Evidence map›Paper›PMID 36142631›Full record

ReviewInternational journal of molecular sciences2022

Malignant Transformation of Giant Cell Tumour of Bone: A Review of Literature and the Experience of a Referral Centre.

Sabrina Vari, Federica Riva, Concetta Elisa Onesti, Antonella Cosimati, Davide Renna, Roberto Biagini, Jacopo Baldi, Carmine Zoccali, Vincenzo Anelli, Alessio Annovazzi and 4 more

Abstract readCase ReportsReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  9. Frontiers in medicine · 2025
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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

14 authors.

Sabrina VariUOSD Sarcomas and Rare Tumors, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Federica RivaUOSD Sarcomas and Rare Tumors, IRCCS Regina Elena National Cancer Institute, Sapienza University of Rome, 00144 Rome, Italy.
Concetta Elisa OnestiUOSD Sarcomas and Rare Tumors, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.ORCID 0000-0002-8360-5026
Antonella CosimatiUOSD Sarcomas and Rare Tumors, IRCCS Regina Elena National Cancer Institute, Sapienza University of Rome, 00144 Rome, Italy.
Davide RennaUOSD Sarcomas and Rare Tumors, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.ORCID 0000-0002-1688-3210
Roberto BiaginiOncological Orthopaedics Unit, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Jacopo BaldiOncological Orthopaedics Unit, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Carmine ZoccaliOncological Orthopaedics Unit, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Vincenzo AnelliRadiology Department, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Alessio AnnovazziNuclear Medicine Department, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Renato CovelloDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.ORCID 0000-0001-8505-4427
Andrea AscioneDepartment of Radiological, Oncological and Pathological Sciences, Sapienza University of Rome, Policlinico Umberto I, 00161 Rome, Italy.
Beatrice CasiniDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
Virginia FerraresiUOSD Sarcomas and Rare Tumors, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Giant cell tumour of bone (GCTB) is a benign, locally aggressive primary bone neoplasm that represents 5% of all bone tumours. The principal treatment approach is surgery. Although generally GCTB is considered only a locally aggressive disease, it can metastasise, and lung metastases occur in 1-9% of patients. To date, only the use of denosumab has been approved as medical treatment for GCTB. Even more rarely, GCTB undergoes sarcomatous transformation into a malignant tumour (4% of all GCTB), but history of this malignant transformation is unclear and unpredictable. Considering the rarity of the event, the data in the literature are few. In this review, we summarise published data of GCTB malignant transformation and we analyse three cases of malignant transformation of GCTB, evaluating histopathology, genetics, and radiological aspects. Despite the rarity of this event, we conclude that a strict follow up is recommended to detect early malignant transformation.

Indexed as

Bone NeoplasmsGiant Cell Tumor of BoneCell Transformation, NeoplasticDenosumabHumansReferral and ConsultationDenosumabbone sarcomadenosumabdiagnosisgiant cell tumour of boneH3F3Amalignant transformationradiological features

Identifiers

PMID36142631
PMCPMC9506170

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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.