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DOI 10.1371/journal.pone.0233046

Медицинская библиотека · PloS one · 2020

Long term term follow-up of tyrosine kinase inhibitors treatments in inoperable or relapsing diffuse type tenosynovial giant cell tumors (dTGCT).

Brahmi Mehdi, Cassier Philippe, Dufresne Armelle, Chabaud Sylvie, Karanian Marie, Meurgey Alexandra, Bouhamama Amine, Gouin Francois, Vaz Gualter, Garret Jerome, Sunyach Marie-Pierre, Dupré Aurélien, Marec-Berard Perrine, Corradini Nadège, Perol David, Ray-Coquard Isabelle, Blay Jean-Yves

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

RATIONALE: 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.

PATIENTS AND

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

Для цитирования: Brahmi Mehdi, Cassier Philippe, Dufresne Armelle, Chabaud Sylvie, Karanian Marie, Meurgey Alexandra, Bouhamama Amine, Gouin Francois, Vaz Gualter, Garret Jerome, Sunyach Marie-Pierre, Dupré Aurélien, Marec-Berard Perrine, Corradini Nadège, Perol David, Ray-Coquard Isabelle, Blay Jean-Yves. Long term term follow-up of tyrosine kinase inhibitors treatments in inoperable or relapsing diffuse type tenosynovial giant cell tumors (dTGCT).. PloS one. 2020. DOI: 10.1371/journal.pone.0233046.

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