Evidence map›Paper›PMID 40579605›Full record

Trial reportCancer chemotherapy and pharmacology2025

Targeting insulin-like growth factor-1 (IGF-1) by using metformin in non-diabetic metastatic breast cancer female patients: a randomized controlled trial.

Hager Salah, Hoda Rabea, Mostafa S Sheemy, Alshaimaa Ibrahim Rabie, Hebatallah Ahmed Mohamed Moustafa, Ahmed A Elberry, Ahmed Hassan

Registry-linked trialAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Cancer chemotherapy and pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04143282 (Evaluation of the Effect of Metformin on Metastatic Breast Cancer as Adjuvant Treatment), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT04143282 phase2completednot on this map

Evaluation of the Effect of Metformin on Metastatic Breast Cancer as Adjuvant Treatment

TypeinterventionalSponsorHager salah el dinRan2019 to 2020Enrolled250ConditionsMetastatic Breast CancerArmsMetformin plus chemotherapy, Chemotherapy
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

7 authors.

Hager SalahClinical pharmacy department, King Hamad University Hospital- Royal Medical Services, Muharraq Governorate, Bahrain.
Hoda RabeaClinical Pharmacy Department, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt.
Mostafa S SheemyMedical Microbiology and Immunology Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.
Alshaimaa Ibrahim RabieClinical Pharmacy Department, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt. Alshaimaa.ph@o6u.edu.eg.
Hebatallah Ahmed Mohamed MoustafaClinical Pharmacy and Pharmacy Practice Department, 319, Faculty of Pharmacy, Badr University in Cairo, 11829, Cairo, Egypt. hebatallah.ahmed@buc.edu.eg.ORCID http://orcid.org/0000-0003-4530-406X
Ahmed A ElberryClinical Pharmacology Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.
Ahmed HassanClinical Oncology Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeInsulin-like growth factor-1 (IGF-1) may play a role in breast cancer (BC) development. Metformin was found to exert anti-cancer function in several studies, partly by interference with the IGF-1 signaling pathway and reducing its blood levels. Therefore, our study aimed primarily to find out how metformin affected both IGF-1 levels and clinical outcomes in metastatic breast cancer patients (MBC) and secondarily to identify the correlation between post-treatment IGF-1 decline rates and BC prognosis and metastasis.

methodsFifty MBC female patients were randomly assigned to either the control group (who were administered conventional chemotherapy) and the intervention group (treated with metformin plus chemotherapy). An enzyme-linked immunosorbent assay (ELISA) was used to detect IGF-1 levels at baseline and three months post-treatment.

resultsIGF-1 levels in the metformin group were significantly lower than in the control group (p = 0.011). Furthermore, the percentage of post-treatment drop in IGF-1 levels differed significantly between the control and metformin groups (p = 0.001). Patients whose IGF-1 levels increased after treatment had a statistically significant occurrence of progressive disease (disease progression) in the control group higher than in the metformin group (92.9% versus 87.5%).

conclusionThe co-administration of metformin with chemotherapy significantly inhibited the IGF-1 signaling pathway, which reduced progressive diseases and reduced mortality in non-diabetic MBC patients. However, while metformin exerts a robust IGF-1 lowering effect, combination chemotherapy and low metastasis burden may further enhance this effect. TRAIL REGISTRATION: Our trial was registered at clinicaltrials.gov (ID no. NCT04143282).

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsInsulin-Like Growth Factor IMetforminAdultAgedFemaleHumansHypoglycemic AgentsInsulin-Like PeptidesMiddle AgedNeoplasm MetastasisPrognosisHypoglycemic AgentsIGF1 protein, humanInsulin-Like Growth Factor IInsulin-Like PeptidesMetforminChemotherapyIGF-1Metastatic breast cancerMetformin

Identifiers

PMID40579605

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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.