Evidence map›Paper›PMID 32210678›Full record

ArticleSaudi journal of biological sciences2020

Therapeutic effect of small molecule targeting drug apatinib on gastric cancer and its role in prognosis and anti-infection mechanism.

Na Wang, Shubo Chen, Dengxiang Liu, Jun Guo, Yawei Sun, Juping Zhang, Qian Kong, Lili He

Open access · hybridAbstract read
In one paragraph

Article in Saudi journal of biological sciences, 2020. 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
0.9field-weighted citation impact, top 22% 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, 10 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

8 authors at 2 institutions in 1 country.

Na WangDepartment of Oncology, Xingtai People's Hospital, No 16 Hongxing Street, Xingtai 054001, Hebei Province, PR China.
Shubo ChenDepartment of Oncology, Xingtai People's Hospital, No 16 Hongxing Street, Xingtai 054001, Hebei Province, PR China.
Dengxiang LiuDepartment of Oncology, Xingtai People's Hospital, No 16 Hongxing Street, Xingtai 054001, Hebei Province, PR China.
Jun GuoMedical Oncology, Xingtai People's Hospital, No 16 Hongxing Street, Xingtai 054001, Hebei Province, PR China.
Yawei SunMedical Oncology, Xingtai People's Hospital, No 16 Hongxing Street, Xingtai 054001, Hebei Province, PR China.
Juping ZhangMedical Oncology, Xingtai People's Hospital, No 16 Hongxing Street, Xingtai 054001, Hebei Province, PR China.
Qian KongMedical Oncology, Xingtai People's Hospital, No 16 Hongxing Street, Xingtai 054001, Hebei Province, PR China.
Lili HeMedical Oncology, Xingtai People's Hospital, No 16 Hongxing Street, Xingtai 054001, Hebei Province, PR China.
Xingtai People's Hospital · CNHebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the effect of apatinib when treating advanced gastric cancer (GC) as well as the mechanism of preventing infection.

methodsFrom January 2017 to December 2018, 100 advanced GC patients had failed to receive second-line or above treatment in XX Hospital were divided into two groups according to the experimental requirements: the experimental group and the blank group. The experimental group was treated with small molecule targeted drug apatinib, while the blank group was only treated with ordinary drugs. After 4 weeks of treatment, the diagnosis and evaluation were carried out every eight weeks. In this study, the mechanism of infection prevention and prognosis was studied through the internal treatment of GC patients with apatinib.

resultsuntil the end of the fourth week, a significant difference can be seen in the treatment effect between the experimental group as well as the blank group. In the experimental group, the proportion of partial remission + disease stability reached about 73%, while that in the blank group was only about 33%. In addition, apatinib was better than the blank group in the control of adverse reactions like hypertension, proteinuria, myelosuppression as well as diarrhea. In addition, apatinib was better than the blank group when treating AFP positive GC. In terms of the therapeutic effect of apatinib, it is much better than that of the negative group. In addition, apatinib is also better than the blank group in drug resistance for GC patients. It is found that apatinib's anti infection mechanism is to prevent the phosphorylation of vascular endothelial growth factor receptor-2 (VEGFR-2) as well as stop the downstream signal pathway, so as to inhibit the tumor angiogenesis, tumor growth and metastasis, so as to achieve treatment and reduce the probability of infection.

conclusionthe therapeutic effect of small molecule targeting drug apatinib on gastric cancer is better than that of other drugs, whether in therapeutic effect, drug resistance, adverse reactions or infection control. This study has important reference significance for the follow-up treatment of apatinib and cancer.

Indexed as

ApatinibInfectionMechanismResponseTreatment

Identifiers

PMID32210678
PMCPMC6997852
OpenAlexW2993486303

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.