Evidence map›Paper›PMID 36516370›Full record

Trial reportJCO precision oncology2022

Monitoring PD-L1 Expression on Circulating Tumor-Associated Cells in Recurrent Metastatic Non-Small-Cell Lung Carcinoma Predicts Response to Immunotherapy With Radiation Therapy.

Jillian A Moran, Daniel L Adams, Martin J Edelman, Pablo Lopez, Jianzhong He, Yawei Qiao, Ting Xu, Zhongxing Liao, Kirby P Gardner, Cha-Mei Tang and 1 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in JCO precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pembrolizumab in Combination with Binimetinib in Patients with Unresectable Locally Advanced or Metastatic Triple-Negative Breast Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
  4. Trial
  5. Review
  6. Article
  7. Observational
  8. Review
  9. Single-Cell RNA Sequencing of Ewing Sarcoma Tumors Demonstrates Transcriptional Heterogeneity and Clonal Evolution.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Liquid biopsy techniques and lung cancer: diagnosis, monitoring and evaluation.Journal of experimental & clinical cancer research : CR · 2024
    Review
  16. Article
  17. Article
  18. Biomarkers for Immunotherapy in Driver-Gene-Negative Advanced NSCLC.International journal of molecular sciences · 2023
    Review
  19. Article
  20. 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

11 authors at 4 institutions in 1 country.

Jillian A MoranRutgers, The State University of New Jersey, New Brunswick, NJ.ORCID 0000-0002-8686-2714
Daniel L AdamsRutgers, The State University of New Jersey, New Brunswick, NJ.ORCID 0000-0002-1916-9637
Martin J EdelmanFox Chase Cancer Center, Philadelphia, PA.ORCID 0000-0002-3752-0726
Pablo LopezMD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-4282-3123
Jianzhong HeMD Anderson Cancer Center, Houston, TX.
Yawei QiaoMD Anderson Cancer Center, Houston, TX.
Ting XuMD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-7851-3389
Zhongxing LiaoMD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-2224-9478
Kirby P GardnerCreatv MicroTech, Inc, Monmouth Junction, NJ.ORCID 0000-0003-4537-1465
Cha-Mei TangCreatv MicroTech, Inc, Rockville, MD.ORCID 0000-0003-3017-0732
Steven H LinFox Chase Cancer Center, Philadelphia, PA.ORCID 0000-0003-4411-0634
The University of Texas MD Anderson Cancer Center · USRutgers, The State University of New Jersey · USFox Chase Cancer Center · USCreatv MicroTech (United States) · US

Funding

I-Corps for SBIR Phase I: Giant Macrophage-like Cells as a blood-based Biomarker for Lung Cancer RecurrenceR43CA206840 · NCI · CREATV MICROTECH, INC. · PI LIN, STEVEN HSESHENG, TANG, CHA-MEI · 2017 to 2019
$305k
NCI NIH HHS R43 CA206840
6 · The paper itself

Abstract

purposeCurrent diagnostic methods to determine programmed death 1 (PD-1) receptor and its ligand (PD-L1)/PD-1 immunotherapy (immune checkpoint inhibitor [ICI]) efficacy in recurrent or metastatic non-small-cell lung carcinoma (rmNSCLC) are imprecise. Although previously shown that patients with high tumor PD-L1 (≥ 50%) demonstrate clinical benefit in the form of disease reduction and improved survival, patients with low PD-L1 (< 50%) sometimes benefit from treatment. Since the PD-L1/PD-1 pathway is dynamic, monitoring PD-L1 levels during treatment may be more accurate than a static baseline tumor biopsy; however, rebiopsying the primary or metastatic disease is rarely feasible. Liquid biopsies that measure the upregulation of PD-L1 on tumor-associated cells (TACs), ie, cancer-associated macrophage-like cells and circulating tumor cells, have been performed, but their predictive value for ICI therapy efficacy is unknown. MATERIALS AND

methodsWe initiated a single-blind prospective study to evaluate TAC PD-L1 expression changes in rmNSCLC from blood samples before (T0) and after (T1) treatment with ICI (ICI, n = 41) or without ICI (no ICI, n = 41). Anonymized blood was filtered to isolate TACs, which were then quantified for high/low PD-L1 expression. Progression-free survival (PFS) or overall survival (OS) hazard ratios (HRs) were evaluated at 18 and 24 months by censored univariate analysis.

resultsIncreased TAC PD-L1 expression between T0 and T1 in patients who were not treated with ICI had no relationship with PFS or OS. However, increased TAC PD-L1 expression between T0 and T1 in patients treated with ICI had significantly better PFS (HR, 3.49; 95% CI, 1.5 to 8.3;

conclusionBlood-based monitoring of dynamic changes in PD-L1 in TACs appears to identify patients with rmNSCLC who may benefit from ICI.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungLung NeoplasmsNeoplastic Cells, CirculatingB7-H1 AntigenBiomarkers, TumorHumansImmunotherapyNeoplasm Recurrence, LocalProgrammed Cell Death 1 ReceptorProspective StudiesSingle-Blind MethodAntineoplastic Agents, ImmunologicalB7-H1 AntigenBiomarkers, TumorProgrammed Cell Death 1 Receptor

Identifiers

PMID36516370
PMCPMC10166406
OpenAlexW4311452532

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.