Evidence map›Paper›PMID 27431499›Full record

ArticleProstate cancer and prostatic diseases2016

PSA nadir as a predictive factor for biochemical disease-free survival and overall survival following whole-gland salvage HIFU following radiotherapy failure.

T T Shah, M Peters, A Kanthabalan, N McCartan, Y Fatola, J van der Voort van Zyp, M van Vulpen, A Freeman, C M Moore, M Arya and 2 more

Open access · hybridAbstract read
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Article in Prostate cancer and prostatic diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 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

12 authors at 3 institutions in 2 countries.

T T ShahDivision of Surgery and Interventional Science, UCL, London, UK.ORCID 0000-0003-1642-1208
M PetersDepartment of Radiation Oncology, University Medical Centre Utrecht, Utrecht, The Netherlands.
A KanthabalanDivision of Surgery and Interventional Science, UCL, London, UK.
N McCartanDivision of Surgery and Interventional Science, UCL, London, UK.
Y FatolaDivision of Surgery and Interventional Science, UCL, London, UK.
J van der Voort van ZypDepartment of Radiation Oncology, University Medical Centre Utrecht, Utrecht, The Netherlands.
M van VulpenDepartment of Radiation Oncology, University Medical Centre Utrecht, Utrecht, The Netherlands.
A FreemanDepartment of Histopathology, UCLH NHS Foundation Trust, London, UK.
C M MooreDivision of Surgery and Interventional Science, UCL, London, UK.
M AryaDepartment of Urology, UCLH NHS Foundation Trust, London, UK.
M EmbertonDivision of Surgery and Interventional Science, UCL, London, UK.
H U AhmedDivision of Surgery and Interventional Science, UCL, London, UK.
University College Hospital · GBUniversity Medical Center Utrecht · NLWhittington Hospital · GB

Funding

Medical Research Council G0701302Medical Research Council G1002509Medical Research Council MR/M009092/1Wellcome Trust
6 · The paper itself

Abstract

backgroundTreatment options for radio-recurrent prostate cancer are either androgen-deprivation therapy or salvage prostatectomy. Whole-gland high-intensity focussed ultrasound (HIFU) might have a role in this setting.

methodsAn independent HIFU registry collated consecutive cases of HIFU. Between 2005 and 2012, we identified 50 men who underwent whole-gland HIFU following histological confirmation of localised disease following prior external beam radiotherapy (2005-2012). No upper threshold was applied for risk category, PSA or Gleason grade either at presentation or at the time of failure. Progression was defined as a composite with biochemical failure (Phoenix criteria (PSA>nadir+2 ng ml(-1))), start of systemic therapies or metastases.

resultsMedian age (interquartile range (IQR)), pretreatment PSA (IQR) and Gleason score (range) were 68 years (64-72), 5.9 ng ml(-1) (2.2-11.3) and 7 (6-9), respectively. Median follow-up was 64 months (49-84). In all, 24/50 (48%) avoided androgen-deprivation therapies. Also, a total of 28/50 (56%) achieved a PSA nadir <0.5 ng ml(-1), 15/50 (30%) had a nadir ⩾0.5 ng ml(-1) and 7/50 (14%) did not nadir (PSA non-responders). Actuarial 1, 3 and 5-year progression-free survival (PFS) was 72, 40 and 31%, respectively. Actuarial 1, 3 and 5-year overall survival (OS) was 100, 94 and 87%, respectively. When comparing patients with PSA nadir <0.5 ng ml(-1), nadir ⩾0.5 and non-responders, a statistically significant difference in PFS was seen (P<0.0001). Three-year PFS in each group was 57, 20 and 0%, respectively. Five-year OS was 96, 100 and 38%, respectively. Early in the learning curve, between 2005 and 2007, 3/50 (6%) developed a fistula. Intervention for bladder outlet obstruction was needed in 27/50 (54%). Patient-reported outcome measure questionnaires showed incontinence (any pad-use) as 8/26 (31%).

conclusionsIn our series of high-risk patients, in whom 30-50% may have micro-metastases, disease control rates were promising in PSA responders, however, with significant morbidity. Additionally, post-HIFU PSA nadir appears to be an important predictor for both progression and survival. Further research on focal salvage ablation in order to reduce toxicity while retaining disease control rates is required.

Indexed as

AgedCombined Modality TherapyDisease ProgressionFollow-Up StudiesHigh-Intensity Focused Ultrasound AblationHumansMaleMiddle AgedMultimodal ImagingNeoplasm GradingPrognosisProstate-Specific AntigenProstatic NeoplasmsRadiotherapy, AdjuvantSurvival AnalysisTreatment OutcomeProstate-Specific Antigen

Identifiers

PMID27431499
PMCPMC4983180
OpenAlexW2505378956

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.