Evidence map›Paper›PMID 34337093›Full record

ArticleOpen forum infectious diseases2021

High Cure Rates for Hepatitis C Virus Genotype 6 in Advanced Liver Fibrosis With 12 Weeks Sofosbuvir and Daclatasvir: The Vietnam SEARCH Study.

Barnaby Flower, Leanne McCabe, Chau Le Ngoc, Hung Le Manh, Phuong Le Thanh, Thuan Dang Trong, Thu Vo Thi, Hang Vu Thi Kim, Thanh Nguyen Tat, Dao Phan Thi Hong and 17 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Frontiers in microbiology · 2024
    Article
  7. SASLT guidelines: Update in treatment of hepatitis C virus infection, 2024.Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association · 2024
    Review
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 6 institutions in 3 countries.

Barnaby FlowerOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0000-0002-2659-544X
Leanne McCabeMRC Clinical Trials Unit at UCL, University College London, United Kingdom.
Chau Le NgocOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
Hung Le ManhHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Phuong Le ThanhHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Thuan Dang TrongHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Thu Vo ThiOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
Hang Vu Thi KimOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
Thanh Nguyen TatOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
Dao Phan Thi HongOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
An Nguyen Thi ChauOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
Tan Dinh ThiOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
Nga Tran Thi TuyetOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
Joel TarningMahidol-Oxford Tropical Medicine Research Unit (MORU), Mahidol University, Bangkok, Thailand.ORCID https://orcid.org/0000-0003-4566-4030
Cherry KingsleyDepartment of Infectious Disease, Imperial College London, United Kingdom.
Evelyne KestelynOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0000-0002-5728-0918
Sarah L PettMRC Clinical Trials Unit at UCL, University College London, United Kingdom.
Guy ThwaitesOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
Vinh Chau Nguyen VanHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
David SmithUniversity of Oxford, United Kingdom.
Eleanor BarnesUniversity of Oxford, United Kingdom.
M Azim AnsariUniversity of Oxford, United Kingdom.
Hugo TurnerMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, United Kingdom.ORCID https://orcid.org/0000-0002-8428-3874
Motiur RahmanOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.
Ann Sarah WalkerDepartment of Infectious Disease, Imperial College London, United Kingdom.
Jeremy DayOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0000-0002-7843-6280
Graham S CookeDepartment of Infectious Disease, Imperial College London, United Kingdom.
Oxford University Clinical Research Unit · VNHospital for Tropical Diseases · VNImperial College London · GBUniversity of Oxford · GBMRC Clinical Trials Unit at UCL · GBMahidol University · TH

Funding

Medical Research Council MR/P025064/1Medical Research Council MR/R015600/1Wellcome Trust 206296/Z/17/Z
6 · The paper itself

Abstract

backgroundGenotype 6 is the most genetically diverse lineage of hepatitis C virus, and it predominates in Vietnam. It can be treated with sofosbuvir with daclatasvir (SOF/DCV), the least expensive treatment combination globally. In regional guidelines, longer treatment durations of SOF/DCV (24 weeks) are recommended for cirrhotic individuals, compared with other pangenotypic regimens (12 weeks), based on sparse data. Early on-treatment virological response may offer means of reducing length and cost of therapy in patients with liver fibrosis.

methodsIn this prospective trial in Vietnam, genotype 6-infected adults with advanced liver fibrosis or compensated cirrhosis were treated with SOF/DCV. Day 14 viral load was used to guide duration of therapy: participants with viral load <500 IU/mL at day 14 were treated with 12 weeks of SOF/DCV and those ≥500 IU/mL received 24 weeks. Primary endpoint was sustained virological response (SVR).

resultsOf 41 individuals with advanced fibrosis or compensated cirrhosis who commenced treatment, 51% had genotype 6a and 34% had 6e. The remainder had 6h, 6k, 6l, or 6o. One hundred percent had viral load <500 IU/mL by day 14, meaning that all received 12 weeks of SOF/DCV. One hundred percent achieved SVR12 despite a high frequency of putative NS5A inhibitor resistance-associated substitutions at baseline.

conclusionsPrescribing 12 weeks of SOF/DCV results in excellent cure rates in this population. These data support the removal of costly genotyping in countries where genotype 3 prevalence is <5%, in keeping with World Health Organization guidelines. NS5A resistance-associated mutations in isolation do not affect efficacy of SOF/DCV therapy. Wider evaluation of response-guided therapy is warranted.

Indexed as

cirrhosisdirect-acting antiviralsgenotype 6hepatitis Cresponse-guided therapy

Identifiers

PMID34337093
PMCPMC8320300
OpenAlexW3173011500

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.