Evidence map›Paper›PMID 32481407›Full record

Observational studyMedicine2020

Efficacy of telbivudine and entecavir against virus reactivation in HBeAg-patients undergoing chemotherapy.

Chih-Jen Chen, Hsien-Chung Yu, Chen-Wang Chang, Ming-Jong Bair, Ching-Chung Lin, Yang-Sheng Lin, Zong-Sian Cai, Ming-Jen Chen

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 49% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 2 institutions in 3 countries.

Chih-Jen ChenDivision of Gastroenterology and Hepatology, Department of Internal Medicine, MacKay Memorial Hospital, Taipei City.
Hsien-Chung YuDivision of Gastroenterology, Department of Internal Medicine, Kaohsiung Veterans General Hospital, Kaohsiung City.
Chen-Wang ChangDivision of Gastroenterology and Hepatology, Department of Internal Medicine, MacKay Memorial Hospital, Taipei City.
Ming-Jong BairDepartment of Medicine, MacKay Medical College, New Taipei City.
Ching-Chung LinDivision of Gastroenterology and Hepatology, Department of Internal Medicine, MacKay Memorial Hospital, Taipei City.
Yang-Sheng LinDivision of Gastroenterology and Hepatology, Department of Internal Medicine, MacKay Memorial Hospital, Taipei City.
Zong-Sian CaiDivision of Gastroenterology and Hepatology, Department of Internal Medicine, MacKay Memorial Hospital, Taipei City.
Ming-Jen ChenDivision of Gastroenterology and Hepatology, Department of Internal Medicine, MacKay Memorial Hospital, Taipei City.ORCID 0000-0001-5849-4259
Mackay Memorial Hospital · TWNational Sun Yat-sen University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The renal protective effect of telbivudine (LdT) was verified by a previous meta-analysis. It was left unclear, however if this effect offsets the associated risk of virological breakthrough in hepatitis B e-antigen-negative (HBeAg-) patients receiving chemotherapy (C/T).Records of 260 HBeAg-, non-cirrhotic cancer patients undergoing systemic C/T with prophylactic LdT or entecavir (ETV) were retrospectively investigated. The investigation was conducted 6 months after completion of C/T, patient death from cancer, or antiviral modification. Treatment duration, outcome, change of renal function, and reason for antiviral modification were analyzed. The primary endpoint was the occurrence of virological breakthrough during prophylaxis C/T and the change in renal function.Of the 126 HBeAg- patients treated with LdT, 3 (2.38%) experienced HBV virological breakthroughs, whereas none of the patients treated with ETV (P = .07) did. The estimated glomerular filtration rate for the patients treated with LdT was essentially unaltered, decreasing only slightly from 87.5 ± 23.1 to 87.3 ± 21.3 ml/minute/1.73 m (P = .55), while the rate for the ETV-treated patients was significantly lowered from 95.7 ± 32.2 to 85.5 ± 85.7 ml/minute/1.73 m (P = .0009).The absolute risk reduction ARR is 27.8% - 21.2% = 6.6%, comparing ETV with LdT for reduction of renal function impairment and the absolute risk increase for virological breakthrough during C/T, the absolute risk increase (ARI) is 2.38% - 0% = 2.38%. The overall likelihood of being helped over being harmed was 2.77. With careful selection of patients with the criteria of HBeAg-status and non-hematologic cancer, it is feasible that telbivudine raise lower probability of virological breakthroughs during prophylaxis treatment.

Indexed as

Acute Kidney InjuryAdultAgedAntineoplastic AgentsAntiviral AgentsFemaleGlomerular Filtration RateGuanineHepatitis B e AntigensHumansKidney Function TestsMaleMiddle AgedNeoplasmsRetrospective StudiesTelbivudineAntineoplastic AgentsAntiviral AgentsentecavirGuanineHepatitis B e AntigensTelbivudine

Identifiers

PMID32481407
PMCPMC12245244
OpenAlexW3031766068

What OpenQuestion holds

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LicenceCC BY-NC
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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.