Evidence map›Paper›PMID 30886395›Full record

ReviewNature reviews. Gastroenterology & hepatology2019

Immunotherapy in colorectal cancer: rationale, challenges and potential.

Karuna Ganesh, Zsofia K Stadler, Andrea Cercek, Robin B Mendelsohn, Jinru Shia, Neil H Segal, Luis A Diaz

Open access · bronzeAbstract readReview
In one paragraph

Review in Nature reviews. Gastroenterology & hepatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,191 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,191citing papers in PubMed, 4 pooled it
82.6field-weighted citation impact, top 1% 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

1,191 citing papers in PubMed, 4 syntheses or guidelines pooled it, 1,952 citations in OpenAlex.

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  18. TIGITCancers · 2026
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1,131 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

Karuna GaneshDepartment of Medicine, Memorial Sloan Kettering Cancer Center, York Avenue, New York, NY, USA. ganeshk@mskcc.org.
Zsofia K StadlerDepartment of Medicine, Memorial Sloan Kettering Cancer Center, York Avenue, New York, NY, USA.
Andrea CercekDepartment of Medicine, Memorial Sloan Kettering Cancer Center, York Avenue, New York, NY, USA.
Robin B MendelsohnDepartment of Medicine, Memorial Sloan Kettering Cancer Center, York Avenue, New York, NY, USA.
Jinru ShiaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, York Avenue, New York, NY, USA.ORCID http://orcid.org/0000-0002-4351-2511
Neil H SegalDepartment of Medicine, Memorial Sloan Kettering Cancer Center, York Avenue, New York, NY, USA.
Luis A DiazDepartment of Medicine, Memorial Sloan Kettering Cancer Center, York Avenue, New York, NY, USA.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Investigating L1CAM-dependent stem cell regeneration in metastasisK08CA230213 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI GANESH, KARUNA · 2018 to 2022
$1.3M
NCI NIH HHS K08 CA230213NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Following initial successes in melanoma treatment, immunotherapy has rapidly become established as a major treatment modality for multiple types of solid cancers, including a subset of colorectal cancers (CRCs). Two programmed cell death 1 (PD1)-blocking antibodies, pembrolizumab and nivolumab, have shown efficacy in patients with metastatic CRC that is mismatch-repair-deficient and microsatellite instability-high (dMMR-MSI-H), and have been granted accelerated FDA approval. In contrast to most other treatments for metastatic cancer, immunotherapy achieves long-term durable remission in a subset of patients, highlighting the tremendous promise of immunotherapy in treating dMMR-MSI-H metastatic CRC. Here, we review the clinical development of immune checkpoint inhibition in CRC leading to regulatory approvals for the treatment of dMMR-MSI-H CRC. We focus on new advances in expanding the efficacy of immunotherapy to early-stage CRC and CRC that is mismatch-repair-proficient and has low microsatellite instability (pMMR-MSI-L) and discuss emerging approaches for targeting the immune microenvironment, which might complement immune checkpoint inhibition.

Indexed as

Colorectal NeoplasmsHumansImmunologic FactorsImmunotherapyMolecular Targeted TherapyTreatment OutcomeImmunologic Factors

Identifiers

PMID30886395
PMCPMC7295073
OpenAlexW2920863623

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.