Evidence map›Paper›PMID 37247180›Full record

ArticleJournal of neuro-oncology2023

Identification of incidental brain tumors in prostate cancer patients via PSMA PET/CT.

Lily A McLaughlin, Onur Yildirim, Marc K Rosenblum, Brandon S Imber, Justin M Haseltine, Michael J Zelefsky, Heiko Schöder, Michael J Morris, William M Rafelson, Simone Krebs and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of neuro-oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 21 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

11 authors at 1 institution in 1 country.

Lily A McLaughlinGeorgetown University School of Medicine, Washington, DC, USA.
Onur YildirimDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Marc K RosenblumDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Brandon S ImberDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Justin M HaseltineDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Michael J ZelefskyDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Heiko SchöderDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Michael J MorrisDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
William M RafelsonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Simone KrebsDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Nelson S MossDepartment of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA. mossn@mskcc.org.ORCID http://orcid.org/0000-0002-0930-1681
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeBrain metastases are rare in patients with prostate cancer and portend poor outcome. Prostate-specific membrane antigen positron emission tomography (PSMA PET)/CT scans including the brain have identified incidental tumors. We sought to identify the incidental brain tumor detection rate of PSMA PET/CT performed at initial diagnosis or in the setting of biochemical recurrence.

methodsAn institutional database was queried for patients who underwent

resultsTwo-thousand seven hundred and sixty-three patients underwent 3363 PSMA PET/CT scans in the absence of neurologic symptoms. Forty-four brain lesions were identified, including 33 PSMA-avid lesions: 10 intraparenchymal metastases (30%), 4 dural-based metastases (12%), 16 meningiomas (48%), 2 pituitary macroadenomas (6%), and 1 epidermal inclusion cyst (3%) (incidences of 0.36, 0.14, 0.58, 0.07, and 0.04%). The mean parenchymal metastasis diameter and mean SUVmax were 1.99 cm (95%CI:1.25-2.73) and 4.49 (95%CI:2.41-6.57), respectively. At the time of parenchymal brain metastasis detection, 57% of patients had no concurrent extracranial disease, 14% had localized prostate disease only, and 29% had extracranial metastases. Seven of 8 patients with parenchymal brain metastases remain alive at a median 8.8 months follow-up.

conclusionProstate cancer brain metastases are rare, especially in the absence of widespread metastatic disease. Nevertheless, incidentally detected brain foci of PSMA uptake may represent previously unknown prostate cancer metastases, even in small lesions and in the absence of systemic disease.

Indexed as

Brain NeoplasmsProstatic NeoplasmsHumansMalePositron-Emission TomographyPositron Emission Tomography Computed Tomography18F-piflufolastat68Ga-PSMA-11Brain metastasisProstate cancerPSMA PET/CT scan

Identifiers

PMID37247180
PMCPMC10746351
OpenAlexW4378640486

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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.