Evidence map›Paper›PMID 40893177›Full record

ArticleJTO clinical and research reports2025

Brief Report: Prospective Trial of Pembrolizumab Monotherapy in Metastatic NSCLC Evaluating Circulating Tumor DNA as a Surrogate Biomarker of Response.

Iris van 't Erve, Isabelle Blanchard, Judy Y Pagtama, Alison J Holmes Tisch, Ash A Alizadeh, Kavitha Ramchandran, Heather A Wakelee, Sukhmani K Padda, Maximilian Diehn, Joel W Neal

Registry-linked trialAbstract read
In one paragraph

Article in JTO clinical and research reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02955758 (A Phase 2 Trial of Pembrolizumab in Metastatic Non-squamous NSCLC Examining Circulating Tumor DNA Levels as a Surrogate Biomarker of Response), 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.

NCT02955758 phase2completednot on this map

A Phase 2 Trial of Pembrolizumab in Metastatic Non-squamous NSCLC Examining Circulating Tumor DNA Levels as a Surrogate Biomarker of Response

TypeinterventionalSponsorJoel NealRan2016 to 2024Enrolled25ConditionsMetastatic Non-Squamous Non-Small Cell Lung CarcinomaArmsPembrolizumab
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

10 authors.

Iris van 't ErveStanford Cancer Institute, Stanford University, Stanford, California.
Isabelle BlanchardDivision of Oncology, Department of Medicine, Stanford University, Stanford, California.
Judy Y PagtamaStanford Thoracic Oncology, Stanford Health Care, Stanford, California.
Alison J Holmes TischStanford Thoracic Oncology, Stanford Health Care, Stanford, California.
Ash A AlizadehStanford Cancer Institute, Stanford University, Stanford, California.
Kavitha RamchandranDivision of Oncology, Department of Medicine, Stanford University, Stanford, California.
Heather A WakeleeStanford Cancer Institute, Stanford University, Stanford, California.
Sukhmani K PaddaFox Chase Cancer Center/Temple Health, Philadelphia, Pennsylvania.
Maximilian DiehnStanford Cancer Institute, Stanford University, Stanford, California.
Joel W NealStanford Cancer Institute, Stanford University, Stanford, California.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors provide clinical benefit to a subset of patients with metastatic NSCLC, yet the reliable prediction of long-term outcomes remains challenging. We conducted a prospective phase 2 clinical trial to evaluate circulating tumor DNA (ctDNA) as a surrogate biomarker for early clinical response to pembrolizumab monotherapy (NCT02955758). Tumor-informed targeted sequencing of pretreatment and early on-treatment plasma ctDNA in 25 patients with metastatic NSCLC was performed. On-treatment ctDNA response, defined as at least a threefold ctDNA variant allele frequency decrease after three cycles of pembrolizumab versus baseline, was able to predict with 100%, 66%, and 100% accuracy partial response, stable disease, and progressive disease radiologic response, respectively. Molecular response was also correlated with progression-free survival. This study confirms the potential clinical utility of early on-treatment ctDNA-based response evaluation in patients treated with immune checkpoint inhibitors, creating the opportunity for early treatment intervention in nonresponders.

Indexed as

BiomarkersctDNALiquid biopsiesLung cancerNSCLCTranslational research

Identifiers

PMID40893177
PMCPMC12396422

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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 OpenQuestion graph.