Evidence map›Paper›PMID 32047958›Full record

ArticleCancer immunology, immunotherapy : CII2020

Tumor mutational load, CD8

Daan P Hurkmans, Merian E Kuipers, Jasper Smit, Ronald van Marion, Ron H J Mathijssen, Piet E Postmus, Pieter S Hiemstra, Joachim G J V Aerts, Jan H von der Thüsen, Sjoerd H van der Burg

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% 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

69 citing papers in PubMed, 1 synthesis or guideline pooled it, 101 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Translational lung cancer research · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Next-generation immunotherapy: igniting new hope for lung cancer.Therapeutic advances in medical oncology · 2024
    Review
  18. Article
  19. Review
  20. Review

9 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Daan P HurkmansDepartment of Pulmonary Medicine, Erasmus University Medical Center, Doctor Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands. d.hurkmans@erasmusmc.nl.ORCID http://orcid.org/0000-0002-8750-5188
Merian E KuipersDepartment of Pulmonology, Leiden University Medical Center, Leiden, The Netherlands.
Jasper SmitDepartment of Pulmonology, Leiden University Medical Center, Leiden, The Netherlands.
Ronald van MarionDepartment of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Ron H J MathijssenDepartment of Medical Oncology, Erasmus University Medical Center, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Piet E PostmusDepartment of Pulmonology, Leiden University Medical Center, Leiden, The Netherlands.
Pieter S HiemstraDepartment of Pulmonology, Leiden University Medical Center, Leiden, The Netherlands.
Joachim G J V AertsDepartment of Pulmonary Medicine, Erasmus University Medical Center, Doctor Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
Jan H von der ThüsenDepartment of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Sjoerd H van der BurgDepartment of Medical Oncology, Leiden University Medical Center, Leiden, The Netherlands.
Erasmus MC · NLLeiden University Medical Center · NL

Funding

Bristol-Myers Squibb OT123-361
6 · The paper itself

Abstract

objectivesA minority of NSCLC patients benefit from anti-PD1 immune checkpoint inhibitors. A rational combination of biomarkers is needed. The objective was to determine the predictive value of tumor mutational load (TML), CD8 MATERIALS AND

methodsMetastatic NSCLC patients were prospectively included in an immune-monitoring trial (NTR7015) between April 2016-August 2017, retrospectively analyzed in FFPE tissue for TML (NGS: 409 cancer-related-genes) and by IHC staining to score PD-L1, CD8

results30 patients with adenocarcinoma (67%) or squamous cell carcinoma (33%) were included. High TML was associated with better PFS (p = 0.004) and OS (p = 0.025). Interaction analyses revealed that patients with both high TML and high total CD8

conclusionThis proof-of-concept study suggests that a combination of PD-L1 expression, TML, CD8

Indexed as

AgedAntineoplastic Agents, ImmunologicalB7-H1 AntigenBiomarkers, TumorBiopsyCarcinoma, Non-Small-Cell LungCD8-Positive T-LymphocytesClinical Decision-MakingDisease ProgressionFemaleFollow-Up StudiesHistocompatibility Antigens Class IHumansLungLung NeoplasmsLymphocytes, Tumor-InfiltratingAntineoplastic Agents, ImmunologicalB7-H1 AntigenBiomarkers, TumorCD274 protein, humanHistocompatibility Antigens Class INivolumabBiomarkerNivolumabNSCLCTMBTumor microenvironment

Identifiers

PMID32047958
PMCPMC7183487
OpenAlexW3006011106

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.