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
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