Evidence map›Paper›PMID 42467100›Full record

ReviewWorld journal of urology2026

Neoadjuvant therapies for clear cell renal cell carcinoma: review of current evidence and future applications.

Thomas McMaster, Niall McVeigh, David C Chen, Abdullah Al-Khanaty, Kieran Sandhu, Jonathon Carll, Dixon T Woon, Declan G Murphy, Nathan Lawrentschuck, Lewis Au and 3 more

Abstract readReview
In one paragraph

Review in World journal of urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Thomas McMasterDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia. tom.mac.1996@outlook.com.ORCID http://orcid.org/0000-0002-8558-7028
Niall McVeighDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
David C ChenDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Abdullah Al-KhanatyDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Kieran SandhuDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Jonathon CarllDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Dixon T WoonDepartment of Surgery, University of Melbourne, Melbourne, VIC, Australia.
Declan G MurphyDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Nathan LawrentschuckDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Lewis AuDepartment of Oncology, University of Melbourne, Melbourne, VIC, Australia.
Muhammad AliDepartment of Radiation Oncology, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, VIC, Australia.
Shankar SivaDepartment of Radiation Oncology, Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, VIC, Australia.
Marlon PereraDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeNeoadjuvant systemic therapy for clear cell renal cell carcinoma (ccRCC) aim to improve oncological and survival outcomes in patients with high-risk disease. This review evaluates contemporary evidence for neoadjuvant and perioperative systemic therapies in ccRCC, with a focus on localised high-risk disease, venous tumour thrombus and metastatic or cytoreductive settings.

methodsA review of the literature was performed using PubMed, Embase and Web of Science from database inception to February 2026. Eligible studies included randomised controlled trials, prospective and retrospective clinical studies, and translational research evaluating neoadjuvant therapies in RCC. Evidence was synthesised by therapeutic class, with emphasis on prospective trials and clinically relevant outcomes.

resultsNeoadjuvant TKIs demonstrate mild to moderate tumour shrinkage and reduction in tumour thrombus burden, with a resultant improvement in operative complexity and an increase in the number of patients eligible for surgical intervention. ICI monotherapy has shown limited efficacy in early-phase studies. However, combination ICI-TKI regimens report higher objective response rates on interval imaging, with tumour downstaging and encouraging early disease-free survival results. Perioperative complication rates appear acceptable across studies, with no consistent increase in surgical morbidity. However, discordance between radiological and pathological responses remains a limitation. Translational studies further highlight the potential role of immune profiling, genomic biomarkers, microbiome modulation and theranostic approaches, although prospective validation remains lacking.

conclusionNeoadjuvant therapy in ccRCC is feasible and demonstrates promising early efficacy, particularly with combination regimens. However, current evidence is limited by heterogeneity and lack of long-term outcomes. Larger prospective trials incorporating translational endpoints are required to define optimal treatment strategies and establish survival benefit.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsNeoadjuvant TherapyHumansccRCCImmune checkpoint inhibitorsNeoadjuvant therapyTyrosine kinase inhibitors

Identifiers

PMID42467100
PMCPMC13379452

What OpenQuestion holds

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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.