Evidence map›Paper›PMID 29709495›Full record

ArticleHuman pathology2018

Morphological changes induced by intraprostatic PSA-based vaccine in prostate cancer biopsies (phase I clinical trial).

Maria J Merino, Peter A Pinto, Vanessa Moreno, Sara Gil, Jeffrey Schlom, James L Gulley

Open access · greenAbstract read
In one paragraph

Article in Human pathology, 2018. 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
0.1field-weighted citation impact, top 55% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
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.

Maria J MerinoTranslational Surgical Pathology, Laboratory of Pathology, CCR, NCI, NIH, Bethesda, MD 20892. Electronic address: mjmerino@mail.nih.gov.
Peter A PintoUrologic Oncology Branch, CCR, NCI, NIH, Bethesda, MD 20892.
Vanessa MorenoTranslational Surgical Pathology, Laboratory of Pathology, CCR, NCI, NIH, Bethesda, MD 20892.
Sara GilTranslational Surgical Pathology, Laboratory of Pathology, CCR, NCI, NIH, Bethesda, MD 20892.
Jeffrey SchlomLaboratory of Tumor Immunology and Biology, CCR, NCI, NIH, Bethesda, MD 20892.
James L GulleyLaboratory of Tumor Immunology and Biology, CCR, NCI, NIH, Bethesda, MD 20892.
Center for Cancer Research · US

Funding

Human T Cell Responses to Tumor Antigens for Cancer Vaccine DevelopmentZIABC010598 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SCHLOM, JEFFREY · 2009 to 2025
$19.3M
miRNA profiling of prostate cancer in young and older male patientsZIABC011406 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MERINO, MARIA · 2011 to 2023
$1.8M
Vaccine Clinical TrialsZ01BC010666 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GULLEY, JAMES L. · 2005 to 2008
$1.7M
Clinical trials employing cancer vaccine combination therapiesZ01BC010945 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GULLEY, JAMES L. · 2008 to 2008
$517k
Intramural NIH HHS Z01 BC010666Intramural NIH HHS Z01 BC010945Intramural NIH HHS ZIA BC011406
6 · The paper itself

Abstract

Immunotherapy is a novel treatment for many tumors including prostate cancer. Little is known about the histological changes in prostate biopsies caused by the prostate-specific antigen (PSA)-based vaccine. This study evaluated the histopathological effects in prostate biopsies of recombinant fowlpox (rF) virus-based vaccine engineered to present the PSA and 3 costimulatory molecules (collectively labeled as PSA-TRICOM). This vaccine has shown that it can break tolerance of the PSA, and its administration directly into a tumor enables the affected tumor cells to act as antigen-presenting cells activating new T cells and broadening the immune response to recognize and kill tumor. We studied 10 patients with recurrent prostate cancer who had failed radiation therapy and/or androgen-deprivation therapy. Pre- and posttreatment biopsies were compared. Posttreatment biopsies induced 8 cases with residual adenocarcinoma despite evidences of treatment effect and inflammation, 2 cases did not show any residual tumor, and 1 one case did not have any inflammatory infiltrate or any evidence of treatment effect. The inflammatory infiltrate varied from mild to severe and was composed of mononuclear cells. Greater numbers of infiltrating CD8+ lymphocytes were identified around prostatic glands and within the epithelial lining. The most remarkable feature was the presence of increased eosinophils around the glands and stroma. Three cases showed areas of necrosis surrounded by lymphocytes and palisading epithelioid macrophages arranged in granuloma-like pattern with multinucleated giant cells. This description of these morphological changes induced by the PSA-TRICOM will help to interpret the results of future intratumoral vaccine therapy trials.

Indexed as

AdenocarcinomaAgedBiopsyHumansMaleMiddle AgedNeoplasm Recurrence, LocalProstateProstate-Specific AntigenProstatic NeoplasmsVaccinesProstate-Specific AntigenVaccinesEosinophilsInflammationProstate adenocarcinomaPSA-based vaccinationTreatment effect

Identifiers

PMID29709495
PMCPMC8054308
OpenAlexW2802695018

What OpenQuestion holds

Textmetadata
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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.