Evidence map›Paper›PMID 33231381›Full record

ArticleCancer medicine2021

Investigation of drugs affecting hypertension in bevacizumab-treated patients and examination of the impact on the therapeutic effect.

Kenta Yagi, Marin Mitstui, Yoshito Zamami, Takahiro Niimura, Yuki Izawa-Ishizawa, Mitsuhiro Goda, Masayuki Chuma, Kimiko Fukunaga, Takahiro Shibata, Shunsuke Ishida and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 20 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

17 authors at 2 institutions in 1 country.

Kenta YagiClinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.ORCID 0000-0003-0869-5786
Marin MitstuiDepartment of Clinical Pharmacology and Therapeutics, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.
Yoshito ZamamiDepartment of Clinical Pharmacology and Therapeutics, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.
Takahiro NiimuraDepartment of Clinical Pharmacology and Therapeutics, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.
Yuki Izawa-IshizawaDepartment of Pharmacology, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.
Mitsuhiro GodaDepartment of Pharmacy, Tokushima University Hospital, Tokushima, Japan.
Masayuki ChumaClinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
Kimiko FukunagaDepartment of Clinical Pharmacology and Therapeutics, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.
Takahiro ShibataDepartment of Pharmacy, Tokushima University Hospital, Tokushima, Japan.
Shunsuke IshidaDepartment of Pharmacy, Tokushima University Hospital, Tokushima, Japan.
Takumi SakuradaDepartment of Pharmacy, Tokushima University Hospital, Tokushima, Japan.
Naoto OkadaDepartment of Pharmacy, Tokushima University Hospital, Tokushima, Japan.ORCID 0000-0003-2476-9191
Hirofumi HamanoDepartment of Pharmacy, Tokushima University Hospital, Tokushima, Japan.
Yuya HorinouchiDepartment of Pharmacology, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.
Yasumasa IkedaDepartment of Pharmacology, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.
Hiroaki YanagawaClinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
Keisuke IshizawaDepartment of Clinical Pharmacology and Therapeutics, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.
Tokushima University Hospital · JPTokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn patients treated with bevacizumab, hypertension may be a biomarker of therapeutic efficacy. However, it is not clear whether drugs that control blood pressure influence bevacizumab's efficacy. In this study, we investigated drugs that may affect hypertension in bevacizumab-treated patients and examined the impact on the therapeutic effect. PATIENTS AND

methodsWe analyzed 3,724,555 reports from the third quarter of 2010 to the second quarter of 2015. All data were obtained from the Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) analysis. In this retrospective cohort study, we investigated a total of 58 patients diagnosed with colorectal cancer and treated for the first time with bevacizumab containing XELOX or mFOLFOX6 at The University of Tokushima Hospital between January 2010 and December 2015. The effect of the treatment was evaluated according to Response Evaluation Criteria in Solid Tumors version 1.0. Thereafter, the effect was confirmed using Gene Expression Omnibus (GEO) and cultured cells.

resultsThere are few reports in FAERS of hypertension in patients treated with omeprazole on bevacizumab. Based on the chart review, patients who used proton pump inhibitors (PPI) had a lower response to treatment than those who did not (response rate: 25% vs 50%). Furthermore, experiments on GEO and cell lines suggested that induction of vascular endothelial growth factor (VEGF) gene expression by PPIs is the cause of the reduced therapeutic effect.

conclusionPPIs prevent hypertension in bevacizumab-treated patients but may reduce bevacizumab's anti-tumoral effects by inducing VEGF expression.

Indexed as

AdultAdverse Drug Reaction Reporting SystemsAgedAged, 80 and overAngiogenesis InhibitorsAntihypertensive AgentsAntineoplastic Agents, ImmunologicalBevacizumabBlood PressureCell Line, TumorColorectal NeoplasmsDatabases, FactualDrug InteractionsFemaleHumansHuman Umbilical Vein Endothelial CellsAngiogenesis InhibitorsAntihypertensive AgentsAntineoplastic Agents, ImmunologicalBevacizumabProton Pump InhibitorsVascular Endothelial Growth Factor AVEGFA protein, humanbevacizumabcolorectal cancerFAERSgene expression omnibushypertensionproton pump inhibitor

Identifiers

PMID33231381
PMCPMC7826469
OpenAlexW3110137591

What OpenQuestion holds

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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.