TY - JOUR
T1 - Role of chemotherapy, VEGFR inhibitors, and mTOR inhibitors in advanced perivascular epithelioid cell tumors (PEComas)
AU - Sanfilippo, Roberta
AU - Jones, Robin L.
AU - Blay, Jean Yves
AU - Cesne, Axel Le
AU - Provenzano, Salvatore
AU - Antoniou, Georgios
AU - Mir, Olivier
AU - Fucà, Giovanni
AU - Fumagalli, Elena
AU - Bertulli, Rossella
AU - Stacchiotti, Silvia
AU - Brahmi, Mehdi
AU - Grosso, Federica
AU - Dufresne, Armelle
AU - Hindi, Nadia
AU - Sbaraglia, Marta
AU - Gronchi, Alessandro
AU - Collini, Paola
AU - Dei Tos, Angelo P.
AU - Casali, Paolo G.
N1 - Publisher Copyright:
© 2019 American Association for Cancer Research Inc.. All rights reserved.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - Purpose: Perivascular epitheliod cell tumors (PEComas) are rare mesenchymal neoplasms for which the role of systemic treatments is not established as there are no published prospective clinical trials or sufficiently large retrospective case series. The aim of this study is to clarify the activity of conventional chemotherapy and biological agents in advanced/metastatic PEComas. Experimental Design: This was an observational, retrospective, international study that included patients with advanced/ metastatic PEComa treated with systemic therapy at 5 European sarcoma reference centers and within the Italian Rare Cancer Network. Survival analyses were performed using the Kaplan-Meier method and the Cox hazards regression models. Results: A total of 53 patients were included. Cytotoxic chemotherapy regimens were active only in a small proportion of PEComas. Gemcitabine-based regimens [objective response rate (ORR): 20%, median progression-free survival (PFS): 3.4 months] seemed to have the same activity of anthracycline- based regimens (ORR: 13%, median PFS: 3.2 months). Antiangiogenic agents resulted in disease stabilization in some patients, with a number having density changes/tissue response on imaging, with an ORR of 8.3% and a median PFS of 5.4 months. mTOR inhibitors were the most active agents, with an ORR of 41% and a median PFS of 9 months. Conclusions: Our study provides data for the selection of systemic therapy in patients with advanced/metastatic PEComa: mTOR inhibitors are the most active agents. Antiangiogenics and chemotherapy with gemcitabine-based regimens or anthracycline-based regimens are options in further line, but with a lower response rate and PFS.
AB - Purpose: Perivascular epitheliod cell tumors (PEComas) are rare mesenchymal neoplasms for which the role of systemic treatments is not established as there are no published prospective clinical trials or sufficiently large retrospective case series. The aim of this study is to clarify the activity of conventional chemotherapy and biological agents in advanced/metastatic PEComas. Experimental Design: This was an observational, retrospective, international study that included patients with advanced/ metastatic PEComa treated with systemic therapy at 5 European sarcoma reference centers and within the Italian Rare Cancer Network. Survival analyses were performed using the Kaplan-Meier method and the Cox hazards regression models. Results: A total of 53 patients were included. Cytotoxic chemotherapy regimens were active only in a small proportion of PEComas. Gemcitabine-based regimens [objective response rate (ORR): 20%, median progression-free survival (PFS): 3.4 months] seemed to have the same activity of anthracycline- based regimens (ORR: 13%, median PFS: 3.2 months). Antiangiogenic agents resulted in disease stabilization in some patients, with a number having density changes/tissue response on imaging, with an ORR of 8.3% and a median PFS of 5.4 months. mTOR inhibitors were the most active agents, with an ORR of 41% and a median PFS of 9 months. Conclusions: Our study provides data for the selection of systemic therapy in patients with advanced/metastatic PEComa: mTOR inhibitors are the most active agents. Antiangiogenics and chemotherapy with gemcitabine-based regimens or anthracycline-based regimens are options in further line, but with a lower response rate and PFS.
UR - http://www.scopus.com/inward/record.url?scp=85071788034&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-19-0288
DO - 10.1158/1078-0432.CCR-19-0288
M3 - Article
C2 - 31217199
AN - SCOPUS:85071788034
SN - 1078-0432
VL - 25
SP - 5295
EP - 5300
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 17
ER -