Evidence map›Paper›PMID 33291528›Full record

ArticleJournal of personalized medicine2020

Oligometastatic Prostate Adenocarcinoma. Clinical-Pathologic Study of a Histologically Under-Recognized Prostate Cancer.

Claudia Manini, Alba González, David Büchser, Jorge García-Olaverri, Arantza Urresola, Ana Ezquerro, Iratxe Fernández, Roberto Llarena, Iñaki Zabalza, Rafael Pulido and 3 more

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2020. 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
–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

3 citing papers in PubMed.

  1. Review
  2. Review
  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

13 authors.

Claudia ManiniDepartment of Pathology, San Giovanni Bosco Hospital, 10154 Turin, Italy.
Alba GonzálezDepartment of Radiation Oncology, Cruces University Hospital, 48903 Barakaldo, Spain.
David BüchserDepartment of Radiation Oncology, Cruces University Hospital, 48903 Barakaldo, Spain.
Jorge García-OlaverriDepartment of Urology, Cruces University Hospital, 48903 Barakaldo, Spain.
Arantza UrresolaDepartment of Radiodiagnostics, Cruces University Hospital, 48903 Barakaldo, Spain.
Ana EzquerroDepartment of Radiodiagnostics, Cruces University Hospital, 48903 Barakaldo, Spain.
Iratxe FernándezDepartment of Nuclear Medicine, Cruces University Hospital, 48903 Barakaldo, Spain.
Roberto LlarenaDepartment of Urology, Cruces University Hospital, 48903 Barakaldo, Spain.
Iñaki ZabalzaDepartment of Pathology, Galdakao Hospital, 48960 Galdakao, Spain.
Rafael PulidoBiocruces-Bizkaia Health Research Institute, 48903 Barakaldo, Spain.ORCID 0000-0001-9100-248X
Arkaitz CarracedoIkerbasque, The Basque Foundation for Science, 48009 Bilbao, Spain.ORCID 0000-0001-5957-1260
Alfonso Gómez-IturriagaDepartment of Radiation Oncology, Cruces University Hospital, 48903 Barakaldo, Spain.
José I LópezBiocruces-Bizkaia Health Research Institute, 48903 Barakaldo, Spain.ORCID 0000-0003-0842-5348

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical parameters and the histological and immunohistochemical findings of a prospective protocolized series of 27 prostate carcinoma patients with oligometastatic disease followed homogeneously were analyzed. Lymph nodes (81.5%) and bones (18.5%) were the only metastatic sites. Local control after metastatic directed treatment was achieved in 22 (81.5%) patients. A total of 8 (29.6%) patients developed castration-resistant prostate cancer. Seventeen (63%) patients presented with non-organ confined disease. The Gleason index 8-10 was the most frequently observed (12 cases, 44.4%) combined grade. Positive immunostainings were detected with androgen receptor (100%), PGP 9.5 (74%), ERG (40.7%), chromogranin A (29.6%), and synaptophysin (18.5%) antibodies. The Ki-67 index value > 5% was observed in 15% of the cases. L1CAM immunostaining was negative in all cases. Fisher exact test showed that successful local control of metastases was associated to mild inflammation, organ confined disease, Ki-67 index < 5%, and Gleason index 3 + 3. A castration resistant status was associated with severe inflammation, atrophy, a Gleason index higher than 3 + 3, Ki-67 index ≥ 5%, and positive PGP 9.5, chromogranin A, and synaptophysin immunostainings. In conclusion, oligometastatic prostate adenocarcinoma does not have a specific clinical-pathologic profile. However, some histologic and immunohistochemical parameters of routine use may help with making therapeutic decisions.

Indexed as

atrophygleason indexhistopathologyimmunohistochemistryinflammationoligometastatic diseasepathologic stagingprognosisprostate cancer

Identifiers

PMID33291528
PMCPMC7761807

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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.