Transmission of Chronic Hepatitis C in Pregnancy

The treatment of chronic hepatitis C virus infection has dramatically advanced in recent years, with the availability of multiple interferon-free treatment regimens that result in cure in over 95% of treatment naïve individuals with 8 -12 weeks of therapy. Despite these advances, however, the natural history and treatment of HCV remains undefined in several populations, including pregnancy. In particular, rates of vertical (mother to child) transmission, perinatal and neonatal morbidity, assessment of disease severity (fibrosis) in pregnancy and timing of treatment are not well understood. At least 2.3 million people in the United States and 185 million people worldwide are believed to have chronic HCV infection, although as it is frequently asymptomatic until the development of end-stage liver disease (ESLD), this may be a significant underestimate. Between 2012 and 2014 the HCV detection rate among women of childbearing age increased by 22% nationally and over 200% in Kentucky, while the proportion of children born to HCV infected women increased 68% nationally and 128% in Kentucky. Currently, in the United States, the overall rate of children born to HCV infected women is 3.4 per 1,000 live births, with the highest rate in West Virginia, with 22.4 per 1,000 live births occurring to HCV-infected women. Overall, the number of HCV infected reproductive age women has doubled from 2006 to 2014, with an estimated 29,000 HCV infected women giving birth and 1,700 infants vertically infected each year, according to previous estimates of vertical transmission.The true incidence of vertical transmission of HCV is unknown, although the most commonly cited meta-analysis reported a mean transmission rate of 5.8% in HIV-negative women and 10.8% in HIV-positive women. The timing of vertical transmission is also not well characterized. There is limited data regarding the course of chronic hepatitis C during pregnancy, HCV viral loads appear to peak during third trimester. Both utero and peripartum transmission appear possible, while breastfeeding does not appear to be a risk factor. It appears that between 80 and 90% of children who acquire hepatitis C via vertical transmission will develop chronic infection. However, as sequelae of infection are not commonly observed in childhood, and appropriate testing of exposed children is poor, this may not be a true reflection of actual prevalence. The current AASLD/IDSA HCV Guidelines recommend all children born to HCV infected women be tested, but they do not specify when or in what manner. Maternal HCV infection has been shown to contribute to worsened perinatal and neonatal outcomes in the absence of vertical transmission. It is associated with increased rates of intrauterine fetal death, preterm delivery, low birth rate, increased risk for adverse neonatal neurological outcomes, increased infant feeding difficulties and subsequent maternal infertility. Although there is sufficient time between the end of the first trimester and delivery to provide curative therapy during pregnancy, no safety studies in pregnancy have been done. Therefore, this study will offer curative DAA therapy to HCV infected Moms with the fixed dose combination of sofosbuvir/velpatasvir (SOF/VEL) after the cessation of breastfeeding. This combination of sofosbuvir, a nucleotide inhibitor of the NS5B RNA-dependent RNA polymerase, and velpatasvir, an inhibitor of the NS5A transcriptional activator, is approved for the treatment of chronic HCV infection due to genotypes 1 through 6. Given the gaps in the investigator's understanding of HCV vertical transmission rates, HCV-associated perinatal complications, and marked increases in both the number of women with chronic HCV infection giving birth and the number of children under two years old testing positive for HCV, this study will help to both better characterize the natural history of HCV in pregnancy and ultimately, to facilitate its elimination when women are screened for chronic HCV as part of routine gynecologic care and are offered curative therapy prior to conception (or as part of prenatal care and when dosing during pregnancy can be safely undertaken). All participants will be offered curative therapy with sofosbuvir/velpatasvir (Epclusa ®) after delivery and the cessation of breastfeeding. Subjects may be enrolled at any time after conception up through 36 weeks gestation. The management of subjects in pregnancy will be in accordance with ACOG guidelines and individual clinical judgment, however testing will include, but not be limited to, testing for HCV infection, HIV infection, HBV infection, HSV infection, group B Streptococcal colonization, HCV genotype, HCV viral load, as well as assessment of hepatic and renal function. Staging of hepatic fibrosis must be performed within 12 months prior to initiation of SOF/VEL. Acceptable methods of staging include transient elastography or liver biopsy. If elastography is performed, it must be performed either prior to pregnancy or at least 12 weeks following delivery, due to pregnancy-related changes in hepatic stiffness. Subjects will be followed on a schedule that is determined by their obstetric care providers throughout their pregnancy. Data from clinical and laboratory records regarding the participants pregnancy and delivery, and their infant's medical record from the infant's pediatrician from birth to 12 months of age will be collected. Following delivery, infants will be evaluated at 12, 24 and 48 weeks of age, with testing for HCV RNA to be obtained at each evaluation. Vertical transmission is defined as two positive HCV RNA PCR tests, at least one before the 48 week visit, and again at the 12-month follow-up infant visit.At 24 weeks following delivery, participants will begin therapy with sofosbuvir/velpatasvir (SOF/VEL) once daily for 12 weeks. Therapy will not be initiated until cessation of breastfeeding. Participants will be evaluated at the initiation of SOF/VEL therapy, at 4 and 8 weeks after starting therapy, as well as 12 weeks following completion of therapy for determination of SVR-12. Quantitative measurement of HCV RNA will be obtained at each visit, as well as evaluation of renal and hepatic function.