Evidence map›Paper›PMID 37009977›Full record

ReviewJournal of gastrointestinal cancer2023

Immune Checkpoint Inhibitors in pMMR/MSS Colorectal Cancer.

Joanna El Hajj, Sarah Reddy, Nilesh Verma, Emina H Huang, Syed M Kazmi

Abstract readReview
In one paragraph

Review in Journal of gastrointestinal cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
5.5field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

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  17. Digestive cancers: mechanisms, therapeutics and management.Signal transduction and targeted therapy · 2025
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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

5 authors at 2 institutions in 1 country.

Joanna El HajjDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-8675-1766
Sarah ReddyDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
Nilesh VermaDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
Emina H HuangDepartment of Surgery, Division of Surgical Oncology, UT Southwestern Medical Center, Dallas, TX, USA.
Syed M KazmiDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA. Syed.Kazmi@UTSouthwestern.edu.
Southwestern Medical Center · USSouthwestern Medical Center

Funding

Center for Clinical and Translational Sciences (CCTS)UL1TR000371 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$13.4M
The miR-20/c-Myc/E2F Regulatory Axis is Critical for the Tumor Promoting Activity of Inflammatory Fibroblasts in Colitis-Associated CancerR01CA237304 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HUANG, EMINA HUI-NA, WESSELY, OLIVER · 2019 to 2023
$2.9M
NCATS NIH HHS R01 CA237304NCATS NIH HHS UL1 TR000371
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors have recently replaced over chemotherapy as the first-line treatment for microsatellite instability-high or mismatch repair deficient (dMMR/MSI-H) stage 4 colorectal cancers. Considering this success, many studies have tried to replicate the use of immune checkpoint inhibitors, either as a single agent or in combination with other therapeutic agents, in the treatment of proficient mismatch repair (pMMR/MSS) stage 4 colorectal cancers. This review summarizes the seminal clinical data about the immune checkpoint inhibitors used in pMMR/MSS colorectal cancers and some future directions.

resultsStudies concerning the use of immune checkpoint inhibitors as a single agent or in combination with other immune checkpoint inhibitors, targeted therapy, chemotherapy, or radiotherapy have proven inefficient in the treatment of pMMR/MSS colorectal cancer. However, a small subset of patients with pMMR/MSS colorectal cancer who has a mutation in POLE and POLD1 enzymes may respond to immunotherapy. Moreover, patients without liver metastasis appear to have a better chance of response. New immune checkpoint targets are being identified, such as VISTA, TIGIT, LAG3, STING signal pathway, and BTLA, and studies are ongoing to determine their efficiency in this disease type.

conclusionImmune checkpoint inhibitor-based regimens have not yet shown any meaningful positive outcomes for most pMMR/MSS colorectal cancers. A beneficial effect among a minority of these patients has been observed, but concrete biomarkers of response are lacking. Understanding the underlying mechanisms of immune resistance should guide further research for overcoming these obstacles.

Indexed as

Colonic NeoplasmsColorectal NeoplasmsBrain NeoplasmsDNA Mismatch RepairHumansImmune Checkpoint InhibitorsImmunotherapyMicrosatellite InstabilityNeoplastic Syndromes, HereditaryImmune Checkpoint InhibitorsColorectal cancerImmunotherapyMicrosaetllite stable

Identifiers

PMID37009977
PMCPMC13200515
OpenAlexW4362506349

What OpenQuestion holds

Textmetadata
LicenceTDM
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.