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Table 3 Characteristics of CHB patients who showed non-response to re-treatment with the same oral nucleos(t)ide analog that had induced initial complete virologic response

From: Off-treatment virologic relapse and outcomes of re-treatment in chronic hepatitis B patients who achieved complete viral suppression with oral nucleos(t)ide analogs

Patients

Medication

HBeAg status

Baseline DNA level (IU/ml)

Liver cirrhosis

Total treatmenta(months)

Additional treatmentb(months)

Time to relapsec(months)

Genotypic resistance

Rescue therapy after second treatment failure

Response to rescue therapy

Patient 1

Clevudine

Positive

20,000,000

Negative

13

7

5

rtM204I

Entecavir

Sustained VR

Patient 2

Lamivudine

Negative

2,099,619

Positive

24

18

2

rtM204I

Entecavir

PartialVR

Patient 3

Lamivudine

Negative

257,039

Negative

20

7

3

rtM204I

Entecavir

Sustained VR

Patient 4

Entecavir

Positive

20,000,000

Negative

33

16

6

rtM204I

Entecavir + Adefovir

Partial VR

  1. aTotal duration of initial oral nucleos(t)ide analog therapy.
  2. bAdditional treatment duration of initial oral nucleos(t)ide analog therapy after undetectable HBV DNA.
  3. cTime to relapse after discontinuation of initial oral nucleos(t)ide analog therapy.
  4. VR, virologic response.