Evidence map›Paper›PMID 38275869›Full record

ReviewCancers2024

The Immune Landscape and Immunotherapeutic Strategies in Platinum-Refractory Testicular Germ Cell Tumors.

Konstantinos Evmorfopoulos, Konstantinos Marsitopoulos, Raphael Karachalios, Athanasios Karathanasis, Konstantinos Dimitropoulos, Vassilios Tzortzis, Ioannis Zachos, Panagiotis J Vlachostergios

Abstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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.

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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
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

8 authors.

Konstantinos EvmorfopoulosDepartment of Urology, School of Health Sciences, Faculty of Medicine, University of Thessaly, 41110 Larissa, Greece.ORCID 0000-0002-5634-9944
Konstantinos MarsitopoulosDepartment of Urology, School of Health Sciences, Faculty of Medicine, University of Thessaly, 41110 Larissa, Greece.
Raphael KarachaliosDepartment of Urology, School of Health Sciences, Faculty of Medicine, University of Thessaly, 41110 Larissa, Greece.
Athanasios KarathanasisDepartment of Urology, School of Health Sciences, Faculty of Medicine, University of Thessaly, 41110 Larissa, Greece.
Konstantinos DimitropoulosDepartment of Urology, Aberdeen Royal Infirmary, Aberdeen AB25 2ZN, UK.
Vassilios TzortzisDepartment of Urology, School of Health Sciences, Faculty of Medicine, University of Thessaly, 41110 Larissa, Greece.ORCID 0000-0002-9993-5943
Ioannis ZachosDepartment of Urology, School of Health Sciences, Faculty of Medicine, University of Thessaly, 41110 Larissa, Greece.
Panagiotis J VlachostergiosDepartment of Urology, School of Health Sciences, Faculty of Medicine, University of Thessaly, 41110 Larissa, Greece.ORCID 0000-0002-1704-1517

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Testicular germ cell tumors (TGCTs) are cancers with very good prognosis, even in the metastatic setting, with high curative potential mainly attributed to the introduction of cisplatin-based chemotherapy. However, approximately 15% of the patients develop platinum-refractory disease and suffer multiple relapses. Therefore, there is an unmet need for novel therapeutic agents with improved efficacy and minimal long-term side effects. Recent advances in the development of immunotherapeutic agents, particularly immune checkpoint inhibitors (ICIs), have offered an opportunity to test their activity in various tumor types, including GCTs. This review aims to analyze the immune microenvironment of these tumors and present the most recently available data from studies that have tested immunotherapeutic agents against GCTs. The majority of the available knowledge derives from case reports or small cohort studies, particularly those involving ICIs of the PD-1/PD-L1 axis alone or in combination with anti-CTLA-4 monoclonal antibodies. Other immunotherapeutic targeted approaches, including antibody-drug conjugates, antibody prodrugs, vaccines, tyrosine kinase inhibitors, chimeric antigen receptor (CAR) T-cell therapy, have biological rationales and have shown preliminary activity or are currently being tested. Growing evidence on these and other approaches will assist in broadening the currently limited treatment armamentarium against platinum-refractory TGCTs.

Indexed as

anti-CTLA-4anti-PD-1/PD-L1immunotherapyplatinum-refractorytesticular germ cell tumors

Identifiers

PMID38275869
PMCPMC10814346

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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.