Evidence map›Paper›PMID 37568759›Full record

ReviewCancers2023

MicroRNA-371a-3p-The Novel Serum Biomarker in Testicular Germ Cell Tumors.

Tim Nestler, Justine Schoch, Gazanfer Belge, Klaus-Peter Dieckmann

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07601672 (PRISTINE Trial), which is not on this map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
7.0field-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.

NCT07601672 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

PRISTINE Trial: PRoton Beam Therapy In Seminoma - Toxicity INvestigation and Evaluation of Outcome

TypeinterventionalSponsorIstituto Clinico HumanitasRan2026 to 2031Enrolled20ConditionsSeminomaArmsprotontherapy
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 3 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. SEOM-GG clinical guidelines for the management of germ-cell testicular cancer (2023).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Guideline
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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

4 authors at 3 institutions in 1 country.

Tim NestlerDepartment of Urology, Federal Armed Forces Hospital Koblenz, 56072 Koblenz, Germany.ORCID 0000-0001-6033-6364
Justine SchochDepartment of Urology, Federal Armed Forces Hospital Koblenz, 56072 Koblenz, Germany.
Gazanfer BelgeDepartment of Tumour Genetics, University Bremen, 28359 Bremen, Germany.ORCID 0000-0001-8613-3450
Klaus-Peter DieckmannDepartment of Urology, Asklepios Klinik Altona, 22763 Hamburg, Germany.ORCID 0000-0002-3821-7956
Bundeswehrzentralkrankenhaus Koblenz · DEAsklepios Klinik Altona · DEUniversity of Bremen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTesticular germ cell tumors (TGCTs) are a paradigm for the use of serum tumor markers in clinical management. However, conventional markers such as alpha-fetoprotein (AFP), beta-human chorionic gonadotropin (hCG), and lactate dehydrogenase (LDH) have quite limited sensitivities and specificities. Within the last decade, the microRNA-371a-3p (miR371) emerged as a possible new biomarker with promising features. AREAS COVERED: This review covers the typical features as well as possible clinical applications of miR371 in TGCT patients, such as initial diagnosis, therapy monitoring, and follow-up. Additionally, technical issues are discussed. EXPERT OPINION: With a sensitivity of around 90% and specificity >90%, miR371 clearly outperforms the classical serum tumor markers in TGCTs. The unique features of the test involve the potential of modifying recent standards of care in TGCT. In particular, miR371 is expected to aid clinical decision-making in scenarios such as discriminating small testicular TGCT masses from benign ones prior to surgery, assessing equivocal lymphadenopathies, and monitoring chemotherapy results. Likewise, it is expected to make follow-up easier by reducing the intensity of examinations and by sparing imaging procedures. Overall, the data presently available are promising, but further prospective studies are required before the test can be implemented in standard clinical care.

Indexed as

biomarkergerm cell tumorMicroRNAmiRNAtesticular cancer

Identifiers

PMID37568759
PMCPMC10417034
OpenAlexW4385555612

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.