Evidence map›Paper›PMID 37639010›Full record

ReviewJournal of cancer research and clinical oncology2023

Clinical research progress on BRAF V600E-mutant advanced colorectal cancer.

Chuanxiu Zeng, Mengchao Wang, Shuqi Xie, Na Wang, Zhen Wang, Dan Yi, Fanming Kong, Liwei Chen

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cancer research and clinical oncology, 2023. 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
1.2field-weighted citation impact, top 18% 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, 5 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 1 institution in 1 country.

Chuanxiu Zeng *Oncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Mengchao Wang *Oncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Shuqi XieOncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Na WangOncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Zhen WangOncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Dan YiOncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Fanming KongOncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Liwei ChenOncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China. c17361048061@163.com.
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine · CN

Funding

National Natural Science Foundation of China 82104553
6 · The paper itself

Abstract

Colorectal cancer is one of the malignant tumors that pose a serious threat to human health. A particularly bad prognosis might be expected for colorectal tumors with the unique molecular subtype BRAF V600E mutation. With the development of precision therapy, the advent of molecularly targeted therapies and immune checkpoint inhibitors has improved the outcome of intermediate to advanced colorectal cancer. However, the duration of drug benefit is usually short, and overall survival and progression-free survival remain suboptimal. Therefore, investigators are exploring more rational, safe, and effective drug combination regimens through clinical trials to provide longer survival for patients with such genetic mutations with metastatic colorectal cancer (mCRC). This article reviews the progress of clinical research on molecularly targeted drugs, immune checkpoint inhibitors, first-line chemotherapeutic agents, and different combination therapy regimens (including different targeted drug combinations, immune combination targeting, and chemotherapy combination targeting) for colorectal cancer patients with BRAF V600E mutation, which provides a reference for further in-depth clinical exploration of the treatment of colorectal cancer patients with BRAF V600E mutation.

Indexed as

Colorectal NeoplasmsProto-Oncogene Proteins B-rafHumansImmune Checkpoint InhibitorsMutationPrognosisBRAF protein, humanImmune Checkpoint InhibitorsProto-Oncogene Proteins B-rafBRAF V600E mutationClinical researchColorectal cancerReview

Identifiers

PMID37639010
PMCPMC11797460
OpenAlexW4386209688

What OpenQuestion holds

Textmetadata
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.