Evidence map›Paper›PMID 32160899›Full record

ArticleJournal of translational medicine2020

Frequency of circulating CD8+CD73+T cells is associated with survival in nivolumab-treated melanoma patients.

Mariaelena Capone, Federica Fratangelo, Diana Giannarelli, Claudia Sorrentino, Roberta Turiello, Serena Zanotta, Domenico Galati, Gabriele Madonna, Marilena Tuffanelli, Luigi Scarpato and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.3field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 37 citations in OpenAlex.

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  13. Low Pretreatment CD4International journal of molecular sciences · 2023
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  19. Oral alloantigen exposure promotes donor-specific tolerance in a mouse model of minor-mismatched skin transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Article
  20. Methods for the Detection of Circulating Biomarkers in Cancer Patients.Advances in experimental medicine and biology · 2022
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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

18 authors at 4 institutions in 1 country.

Mariaelena CaponeIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy. me.capone@istitutotumori.na.it.
Federica FratangeloIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Diana GiannarelliIstituto Nazionale Tumori Regina Elena, IRCCS, Rome, Italy.
Claudia SorrentinoDepartment of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, 84084, Fisciano, SA, Italy.
Roberta TurielloDepartment of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, 84084, Fisciano, SA, Italy.
Serena ZanottaIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Domenico GalatiIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Gabriele MadonnaIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Marilena TuffanelliIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Luigi ScarpatoIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Antonio M GrimaldiIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Assunta EspositoIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Rosa AzzaroIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Antonio PintoIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Ernesta CavalcantiIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Aldo PintoDepartment of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, 84084, Fisciano, SA, Italy.
Silvana MorelloDepartment of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, 84084, Fisciano, SA, Italy. smorello@unisa.it.
Paolo A AsciertoIstituto Nazionale Tumori - IRCCS - Fondazione "G. Pascale", Naples, Italy.
Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITUniversity of Salerno · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPD-1 blocking agents, such as nivolumab, have demonstrated clear anti-tumor effects and clinical benefits in a subset of patients with advanced malignancies. Nonetheless, more efforts are needed to identify reliable biomarkers for outcome, to correctly select patients who will benefit from anti-PD-1 treatment. The aim of this study was to investigate the role of peripheral CD8+T cells expressing CD73, involved in the generation of the immune suppressive molecule adenosine, in predicting outcome after nivolumab treatment in advanced melanoma patients.

methodsPBMCs from 100 melanoma patients treated with nivolumab were collected at National Cancer Institute "G. Pascale" of Naples. Frequencies of CD8+ lymphocytes phenotypes were assessed by flow cytometry at baseline before nivolumab treatment, along with clinical characteristics and blood count parameters. Healthy controls (n = 20) were also analysed. Percentages of baseline T cells expressing PD-1 and CD73 were correlated with outcome after nivolumab treatment.

resultsMelanoma patients presented a lower frequency of total circulating CD8+ lymphocytes than control subjects (p = 0.008). Patients with low baseline percentage of circulating CD8+PD-1+CD73+ lymphocytes (< 2.3%) had better survival (22.4 months vs 6.9 months, p = 0.001). Patients (39%) with clinical benefit from nivolumab therapy presented a significantly lower frequency of circulating CD8+PD-1+CD73+ lymphocytes than patients who progressed to nivolumab treatment (p = 0.02).

conclusionsOur observations suggest that baseline CD73 expression on circulating CD8+PD-1+ lymphocytes appear a promising biomarker of response to anti-PD-1 treatment in melanoma patients. Further investigations are needed for validation and for clarifying its role as prognostic or predictive marker.

Indexed as

MelanomaNivolumabCD8-Positive T-LymphocytesHumansPrognosisProgrammed Cell Death 1 ReceptorNivolumabProgrammed Cell Death 1 ReceptorCD73Circulating CD8+ lymphocytesImmunotherapyMetastatic melanomaNivolumab

Identifiers

PMID32160899
PMCPMC7065327
OpenAlexW3011603183

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Registered trials

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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.