Evidence map›Paper›PMID 37261532›Full record

Trial reportMedical oncology (Northwood, London, England)2023

A phase II study of metformin plus pemetrexed and carboplatin in patients with non-squamous non-small cell lung cancer (METALUNG).

S Verma, S Chitikela, V Singh, S Khurana, D Pushpam, D Jain, S Kumar, Y Gupta, P S Malik

Abstract readClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in Medical oncology (Northwood, London, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Drug repurposing in oncology: a path beyond the bottleneck.Medical oncology (Northwood, London, England) · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
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 1 institution in 1 country.

S VermaDepartment of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India.
S ChitikelaDepartment of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India.
V SinghDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
S KhuranaDepartment of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India.
D PushpamDepartment of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India.
D JainDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
S KumarDepartment of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India.
Y GuptaDepartment of Endocrinology, All India Institute of Medical Sciences, New Delhi, India.
P S MalikDepartment of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India. drprabhatsm@gmail.com.ORCID http://orcid.org/0000-0003-0205-8559
All India Institute of Medical Sciences · IN

Funding

All-India Institute of Medical Sciences 8-688/A-688/2019
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) ± chemotherapy is the standard treatment for driver mutation-negative non-small cell lung cancer (NSCLC). However, accessibility to ICIs in LMICs is limited due to high cost, and platinum-based chemotherapy remains the mainstay of treatment. Metformin has anticancer properties, and studies suggest synergism between metformin and pemetrexed. Based on preclinical evidence, this combination may be more beneficial for STK11-mutated NSCLC, a subgroup, inherently resistant to ICIs. In this Simon two-stage, single-arm phase 2 trial, we investigated metformin with pemetrexed-carboplatin (PC) in patients with treatment-naive stage IV non-squamous NSCLC. The primary outcome was 6-month progression-free survival (PFS) rate. Secondary outcomes were safety, overall survival (OS), overall response rate (ORR), proportion of STK11 mutation, and effect of STK11 mutation on 6-month PFS rate. The study was terminated for futility after interim analysis. The median follow-up was 34.1 months. The 6-month PFS rate was 28% (95% CI 12.4-0.46). The median PFS and OS were 4.5 (95% CI 2.2-6.1) and 7.4 months (95% CI 5.3-15.3), respectively. The ORR was 72%. Gastrointestinal toxicities were the most common. No grade 4/5 toxicities were reported. Targeted sequencing was possible in nine cases. Two patients had STK11 mutation and a poor outcome (PFS < 12 weeks). We could not demonstrate the benefit of metformin with CP in terms of improvement in 6-month PFS rate; however, the combination was safe (CTRI/2019/02/017815).

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsMetforminAntineoplastic Combined Chemotherapy ProtocolsCarboplatinHumansPemetrexedCarboplatinMetforminPemetrexedDrug repositioningDrug repurposingMetforminNSCLCSTK11

Identifiers

PMID37261532
OpenAlexW4378952314

What Socratic holds

Textmetadata
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.