Evidence map›Paper›PMID 39301179›Full record

ArticleJCEM case reports2024

A Potential Role for Nivolumab in the Treatment of Fibrous Dysplasia-Related Pain.

Mohammad Jay, Cassandra Hawco, Kristin K Clemens, Stan Van Uum

Abstract readCase Reports
In one paragraph

Article in JCEM case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Mohammad JayDivision of Endocrinology, Department of Medicine, University of Toronto, Toronto, ON M5S 1A1, Canada.ORCID https://orcid.org/0009-0002-7299-4342
Cassandra HawcoDivision of Endocrinology, Department of Medicine, Western University, London, ON N6A 5C1, Canada.
Kristin K ClemensDivision of Endocrinology, Department of Medicine, Western University, London, ON N6A 5C1, Canada.
Stan Van UumDivision of Endocrinology, Department of Medicine, Western University, London, ON N6A 5C1, Canada.ORCID https://orcid.org/0000-0002-0150-8223

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrous dysplasia (FD) is a chronic and progressive disorder of bone growth because of decreased osteoblast formation and osteoclast overactivity. Its main symptoms include pain, fracture, and irregular bone growth. Bisphosphonates are the mainstay of therapy for FD with a primary goal of pain relief. A 50-year-old woman presented to ophthalmology in March 2011 with intermittent proptosis, vertical diplopia, and orbital pain. A computed tomography scan of the head revealed a skull base lesion, which was confirmed to be fibrous dysplasia on bone biopsy. Because of significant headache, she was treated with IV pamidronate monthly starting November 2011, which led to pain reduction. Repeated attempts to decrease the frequency of pamidronate were unsuccessful because of breakthrough pain. Oral alendronate and risedronate did not control her symptoms. She remained on risedronate however because of its convenience. In August 2021, she was diagnosed with metastatic melanoma and started nivolumab. Her headache completely resolved for the first time in 10 years. Although nivolumab, a programmed death-1 blocker, has been used in the treatment of bone malignancy, it has not been previously studied in FD. By suppressing RANK ligand-related osteoclastogenesis, nivolumab decreases cancer-associated bone pain. Our case suggests a potential role for nivolumab in treating FD-associated pain.

Indexed as

fibrous dysplasianivolumabRANK ligand

Identifiers

PMID39301179
PMCPMC11408923

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