Evidence map›Paper›PMID 40527402›Full record

ReviewCritical reviews in oncology/hematology2025

IGF-1R inhibitors in cancer: A review of available evidence and future outlook.

Deniz Can Guven, Jibran Ahmed, Bettzy Stephen, Aung Naing

Erratum issuedAbstract readReview
In one paragraph

Review in Critical reviews in oncology/hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Deniz Can GuvenHacettepe University Cancer Institute, Ankara, Turkey.
Jibran AhmedDevelopmental Therapeutics Clinic, Early Phase Clinical Trials Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Bettzy StephenDepartment of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Aung NaingDepartment of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. Electronic address: anaing@mdanderson.org.

Funding

TRANSLATIONAL AND ANALYTICAL CHEMISTRY COREP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI PETER W PISTERS · 1985 to 2026
$279.3M
Integrating patient-reported outcomes and T-cell receptor sequencing to predict immune-related adverse eventsR01CA279749 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Aung Naing · 2024 to 2026
$1.9M
NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA279749
6 · The paper itself

Abstract

The insulin-like growth factor-1 receptor (IGF-1R) has emerged as a critical target in oncology due to its pivotal role in tumor growth, progression, and therapeutic resistance. Despite encouraging preclinical findings, clinical trials utilizing IGF-1R inhibitors as monotherapies have largely been unsuccessful. Herein, we reviewed the available data with IGF-1R inhibitors and the potential of IGF-1R inhibitors when used in combination therapies, an approach supported by advances in precision medicine and immuno-oncology. We aimed to provide comprehensive analysis of the preclinical rationale underpinning the combination of IGF-1R inhibitors with immune checkpoint inhibitors, mTOR/AKT, CDK 4/6, BRAF/MEK, and DNA-damage repair pathway inhibitors. Furthermore, we discussed the development of biomarkers, such as IGF-1R expression levels and hyperglycemia, to predict therapeutic response. Despite initial challenges, the strategic integration of IGF-1R inhibitors within combination therapies holds promise for significantly improving patient outcomes by overcoming resistance. This review highlights the need for ongoing research to optimize these combination strategies and fully harness the therapeutic potential of IGF-1R inhibitors in cancer treatment.

Indexed as

Antineoplastic AgentsNeoplasmsProtein Kinase InhibitorsReceptor, IGF Type 1AnimalsAntineoplastic Combined Chemotherapy ProtocolsHumansMolecular Targeted TherapySignal TransductionAntineoplastic AgentsIGF1R protein, humanProtein Kinase InhibitorsReceptor, IGF Type 1BiomarkerCombinationIGF-1RImmunotherapyMTOR/AKTResistance

Identifiers

PMID40527402
PMCPMC12320188

What Socratic 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 Socratic graph.