TY - JOUR
T1 - Multiple systemic treatment options in a patient with malignant tenosynovial giant cell tumour
AU - Rebuzzi, Sara Elena
AU - Grassi, Massimiliano
AU - Catalano, Fabio
AU - Buscaglia, Michele
AU - Bertulli, Rossella
AU - Satragno, Camilla
AU - Belgioia, Liliana
AU - Comandini, Danila
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Tenosynovial giant cell tumour (TGCT) is a group of rare soft tissues neoplasia affecting synovial joints, bursae and tendon sheaths and is classified as localized type or diffuse type. The diffuse type (TGCT-D), also known as 'pigmented villonodular (teno)synovitis' is characterized by local aggressivity, with invasion and destruction of adjacent soft-tissue structures, and high local recurrence rate. Radical surgery remains the standard therapy while adjuvant radiotherapy may help to control local spread. Malignant TGCT is characterized by high rate of local recurrences and distant metastasis. Few cases of malignant TGCT and very few evidences on systemic therapies are described in the literature, so, to date, no systemic treatment is approved for this rare disease. We report the case of a malignant TGCT patient treated with many different systemic therapies, including chemotherapy and tyrosine-kinase inhibitors, and performed a review of the literature on the systemic treatment options of this rare tumour.
AB - Tenosynovial giant cell tumour (TGCT) is a group of rare soft tissues neoplasia affecting synovial joints, bursae and tendon sheaths and is classified as localized type or diffuse type. The diffuse type (TGCT-D), also known as 'pigmented villonodular (teno)synovitis' is characterized by local aggressivity, with invasion and destruction of adjacent soft-tissue structures, and high local recurrence rate. Radical surgery remains the standard therapy while adjuvant radiotherapy may help to control local spread. Malignant TGCT is characterized by high rate of local recurrences and distant metastasis. Few cases of malignant TGCT and very few evidences on systemic therapies are described in the literature, so, to date, no systemic treatment is approved for this rare disease. We report the case of a malignant TGCT patient treated with many different systemic therapies, including chemotherapy and tyrosine-kinase inhibitors, and performed a review of the literature on the systemic treatment options of this rare tumour.
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U2 - 10.1097/CAD.0000000000000844
DO - 10.1097/CAD.0000000000000844
M3 - Article
C2 - 31567307
SN - 0959-4973
VL - 31
SP - 80
EP - 84
JO - Anti-Cancer Drugs
JF - Anti-Cancer Drugs
IS - 1
ER -