Evidence map›Paper›PMID 30200242›Full record

ReviewDiagnostics (Basel, Switzerland)2018

The Interplay between Circulating Tumor Cells and the Immune System: From Immune Escape to Cancer Immunotherapy.

Kevin Leone, Cristina Poggiana, Rita Zamarchi

Registry-linked trialAbstract readReview
In one paragraph

Review in Diagnostics (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05810402 (Liver Cancer and Immunotherapy), which is not on this map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing 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.

NCT05810402 narecruitingnot on this mapstarted 2023, after this paper: background citation

Liver Cancer and Immunotherapy : Clinical Relevance of LIquid BioPSY

TypeinterventionalSponsorUniversity Hospital, MontpellierRan2023 to 2027Enrolled60ConditionsHepatocellular Carcinoma, BCLC Stage B Hepatocellular Carcinoma, BCLC Stage C Hepatocellular Carcinoma, Immune Checkpoint InhibitorArmsLiquid Biopsy
3 · Its place in the literature

Who cites it

57 citing papers in PubMed.

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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

3 authors.

Kevin LeoneVeneto Institute of Oncology IOV-IRCCS, Padua, Italy. kevin.leone@iov.veneto.it.
Cristina PoggianaVeneto Institute of Oncology IOV-IRCCS, Padua, Italy. cristinapoggiana@gmail.com.
Rita ZamarchiVeneto Institute of Oncology IOV-IRCCS, Padua, Italy. rita.zamarchi@unipd.it.

Funding

IMI - Innovative Medicines Initiative IMI [115749] CANCER-IDIOV-IRCCS Intramural call [DGRV 2980/12, 5x1000 IOV - Translational Oncology: from benchtop to bedside; PI R. Zamarchi]
6 · The paper itself

Abstract

Circulating tumor cells (CTCs) have aroused increasing interest not only in mechanistic studies of metastasis, but also for translational applications, such as patient monitoring, treatment choice, and treatment change due to tumor resistance. In this review, we will assess the state of the art about the study of the interactions between CTCs and the immune system. We intend to analyze the impact that the cells of the immune system have in limiting or promoting the metastatic capability of CTCs. To this purpose, we will examine studies that correlate CTCs, immune cells, and patient prognosis, and we will also discuss relevant animal models that have contributed to the understanding of the mechanisms of immune-mediated metastasis. We will then consider some studies in which CTCs seem to play a promising role in monitoring cancer patients during immunotherapy regimens. We believe that, from an accurate and profound knowledge of the interactions between CTCs and the immune system, new immunotherapeutic strategies against cancer might emerge in the future.

Indexed as

cancer biomarkerscirculating tumor cellsimmune systemimmunotherapyliquid biopsymetastasis

Identifiers

PMID30200242
PMCPMC6164896

What OpenQuestion holds

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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.