Evidence map›Paper›PMID 38191608›Full record

ReviewBritish journal of cancer2024

Systemic anticancer therapy for urothelial carcinoma: UK oncologists' perspective.

Robert J Jones, Simon J Crabb, Mark Linch, Alison J Birtle, John McGrane, Deborah Enting, Robert Stevenson, Kin Liu, Bihani Kularatne, Syed A Hussain

Open access · hybridAbstract readReview
In one paragraph

Review in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
12.6field-weighted citation impact, top 1% 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.

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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

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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

10 authors at 10 institutions in 1 country.

Robert J JonesUniversity of Glasgow, Beatson West of Scotland Cancer Centre, Glasgow, UK.ORCID 0000-0002-2904-6980
Simon J CrabbSchool of Cancer Sciences, University of Southampton, Southampton, UK.ORCID 0000-0003-3521-9064
Mark LinchUCL Cancer Institute, University College London, London, UK.
Alison J BirtleRosemere Cancer Centre, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK.
John McGraneRoyal Cornwall Hospital NHS Trust, Truro, UK.
Deborah EntingGuy's and St Thomas' NHS Foundation Trust, London, UK.
Robert StevensonUniversity Hospital Birmingham, Birmingham, UK.
Kin LiuMerck Serono Ltd., an affiliate of Merck KGaA, Feltham, UK.
Bihani KularatnePfizer Ltd., Tadworth, UK.
Syed A HussainUniversity of Sheffield and Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK. syed.hussain@sheffield.ac.uk.ORCID 0000-0003-1552-511X
Beatson West of Scotland Cancer Centre · GBCRUK Lung Cancer Centre of Excellence · GBGuy's and St Thomas' NHS Foundation Trust · GBLancashire Teaching Hospitals NHS Foundation Trust · GBMerck (United Kingdom) · GBNIHR Surgical Reconstruction and Microbiology Research Centre · GBPfizer (United Kingdom) · GBRoyal Cornwall Hospital Trust · GBSheffield Teaching Hospitals NHS Foundation Trust · GBUniversity of Southampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Urothelial carcinoma (UC) is a common cancer associated with a poor prognosis in patients with advanced disease. Platinum-based chemotherapy has remained the cornerstone of systemic anticancer treatment for many years, and recent developments in the treatment landscape have improved outcomes. In this review, we provide an overview of systemic treatment for UC, including clinical data supporting the current standard of care at each point in the treatment pathway and author interpretations from a UK perspective. Neoadjuvant cisplatin-based chemotherapy is recommended for eligible patients with muscle-invasive bladder cancer and is preferable to adjuvant treatment. For first-line treatment of advanced UC, platinum-eligible patients should receive cisplatin- or carboplatin-based chemotherapy, followed by avelumab maintenance in those without disease progression. Among patients unable to receive platinum-based chemotherapy, immune checkpoint inhibitor (ICI) treatment is an option for those with programmed death ligand 1 (PD-L1)-positive tumours. Second-line or later treatment options depend on prior treatment, and enfortumab vedotin is preferred after prior ICI and chemotherapy, although availability varies between countries. Additional options include rechallenge with platinum-based chemotherapy, an ICI, or non-platinum-based chemotherapy. Areas of uncertainty include the optimal number of first-line chemotherapy cycles for advanced UC and the value of PD-L1 testing for UC.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Transitional CellUrinary Bladder NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenCisplatinHumansPlatinumUnited KingdomAntineoplastic Agents, ImmunologicalB7-H1 AntigenCisplatinPlatinum

Identifiers

PMID38191608
PMCPMC10951251
OpenAlexW4390661934

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.