Evidence map›Paper›PMID 30510970›Full record

ArticleAmerican journal of clinical and experimental urology2018

NKX3.1 and PSMA are sensitive diagnostic markers for prostatic carcinoma in bone metastasis after decalcification of specimens.

Hongying Huang, Sergei R Guma, Jonathan Melamed, Ming Zhou, Peng Lee, Fang-Ming Deng

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In one paragraph

Article in American journal of clinical and experimental urology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 16 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

6 authors at 1 institution in 1 country.

Hongying HuangDepartment of Pathology, School of Medicine, New York University New York, NY, USA.
Sergei R GumaDepartment of Pathology, School of Medicine, New York University New York, NY, USA.
Jonathan MelamedDepartment of Pathology, School of Medicine, New York University New York, NY, USA.
Ming ZhouDepartment of Pathology, School of Medicine, New York University New York, NY, USA.
Peng LeeDepartment of Pathology, School of Medicine, New York University New York, NY, USA.
Fang-Ming DengDepartment of Pathology, School of Medicine, New York University New York, NY, USA.
New York University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate specific antigen (PSA), prostate specific membrane antigen (PSMA), and NKX3.1 are sensitive and prostate-specific markers frequently used for the diagnosis of metastatic prostate cancer (mPCa). International Society of Urological Pathology recommends use of PSA as the initial immunohistochemical (IHC) marker to identify PCa. If the tumor is equivocal/weak/negative for PSA, then P501S and NKX3.1 stains are suggested. However, no specific studies have attempted to compare the staining sensitivity of these markers post specimen decalcification of bone specimens. In this study, we analyze the staining sensitivity of PSA, PSMA and NKX3.1 in bone specimens with mPCa after decalcification.

designWe studied 24 cases of mPCa to the bone. All cases were decalcified for 24 to 48 hours prior to H&E staining and IHC workup. Eight cases were biopsies from vertebral bodies, five were from the femur, four came from the iliac bone, two were from ribs, three were from the pubic ramus, one was from the sacrum and one was from the skull. IHC staining pattern of PSA, PSMA and NKX3.1 was defined as follows: negative (no staining), focally positive (≤ 10%) and diffusely positive (≥ 10%). Focal and diffuse positivity are both considered positive.

resultsPSA was positive in 64% (14/22) cases, while PSMA and NKX3.1 were positive in all cases (17/17 and 24/24, respectively). The frequency of positive PSMA staining in decalcified samples of prostatic carcinoma metastatic to the bone is statistically higher than that of PSA staining, when analyzed by the Chi-square test (Chi-square statistic: 5.389; P = 0.0203). The frequency of positive NKX3.1 staining in decalcified samples of prostatic carcinoma metastatic to the bone is also statistically higher than that of PSA staining, when analyzed by the Chi-square test (Chi-square statistic: 10.56; P = 0.0012). When comparing PSMA and NKX3.1 positive staining, NKX3.1 tended to be diffusely positive at a higher frequency. However, this difference was not statistically significant.

conclusionThis study demonstrates that PSMA and NKX3.1 are more sensitive markers than PSA for mPCa to the bone following decalcification. We recommend use of PSMA and NKX3.1, rather than PSA, as the IHC markers to confirm mPCa to the bone.

Indexed as

bone metastasisNKX3.1prostatic carcinomaPSMA

Identifiers

PMID30510970
PMCPMC6261873
OpenAlexW2991202971

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.