Evidence map›Paper›PMID 26442515›Full record

ArticleMedical oncology (Northwood, London, England)2015

Clinicopathologic characteristics of anterior prostate cancer (APC), including correlation with previous biopsy pathology.

Martin J Magers, Tianyu Zhan, Aaron M Udager, John T Wei, Scott A Tomlins, Angela J Wu, Lakshmi P Kunju, Madelyn Lew, Felix Y Feng, Daniel A Hamstra and 10 more

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

20 authors at 3 institutions in 1 country.

Martin J MagersDepartment of Pathology, University of Michigan Health System, Room 2G332 UH, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Tianyu ZhanDepartment of Biostatistics, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI, 48109, USA.
Aaron M UdagerDepartment of Pathology, University of Michigan Health System, Room 2G332 UH, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
John T WeiDepartment of Urology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Scott A TomlinsDepartment of Pathology, University of Michigan Health System, Room 2G332 UH, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Angela J WuDepartment of Pathology, University of Michigan Health System, Room 2G332 UH, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Lakshmi P KunjuDepartment of Pathology, University of Michigan Health System, Room 2G332 UH, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Madelyn LewDepartment of Pathology, University of Michigan Health System, Room 2G332 UH, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Felix Y FengDepartment of Radiation Oncology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Daniel A HamstraDepartment of Radiation Oncology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Javed SiddiquiDepartment of Pathology, University of Michigan Health System, Room 2G332 UH, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Arul M ChinnaiyanDepartment of Pathology, University of Michigan Health System, Room 2G332 UH, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Jeffrey S MontgomeryDepartment of Urology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Alon Z WeizerDepartment of Urology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Todd M MorganDepartment of Urology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Brent K HollenbeckDepartment of Urology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
David C MillerDepartment of Urology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Ganesh S PalapattuDepartment of Urology, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.
Hui JiangDepartment of Biostatistics, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI, 48109, USA.
Rohit MehraDepartment of Pathology, University of Michigan Health System, Room 2G332 UH, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA. mrohit@med.umich.edu.
Michigan Medicine · USUniversity of Michigan–Ann Arbor · USMichigan Center for Translational Pathology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anterior-predominant prostate cancer (APC) is an incompletely understood entity which can be difficult to sample via transrectal biopsy. Seemingly favorable biopsy results may belie the potential aggressiveness of these tumors. Here, we attempt to characterize APC by retrospectively examining the clinicopathologic features of APC at radical prostatectomy and comparing our findings with prior biopsy information. We found that 17.4 % of patients in our study had APC. APC demonstrated a significantly lower (P value < 0.05) Gleason score (GS) and pathologic stage than non-APC tumors, including the absence of seminal vesicle invasion by APC. A subset (5.6 %) of APC consisted of high-grade tumors (GS ≥ 8), and these tumors were more often detected on transperineal saturation biopsy than non-transperineal saturation (i.e., transrectal ultrasound guided) biopsy strategies. Four patients (7 %) without transperineal saturation biopsy exhibited a significantly worse GS at RP than biopsy, compared to five patients (36 %) with transperineal saturation biopsy. Our findings corroborate the difficulty in detecting APC and suggest that APC is not a uniform disease with a wholly indolent phenotype. Dedicated long-term outcome data are needed in these patients. Additionally, alternative pathologic staging parameters may be necessary.

Indexed as

BiopsyCohort StudiesHumansMaleMiddle AgedNeoplasm GradingProstateProstatic NeoplasmsRetrospective StudiesAnterior prostateBiopsyProstate cancerRadical prostatectomy

Identifiers

PMID26442515
OpenAlexW1954801305

What OpenQuestion holds

Textmetadata
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.