Evidence map›Paper›PMID 35063062›Full record

ArticleOncology research2022

Real-World Data: Fruquintinib in Treating Metastatic Colorectal Cancer.

Shuai Liu, Lu Lu, Feng Pan, Chunsheng Yang, Jing Liang, Jinfeng Liu, Jian Wang, Rong Shen, Fu-Ze Xin, Nan Zhang

Abstract read
In one paragraph

Article in Oncology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–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

12 citing papers in PubMed.

  1. Trial
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  6. Review
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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

10 authors.

Shuai LiuDepartment of Breast Disease Diagnosis and Treatment Center, Central Hospital Affiliated to Shandong First Medical UniversityJinanP.R. China.
Lu LuDepartment of Breast Disease Diagnosis and Treatment Center, Central Hospital Affiliated to Shandong First Medical UniversityJinanP.R. China.
Feng PanEthics Committee Office, Jinan Central Hospital, Cheeloo College of Medicine, Shandong UniversityJinanP.R. China.
Chunsheng YangDepartment of Breast Disease Diagnosis and Treatment Center, Central Hospital Affiliated to Shandong First Medical UniversityJinanP.R. China.
Jing LiangDepartment of Oncology, Shandong Provincial Qianfoshan HospitalJinanP.R. China.
Jinfeng LiuDepartment of Oncology, Rizhao Hospital of Traditional Chinese MedicineRizhaoP.R. China.
Jian WangDepartment of Medical Oncology, Qilu Hospital of Shandong UniversityJinanP.R. China.
Rong ShenDepartment of Chemotherapy, Shandong Provincial Hospital Affiliated to Shandong First Medical UniversityJinanP.R. China.
Fu-Ze XinDepartment of Gastrointestinal Surgery, Liao Cheng Peoples HospitalLiaochengP.R. China.
Nan ZhangDepartment of Breast Disease Diagnosis and Treatment Center, Central Hospital Affiliated to Shandong First Medical UniversityJinanP.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fruquintinib, also called HMPL-013, was first discovered by Hutchison Whampoa Pharmaceuticals Co. Ltd., Shanghai, China, and it is an oral vascular endothelial growth factor receptor (VEGFR) inhibitor. In clinical trials, fruquintinib has demonstrated a survival benefit in metastatic colorectal cancer (mCRC) patients. The purpose of this study was to retrospectively evaluate the efficacy and toxicity of fruquintinib in real-world patients. We collected data from patients with mCRC treated with oral fruquintinib from 2018 to 2020 in six different institutions. Patients with mCRC initially received 5 mg of oral fruquintinib daily for 3 weeks. Progression-free survival (PFS) was evaluated using the KaplanMeier method. The efficacy and safety of fruquintinib were also assessed. Seventy-five patients were involved in our study, and 29.3% of patients achieved stable disease (SD). Median PFS was 5.4 months (95% CI: 4.8415.959). The treatment-emergent adverse events (TEAEs) with fruquintinib were acceptable with grade 3 TEAEs of 6%. The grade 3 TEAEs were handfoot skin reaction (HFSR), fatigue, and stomatitis. The ECOG performance status was associated with PFS. In this real-world study, the clinical activity of fruquintinib was consistent with what has been reported in previous clinical trials. The level of safety was acceptable, and the side effects were manageable.

Indexed as

Colonic NeoplasmsColorectal NeoplasmsBenzofuransChinaHumansQuinazolinesRetrospective StudiesVascular Endothelial Growth Factor ABenzofuransHMPL-013QuinazolinesVascular Endothelial Growth Factor A

Identifiers

PMID35063062
PMCPMC9110705

What OpenQuestion holds

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Registered trials

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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.