Evidence map›Paper›PMID 37357741›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2023

SS18-SSX Antibody: A Useful Tool to Save Time and Reduce Costs in Synovial Sarcoma Diagnosis. Proposal of a Novel Diagnostic Algorithm.

Giulia Orlando, Federica Santoro, Alessandra Linari, Cristian Tampieri, Ludovica Verdun di Cantogno, Simone De Meo, Nicola Ratto, Giovanni Grignani, Mauro Papotti, Rebecca Senetta

Open access · bronzeAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 4 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

10 authors at 2 institutions in 1 country.

Giulia OrlandoPathology Unit, Department of Oncology, Città della Salute e della Scienza Hospital, University of Turin, Turin, Italy.ORCID 0000-0002-8917-0246
Federica SantoroPathology Unit, Department of Medical Sciences, Città della Salute e della Scienza Hospital, University of Turin, Turin, Italy.ORCID 0000-0002-4048-1078
Alessandra LinariPathology Unit, Città della Salute e della Scienza Hospital, Turin, Italy.
Cristian TampieriPathology Unit, Department of Medical Sciences, Città della Salute e della Scienza Hospital, University of Turin, Turin, Italy.ORCID 0000-0002-6515-7338
Ludovica Verdun di CantognoPathology Unit, Città della Salute e della Scienza Hospital, Turin, Italy.
Simone De MeoFondazione per la ricerca sui tumori dell'apparato muscoloscheletrico e rari Onlus, Turin, Italy.ORCID 0000-0001-7542-8077
Nicola RattoOrthopaedic Oncological Surgery, Città della Salute e della Scienza Hospital, Turin, Italy.
Giovanni GrignaniMedical Oncology Unit, Città della Salute e della Scienza Hospital, Turin, Italy.
Mauro PapottiPathology Unit, Department of Oncology, Città della Salute e della Scienza Hospital, University of Turin, Turin, Italy.
Rebecca SenettaPathology Unit, Department of Oncology, Città della Salute e della Scienza Hospital, University of Turin, Turin, Italy.ORCID 0000-0001-8419-4591
University of Turin · ITAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synovial sarcoma is a rare malignant mesenchymal neoplasm mostly affecting young adults, characterized by a specific translocation which results in the fusion of the SS18 gene on chromosome 18 with one of the three highly homologous SSX genes on chromosome X. Its morphological diagnosis, especially in monophasic or poorly differentiated variants, can be challenging because histological features often overlap with other malignant mesenchymal tumors. Until recently, the differential diagnosis mostly relied on the use of cytogenetic or molecular analyses to detect the specific t(X;18)(p11;q11) translocation, thus virtually restricting its correct identification to referral centers with a high histological and molecular pathology workflow. The recently commercialized highly sensitive and fusion-specific SS18-SSX antibody has significantly improved the approach to these tumors, representing a relatively cheap and easy to access tool for synovial sarcoma diagnosis. Through a retrospective analysis of 79 synovial sarcomas and histological mimickers, this study confirms the usefulness of the SS18-SSX antibody in the diagnosis of synovial sarcoma, particularly focusing on its application in the pathological response evaluation after neoadjuvant treatment as well as its time- and cost-saving advantages. Finally, we here propose a new diagnostic algorithm to apply into the routine practice.

Indexed as

Repressor ProteinsSarcoma, SynovialAlgorithmsAntibodiesHumansOncogene Proteins, FusionProto-Oncogene ProteinsRetrospective StudiesYoung AdultAntibodiesOncogene Proteins, FusionProto-Oncogene ProteinsRepressor Proteinsdiagnosisfluorescent in situ hybridizationimmunohistochemistryneoadjuvant treatment response

Identifiers

PMID37357741
PMCPMC10363909
OpenAlexW4382011738

What OpenQuestion holds

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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.