Evidence map›Paper›PMID 30619941›Full record

ArticleJGH open : an open access journal of gastroenterology and hepatology2018

Real-world safety and efficacy of sofosbuvir and ledipasvir for elderly patients.

Hideyuki Tamai, Naoki Shingaki, Yoshiyuki Ida, Ryo Shimizu, Shuya Maeshima, Junpei Okamura, Akira Kawashima, Taisei Nakao, Takeshi Hara, Hiroyoshi Matsutani and 2 more

Open access · goldAbstract read
In one paragraph

Article in JGH open : an open access journal of gastroenterology and hepatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

12 authors at 4 institutions in 1 country.

Hideyuki TamaiDepartment of Hepatology Wakayama Rosai Hospital Wakayama-shi Japan.ORCID 0000-0003-4511-4573
Naoki ShingakiDepartment of Hepatology Wakayama Rosai Hospital Wakayama-shi Japan.
Yoshiyuki IdaSecond Department of Internal Medicine Wakayama Medical University Wakayama-shi Japan.
Ryo ShimizuSecond Department of Internal Medicine Wakayama Medical University Wakayama-shi Japan.
Shuya MaeshimaSecond Department of Internal Medicine Wakayama Medical University Wakayama-shi Japan.
Junpei OkamuraDepartment of Internal Medicine Naga Municipal Hospital Naga Japan.
Akira KawashimaDepartment of Internal Medicine Naga Municipal Hospital Naga Japan.
Taisei NakaoDepartment of Internal Medicine Naga Municipal Hospital Naga Japan.
Takeshi HaraDepartment of Gastroenterology Wakayama Rosai Hospital Wakayama-shi Japan.
Hiroyoshi MatsutaniFirst Department of Internal Medicine Hidaka General Hospital Gobō Japan.
Izumi NishikawaFirst Department of Internal Medicine Hidaka General Hospital Gobō Japan.
Katsuhiko HigashiFirst Department of Internal Medicine Hidaka General Hospital Gobō Japan.
Wakayama Medical University · JPHidaka Hospital · JPNaga Municipal Hospital · JPWakayama Rosai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimIn September 2015, sofosbuvir and ledipasvir were approved for clinical use in Japan for patients infected with genotype 1 hepatitis C virus. We conducted a postmarketing prospective cohort study to elucidate the safety and efficacy of this therapy in a real-world setting.

methodsWe treated 509 patients using standard doses of sofosbuvir and ledipasvir for 12 weeks. As sustained virological response (SVR) in 2 patients could not be evaluated, 507 patients were finally analyzed. Patients with daclatasvir plus asunaprevir failure were excluded.

resultsFour patients (0.8%) discontinued treatment due to adverse events. SVR rates for the overall cohort, patients <65 years old, ≥65 and <75 years old, and ≥75 years old were 98% (495/507), 98% (161/163), 96% (179/186), and 98% (155/158), respectively. SVR rates among cirrhotic patients, patients with moderate chronic kidney disease (CKD), patients with a history of hepatocellular carcinoma (HCC) treatment, patients with protease inhibitor (PI) triple therapy failure, and patients with resistance-associated substitutions (RASs) to nonstructural protein 5A (NS5A) were 97% (228/235), 98% (117/119), 95% (95/100), 94% (46/49), and 92% (44/48), respectively. In the comparison of factors between patients with and without SVR, high body weight, discontinuation of therapy, and NS5A RASs were significantly associated with non-SVR.

conclusionsIn this real-world setting, sofosbuvir and ledipasvir were a safe treatment even in patients ≥75 years old. When patients without pre-existing NS5A RASs and daclatasvir plus asunaprevir failure are selected, extremely high SVR rates can be achieved irrespective of age.

Indexed as

genotype 1hepatitis C virusledipasvirsofosbuvir

Identifiers

PMID30619941
PMCPMC6308062
OpenAlexW2890297610

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.