Evidence map›Paper›PMID 30740581›Full record

ArticleKidney cancer (Clifton, Va.)2018

What Survival Benefits are Needed to Make Adjuvant Sorafenib Worthwhile After Resection of Intermediate- or High-Risk Renal Cell Carcinoma? Clinical Investigators' Preferences in the SORCE Trial.

Nicola J Lawrence, Andrew Martin, Ian D Davis, Simon Troon, Shomik Sengupta, Elizabeth Hovey, Xanthi Coskinas, Richard Kaplan, Benjamin Smith, Alastair Ritchie and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Kidney cancer (Clifton, Va.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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  5. 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

14 authors at 9 institutions in 2 countries.

Nicola J LawrenceNHMRC Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.
Andrew MartinNHMRC Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.
Ian D DavisAustralian and New Zealand Urogenital and Prostate Cancer Trials Group, Sydney, NSW, Australia.
Simon TroonFiona Stanley Hospital, Perth, WA, Australia.
Shomik SenguptaAustralian and New Zealand Urogenital and Prostate Cancer Trials Group, Sydney, NSW, Australia.
Elizabeth HoveyAustralian and New Zealand Urogenital and Prostate Cancer Trials Group, Sydney, NSW, Australia.
Xanthi CoskinasNHMRC Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.
Richard KaplanMRC Clinical Trials Unit, University College London, London, UK.
Benjamin SmithMRC Clinical Trials Unit, University College London, London, UK.
Alastair RitchieGloucestershire Royal Hospital, Gloucester, UK.
Angela MeadeMRC Clinical Trials Unit, University College London, London, UK.
Tim EisenCambridge University Hospital NHS Foundation Trust, Cambridge, UK.
Prunella BlinmanAustralian and New Zealand Urogenital and Prostate Cancer Trials Group, Sydney, NSW, Australia.
Martin R StocklerNHMRC Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.
The University of Sydney · AUMRC Clinical Trials Unit at UCL · GBCambridge University Hospitals NHS Foundation Trust · GBConcord Repatriation General Hospital · AUEastern Health · AUFiona Stanley Hospital · AUGloucestershire Royal Hospital · GBThe University of Melbourne · AUUNSW Sydney · AU

Funding

Cancer Research UK 6858Medical Research Council MC_U122861326Medical Research Council MC_UU_12023/20Medical Research Council MC_UU_12023/4
6 · The paper itself

Abstract

backgroundDecisions about adjuvant therapy involve trade-offs between possible benefits and harms.

objectiveWe sought to determine the survival benefits that clinical investigators would judge as sufficient to warrant treatment with adjuvant sorafenib in the SORCE trial after nephrectomy for apparently localised renal cell carcinoma (RCC).

methodsA subset of clinical investigators in the SORCE trial completed a validated questionnaire that elicited the minimum survival benefits they judged sufficient to warrant one year of adjuvant sorafenib in scenarios with hypothetical baseline survival times of 5 years and 15 years, and baseline survival rates at 5 years of 65% and 85%.

resultsThe 100 participating SORCE investigators had a median age of 42 years, and 74 were male. For one year of sorafenib versus no therapy, the median benefits in survival times the investigators judged sufficient to warrant treatment were an extra nine months beyond five years and an extra 12 months beyond 15 years; the median benefits in survival rates were an extra 5% beyond baseline survival rates of both 65% and 85% at five years. The patients recruited in the SORCE trial by these investigators judged smaller benefits sufficient to warrant adjuvant sorafenib for both survival rate scenarios (

conclusionSORCE investigators judged larger benefits necessary to warrant adjuvant sorafenib than their patients. The benefits required by the investigators were similar or smaller than those other clinicians considered sufficient to warrant adjuvant chemotherapy for other cancers. Clinicians should recognise that their patients and colleagues may have preferences that differ from their own when considering the potential benefits and harms of adjuvant treatment.

Indexed as

adjuvant therapydecision makinginvestigators’ preferencesRenal cell carcinomasorafenib

Identifiers

PMID30740581
PMCPMC6364092
OpenAlexW2883461158

What OpenQuestion holds

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LicenceCC BY-NC
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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.