Active surveillance of diffuse-type tenosynovial giant cell tumors: A retrospective, multicenter cohort study.


Journal

European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
ISSN: 1532-2157
Titre abrégé: Eur J Surg Oncol
Pays: England
ID NLM: 8504356

Informations de publication

Date de publication:
06 Jan 2024
Historique:
received: 17 10 2023
revised: 19 12 2023
accepted: 05 01 2024
medline: 13 1 2024
pubmed: 13 1 2024
entrez: 12 1 2024
Statut: aheadofprint

Résumé

Diffuse-type tenosynovial giant cell tumor (D-TGCT) is a mono-articular, soft-tissue tumor. Although it can behave locally aggressively, D-TGCT is a non-malignant disease. This is the first study describing the natural course of D-TGCT and evaluating active surveillance as possible treatment strategy. This retrospective, multicenter study included therapy naïve patients with D-TGCT from eight sarcoma centers worldwide between 2000 and 2019. Patients initially managed by active surveillance following their first consultation were eligible. Data regarding the radiological and clinical course and subsequent treatments were collected. Sixty-one patients with primary D-TGCT were initially managed by active surveillance. Fifty-nine patients had an MRI performed around first consultation: D-TGCT was located intra-articular in most patients (n = 56; 95 %) and extra-articular in 14 cases (24 %). At baseline, osteoarthritis was observed in 13 patients (22 %) on MRI. Most of the patients' reported symptoms: pain (n = 43; 70 %), swelling (n = 33; 54 %). Eight patients (13 %) were asymptomatic. Follow-up data were available for 58 patients; the median follow-up was 28 months. Twenty-one patients (36 %) had radiological progression after 21 months (median). Eight of 45 patients (18 %) without osteoarthritis at baseline developed osteoarthritis during follow-up. Thirty-seven patients (64 %) did not clinically deteriorate during follow-up. Finally, eighteen patients (31 %) required a subsequent treatment. Active surveillance can be considered adequate for selected therapy naïve D-TGCT patients. Although follow-up data was limited, almost two-thirds of the patients remained progression-free, and 69 % did not need treatment during the follow-up period. However, one-fifth of patients developed secondary osteoarthritis. Prospective studies on active surveillance are warranted.

Sections du résumé

BACKGROUND BACKGROUND
Diffuse-type tenosynovial giant cell tumor (D-TGCT) is a mono-articular, soft-tissue tumor. Although it can behave locally aggressively, D-TGCT is a non-malignant disease. This is the first study describing the natural course of D-TGCT and evaluating active surveillance as possible treatment strategy.
METHODS METHODS
This retrospective, multicenter study included therapy naïve patients with D-TGCT from eight sarcoma centers worldwide between 2000 and 2019. Patients initially managed by active surveillance following their first consultation were eligible. Data regarding the radiological and clinical course and subsequent treatments were collected.
RESULTS RESULTS
Sixty-one patients with primary D-TGCT were initially managed by active surveillance. Fifty-nine patients had an MRI performed around first consultation: D-TGCT was located intra-articular in most patients (n = 56; 95 %) and extra-articular in 14 cases (24 %). At baseline, osteoarthritis was observed in 13 patients (22 %) on MRI. Most of the patients' reported symptoms: pain (n = 43; 70 %), swelling (n = 33; 54 %). Eight patients (13 %) were asymptomatic. Follow-up data were available for 58 patients; the median follow-up was 28 months. Twenty-one patients (36 %) had radiological progression after 21 months (median). Eight of 45 patients (18 %) without osteoarthritis at baseline developed osteoarthritis during follow-up. Thirty-seven patients (64 %) did not clinically deteriorate during follow-up. Finally, eighteen patients (31 %) required a subsequent treatment.
CONCLUSION CONCLUSIONS
Active surveillance can be considered adequate for selected therapy naïve D-TGCT patients. Although follow-up data was limited, almost two-thirds of the patients remained progression-free, and 69 % did not need treatment during the follow-up period. However, one-fifth of patients developed secondary osteoarthritis. Prospective studies on active surveillance are warranted.

Identifiants

pubmed: 38215550
pii: S0748-7983(24)00005-2
doi: 10.1016/j.ejso.2024.107953
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107953

Informations de copyright

© 2024 Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: G. and M.A.J.v.d.S. report research funding from Daiichi-Sankyo to the department of Orthopedic Surgery of the Leiden University Medical Center outside the submitted work. E.S, E.P, R.L R., S.W.T, J.S.W., P.C.F., F.G.M.V, M.T.H., N.M.B., B.H.W.B.S., H.G. and L.v.d.H. declare no conflict of interest.

Auteurs

Geert Spierenburg (G)

Department of Orthopedic Surgery, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: G.Spierenburg@lumc.nl.

Eric L Staals (EL)

Third Orthopaedic Clinic and Traumatology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.

Emanuela Palmerini (E)

Osteooncology, Soft Tissue and Bone Sarcomas, Innovative Therapy Unit, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.

Robert Lor Randall (RL)

Department of Orthopaedic Surgery, University of California-Davis, Sacramento, CA, USA.

Steven W Thorpe (SW)

Department of Orthopaedic Surgery, University of California-Davis, Sacramento, CA, USA.

Jay S Wunder (JS)

Division of Orthopaedic Surgery, University Musculoskeletal Oncology Unit, Mount Sinai Hospital, Toronto, Ontario, Canada.

Peter C Ferguson (PC)

Division of Orthopaedic Surgery, University Musculoskeletal Oncology Unit, Mount Sinai Hospital, Toronto, Ontario, Canada.

Floortje G M Verspoor (FGM)

Department of Orthopedic Surgery, Amsterdam University Medical Centers, Amsterdam, the Netherlands.

Matthew T Houdek (MT)

Department of Orthopaedic Surgery, Mayo Clinic, Rochester, MN, USA.

Nicholas M Bernthal (NM)

Department of Orthopaedic Surgery, University of California-Los Angeles, Los Angeles, CA, USA.

Bart H W B Schreuder (BHWB)

Department of Orthopaedics, Radboudumc, Nijmegen, the Netherlands.

Hans Gelderblom (H)

Department of Medical Oncology, Leiden University Medical Center, Leiden, the Netherlands.

Michiel A J van de Sande (MAJ)

Department of Orthopedic Surgery, Leiden University Medical Center, Leiden, the Netherlands.

Lizz van der Heijden (L)

Department of Orthopedic Surgery, Leiden University Medical Center, Leiden, the Netherlands.

Classifications MeSH