Evidence map›Paper›PMID 31807967›Full record

Observational studyInternational journal of clinical oncology2020

Therapeutic drug monitoring of regorafenib and its metabolite M5 can predict treatment efficacy and the occurrence of skin toxicities.

Daiki Taguchi, Masahiro Inoue, Koji Fukuda, Taichi Yoshida, Kazuhiro Shimazu, Kazuma Fujita, Hiroyuki Okuyama, Nobuhisa Matsuhashi, Akihito Tsuji, Kazuhiro Yoshida and 2 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in International journal of clinical oncology, 2020. 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
–field-weighted citation impact
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.

  1. Article
  2. Risk factor analysis for regorafenib-induced severe hypertension in metastatic colorectal cancer treatment.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2022
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Observational
  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

12 authors.

Daiki TaguchiDepartment of Clinical Oncology, Akita University Graduate School of Medicine, Hondo 1-1-1, Akita, Japan.
Masahiro InoueDepartment of Clinical Oncology, Akita University Graduate School of Medicine, Hondo 1-1-1, Akita, Japan.
Koji FukudaDepartment of Clinical Oncology, Akita University Graduate School of Medicine, Hondo 1-1-1, Akita, Japan.
Taichi YoshidaDepartment of Clinical Oncology, Akita University Graduate School of Medicine, Hondo 1-1-1, Akita, Japan.
Kazuhiro ShimazuDepartment of Clinical Oncology, Akita University Graduate School of Medicine, Hondo 1-1-1, Akita, Japan.
Kazuma FujitaDepartment of Pharmacy, Akita University Hospital, Hondo 1-1-1, Akita, Japan.
Hiroyuki OkuyamaDepartment of Clinical Oncology, Kagawa University, Ikedo 1750-1, Miki-cho, Kida-gun, Kagawa, Japan.
Nobuhisa MatsuhashiDepartment of Surgical Oncology, Gifu University Graduate School of Medicine, Yanagito 1-1, Gifu, Gifu, Japan.
Akihito TsujiDepartment of Clinical Oncology, Kagawa University, Ikedo 1750-1, Miki-cho, Kida-gun, Kagawa, Japan.
Kazuhiro YoshidaDepartment of Surgical Oncology, Gifu University Graduate School of Medicine, Yanagito 1-1, Gifu, Gifu, Japan.
Masatomo MiuraDepartment of Pharmacy, Akita University Hospital, Hondo 1-1-1, Akita, Japan.
Hiroyuki ShibataDepartment of Clinical Oncology, Akita University Graduate School of Medicine, Hondo 1-1-1, Akita, Japan. hiroyuki@med.akita-u.ac.jp.ORCID http://orcid.org/0000-0003-3581-3506

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRegorafenib is a multiple tyrosine kinase inhibitor, and the use of this drug is approved for the treatment of cancers that are resistant to chemotherapy, which include advanced colorectal cancer, gastrointestinal stromal tumor, and hepatocellular carcinoma. However, the drug causes adverse events, including skin toxicities that require dose modification in approximately 75% of cases. At present, the blood concentration of regorafenib is not assessed in clinical settings; thus, we recently developed a method that can assess the blood concentration of the drug using high-performance liquid chromatography.

methodsWe measured the trough blood concentrations (C

resultsIn patients who were receiving regorafenib 40-160 mg/day, the C

conclusionsThe use of regorafenib may not be suitable in patients with a low C

Indexed as

AgedAged, 80 and overAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily BATP Binding Cassette Transporter, Subfamily G, Member 2Colorectal NeoplasmsCytochrome P-450 CYP3ADrug MonitoringFemaleGastrointestinal Stromal TumorsGlucuronosyltransferaseHumansIncidenceMaleMiddle AgedNeoplasm ProteinsABCB1 protein, humanABCG2 protein, humanAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily BATP Binding Cassette Transporter, Subfamily G, Member 2CYP3A5 protein, humanCytochrome P-450 CYP3AGlucuronosyltransferaseNeoplasm ProteinsPhenylurea CompoundsProtein Kinase InhibitorsPyridinesregorafenibUGT1A1 EnzymeColorectal cancerCtroughGastrointestinal stromal tumorRegorafenibTherapeutic drug monitoring

Identifiers

What OpenQuestion holds

Textmetadata
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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.