Pregled bibliografske jedinice broj: 1031056
MOLECULAR AND CLINICAL BASES OF ANTI-HCV DRUG RESISTANCE
MOLECULAR AND CLINICAL BASES OF ANTI-HCV DRUG RESISTANCE // PROGRAM AND ABSTRACTS 6th International Monothematic Conference on Viral Hepatitis C (IMC- HCV- 2019) / Smolić, Robert ; Včev, Aleksandar ; Wu, Y. George (ur.).
Osijek: Fakultet za dentalnu medicinu i zdravstvo Sveučilišta Josipa Jurja Strossmayera u Osijeku ; Hrvatsko društvo za preciznu (personaliziranu) medicinu, 2019. str. 42-42 (pozvano predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1031056 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
MOLECULAR AND CLINICAL BASES OF ANTI-HCV DRUG RESISTANCE
Autori
Smolić, Martina ; Wu Y, George
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
PROGRAM AND ABSTRACTS 6th International Monothematic Conference on Viral Hepatitis C (IMC- HCV- 2019)
/ Smolić, Robert ; Včev, Aleksandar ; Wu, Y. George - Osijek : Fakultet za dentalnu medicinu i zdravstvo Sveučilišta Josipa Jurja Strossmayera u Osijeku ; Hrvatsko društvo za preciznu (personaliziranu) medicinu, 2019, 42-42
ISBN
978-953-57695-6-8
Skup
6th International Monothematic Conference on Viral Hepatitis C (IMC-HCV 2019)
Mjesto i datum
Osijek, Hrvatska, 03.10.2019. - 05.10.2019
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Direct-acting antivirals ; treatment failure ; HCV resistance testing
Sažetak
With excellent efficacy of direct-acting antivirals (DAA) now available, treatment failure is rare, however, when it occurs, it is mostly due to relapse. On treatment failure is very rare. Baseline resistance-associated amino acid (aa) substitutions (RASs) are common, but do not frequently result in treatment failure. Therefore, detection of baseline mutations is not generally predictive of response. In addition, the frequency of resistant mutation data is often underestimated because virus <500 IU/ml cannot be deep sequenced, and therefore, is not included in resistance data. Mutations resulting in resistance have been identified, and involve NS5A and protease inhibitors. Resistance to NS5B polymerase inhibitors is rare. To minimize the development of resistance mutations, it is recommended to limit exposure to reliable compliant patients because missed doses increase the risk of development of resistance mutations. Use of multiple agent combinations with different mechanisms of action including NS5B inhibitors, increases the barriers to resistance and reduce the risk of development of resistance. In recently published real-life studies on DAA failures, RASs prevalence was remarkably high. These findings advocate for HCV resistance testing at failure, in order to optimize the second-line therapeutic options and to overcome treatment failure.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Osijek,
Fakultet za dentalnu medicinu i zdravstvo, Osijek
Profili:
Martina Smolić
(autor)