Clinical utility of ledipasvir/sofosbuvir in the treatment of adolescents and children with hepatitis C

Abstract

Chronic infection with hepatitis C virus (HCV) affects an estimated 0.1%–2% of the pediatric population in the United States. While the clinical course in young children is indolent, adolescents who contract HCV have a disease course similar to adults, with a 26-fold increased risk of chronic liver disease-associated mortality, hepatocellular carcinoma, and need for curative liver transplantation. Furthermore, adolescent patients are entering childbearing age and carry a risk of passing HCV to their offspring via vertical transmission. Pegylated-interferon (PEG-IFN) with ribavirin was previously the only treatment option for pediatric patients with chronic hepatitis C (CHC), but the high likelihood of adverse reactions and subcutaneous route of administration limited its use and efficacy. Recently, the direct-acting antivirals (DAAs) ledipasvir (LDV) and sofosbuvir (SOF) were approved for adolescents with CHC. This review discusses the natural history of CHC in pediatric patients, data supporting LDV/SOF in adolescents, and ongoing studies evaluating DAAs in pediatric patients.

Keywords:

• hepatitis C virus
• chronic hepatitis C
• adolescent
• pediatric
• direct-acting antivirals

Introduction

Hepatitis C virus (HCV) is an RNA virus that affects more than 180 million people worldwide.¹ The HCV seroprevalence rate is 1%–1.5% in North America, with 0.17% in 6–11-year-olds and 0.39% in 12–19-year-olds. HCV is the primary cause of chronic hepatitis of infectious etiology in children in industrialized countries² and is estimated to affect 0.1%–2% of children in the United States.³ Chronic HCV infection (CHC) is defined by the presence of serum HCV RNA for at least 6 months after the onset of infection and includes the ensuing complications from liver injury that may develop.¹ In the USA, it is estimated 23,000–46,000 children have CHC,⁴ and who are thus at risk for cirrhosis, hepatocellular carcinoma, and death.⁵

HCV virology

HCV is from the Flaviviridae family and hepacivirus genus and is a single-stranded, positive sense RNA virus. There are six genotypes, as well as 100 subtypes, which are denoted by lower-case letters.⁶ The six genotypes follow a geographic distribution. Genotype 1 is the most prevalent worldwide and accounts for the majority of HCV infections in North America (genotype 1a) and Europe (genotype1b). Genotype 2 is found in regions of Africa. Genotype 3 is commonly found in Asia, Europe, and Australia. Genotype 4 is mostly found in North Africa and the Middle East. Genotype 5 is found in Southern Sub-Saharan Africa. Lastly, genotype 6 is found mainly in Asia.² Historically, genotype 3 has been considered the most challenging to treat.⁷

Clinical course of HCV infection in pediatric patients

The transmission of HCV is through blood contact. Before widespread blood screening efforts were established in 1992, transmission of HCV to pediatric patients occurred mostly through blood transfusions and organ transplantations. After 1992, vertical transmission has become the most common means of HCV transmission in children.⁸ Approximately 7,500 new cases of CHC occur annually in the US from vertical transmission.⁹ There is increasing concern for horizontal transmission through injection drug use, especially among adolescents.¹⁰ HCV infection rates are rising among adolescents and young adults in the US, especially in eastern rural regions of the country. This is associated with the opioid epidemic and increased use of injected opiates.¹¹ As these individuals are entering childbearing age, the risk of vertical transmission will also increase.¹² Spontaneous clearance of infection occurs in 25%–40% of infected infants but occurs far less frequently in older children (6%–12%).⁵ Thus, the majority of children (54%–86%) exposed to HCV will progress to develop CHC.²

For CHC acquired in childhood, the clinical course is indolent and usually asymptomatic. However, adolescents who acquire CHC have a clinical course similar to adults,¹³ with at 26-fold increased risk of liver-associated mortality, hepatocellular carcinoma, and need for liver transplantation, compared to age-matched controls.^14,15 Additionally, the 10-year cost associated with pediatric HCV infection is estimated to be $199–336 million⁴ as pediatric patients with CHC have decreased quality of life from learning disorders, developmental delay, and cognitive deficits reflective of decreased executive function.¹⁶ Thus, it is critical to treat HCV infection in pediatric patients, in order to prevent progression of liver disease, development of hepatocellular carcinoma, transmission to subsequent generations, and to improve childhood development.¹⁷

Medical therapy for pediatric patients with CHC

Prior to 2017, the only US Food and Drug Administration (FDA) approved therapy for CHC in pediatric patients aged three and older was pegylated-interferon-alpha (PEG-IFN) given in combination with ribavirin.¹⁸ However, in 2017, both the European Medicines Agency (EMA) and the FDA approved the use of fixed-dose ledipasvir/sofosbuvir (LDV/SOF) 90 mg/400 mg once daily to treat adolescents (ages 12–17 or weight >35 kg) with CHC with genotypes 1 and 4. Treatment duration is 12 weeks, unless patients have cirrhosis and previously failed therapy with PEG-IFN/ribavirin, in which case treatment duration is 24 weeks. Sofosbuvir with ribavirin is also approved to treat adolescents with CHC with genotypes 2 and 3. For patients with genotype 2, treatment is SOF 400 mg once daily with weight-based ribavirin (15 mg/kg in two divided doses) for 12 weeks. For patients with genotype 3, doses are the same but duration is 24 weeks (Table 1).¹⁰ There are ongoing trials for treatment with these agents for younger children. The current recommendation from the Hepatology Committee of the European Society of Pediatric Gastroenterology, Hepatology, and Nutrition (ESP-GHAN) is to consider waiting until younger children are old enough to receive approved therapy, or use these medications off-label in young children with severe disease (Table 2).¹⁰

Table 1 Drugs approved by the EMA and FDA for the treatment of children with CHC

Drug	Age (years)	HCV genotype	Dose
Ledipasvir/sofosbuvir	12–17	1, 4, 5, 6	90/400 mg PO daily
Sofosbuvir	12–17	2, 3	400 mg PO daily
Ribavirin	1–18	1–6	15 mg/kg PO daily divided in two doses
Interferon α–2b	3–18	1–6	six× 10^Citation6 IU/m^2 SQ three times weekly
Pegylated interferon α–2b	3–18	1–6	1.5 mg/kg SQ once weekly
Pegylated interferon α–2a	5–18	1–6	100 mg/m^2 SQ once weekly

Abbreviations: CHC, chronic hepatitis C; EMA, European Medicines Agency; FDA, US Food and Drug Administration; HCV, hepatitis C virus; PO, per os; SQ, subcutaneous.

Table 2 Current recommendations from ESPGHAN’s hepatology committee for the treatment of CHC in adolescents (children >12 years or weight >35 kg)

Recommendation	Quality of evidence and strength of recommendation per GRADE system
HCV genotypes 1 and 4 should be treated with LDV/SOF 90/400 mg once daily for 12 weeks	C1
HCV genotype 1 with cirrhosis should be treated with LDV/SOF 90/400 mg once daily for 24 weeks	C2
HCV genotype 2 should be treated with SOF 400 mg once daily and weight-based ribavirin (15 mg/kg in two divided doses) for 12 weeks	C1
HCV genotype 3 should be treated with SOF 400 mg once daily and weight-based ribavirin (15 mg/kg in two divided doses) for 24 weeks	C1
IFN-free regimens are the best options for HCV-infected adolescents, regardless of liver disease stage and co-morbidities, and PEG-IFN with ribavirin is no longer recommended as of 2017 for the treatment of HCV in adolescents	C1

Abbreviations: C1, low quality of evidence, strong recommendation; C2, low quality of evidence, weak recommendation; CHC, chronic hepatitis C; ESPGHAN, European Society of Pediatric Gastroenterology, Hepatology and Nutrition; GRADE, Grading of Recommendations Assessment, Development, and Evaluation; HCV, hepatitis C virus; IFN, interferon; LDV/SOF, ledipasvir/sofosbuvir; PEG-IFN, pegylated interferon.

LDV and SOF are small molecules classified as direct-acting antivirals (DAAs). DAAs target a variety of viral enzymes, which are responsible for different parts of the HCV life cycle. The HCV genome encodes a precursor polyprotein, which is then processed by host peptidases and HCV proteases into structural (core, envelope E1, E2/p7) and non-structural (NS2: protease, NS3: protease, NS4A: NS3 cofactor, NS5A: involved in viral replication, NS5B: RNA polymerase) proteins.^19,20 DAAs attack non-structural proteins, and are classified based on the non-structural proteins they inhibit.

LDV is an NS5A inhibitor and SOF is an NS5B nucleoside analog polymerase inhibitor. NS5A is an RNA binding protein involved in viral assembly.^21,22 NS5A inhibitor monotherapy was found to be effective in decreasing HCV RNA, but viral resistance to NS5A monotherapy quickly developed.²³ Hence, NS5A inhibitors are used in combination with other agents.²⁴ NS5B is an RNA-dependent polymerase,²⁵ and inhibitors of NS5B are labeled either as nucleoside analog inhibitors (these are incorporated into RNA to cause termination) or non-nucleoside inhibitors (these bind to allosteric sites and cause conformational change in RNA polymerase).²⁶ As NS5B nucleoside analog inhibitors inhibit a highly conserved region among genotypes, this gives them broad activity against many genotypes. It is also difficult for HCV to develop mutations to resist NS5B inhibitors, as mutations in the viral RNA polymerase result in loss of function.²⁵

LDV/SOF use in adults

The introduction of DAAs in 2011 revolutionized CHC treatment in adults, and nowadays CHC in adults is considered curable. There are currently ten different oral regimens licensed by the EMA and FDA for treatment of CHC in adults. All regimens achieve high (>90%) sustained virologic response (SVR) rates with 12 weeks of therapy, regardless of genotype, stage of fibrosis, or presence of human immunodeficiency virus (HIV) infection. SVR is defined as undetectable HCV RNA after completion of therapy, usually evaluated 12 weeks after treatment completion and coined “SVR12”. Certain populations can even achieve equally high SVR rates with only 8 weeks of therapy.²⁷

The efficacy of LDV/SOF in treating adults with CHC genotype 1 was established in multiple Phase III trials, including ION-1,²⁸ −2,²⁹ and –3,²⁷ along with a Japanese Phase III trial.³⁰ The oral, once daily fixed dose pill of LDV/SOF 90 mg/400 mg was used in all four trials that ranged from 341 to 865 patients. These trials found SVR12 rates of ≥93% in both treatment-naïve and treatment-experienced patients, regardless of treatment duration (8, 12, or 24 weeks), as well as whether it was administered with or without ribavirin. Rates of virologic breakthrough (reappearance of HCV RNA while on therapy) or relapse (reappearance of HCV RNA after completion of therapy) were low in all four studies, ranging from 0%–6%.³¹ These findings have been corroborated in several large real-world observational and registry studies ranging from 600 to 14,000 patients.^32–40 The efficacy of LDV/SOF for treating adults with CHC from other genotypes has also been supported by multiple Phase II trials,^41–47 a Japanese Phase III trial, and real-world data from a French cohort.³¹

LDV/SOF has shown great safety and in treatment-naïve and treatment-experienced adult patients with CHC with all genotypes. Pooled analysis of the ION trials found that treatment-emergent adverse events (TEAEs) occurred in 74% of 1,080 LDV/SOF patients, and 85% of LDV/SOF with ribavirin patients, with most TEAEs mild to moderate in severity.⁴⁸ Very few (0%–2%) of patients discontinued treatment due to TEAEs. The most common treatment-related adverse events (TRAEs) were fatigue (13%–18%), headache (11%–17%), nausea (6%–9%), diarrhea (3%–7%), and insomnia (3%–6%), most of which were grade 1 in severity.³¹ Treatment-emergent serious adverse events (SAEs) occurred in 2% of LDV/SOF patients and 3% of LDV/SOF with ribavirin patients; of these, ≤0.4% were considered treatment-related.⁴⁸

LDV/SOF use in adolescents

In children, SVR24 (sustained virologic response 24 weeks after completion of therapy) corresponds to definitive cure in 98%–100% of cases.^49,50 With the successful use of DAAs in adults with CHC, there is now great interest in their use in children. In the US, there are currently eight clinical trials evaluating DAAs in pediatric patients (Table 3).¹⁰

Table 3 Clinical trials evaluating DAA use in pediatric patients with CHC

Drug	HCV genotype	Study identifier	Estimated completion
Glecaprevir/pibrentasvir	1–6	NCT 03067129	May 2022
Gratisovir + ribavirin	1–6	NCT 02486406	June 2018
Ledipasvir/sofosbuvir	1, 4	NCT 02868242	April 2019
Ledipasvir/sofosbuvir ±ribavirin	1, 4, 5, 6	NCT 02249182	July 2018
Ombitasvir/paritaprevir/ritonavir ± dasabuvir ± ribavirin	1, 4	NCT 02486406	September 2019
Sofosbuvir + daclatasvir	4	NCT 03080415	June 2018
Sofosbuvir + ribavirin	2, 3	NCT 021755758	April 2018
Sofosbuvir/velpatasvir	1–6	NCT 03022981	December 2019

Abbreviations: CHC, chronic hepatitis C; DAA, direct-acting antivirals; HCV, hepatitis C virus.

Data from a Phase II, multicenter open-label study (NCT 02249182) evaluating safety and efficacy of LDV/SOF in 100 adolescent patients aged 12–17 years with CHC genotype 1 showed an excellent SVR rate of 98%.¹¹ In this study, patients received fixed-dose LDV/SOF 90 mg/400 mg once daily for 12 weeks. Patient demographics were: 37% were males and 63% were females, 90% were white, and average weight was 61 kg (range 33–126 kg). HCV history was: average baseline HCV RNA log₁₀ IU/mL 6.0 (range 4.7–7.0) with 55% having HCV RNA >800,000 IU/mL, 81% genotype 1a, 80% treatment-naïve, 1% with cirrhosis, and 84% infected through vertical transmission. Pharmacokinetic evaluation of LDV, SOF, and the SOF metabolite GS-331007 was comparable to those of adult patients receiving the same dose in Phase II and III trials. The primary efficacy endpoint was percentage of patients achieving SVR12, which occurred in 98/100 (98%) patients, including the one patient with cirrhosis. The two patients in which SVR12 was not achieved were lost to follow-up either during or after treatment, but both had undetectable viral loads at the time of their last visit. None of the 98 patients achieving SVR experienced virologic breakthrough or relapse. Adverse reactions were similar to the adult population, including headache (27%), diarrhea (14%), and fatigue (13%), with no serious adverse events or treatment discontinuation reported. Nine patients developed transient grade 3–4 (severe or life threatening) laboratory abnormalities which later resolved after treatment completion. There was no effect on child development through the 12 weeks of follow-up as evaluated by Tanner staging.¹¹ Quality of life was also found to improve significantly both during and after treatment.¹⁷ Currently, follow-up to evaluate for SVR24 after treatment is in process,⁵¹ as are studies in other age groups (3–11 years) and genotypes (4, 5, and 6). Estimated date of study completion is July 2018.¹⁰

A prospective, multicenter open-label study in Egypt of 144 adolescents (mean age 14 years, range 12–16 years, 69% males) with CHC with genotype 4 treated with fixed dose LDV/SOF 90 mg/400 mg once daily for 12 weeks also showed promising results.¹⁴ In this cohort, 128/144 (89%) were treatment-naïve with mean baseline HCV RNA log₁₀ IU/mL 5.26 (range 3.70–6.73). Transient elastography measurements revealed 96/144 (67%) had F0/F1 fibrosis, 48/144 (33%) had F2 fibrosis, and there were no patients with F3–4 fibrosis or cirrhosis. Virologic monitoring was performed before treatment, at weeks 4 and 12 of treatment, and 12 weeks after treatment. SVR12 was achieved in 142/144 (99%) of patients. The two patients that did not achieve SVR12 were treatment naïve and had early virologic response to LDV/SOF but relapsed. No serious adverse events were observed, and no patients discontinued therapy due to adverse events. Headache was the most common side effect (20%), and treatment-experienced patients had significantly higher rates of pruritus (31%, P=0.007), diarrhea (44%, P<0.001), and rash (19%, P=0.002) compared to treatment-naïve patients. One treatment-naïve patient developed hyperbilirubinemia and anemia, and one treatment-experienced patient developed anemia. Both of these laboratory abnormalities resolved after the end of treatment.¹⁴

Other published DAA data in adolescents

SOF and ribavirin use in adolescents

Data from a Phase II, multicenter, open-label study (NCT 02175758) evaluating safety and efficacy of SOF with ribavirin in 52 patients aged 12–17 years (median age 15 years) with CHC with genotype 2 or 3 also showed promising results.⁵² Thirteen patients genotype 2 (25%) and 39 with genotype 3 (75%) infection were recruited from 30 study sites in Australia, Germany, Italy, New Zealand, Russia, the UK, and the US. Most patients (43/52, 83%) were treatment-naïve, 60% (31/52) were male, and 90% (47/52) were white. No patients had known cirrhosis; 21/52 (40%) were documented as not having cirrhosis, and the remainder were not assessed for presence or absence of cirrhosis. All received SOF 400 mg once daily, and weight-based ribavirin (15 mg/kg divided into two doses), either for 12 weeks (genotype 2) or 24 weeks (genotype 3).⁵² The adult dose of SOF 400 mg was given as pharmacokinetic results showed similar plasma exposure and safety profiles.⁵³ Pharmacokinetic studies for SOF and GS-331007 were also done at day seven in the first 10 patients enrolled, as well as with sparse sampling throughout treatment, and were found to be comparable to prior SOF studies with adults. The primary efficacy endpoint was the percentage of patients achieving SVR12, which was achieved in 98% (51/52) of patients. The single patient who did not achieve SVR12 had HCV genotype 3 and was lost to follow-up after 4 weeks of treatment during which the viral load was already undetectable. The most common adverse events were nausea (27%) and headache (23%), and no patients discontinued treatment due to adverse events. Only one patient reported a grade 3 (severe) adverse event, which was a shoulder joint injury that was not considered related to the study drug.⁵² The study is ongoing in younger children. The dose of SOF for patients aged 6–11 will be 200 mg. This dosing is from pharmacokinetic data in adults, along with a lead-in group of patients in the 6–11 age group.⁵⁴ Pharmacokinetic lead-in results for patients aged 3–5 are pending.

In addition, there is an ongoing study Phase II/III in Egypt evaluating the safety and efficacy of gratisovir (a generic of sofosbuvir) and ribavirin in pediatric patients with CHC 10–18 years in age (NCT 02985281).⁵⁵ Generic versions of sofosbuvir have been studied in adults with CHC genotype 4 in Egypt. One study found no significant difference in SVR12 rates between patients treated with ribavirin and either gratisovir or grateziano, which are both generic versions of sofosbuvir.⁵⁶ Another study found that dual gratisovir/daclatasvir treatment duration tailored according to vRVR at 8 or 12 weeks was non-inferior compared to a fixed 12-week treatment duration.²⁷

Sofosbuvir and daclatasvir use in adolescents

Sofosbuvir and daclatasvir therapy for 12 weeks is an option for the treatment of CHC (all genotypes) in adults.⁵⁷ Furthermore, a study in adults who achieved very rapid virologic response (vRVR, defined as undetectable serum HCV RNA by week 2 of treatment) showed that decreasing the duration of therapy to 8 weeks was non-inferior to the standard 12-week treatment course.²⁷ In adolescents, there has been a pilot study of a cohort of 10 adolescents from Egypt with CHC from any genotype treated with SOF and daclatasvir.⁵⁸ The first ten consecutive adolescent patients who fulfilled eligibility criteria were treated with weight-based SOF and weight-based daclatasvir; as all patients weighed >40 kg, they all received the adult doses of 400 mg and 60 mg once daily, respectively. All achieved vRVR at week 2, thus all received 8 weeks of treatment instead of 12 weeks. All patients completed 8 weeks of treatment, and SVR12 was achieved in all patients. Six patients reported adverse events, including nausea, abdominal pain, fatigue, and headache; all were mild to moderate in severity.⁵⁸

LDV/SOF use in children

There is preliminary data from 90 children (aged 6–11 years) treated with SOF/LDV 45 mg/200 mg, with or without ribavirin.⁵⁹ Of the 90 children, there were 86, 3, and 2 with genotypes 1, 3, and 4 respectively; 59% were male, 79% were whites, and 80% were treatment-naïve. Median age was 9 years, median weight was 33 kg, and median BMI was 18 kg/m². Pharmacokinetic evaluation was done on day 10 in the first 12 participants, and found that LDV, SOF, and GS-331007 exposures were equivalent to those in adults. At the time of this review, 88/90 patients had completed therapy, and the rate of SVR at 4 weeks post-treatment (SVR4) in these 88 patients was 99% (87/88); one genotype 1a patient relapsed at 12 weeks of LDV/SOF therapy. No patients experienced grade 3 or 4 adverse events, and the only serious adverse events reported were a tooth abscess, abdominal pain, and gastroenteritis not believed to be related to the study drug. The most common adverse events were abdominal pain, headache, diarrhea, vomiting, nausea, fatigue, fever, cough, and oropharyngeal pain.⁶⁰

Ongoing DAA trials for pangenotype CHC in pediatric patients

Of the ongoing clinical trials evaluating DAAs in pediatric patients with CHC, there are two which are evaluating CHC from all genotypes: sofosbuvir/velpatasvir and glecaprevir/pibrentasvir.

Sofosbuvir/velpatasvir (SOF/VEL)

Velpatasvir (VEL) is an NS5A inhibitor and is given with SOF as a single-tablet combination DAA. This was the first single-tablet pangenotype DAA therapy for CHC. In adults, SVR12 rates range between 95% and 100% in a variety of populations, including those with compensated cirrhosis and prior treatment failures. Duration of treatment is 12 weeks, regardless of genotype, prior treatment, cirrhosis, or presence of NS5A-resistant mutations. Patients with uncompensated cirrhosis are also treated with ribavirin. Adverse reactions include fatigue, headache, nausea, and nasopharyngitis, but it is overall well tolerated.⁶¹ The pediatric clinical trial (NCT03022981) is ongoing and is a Phase II trial with two parts: pharmacokinetics lead-in phase and treatment phase. The pharmacokinetic phase will evaluate pediatric SOF/VEL dosing; the treatment phase will evaluate safety and efficacy of a 12-week course of treatment. Patients will be divided into three cohorts for the pharmacokinetic phase (ages 12 to <18, 6 to <12, and 3 to <6 years), and two cohorts for the treatment phase (ages 12 to <18, and 3 to <12 years). Estimated enrollment is 200 patients, with estimated primary completion date December 2019.⁶²

Glecaprevir/pibrentasvir (GLE/PIB)

Glecaprevir is an NS3/4A protease inhibitor, and pibrentasvir (PIB) is an NS5A inhibitor. GLE/PIB is effective across all HCV genotypes, including in patients with chronic kidney disease (as it is minimally excreted by the kidneys), HIV infection, and compensated cirrhosis, as well as those who have failed a previous NS5A treatment regimen. In addition, treatment duration is shortened to 8 weeks in treatment-naïve patients without cirrhosis.^63,64 The pediatric clinical trial (NCT03067129) is a Phase III trial evaluating the pharmacokinetics, safety, and efficacy of GLE/PIB. Patients will be divided into four age groups: 12 to <18, 9 to <12, 6 to <9, and 3 to <6 years. Some patients in all age groups will undergo pharmacokinetic evaluation to determine the pharmacokinetics of GLE/PIB in each age group, with the rest undergoing evaluation of safety and efficacy of GLE/PIB. Estimated enrollment is 110 patients, with estimated primary completion date September 2019.⁶⁵

Conclusion

The development of DAAs has dramatically changed the landscape of HCV treatment in adults with CHC. LDV/SOF and SOF with ribavirin are now approved treatments for adolescents with CHC. There are few published studies examining DAAs in the pediatric population, and none with long-term follow-up. Furthermore, currently there is no data from controlled trials regarding DAA use in children with co-infections (such as hepatitis B virus or HIV), co-morbidities, or those who are nonsustained virological responders to DAAs.¹⁰ However, the results of DAAs in the adult population are encouraging for their expanded use in the younger population, and there have been promising cases of children successfully treated with DAAs who had cirrhosis.^10,66,67 There are several ongoing clinical trials evaluating LDV/SOF and SOF with ribavirin in younger children. It is anticipated that more treatment options will become available to treat CHC in pediatric patients in the upcoming years.

Disclosure

Aijaz Ahmed is a consultant and advisory board member for AbbVie Pharmaceuticals, Gilead Sciences, and Janssen Pharmaceutical. Aijaz Ahmed has research funding/grant from Gilead Sciences. The authors report no other conflicts of interest in this work.