Evidence map›Paper›PMID 41280159›Full record

ReviewEuropean urology open science2025

Genetic Testing and Counselling for Hereditary Renal Carcinoma: What Do Clinicians Need to Know?

Chiara Re, Angela Pecoraro, Grant D Stewart, Anna Caliò, Selcuk Erdem, Tugba Kalayci, Zehra Oya Uyguner, Alessandro Larcher, Riccardo Campi, Daniele Amparore and 3 more

Abstract readReview
In one paragraph

Review in European urology open science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Review
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

13 authors.

Chiara ReDivision of Experimental Oncology, Unit of Urology; Urological Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Angela PecoraroDepartment of Urology, Pederzoli Hospital, Peschiera del Garda, Italy.
Grant D StewartDepartment of Surgery, University of Cambridge, Cambridge Biomedical Centre, Cambridge, UK.
Anna CaliòDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Selcuk ErdemDivision of Urologic Oncology, Department of Urology, Istanbul University, Istanbul, Turkey.
Tugba KalayciDepartment of Medical Genetics, Istanbul University, Istanbul, Turkey.
Zehra Oya UygunerDepartment of Medical Genetics, Istanbul University, Istanbul, Turkey.
Alessandro LarcherDivision of Experimental Oncology, Unit of Urology; Urological Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Riccardo CampiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Daniele AmparoreDepartment of Oncology, University of Turin, Orbassano, Turin, Italy.
James WhitworthCancer Research UK Cambridge Centre, Cambridge Biomedical Campus, Cambridge, UK.
Laura MarandinoDepartment of Medical Oncology, The Royal Marsden NHS Foundation Trust, London, UK.
European Association of Urology Young Academic Urologists Renal Cancer Working Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and objective: Hereditary renal cell carcinoma (H-RCC) accounts for 5-8% of kidney cancers and has important clinical implications. However, H-RCC is frequently underdiagnosed, and genetic counselling is underutilised in clinical practice. This review provides an overview of the main H-RCC syndromes and offers a step-by-step clinical guide to support clinicians in the identification, counselling, and management of affected individuals. Methods: A nonsystematic search of PubMed/MEDLINE was performed in June 2024 and updated in February 2025, covering guidelines, consensus statements, and original studies. Additional sources were identified via manual reference screening. Key findings and limitations: Although H-RCC syndromes may present with overlapping features, they vary significantly in genetics, histology, and aggressiveness. While referral criteria for genetic testing in RCC are outlined in multiple international guidelines, certain criteria are still debated. Genetic counselling is essential both before and after testing. Pretest counselling ensures informed consent and helps patients to understand the implications of results. Post-test counselling discusses medical and psychological implications, and guides cascade testing for at-risk relatives. Mainstream genetic testing led by clinicians other than genetic specialists is increasingly adopted, but adequate training and structured collaboration with genetics services are required. Clinical management differs across syndromes: while aggressive entities such as FH-associated RCC warrant prompt surgical intervention, others such as clear-cell RCC associated with von Hippel-Lindau disease benefit from active surveillance, with nephron-sparing approaches typically recommended when the largest tumour reaches a threshold of 3 cm to balance oncological control and renal preservation. The main limitation of this review is its nonsystematic design. Conclusions and clinical implications: Genetic assessment is a key component of RCC management. Enhancement of clinician awareness and fostering of multidisciplinary collaboration are key to improving care and outcomes. Patient summary: For patients with kidney cancer, genetic risk assessment and testing are crucial for improving patient care, guiding surveillance, and offering tailored treatments to those who might have a hereditary form of cancer. Collaboration among different specialists is vital to provide the best care for patients with hereditary kidney cancer syndromes.

Indexed as

Genetic counsellingGenetic testingGermline variantHereditary syndromeRecommendationsRenal cell carcinoma

Identifiers

PMID41280159
PMCPMC12630327

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.