Undetectable HCV-RNA at treatment-week 8 results in high-sustained virological response in HCV G1 treatment-experienced patients with advanced liver disease: the International Italian/Spanish Boceprevir/Peginterferon/Ribavirin Name Patients Program

被引:8
|
作者
Bruno, S. [1 ]
Bollani, S. [1 ]
Zignego, A. L. [2 ]
Pascasio, J. M. [3 ]
Magni, C. [4 ]
Ciancio, A. [5 ]
Caremani, M. [6 ]
Mangia, A. [7 ]
Marenco, S. [8 ]
Piovesan, S. [9 ]
Chemello, L. [9 ]
Babudieri, S. [10 ]
Moretti, A. [11 ]
Gea, F. [12 ]
Colletta, C. [13 ]
Perez-Alvarez, R. [14 ]
Forns, X. [15 ]
Larrubia, J. R. [16 ]
Arenas, J. [17 ]
Crespo, J. [18 ]
Calvaruso, V. [19 ]
Silberstein, F. Ceccherini [20 ]
Maisonneuve, P. [21 ]
Craxi, A. [19 ]
Calleja, J. L. [22 ]
机构
[1] AO Fatebenefratelli & Oftalm, Milan, Italy
[2] Univ Florence, Florence, Italy
[3] Hosp Univ Virgen del Rocio, Seville, Spain
[4] AO L Sacco, Milan, Italy
[5] Univ Turin, Turin, Italy
[6] AO Arezzo, Arezzo, Italy
[7] IRCCS Casa Sollievo & Sofferenza, San Giovanni Rotondo, Italy
[8] Univ Genoa, Genoa, Italy
[9] Univ Padua, Padua, Italy
[10] Univ Sassari, I-07100 Sassari, Italy
[11] AO S Filippo Neri, Rome, Italy
[12] Hosp U La Paz, Madrid, Spain
[13] COQ Osped Madonna del Popolo, Omegna, Italy
[14] Hosp Univ Cent Asturias, Oviedo, Spain
[15] Hosp Clin Barcelona, Barcelona, Spain
[16] Hosp Univ Guadalajara, Guadalajara, Spain
[17] Hosp Donostia, Donostia San Sebastian, Spain
[18] Hosp Univ Marques de Valdecilla, Santander, Spain
[19] Univ Palermo, Palermo, Italy
[20] Univ Roma Tor Vergata, Rome, Italy
[21] Ist Europeo Oncol, Milan, Italy
[22] Hosp Univ Puerta de Hierro, Madrid, Spain
关键词
boceprevir; cirrhosis; first-generation protease inhibitors; hepatitis C; IFN-based therapy; CHRONIC HEPATITIS-C; GENOTYPE; INFECTION; TRIPLE THERAPY; BOCEPREVIR; TELAPREVIR; RIBAVIRIN; CIRRHOSIS; PEGINTERFERON; DACLATASVIR; FIBROSIS;
D O I
10.1111/jvh.12342
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In many countries, first-generation protease inhibitors (PIs)/peginterferon/ribavirin (P/R) still represent the only treatment option for HCV-infected patients. Subjects with advanced disease and previous failure to P/R urgently need therapy, but they are under-represented in clinical trials. All treatment-experienced F3/4 Metavir patients who received boceprevir (BOC)+P/R in the Italian-Spanish Name Patient Program have been included in this study. Multivariate logistic regression analysis (MLR) was used to identify baseline and on-treatment predictors of SVR and adverse events (AEs). Four hundred and sixteen patients, mean age 57.7 (range 25-78years), 70% males, 69.5% (289/416) F4, 14% (41/289) Child-Pugh class A6, 24% (70/289) with varices and 42% (173/416) prior null responders to P/R, were analysed. Overall, SVR rate (all 381 patients who received one dose of BOC) was 49%, (58% in F3, 45% in F4, 61% in relapsers, 51% in partial, 38% in null responders, and 72% in subjects with undetectable HCV-RNA at treatment-week (TW)8. Among patients with TW8 HCV-RNA1000IU/L, SVR was 8% (negative predictive value=92%). Death occurred in 3 (0.8%) patients, while decompensation and infections were observed in 2.9% and 11%, respectively. At MLR, SVR predictors were TW4 HCV-RNA1log(10)-decline from baseline, undetectable TW8 HCV-RNA, prior relapse, albumin levels 3.5g/dL and platelet counts 100000/L. Metavir F4, Child-Pugh A6, albumin, platelets, age and female gender were associated with serious and haematological AEs. Among treatment-experienced patients with advanced liver disease eligible for IFN-based therapy, TW8 HCV-RNA characterised the subset with either high or poor likelihood of achieving SVR. Using TW8 HCV-RNA as a futility rule, BOC/P/R appears to have a favourable benefit-risk profile.
引用
收藏
页码:469 / 480
页数:12
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