Evidence map›Paper›PMID 36189266›Full record

ReviewFrontiers in immunology2022

Biomarkers of related driver genes predict anti-tumor efficacy of immune checkpoint inhibitors.

Shuai Jiang, Shuai Geng, Xinyu Luo, Can Zhang, Yang Yu, Mengfei Cheng, Shuo Zhang, Ning Shi, Mei Dong

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
  3. Human leukocyte antigen and tumor immunotherapy (Review).International journal of oncology · 2023
    Review
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

9 authors at 3 institutions in 1 country.

Shuai JiangDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, China.
Shuai GengDepartment of Pharmacy, Strategic Support Force Medical Center, Beijing, China.
Xinyu LuoDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, China.
Can ZhangDepartment of Ultrasound Diagnosis, Strategic Support Force Medical Center, Beijing, China.
Yang YuDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, China.
Mengfei ChengDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, China.
Shuo ZhangDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, China.
Ning ShiDepartment of Pharmacy, Strategic Support Force Medical Center, Beijing, China.
Mei DongDepartment of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, China.
Harbin Medical University · CNAir Force General Hospital PLA · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a disease with high morbidity and mortality in the world. In the past, the main treatment methods for cancer patients were surgery, radiotherapy and chemotherapy. However, with early treatment, the recurrence rate of cancer is higher, and the drug resistance of cancer cells is faster. In recent years, with the discovery of immune escape mechanism of cancer cells, Immunotherapy, especially Immune Checkpoint Inhibitors (ICIs), has made a breakthrough in the treatment of solid tumors, significantly prolonging the overall survival time and disease-free progression in some solid tumors, and its clinical benefits are more prominent than those of traditional anti-tumor drugs, which has become the hope of cancer patients after the failure of multi-line therapy. More and more studies have shown that there is a correlation between cancer driving genes and the clinical benefits of ICIs treatment, and the therapeutic effects and adverse reactions of ICIs can be predicted by the status of driving genes. Therefore, screening potential biomarkers of people who may benefit from immunotherapy in order to maximize the therapeutic benefits is a top priority. This review systematically summarizes the cancer driving genes that may affect the clinical benefits of immune checkpoint inhibitors, and provides accurate scientific basis for clinical practice.

Indexed as

Antineoplastic AgentsNeoplasmsBiomarkersHumansImmune Checkpoint InhibitorsImmunotherapyAntineoplastic AgentsBiomarkersImmune Checkpoint Inhibitorsbiomarkercancerimmune checkpoint inhibitoroverall survivalprogress free survival

Identifiers

PMID36189266
PMCPMC9521273
OpenAlexW4295946049

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.