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©The Author(s) 2021.
World J Gastroenterol. May 28, 2021; 27(20): 2474-2494
Published online May 28, 2021. doi: 10.3748/wjg.v27.i20.2474
Published online May 28, 2021. doi: 10.3748/wjg.v27.i20.2474
Table 1 Pediatric studies of different combinations of direct-acting antivirals
Drug regimen | Age range in yr | Sample size | Genotype(s) | Number of patients with SVR12, % | Ref. |
Sofosbuvir/ledipasvir | 12-17 | 100 | 1 | 98/100 (98) | Balistreri et al[25] |
6-11 | 92 | 1, 3, 4 | 91/92 (99) | Murray et al[26] | |
3-5 | 34 | 1, 4 | 33/34 (97) | Schwarz et al[27] | |
Sofosbuvir plus ribavirin | 12-17 | 52 | 2, 3 | 51/52 (98) | Wirth et al[33] |
6-11 | 41 | 41/41 (100) | Rosenthal et al[34] | ||
3-5 | 13 | 12/13 (92) | Rosenthal et al[34] | ||
Sofosbuvir/velpatasvir | 12-17 | 102 | 1, 2, 3, 4 | 97/102 (95) | Sokal et al[35] |
6-11 | 73 | 68/73 (93) | Sokal et al[35] | ||
3-5 | 41 | 34/41 (83) | Sokal et al[35] | ||
Glecaprevir/pibrentasvir | 12-17 | 47 | 1, 2, 3, 4 | 47/47 (100) | Jonas et al[36] |
6-11 | 32 | 31/32 (97) | Jonas et al[37] | ||
3-5 | 16 | 15/16 (96) | Jonas et al[37] | ||
Ombitasvir/paritaprevir/ritonavir ± dasabuvir ± ribavirin | 12-17 | 38 | 1, 4 | 38/38 (100) | Leung et al[134] |
6-11 | 26 | 1 | 25/26 (95) | Rosenthal et al[135] | |
Elbasvir/grazoprevir | 12-17 | 22 | 1, 4 | 22/22 (100) | Wirth et al[136] |
6-11 | 17 | 17/17 (100) | Wirth et al[136] | ||
3-5 | 18 | 18/18 (100) | Wirth et al[136] | ||
Sofosbuvir/velpatasvir/voxilaprevir | 12-17 | 21 | 1, 2, 3, 4 | 21/21 (100) | Bansal et al[137] |
Sofosbuvir plus daclatasvir | 15-17 | 13 | 4 | 13/13 (100) | El-Sayed et al[138] |
13-17 | 10 | 10/10 (100) | El-Shabrawi et al[139] | ||
12-17 | 30 | 29/29 (100) | Yakoot et al[140] | ||
8-17 | 40 | 1, 4 | 39/39 (100) | Abdel Ghaffar et al[141] | |
7-13 | 14 | 3 | 14/14 (100) | Padhi et al[57] |
Table 2 Direct-acting antiviral regimens approved for treatment of chronic hepatitis C virus infection in children and adolescents
Regimen | Genotype and duration of treatment | Formulations | Dosage |
Sofosbuvir/ledipasvir | GT 1, 4, 5, 6: 12 wk | Tablet (FDC) 400/90 mg | > 35 kg: 400/90 mg/d |
GT 1, treatment-experienced, cirrhosis: 24 wk | 17-35 kg: 200/45 mg/d | ||
< 17 kg, older than 3 yr of age: 150/33.75 mg/d | |||
Tablet (FDC) 200/45 mg | |||
Pellets 200/45 mg and 150/33.75 | |||
Sofosbuvir + ribavirin | GT 2: 12 wk | Sofosbuvir: tablet 400 mg | Sofosbuvir: > 35 kg: 400 mg/d |
GT 3: 24 wk | 17-35 kg: 200 mg/d | ||
Tablet 100 mg | < 17 kg, older than 3 yr of age: 200 mg if ≥ 17 kg | ||
Capsules 50 mg containing granules | |||
150 mg/d if < 17 kg. Ribavirin: 15 mg/kg per day in two divided doses | |||
Sofosbuvir/velpatasvir | All GTs: 12 wkdecompensated cirrhosis: 12 wk + ribavirin | Tablet (FDC) 400/100 mg | > 30 kg: 400/100 mg/d |
17-30 kg, older than 6 yr of age: 200/50 mg/d. Ribavirin: 15 mg/kg per day in two divided doses | |||
Tablet (FDC) 200/50 mg | |||
Glecaprevir/pibrentasvir | All GTs: 8 wk | Tablet (FDC) 100/40 mg/d | 12-17 yr or > 45 kg: 300/120 mg/d |
All GTs, cirrhosis: 12 wk | |||
GT 3 treatment-experienced: 16 wk |
Table 3 Antiviral drugs approved for adolescents and children with chronic hepatitis B virus infection
Drug | Use in children | Dose | Formulation |
Interferon-α-2b | ≥ 1 yr | 6 million IU/m2 3 times a week | Subcutaneous injections |
Pegylated interferon-α-2a | ≥ 3 yr | 180 µg/1.73 m2 once a week | Subcutaneous injections |
Lamivudine | ≥ 3 yr | 3 mg/kg daily (max 100 mg) | Oral solution (5 mg/mL) |
tablets (100 mg) | |||
Entecavir | ≥ 2 yr | 10-30 kg: 0.015 mg/kg daily (max 0·5 mg) | Oral solution (0.05 mg/mL) |
tablets (0.5 mg and 1 mg) | |||
Adefovir | ≥ 12 yr | 10 mg daily | Tablets (10 mg) |
Tenofovir disoproxil fumarate | ≥ 12 yr (FDA) | 300 mg daily | Oral powder (40 mg per 1 g) |
≥ 2 yr (EMA) | tablets (150, 200, 250 and 300 mg) | ||
Tenofovir alafenamide | ≥ 12 yr (EMA) | 25 mg daily | Tablets (25 mg) |
Table 4 Summary of results of clinical trials of hepatitis B antiviral therapy in children
Interferon-α-2b | Lamivudine | Adefovir | Tenofovir DF | Entecavir | Pegylated interferon-α-2a | |
Number treated | 144 | 191 | 173 | 52 | 120 | 101 |
Duration of treatment in wk | 24 | 52 | 48 | 72 | 48 | 48 |
Age, median (range) | 5 (1-17) | 9 (2-17) | 11 | 15.5 (12-17) | 12 (2-17) | 11 (3-7) |
Virological response as HBeAg negative HBV DNA undetectable (% treated vs placebo) | 26 (vs 11) | 23 (vs 13) | 10.6 (vs 0) | 21.2 (vs 0) | 24.2 (vs 3.3) | 19.8 (vs 2) |
HBsAg negative (% treated vs placebo) | 10 (vs 1) | 2 (vs 0) | 0.8 (vs 0) | 1.9 (vs 0) | 5.8 (vs 0) | 8.9 (0) |
Ref. | Sokal et al[97] | Jonas et al[98] | Jonas et al[99] | Murray et al[100] | Jonas et al[101] | Wirth et al[102] |
Table 5 Investigational drugs for chronic hepatitis B infection
Class | Compound | Mechanism | Known side effects | Route | Status | Ref. |
Entry inhibitors | Bulevirtide | Blocks entry via interaction with NTCP | Injection site reactions, cholestasis | Subcutaneous (iv) | Approved for CHD (HBV/HDV) Phase II for HBeAg-CHB | European Association for the Study of the Liver[117] and Bogomolov et al[118] |
Capsid assembly modulators | JNJ-56136379 | Prevents encapsidation of pgRNA Prevents formation of cccDNA | Hypertransaminasemia | Oral | Phase II for CHB ± NA | Zoulim et al[105] |
Capsid assembly modulators | ABI-H0731 (Vebicorvir) | Prevents packaging of pgRNA into capsids | Skin rash, dizziness | Oral | Phase II for CHB ± NA | Yuen et al[106] |
HBsAg secretion inhibitors | REP-2139 | Inhibits the secretion of HBsAg subviral particles | Fever, chills, hypertransaminasemia, leukopenia | iv | Phase II for CHB + NA Phase II for CHD + peg-IFN-α | Bazinet et al[109,110] |
HBsAg secretion inhibitors | REP-2165 | Inhibits the secretion of HBsAg subviral particles | Fever, chills, hypertransaminasemia, leukopenia | iv | Phase II for CHD + peg-IFN-α | Bazinet et al[110] |
RNA interference | JNJ-3989 | Silences the mRNA viral transcripts reducing HBsAg | - | iv | Phase II for CHB | Yuen et al[111] and Gane et al[112] |
RNA interference | VIR-2218 | Silences the mRNA viral transcripts reducing HBsAg | - | iv | Phase II for CHB | VIR Biotechnology[113] |
RIG-1 agonist | Inarigivir (SB9200) | Activates PRR RIG-1 and IFN-I response | Headache, dizziness, UTI, ILI, GI symptoms, hypertransaminasemia | Oral | Phase II for CHB + NA | Yuen et al[114] |
Immune modifier | Selgantolimod (GS-9688) | TLR8 agonist | Nausea, vomiting, chills, headache, UTI | Oral | Phase II for CHB + NA | Gane et al[116] |
- Citation: Nicastro E, Norsa L, Di Giorgio A, Indolfi G, D'Antiga L. Breakthroughs and challenges in the management of pediatric viral hepatitis. World J Gastroenterol 2021; 27(20): 2474-2494
- URL: https://www.wjgnet.com/1007-9327/full/v27/i20/2474.htm
- DOI: https://dx.doi.org/10.3748/wjg.v27.i20.2474