No Difference in Effectiveness of 8 vs 12 Weeks of Ledipasvir and Sofosbuvir for Treatment of Hepatitis C in Black Patients

被引:12
|
作者
Marcus, Julia L. [1 ,2 ]
Hurley, Leo B. [3 ]
Chamberland, Scott [4 ]
Champsi, Jamila H. [5 ]
Gittleman, Laura C. [6 ]
Korn, Daniel G. [7 ]
Lai, Jennifer B.
Lam, Jennifer O. [3 ,8 ]
Pauly, Mary Patricia [9 ]
Quesenberry, Charles P., Jr. [3 ]
Ready, Joanna [10 ]
Saxena, Varun [5 ]
Seo, Suk I. [11 ,12 ]
Witt, David J. [8 ]
Silverberg, Michael J. [3 ]
机构
[1] Harvard Med Sch, Boston, MA USA
[2] Harvard Pilgrim Hlth Care Inst, Boston, MA USA
[3] Kaiser Permanente Div Res, Oakland, CA USA
[4] Kaiser Permanente Northern Calif, Reg Pharm, Oakland, CA USA
[5] Kaiser Permanente South San Francisco Med Ctr, San Francisco, CA USA
[6] Kaiser Permanente Northern Calif, Med Grp Support Serv, Oakland, CA USA
[7] Kaiser Permanente Oakland Med Ctr, Oakland, CA USA
[8] Kaiser Permanente San Rafael Med Ctr, San Rafael, CA USA
[9] Kaiser Permanente Sacramento Med Ctr, Sacramento, CA USA
[10] Kaiser Permanente Santa Clara Med Ctr, Santa Clara, CA USA
[11] Kaiser Permanente Antioch Med Ctr, Antioch, CA USA
[12] Kaiser Permanente Walnut Creek Med Ctr, Walnut Creek, CA USA
关键词
Direct-acting Antiviral Agents; Sustained Virologic Response; Race; Effectiveness; VIRUS-INFECTION; LEDIPASVIR/SOFOSBUVIR; HCV; MARKERS;
D O I
10.1016/j.cgh.2018.03.003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Treatment with the combination of ledipasvir and sofosbuvir for 12 weeks has been approved by the Food and Drug Administration for patients with genotype 1 hepatitis C virus (HCV) infection; some patients can be treated with an 8-week course. Guidelines recommend a 12-week treatment course for black patients, but studies have not compared the effectiveness of 8 vs 12 weeks in black patients who are otherwise eligible for an 8-week treatment regimen. METHODS: We conducted an observational study of Kaiser Permanente Northern California members with HCV genotype 1 infection who were eligible for 8 weeks of treatment with ledipasvir and sofosbuvir (treatment-naive, no cirrhosis, no HIV infection, level of HCV RNA <6 million IU/mL) and were treated for 8 or 12 weeks from October 2014 through December 2016. We used chi(2) analyses to compare sustained virologic response 12 weeks after the end of treatment (SVR12) among patients treated for 8 vs 12 weeks, and adjusted Poisson models to identify factors associated with receipt of 12 weeks of therapy among patients eligible for 8 weeks. RESULTS: Of 2653 patients eligible for 8 weeks of treatment with ledipasvir and sofosbuvir, 1958 (73.8%) received 8 weeks of treatment and 695 (26.2%) received 12 weeks; the proportions of patients with SVR12 were 96.3% and 96.3%, respectively (P = .94). Among 435 black patients eligible for the 8-week treatment regimen, there was no difference in the proportions who achieved an SVR12 following 8 vs 12 weeks' treatment (95.6% vs 95.8%; P = .90). Male sex, higher transient elastography or FIB-4 scores, higher INR and level of bilirubin, lower level of albumin, obesity, diabetes, and >= 15 alcohol drinks consumed/week were independently associated with receiving 12 weeks of treatment among patients eligible for the 8-week treatment regimen, but were not associated with reduced SVR12 after 8 weeks of treatment. CONCLUSION: In an observational study of patients who received ledipasvir and sofosbuvir treatment for HCV genotype 1 infection, we found that contrary to guidelines, 8-week and 12-week treatment regimens do not result in statistically significant differences in SVR12 in black patients. Patient characteristics were associated with receipt of 12-week regimens among patients eligible for 8 weeks, but were not associated with reduced SVR12 after 8 weeks. Shorter treatment courses might therefore be more widely used without compromising treatment effectiveness.
引用
收藏
页码:927 / 935
页数:9
相关论文
共 50 条
  • [31] Effectiveness of ledipasvir/sofosbuvir in real-world patients with chronic hepatitis C: a collaborative treatment approach
    Johnson, Steven W.
    Ammirati, Shelby R.
    Hartis, Charles E.
    Weber, Stephen F.
    Morgan, Michael R.
    Darnell, Timothy A.
    Silwal, Adwait
    Schmidlin, Holly N.
    Priest, David H.
    INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2017, 49 (06) : 778 - 781
  • [32] Ledipasvir/sofosbuvir for 12 weeks is safe and effective in patients with chronic hepatitis C and hepatitis B coinfection: A phase 3 study in Taiwan
    Liu, C. -J.
    Chuang, W. -L.
    Sheen, I-S.
    Wang, H. -Y.
    Chen, C. -Y.
    Tseng, K. -C.
    Chang, T. -T.
    Massetto, B.
    Yang, J.
    Camus, G.
    Zhang, F.
    Brainard, D. M.
    McHutchison, J. G.
    Hu, T. -H.
    Hsu, Y. -C.
    Lo, G. -H.
    Chu, C. -J.
    Chen, J. -J.
    Peng, C. -Y.
    Chien, R. -N.
    Chen, P. -J.
    JOURNAL OF HEPATOLOGY, 2017, 66 (01) : S56 - S56
  • [33] Pharmacokinetics and pharmacodynamics of sofosbuvir and ledipasvir for the treatment of hepatitis C
    Cuenca-Lopez, Francisca
    Rivero, Antonio
    Rivero-Juarez, Antonio
    EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2017, 13 (01) : 105 - 112
  • [34] Treatment of Hepatitis C with Sofosbuvir/Ledipasvir in Elderly Veterans
    Blanquicett, C. J.
    Mirk, A.
    Cartwright, E.
    JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2017, 65 : S100 - S100
  • [35] Higher relapse rate among HIV/HCV-coinfected patients receiving sofosbuvir/ledipasvir for 8 vs 12 weeks
    Corma-Gomez, Anais
    Macias, Juan
    Merino Munoz, Dolores
    Tellez, Francisco
    Granados, Rafael
    Morano, Luis E.
    Santos Gil, Ignacio De Los
    Vera-Mendez, Francisco J.
    Collado, Antonio
    Palacios, Rosario
    Pineda, Juan A.
    JOURNAL OF INFECTION, 2019, 79 (01) : 30 - 35
  • [36] Ledipasvir-Sofosbuvir for 12 Weeks in Children 3 to <6 Years Old With Chronic Hepatitis C
    Schwarz, Kathleen B.
    Rosenthal, Philip
    Murray, Karen F.
    Honegger, Jonathan R.
    Hardikar, Winita
    Hague, Rosie
    Mittal, Naveen
    Massetto, Benedetta
    Brainard, Diana M.
    Hsueh, Chia-Hsiang
    Shao, Jiang
    Parhy, Bandita
    Narkewicz, Michael R.
    Rao, Girish S.
    Whitworth, Suzanne
    Bansal, Sanjay
    Balistreri, William F.
    HEPATOLOGY, 2020, 71 (02) : 422 - 430
  • [37] Ledipasvir/Sofosbuvir versus Daclatasvir/Sofosbuvir for the Treatment of Chronic Hepatitis C Genotype 4 Patients
    Abdelaty, Lamiaa N.
    Elnaggar, Ahmed A.
    Said, Amira A.
    Hussein, Raghda R. S.
    CURRENT DRUG SAFETY, 2020, 15 (01) : 53 - 60
  • [38] Hepatitis B reactivation in chronic hepatitis C patients during treatment with ledipasvir and sofosbuvir
    Ou, Pengcheng
    Chen, Jun
    ANTIVIRAL THERAPY, 2018, 23 (03) : 283 - 284
  • [39] Cost-effectiveness analysis of the use of daclatasvir + sofosbuvir + ribavirin (16 weeks and 12 weeks) vs sofosbuvir + ribavirin (16 weeks and 24 weeks) for the treatment of cirrhotic patients affected with hepatitis C virus genotype 3 in Italy
    Umberto Restelli
    Alfredo Alberti
    Adriano Lazzarin
    Marzia Bonfanti
    Carmela Nappi
    Davide Croce
    The European Journal of Health Economics, 2018, 19 : 37 - 44
  • [40] Safety and efficacy of sofosbuvir/ledipasvir and sofosbuvir/daclatasvir in the treatment of hepatitis C in patients with decompensated cirrhosis
    El Kassas, Mohamed
    Abdeen, Nermeen
    Omran, Dalia
    Alboraie, Mohamed
    Salaheldin, Mohamed
    Eltabbakh, Mohamed
    Farghaly, Rasha
    Emadeldeen, Mohammed
    Afify, Shimaa
    Sweedy, Ahmad
    Ghalwash, Ahmed
    Abbass, Amr
    Ezzat, Sameera
    Tahoon, Marwa
    ELshazly, Helmy M.
    Hamdy, Hassan
    Omar, Heba
    EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2021, 33 : E877 - E882