Evidence map›Paper›PMID 32058619›Full record

Trial reportThe oncologist2020

Administration of Lapatinib with Food Increases Its Plasma Concentration in Chinese Patients with Metastatic Breast Cancer: A Prospective Phase II Study.

Fei Xu, Kaping Lee, Wen Xia, Hai Liao, Qianyi Lu, Jingmin Zhang, Huimin Yuan, Kai Zhang, Qiufan Zheng, Ge Qin and 5 more

Open access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in The oncologist, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Optimising oncology drug expenditure in Ireland.Irish journal of medical science · 2024
    Review
  3. 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

15 authors at 2 institutions in 1 country.

Fei Xu *Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Kaping Lee *Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Wen Xia *Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Hai Liao *Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Qianyi LuMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Jingmin ZhangMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Huimin YuanMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Kai ZhangMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Qiufan ZhengMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Ge QinMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Qinglian ZhaiMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Ruoxi HongMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Kuikui JiangMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Yuan LiMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Shusen WangMedical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Sun Yat-sen University Cancer Center · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

lessons learnedAdministration of lapatinib with food significantly increased its plasma concentration in Chinese patients with metastatic breast cancer. There were no serious adverse events during the study and no significant differences in lapatinib-related adverse events between the fasted and fed states.

backgroundLapatinib, a small molecular reversible dual tyrosine kinase inhibitor of epidermal growth factor receptor (EGFR) and human epidermal growth receptor 2 (HER2), was approved for use in combination with capecitabine to treat metastatic HER2-positive breast cancer. Administration of lapatinib in the fasted state was recommended; however, our preliminary phase II trial data showed that administration of lapatinib with food increased its concentration.

methodsThis study was a single-center, open-label, and prospective self-controlled clinical study. Ten Chinese patients with metastatic breast cancer were enrolled from June 2017 to April 2018. They were required to receive lapatinib plus physician's choice of chemotherapy. Patients were required to take lapatinib orally on an empty stomach continually for 10 days, and then take lapatinib with food continually for the next 10 days. Plasma concentration was measured by liquid chromatography on the 9th and 10th day of each state.

resultsArea under the concentration-time curve (AUC) of the fasted state and the fed state was 21.23 ± 8.91 mg*h/L (coefficient of variation (CV)% 42%) and 60.60 ± 16.64 mg*h/L (CV% 27%), respectively. The mean plasma concentration in the fasted state was 0.88 ± 0.39 mg/L (CV% 45%), and that in the fed state was 2.53 ± 0.77 mg/L (CV% 30%). Compared with taking lapatinib on an empty stomach, receiving lapatinib with food significantly increased the plasma concentration of lapatinib (Wilcoxon match-paired test, p = .005). In addition, there were no serious adverse events during the study or significant difference in lapatinib-related adverse events between the two states.

conclusionOur study shows that receiving lapatinib with food can increase its plasma concentration with no significantly increased drug-related toxicity. We suggest that a larger-sample-size clinical trial is needed to fully understand the effect of administration of lapatinib with food.

Indexed as

Breast NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsChinaErb-b2 Receptor Tyrosine KinasesFemaleHumansLapatinibProspective StudiesQuinazolinesErb-b2 Receptor Tyrosine KinasesLapatinibQuinazolines

Identifiers

PMID32058619
PMCPMC7485350
OpenAlexW3006462769

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.