Evidence map›Paper›PMID 39352649›Full record

SynthesisInvestigational new drugs2024

Clinical research progress of fruquintinib in the treatment of malignant tumors.

Shihao Zhao, Wenhui Wang, Jingyi Li, Zhigang Li, Zhanbo Liu, Shunchao Zhang, Zhaoqi Chen, Hongling Wang, Xiangqi Wang, Juntao Wang

Erratum issuedAbstract readSystematic Review
In one paragraph

Synthesis in Investigational new drugs, 2024. 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 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
–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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Polypharmacology: new drugs in 2023-2024.Pharmacological reports : PR · 2025
    Review
  8. Article
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Shihao Zhao *School of Acupuncture, Moxibustion and Tuina, The Third Affiliated Hospital of Henan University of TCM, Zhengzhou, 450000, Henan, China.
Wenhui Wang *Department of oncology, People's Hospital of Henan University of Chinese Medicine, Zhengzhou, 450014, Henan, China.
Jingyi LiDepartment of oncology, People's Hospital of Henan University of Chinese Medicine, Zhengzhou, 450014, Henan, China.
Zhigang LiDepartment of oncology, The Third Affiliated Hospital of Henan University of TCM, Zhengzhou, Henan, 450000, China.
Zhanbo LiuThe First Clinical Medical College, Henan University of Chinese Medicine, Zhengzhou, 450046, Henan, China.
Shunchao ZhangPublicity Department, Henan University of Chinese Medicine, Zhengzhou, 450046, Henan, China.
Zhaoqi ChenPublicity Department, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China.
Hongling WangDepartment of oncology, Henan General Hospital, Zhengzhou, 450002, Henan, China.
Xiangqi WangDepartment of oncology, The Third Affiliated Hospital of Henan University of TCM, Zhengzhou, Henan, 450000, China.
Juntao WangDepartment of oncology, People's Hospital of Henan University of Chinese Medicine, Zhengzhou, 450014, Henan, China. wjuntao@yeah.net.

Funding

Henan Chief Science Popularization Expert Wang Xiangqi Studio HNKP2024176National Traditional Chinese Medicine Expert Inheritance Studio Construction Project Guozhong Pharmaceutical Renjiao Fa [2022] No. 75Special Project for Research on Traditional Chinese Medicine in Henan Province 2024ZY2100 & 2022ZY2046 & 2023ZY2110
6 · The paper itself

Abstract

Malignant tumors represent an important cause of mortality within the global population. Tumor angiogenesis, recognized as one of the key hallmarks of malignant tumors, is crucial for supplying essential nutrients and oxygen for tumor growth. Vascular endothelial growth factor (VEGF) and its receptor (VEGFR) are key drivers of tumor angiogenesis. Targeted therapeutic interventions not only effectively inhibit tumor growth by specifically blocking tumor angiogenesis but have also made breakthroughs in the treatment of malignant tumors. Fruquintinib, an anti-angiogenic small molecule drug developed independently in China, functions as a potent tyrosine kinase inhibitor with high selectivity. It effectively curtails tumor growth by binding to and inhibiting VEGFR-1, VEGFR-2, and VEGFR-3. Additionally, fruquintinib offers several advantages including minimal off-target toxicity, robust resistance profiles, and commendable efficacy. This agent can be used alone or in combination with other treatments. It has shown high effectiveness and survival benefits across various malignant tumors such as colorectal cancer, gastric cancer, non-small cell lung cancer, breast cancer, and other malignant tumors. Therefore, this article conducts a systematic review encompassing the mechanism of action, pharmacokinetics, clinical efficacy, and safety profile of fruquintinib. Through this review, we aimed to offer a reference for the clinical application and subsequent development of fruquintinib.

Indexed as

BenzofuransNeoplasmsQuinazolinesAngiogenesis InhibitorsAnimalsAntineoplastic AgentsHumansNeovascularization, PathologicReceptors, Vascular Endothelial Growth FactorTyrosine Kinase InhibitorsAngiogenesis InhibitorsAntineoplastic AgentsBenzofuransHMPL-013QuinazolinesReceptors, Vascular Endothelial Growth FactorTyrosine Kinase InhibitorsFruquintinibMalignant tumorTyrosine kinase inhibitorVascular endothelial growth factor

Identifiers

PMID39352649
PMCPMC11625063

What OpenQuestion holds

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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.