Evidence map›Paper›PMID 36006054›Full record

Observational studyJournal of surgical oncology2022

A prospective real-world study of the diffuse-type tenosynovial giant cell tumor patient journey: A 2-year observational analysis.

Nicholas M Bernthal, John H Healey, Emanuela Palmerini, Sebastian Bauer, Hendrik Schreuder, Andreas Leithner, Javier Martin-Broto, Francois Gouin, Julio Lopez-Bastida, Hans Gelderblom and 8 more

Open access · hybridAbstract readObservational StudyMulticenter Study
PubMed Publisher
In one paragraph

Observational study in Journal of surgical oncology, 2022. 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
2.0field-weighted citation impact, top 13% 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, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Observational
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

18 authors at 12 institutions in 8 countries.

Nicholas M BernthalDivision of Musculoskeletal Oncology, David Geffen School of Medicine at UCLA, Santa Monica, California, USA.ORCID http://orcid.org/0000-0003-3338-5878
John H HealeyDepartment of Surgery, Orthopaedic Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID http://orcid.org/0000-0002-0802-1186
Emanuela PalmeriniOsteoncology, Bone and Soft Tissue Sarcomas and Innoviative Therapies Unit, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.ORCID http://orcid.org/0000-0003-3406-6705
Sebastian BauerDepartment of Medical Oncology, Sarcoma Center, West German Cancer Center, University of Duisburg-Essen, Essen, Germany.
Hendrik SchreuderDepartment of Orthopaedics, Radboud University, Nijmegen, The Netherlands.
Andreas LeithnerDeptartment of Orthopaedics and Trauma, Medical University of Graz, Graz, Austria.
Javier Martin-BrotoOncology Department, Fundacíon Jiménez Díaz University Hospital, Madrid, Spain.
Francois GouinDepartment of Surgery, Onco-Orthopedic, Centre Léon Bérard, Lyon, France.
Julio Lopez-BastidaFaculty of Health Sciences, University Castilla-La Mancha, Talavera de la Reina, Spain.
Hans GelderblomDepartment of Medical Oncology, Leiden University Medical Center, Leiden, The Netherlands.
Eric L StaalsDepartment of Orthopaedic Surgery, Musculoskeletal Oncology Department, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Zachary D BurkeDivision of Musculoskeletal Oncology, David Geffen School of Medicine at UCLA, Santa Monica, California, USA.
Erik J GeigerDivision of Musculoskeletal Oncology, David Geffen School of Medicine at UCLA, Santa Monica, California, USA.
Geert SpierenburgDepartment of Orthopaedic Surgery, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-0236-7338
Petra LaeisClinical Operations, Daiichi Sankyo Europe GMbH, Munich, Germany.
Elisabeth BeyerleinBiostatistics & Data Management, Daiichi Sankyo Europe GMbH, Munich, Germany.
Xin YeGlobal Specialty Value, Access & Pricing, Daiichi Sankyo, Inc., Basking Ridge, New Jersey, USA.
Michiel van de SandeDepartment of Orthopaedic Surgery, Leiden University Medical Center, Leiden, The Netherlands.
Carolina Musculoskeletal Institute · USLeiden University Medical Center · NLDaiichi Sankyo (Germany) · DEIstituto Ortopedico Rizzoli · ITCentre Léon Bérard · FRDaiichi Sankyo (United States) · USHospital Universitario Fundación Jiménez Díaz · ESMedical University of Graz · ATMemorial Sloan Kettering Cancer Center · USRadboud University Nijmegen · NLServicio de Salud de Castilla La Mancha · ESWest German Heart and Vascular Center Essen · DE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Daiichi Sankyo, Inc. 20182433NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

BACKGROUND AND

objectivesDiffuse-tenosynovial giant cell tumor (D-TGCT) is a rare, locally aggressive, typically benign neoplasm affecting mainly large joints, representing a wide clinical spectrum. We provide a picture of the treatment journey of D-TGCT patients as a 2-year observational follow-up.

methodsThe TGCT Observational Platform Project registry was a multinational, multicenter, prospective observational study at tertiary sarcoma centers spanning seven European countries and two US sites. Histologically confirmed D-TGCT patients were categorized as either those who remained on initial treatment strategy (determined at baseline visit) or those who changed treatment strategy with specific changes documented (e.g., systemic treatment to surgery) at the 1-year and/or 2-year follow-up visits.

resultsA total of 176 patients were assessed, mean diagnosis age was 38.4 (SD ± 14.6) years; most patients had a knee tumor (120/176, 68.2%). For the 2-year observation period, most patients (75.5%) remained on the baseline treatment strategy throughout, 54/79 patients (68.4%) remained no treatment, 30/45 patients (66.7%) remained systemic treatment, 39/39 patients (100%) remained surgery. Those who changed treatment strategy utilized multimodal treatment options.

conclusionsThis is the first prospectively collected analysis to describe D-TGCT patient treatments over an extended follow-up and demonstrates the need for multidisciplinary teams to determine an optimal treatment strategy.

Indexed as

Giant Cell Tumor of Tendon SheathSoft Tissue NeoplasmsSynovitis, Pigmented VillonodularAdultHumansKnee JointProspective Studiesdiffuse-tenosynovial giant cell tumor (D-TGCT)pexidartinibprospectivereal-worldTGCT observational platform project (TOPP)

Identifiers

PMID36006054
OpenAlexW4293047631

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.