Evidence map›Paper›PMID 29856804›Full record

ArticlePloS one2018

Change in plasma lactate concentration during arctigenin administration in a phase I clinical trial in patients with gemcitabine-refractory pancreatic cancer.

Rumi Fujioka, Nobuo Mochizuki, Masafumi Ikeda, Akihiro Sato, Shogo Nomura, Satoshi Owada, Satoshi Yomoda, Katsuya Tsuchihara, Satoshi Kishino, Hiroyasu Esumi

Open access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in PloS one, 2018. 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
0.6field-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

7 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  3. Review of potential medical treatments for middle ear cholesteatoma.Cell communication and signaling : CCS · 2022
    Review
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  5. The therapeutic potential of mitochondrial toxins.The Journal of antibiotics · 2021
    Review
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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

10 authors at 4 institutions in 1 country.

Rumi FujiokaDivision of Translational Research, Exploratory Oncology and Clinical Trial Center, National Cancer Center, Kashiwa, Japan.
Nobuo MochizukiDepartment of Medication Use Analysis and Clinical Research, Meiji Pharmaceutical University, Tokyo, Japan.
Masafumi IkedaDepartment of Hepatobiliary and Pancreatic Oncology, National Cancer Center, Hospital East, Kashiwa, Japan.
Akihiro SatoClinical Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan.
Shogo NomuraBiostatistics Division, Center for Research Administration and Support, National Cancer Center, Kashiwa, Japan.
Satoshi OwadaResearch Institute for Biomedical Sciences, Tokyo University of Science, Noda, Japan.
Satoshi YomodaKanpo Research Institute, Kracie Pharmaceutical Company, Toyama, Japan.
Katsuya TsuchiharaDivision of Translational Research, Exploratory Oncology and Clinical Trial Center, National Cancer Center, Kashiwa, Japan.
Satoshi KishinoDepartment of Medication Use Analysis and Clinical Research, Meiji Pharmaceutical University, Tokyo, Japan.
Hiroyasu EsumiResearch Institute for Biomedical Sciences, Tokyo University of Science, Noda, Japan.ORCID 0000-0001-9522-2957
National Cancer Center Hospital East · JPMeiji Pharmaceutical University · JPTokyo University of Science · JPKracie (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arctigenin is evaluated for antitumor efficacy in patients with pancreatic cancer. It has an inhibitory activity on mitochondrial complex I.Therefore, plasma lactate level of patients after arctigenin administration was evaluated for biomarker of clinical response and/or adverse effect. Plasma lactate level in 15 patients enrolled in a Phase I clinical trial of GBS-01 rich in arctigenin was analyzed by colorimetric assay. Statistical analyses for association of plasma lactate and clinical responses, pharmacokinetics of arctigenin, and background factors of each patient by multivariate and univariate analyses.In about half of the patients, transient increase of lactate was observed. Correlation between plasma lactate level and pharmacokinetic parameters of arctigenin and its glucuronide conjugate, and clinical outcome was not detected. Regarding to the determinant of lactate level, only slight association with liver function test was detected. Plasma lactate level is primary determined by reutilization rather than production for antitumor effect and dose not serve as a biomarker. Arctigenin, inhibition of mitochondrial complex I, plasma lactate concentration, phase I clinical trial of GBS-01, Cori cycle.

Indexed as

ArctiumAntineoplastic Agents, PhytogenicArea Under CurveBiomarkersCarcinoma, AdenosquamousCarcinoma, Pancreatic DuctalCell Line, TumorDeoxycytidineDrug Resistance, NeoplasmDrugs, Chinese HerbalDrug Screening Assays, AntitumorFuransGemcitabineGluconeogenesisHumansKaplan-Meier EstimateAntineoplastic Agents, PhytogenicarctigeninBiomarkersDeoxycytidineDrugs, Chinese HerbalFuransGemcitabineLactic AcidLignansPlant Extracts

Identifiers

PMID29856804
PMCPMC5983509
OpenAlexW2807599439

What OpenQuestion holds

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LicenceCC BY
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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.