Long term term follow-up of tyrosine kinase inhibitors treatments in inoperable or relapsing diffuse type tenosynovial giant cell tumors (dTGCT).
Adolescent
Adult
Antineoplastic Agents, Immunological
/ therapeutic use
Female
Follow-Up Studies
Humans
Male
Middle Aged
Neoplasm Recurrence, Local
/ drug therapy
Protein Kinase Inhibitors
/ therapeutic use
Retrospective Studies
Survival Analysis
Synovitis, Pigmented Villonodular
/ drug therapy
Treatment Outcome
Young Adult
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2020
2020
Historique:
received:
19
09
2019
accepted:
27
04
2020
entrez:
21
5
2020
pubmed:
21
5
2020
medline:
1
8
2020
Statut:
epublish
Résumé
CSF1R tyrosine kinase inhibitors (TKI) and antibodies yield response rates and tumor control in patients with diffuse type tenosynovial giant cell tumors (dTGCT). The long term management of patients with dTGCT treated with TKI is however not known. We conducted a retrospective single center study on the 39 patients with advanced and/or inoperable dTGCT referred to the Centre Leon Berard for a medical treatment. The clinical characteristics and treatments of patients who had received at least one line of CSF1R TKI or Ab was collected from the electronic patient records and analyzed, after this study was approved by the Institutional Review Board of the Centre Leon Berard. Statistics were conducted using SPSS 23.0. Thirty-nine patients received at least one line of TKI among the 101 patients with histologically confirmed dTGCT refered to this center. Imatinib, nilotinib, pexidartinib, emactuzumab were the most frequently used agents. First line treatment was given for a median duration of 7 months. With a median follow-up from the initiation of TKI of 30 months, the progression-free rate at 30 months is 56% for the 39 patients. 15 patients had recurrent disease after first line CSF1R inhibitor: 12 (80%) received a 2nd line treatment for a median duration of 6 months and a median time to progression (TTP) of 12 months. Six patients had afterwards a recurrent disease and 5 (83%) received a 3rd line treatment for a median duration of 5 months and a median TTP of 9 months. Progression-free rate at 30 months was observed in 3 of 12 (25%) after line 2 and 1 of 5 (20%) after line 3. None of the patients refered died with a median follow-up of 67 months. CSF1R TKI or Ab provide prolonged tumor control and symptom relief for a majority of patients with inoperable or relapsing dTGCT, in first and subsequent lines. Multiple lines are required for close to 50% of patients with relapsing dTGCT.
Identifiants
pubmed: 32433669
doi: 10.1371/journal.pone.0233046
pii: PONE-D-19-26498
pmc: PMC7239463
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Protein Kinase Inhibitors
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0233046Déclaration de conflit d'intérêts
JYB: research support and honoraria from Novartis, Roche, Five Prime, Plexxikon, Daiichi Sankyo, Deciphera. MB, PC, AD, DP, SC Research support from Novartis, Roche, Five Prime, Plexxikon, Daiichi Sankyo, and Deciphera. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
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