Evidence map›Paper›PMID 35146630›Full record

ArticleInternational journal of hematology2022

Long-term follow-up of patients with paroxysmal nocturnal hemoglobinuria treated with eculizumab: post-marketing surveillance in Japan.

Takayuki Ikezoe, Hideyoshi Noji, Yasutaka Ueda, Yoshinobu Kanda, Shinichiro Okamoto, Kensuke Usuki, Takahisa Matsuda, Hirozumi Akiyama, Akihiko Shimono, Yuji Yonemura and 6 more

Abstract read
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In one paragraph

Article in International journal of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

16 authors at 9 institutions in 1 country.

Takayuki IkezoeDepartment of Hematology, Fukushima Medical University, Hikarigaoka-1, Fukushima, Fukushima, 960-1295, Japan. ikezoet@fmu.ac.jp.ORCID http://orcid.org/0000-0002-7858-278X
Hideyoshi NojiDepartment of Hematology, Fukushima Medical University, Hikarigaoka-1, Fukushima, Fukushima, 960-1295, Japan.
Yasutaka UedaOsaka University Graduate School of Medicine, Suita, Japan.
Yoshinobu KandaJichi Medical University, Shimotsuke, Japan.
Shinichiro OkamotoKeio University School of Medicine, Tokyo, Japan.
Kensuke UsukiNTT Medical Center Tokyo, Tokyo, Japan.
Takahisa MatsudaAlexion Pharma G.K., Tokyo, Japan.
Hirozumi AkiyamaAlexion Pharma G.K., Tokyo, Japan.
Akihiko ShimonoAlexion Pharma G.K., Tokyo, Japan.
Yuji YonemuraKumamoto University Hospital, Kumamoto, Japan.
Tatsuya KawaguchiKumamoto University Hospital, Kumamoto, Japan.
Shigeru ChibaUniversity of Tsukuba, Tsukuba, Japan.
Yuzuru KanakuraOsaka University Graduate School of Medicine, Suita, Japan.
Jun-Ichi NishimuraOsaka University Graduate School of Medicine, Suita, Japan.
Haruhiko NinomiyaUniversity of Tsukuba, Tsukuba, Japan.
Naoshi ObaraUniversity of Tsukuba, Tsukuba, Japan.
University of Tsukuba · JPFukushima Medical University · JPThe University of Osaka · JPJichi Medical University · JPKeio University · JPKumamoto Health Science University · JPKumamoto University Hospital · JPNTT Medical Center · JPSumitomo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

All Japanese patients with paroxysmal nocturnal hemoglobinuria (PNH) treated with eculizumab were enrolled in post-marketing surveillance (PMS) between June 2010 and August 2019 to assess the long-term effectiveness and safety of eculizumab. The reduction in intravascular hemolysis, the change in hemoglobin (Hb) level, and the change in renal function were assessed to determine the effectiveness of eculizumab. The types and frequencies of adverse events (AEs) were assessed to determine its safety. A total of 632 patients were enrolled and the median treatment duration was 3.6 years. Treatment with eculizumab significantly reduced lactate dehydrogenase (LDH) levels and significantly increased Hb levels. These changes were maintained for up to 5 years of treatment. An estimated glomerular filtration rate ≥ 60 ml/min/1.73 m

Indexed as

Hemoglobinuria, ParoxysmalAntibodies, Monoclonal, HumanizedFollow-Up StudiesHemolysisHumansJapanProduct Surveillance, PostmarketingAntibodies, Monoclonal, HumanizedeculizumabEculizumabEffectivenessParoxysmal nocturnal hemoglobinuriaPost-marketing surveillanceSafety

Identifiers

PMID35146630
OpenAlexW4211172913

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.