Evidence map›Paper›PMID 32110781›Full record

ArticleNature cancer2020

Immune-awakening revealed by peripheral T cell dynamics after one cycle of immunotherapy.

Sara Valpione, Elena Galvani, Joshua Tweedy, Piyushkumar A Mundra, Antonia Banyard, Philippa Middlehurst, Jeff Barry, Sarah Mills, Zena Salih, John Weightman and 6 more

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Nature cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 160 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
160citing papers in PubMed, 2 pooled it
11.2field-weighted citation impact, top 1% 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.

NCT05236114 recruitingnot on this mapstarted 2022, after this paper: background citation

TEMPUS GEMINI NSCLC STUDY: A Longitudinal Multi-Omic Biomarker Profiling Study of Patients With Non-Small Cell Lung Cancer (NSCLC)

TypeobservationalSponsorTempus AIRan2022 to 2029Enrolled1,200ConditionsNon-Small Cell Lung CancerArmsObservation
NCT06163534 recruitingnot on this mapstarted 2024, after this paper: background citation

TEMPUS PHOENIX HNSCC STUDY: A Longitudinal Multi-Omic Biomarker Profiling Study of Patients With Head & Neck Squamous Cell Carcinoma (HNSCC)

Typeobservational_patient_registrySponsorTempus AIRan2024 to 2028Enrolled500ConditionsHead and Neck Squamous Cell Carcinoma
3 · Its place in the literature

Who cites it

160 citing papers in PubMed, 2 syntheses or guidelines pooled it, 223 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Sequential Immune Activation of Effector T Cells as Biomarkers of Response to Durvalumab in Patients with Locally Advanced NSCLC.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Observational
  12. Article
  13. Article
  14. Article
  15. Early increase of CD103 expression on peripheral PD-1Cancer immunology, immunotherapy : CII · 2026
    Observational
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 3 countries.

Sara ValpioneMolecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
Elena GalvaniMolecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
Joshua TweedyMolecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
Piyushkumar A MundraMolecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.ORCID http://orcid.org/0000-0001-7769-2939
Antonia BanyardAdvanced Imaging and Flow Cytometry, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
Philippa MiddlehurstManchester Cancer Research Centre Biobank, The Christie NHS Foundation Trust, Manchester, UK.
Jeff BarryAdvanced Imaging and Flow Cytometry, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
Sarah MillsManchester Cancer Research Centre Biobank, The Christie NHS Foundation Trust, Manchester, UK.
Zena SalihThe Christie NHS Foundation Trust, Manchester, UK.
John WeightmanMolecular Biology Core Facility, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
Avinash GuptaThe Christie NHS Foundation Trust, Manchester, UK.
Gabriela GremelMolecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
Franziska BaenkeMolecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
Nathalie DhomenMolecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
Paul C LoriganThe Christie NHS Foundation Trust, Manchester, UK. paul.lorigan@christie.nhs.uk.ORCID http://orcid.org/0000-0002-8875-2164
Richard MaraisMolecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK. richard.marais@cruk.manchester.ac.uk.ORCID http://orcid.org/0000-0001-7484-4183
University of Manchester · GBThe Christie NHS Foundation Trust · GBGerman Cancer Research Center · DE

Funding

Cancer Research UK 17240Cancer Research UK 19279Cancer Research UK 22902Cancer Research UK A22902Cancer Research UK A27412Wellcome Trust 100282
6 · The paper itself

Abstract

Our understanding of how checkpoint inhibitors (CPI) affect T cell evolution is incomplete, limiting our ability to achieve full clinical benefit from these drugs. Here we analyzed peripheral T cell populations after one cycle of CPI and identified a dynamic awakening of the immune system revealed by T cell evolution in response to treatment. We sequenced T cell receptors (TCR) in plasma cell-free DNA (cfDNA) and peripheral blood mononuclear cells (PBMC) and performed phenotypic analysis of peripheral T cell subsets from metastatic melanoma patients treated with CPI. We found that early peripheral T cell turnover and TCR repertoire dynamics identified which patients would respond to treatment. Additionally, the expansion of a subset of immune-effector peripheral T cells we call T

Indexed as

Leukocytes, MononuclearMelanomaHumansImmunologic FactorsImmunotherapyReceptors, Antigen, T-CellImmunologic FactorsReceptors, Antigen, T-Cell

Identifiers

PMID32110781
PMCPMC7046489
OpenAlexW3005411249

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.