | C | + | + | + | + | SVR |
12 | C | - | - | - | - | Nonresponder |
13 | C | - | + | + | + | SVR |
14 | C | - | + | + | - | Relapse |
15 | C | - | - | - | - | Nonresponder |
16 | B | + | + | + | + | SVR |
17 | B | - | - | - | - | Nonresponder |
18 | B | + | + | + | - | Relapse |
19 | B | + | + | - | - | Breakthrough |
20 | B | - | - | - | - | Nonresponder |
21 | B | - | + | - | - | Breakthrough |
22 | B | + | + | + | + | SVR |
23 | B | - | - | - | - | Nonresponder |
24 | B | - | - | - | - | Nonresponder |
25 | B | - | - | + | - | Relapse |
26 | B | + | + | + | + | SVR |
27 | B | - | - | - | - | Nonresponder |
28 | B | + | + | + | + | SVR |
29 | B | + | + | + | + | SVR |
Patients 1 to 29 from our previous study,24 all infected with HCV genotype 1, were enrolled in a study of viral kinetics and evolution during therapy with pegylated IFNα and ribavirin. Treatment groups A, B, and C are described in “Patients, materials, and methods.” HCV viral load was recorded at frequent intervals during therapy. + and - refer to positive and negative responses, respectively.
A positive day 29 response was defined as a > 2 log10 drop in viral load; a negative day 29 response was defined as a drop of < 1 log10 in viral load.
Early virologic response, EVR, was defined as a > 2 log10 drop in viral load following 12 weeks of therapy.
A positive end-of-treatment response, ETR, was achieved if HCV RNA was undetectable in patient serum at the end of treatment.
An SVR was achieved if HCV RNA remained undetectable in patient serum 6 months after completion of therapy.
These patients, who both achieved SVRs, declined to donate follow-up blood samples at the 72-week time point.
This patient, who was a nonresponder, discontinued therapy before the 48-week point but remained in the study.