Evidence map›Paper›PMID 39886173›Full record

ArticleBMJ oncology2024

Tale of two zones: investigating the clinical outcomes and research gaps in peripheral and transition zone prostate cancer through a systematic review and meta-analysis.

Amin Ali, Thiraviyam Elumalai, BhanuPrasad Venkatesulu, Lauren Hekman, Hitesh Mistry, Ashwin Sachdeva, Pedro Oliveira, Noel Clarke, Esther Baena, Ananya Choudhury and 1 more

Abstract read
In one paragraph

Article in BMJ oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

11 authors.

Amin AliOncology Department, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK.ORCID 0000-0003-4876-0626
Thiraviyam ElumalaiOncology Department, Addenbrooke's Hospital, Cambridge, UK.
BhanuPrasad VenkatesuluRadiation Oncology Department, Loyola University Chicago, Chicago, Illinois, USA.
Lauren HekmanDepartment of Urology, Loyola University Chicago, Chicago, Illinois, USA.
Hitesh MistrySchool of Health Sciences, The University of Manchester, Manchester, UK.
Ashwin SachdevaDepartment of Surgery, The Christie Hospital NHS Trust, Manchester, UK.
Pedro OliveiraDepartment of Pathology, The Christie Hospital NHS Trust, Manchester, UK.
Noel ClarkeDepartment of Surgery, The Christie Hospital NHS Trust, Manchester, UK.
Esther BaenaProstate Oncobiology, Cancer Research UK Manchester Centre, The University of Manchester, Manchester, UK.
Ananya ChoudhuryDepartment of Clinical Oncology, The Christie NHS Foundation Trust, Manchester, UK.
Robert G BristowTranslational Oncogenomics, Cancer Research UK Manchester Centre, The University of Manchester, Manchester, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To assess pathological characteristics, clinical features and outcomes of patients diagnosed with peripheral zone (PZ) and transition zone (TZ) prostate cancer after prostatectomy. Methods and analysis: We systematically reviewed PubMed, EMBASE and MEDLINE. Primary endpoints were biochemical relapse-free survival (bRFS) and distant metastases rate; secondary endpoints included clinical and pathological features. Results: Ten retrospective cohort studies were identified, six reported HRs for bRFS between PZ and TZ tumours. Patients with TZ tumours had significantly better bRFS (pooled HR 0.57 (0.47, 0.68)) than those with PZ tumours. Two studies reported a lower proportion of distant metastasis in patients diagnosed with TZ tumours compared with PZ tumours (1.5% vs 4.9% (median follow-up 7.0 years) and 0% vs 5% (median follow-up 7.8 years)). PZ tumours presented higher Gleason group and T staging more frequently, while TZ tumours were associated with higher prostate specific antigen levels at diagnosis. Conclusion: PZ tumours were associated with poorer prognostic clinical features and outcomes. Despite adjusting for poor prognostic clinical features, PZ tumours consistently showed worse clinical outcomes than TZ tumours. Our systematic review underscores the need for further research comparing PZ and TZ prostate cancer to understand the underlying differences and refine clinical practice.

Indexed as

Prostate cancer

Identifiers

PMID39886173
PMCPMC11234997

What OpenQuestion holds

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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.