Evidence map›Paper›PMID 30989775›Full record

ArticleCancer science2019

Pharmacokinetic study of the oral fluorouracil antitumor agent S-1 in patients with impaired renal function.

Keiko Goto, Yutaka Fujiwara, Takeshi Isobe, Naoko Chayahara, Naomi Kiyota, Toru Mukohara, Yukari Tsubata, Takamasa Hotta, Kenji Tamura, Noboru Yamamoto and 1 more

Erratum issuedOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Article
  3. Correction.Cancer science · 2020
    Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Keiko GotoDepartment of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Yutaka FujiwaraDepartment of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0001-6981-0800
Takeshi IsobeDivision of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Shimane University, Shimane, Japan.
Naoko ChayaharaDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Naomi KiyotaDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Toru MukoharaDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Yukari TsubataDivision of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Shimane University, Shimane, Japan.
Takamasa HottaDivision of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Shimane University, Shimane, Japan.
Kenji TamuraDepartment of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3514-9927
Noboru YamamotoDepartment of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Hironobu MinamiDepartment of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.ORCID https://orcid.org/0000-0001-8630-9145
Kobe University · JPShimane University · JPNational Cancer Center Hospital East · JPMitsui Memorial Hospital · JP

Funding

Ministry of Health, Labour and Welfare 23-A-16
6 · The paper itself

Abstract

Although dose reduction of S-1 is recommended for patients with impaired renal function, dose modification for such patients has not been prospectively evaluated. The aim of the present study was to investigate the pharmacokinetic parameters of 5-fluorouracil, 5-chloro-2,4 dihydroxypyridine and oteracil potassium, and to review the recommended dose modification of S-1 in patients with renal impairment. We classified patients receiving S-1 into 4 groups according to their renal function, as measured using the Japanese estimated glomerular filtration rate (eGFR) equation. The daily S-1 dose was adjusted based on the patient's eGFR and body surface area. Blood samples were collected for pharmacokinetic analysis. A total of 33 patients were enrolled and classified into 4 groups as follows: 10 patients in cohort 1 (eGFR ≥ 80 mL/min/1.73 m

Indexed as

Administration, OralAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsArea Under CurveCohort StudiesDrug CombinationsFemaleFluorouracilGlomerular Filtration RateHumansMaleMiddle AgedNauseaOxonic AcidDrug CombinationsFluorouracilOxonic AcidS 1 (combination)Tegafur5-fluorouracilCDHPclearanceeGFRS-1

Identifiers

PMID30989775
PMCPMC6550132
OpenAlexW2937370408

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.