Locoregional treatment with radical intent should be considered during therapy with targeted agents in patients with metastatic renal cell carcinoma (mRCC) in order to achieve a complete response, especially in the setting of an oligo-progression in one or more metastatic sites. We retrospectively enrolled 55 patients who experienced a disease oligoprogression after at least 6 months from the beginning of first-line therapy in one or more metastatic sites radically treated with locoregional treatments. Post-first-oligoprogression overall survival (PFOPOS) and post-first-oligo-progression free survival (PFOPFS) were evaluated. The global median PFOPOS and PFOPFS were 37 months and 14 months respectively. Patients who continued the same therapy after a locoregional treatment on a site of progression had a significantly longer mPFOPOS compared to patients who changed therapy (39 vs 11 months, p=0.014). An advantage in mPFOPOS was also observed in patients with a Memorial Sloan-Kettering Cancer Center (MSKCC) good risk score compared to patients of the intermediate risk group (39 vs 29 months, p=0.036); patients with bone metastases had a longer mPFOPOS compared to those with visceral metastases (not reached vs 31 months, p=0.045). The only independent predictor of poor prognosis, in terms of PFOPOS at multivariate analysis (p=0.007), proved out to be change of treatment after first progression.

Outcome of oligoprogressing metastatic renal cell carcinoma patients treated with locoregional therapy. A multicenter retrospective analysis / Santini, D; Ratta, R; Pantano, F; De Lisi, D; Maruzzo, M; Galli, L; Biasco, E; Farnesi, A; Buti, S; Sternberg, Cn; Cerbone, L; Di Lorenzo, G; Spoto, S; Sterpi, M; De Giorgi, U; Berardi, R; Torniai, M; Camerini, A; Massari, F; Procopio, G; Tonini, G. - In: ONCOTARGET. - ISSN 1949-2553. - 8:59(2017), pp. 100708-100716. [10.18632/oncotarget.20022]

Outcome of oligoprogressing metastatic renal cell carcinoma patients treated with locoregional therapy. A multicenter retrospective analysis

Santini D;
2017

Abstract

Locoregional treatment with radical intent should be considered during therapy with targeted agents in patients with metastatic renal cell carcinoma (mRCC) in order to achieve a complete response, especially in the setting of an oligo-progression in one or more metastatic sites. We retrospectively enrolled 55 patients who experienced a disease oligoprogression after at least 6 months from the beginning of first-line therapy in one or more metastatic sites radically treated with locoregional treatments. Post-first-oligoprogression overall survival (PFOPOS) and post-first-oligo-progression free survival (PFOPFS) were evaluated. The global median PFOPOS and PFOPFS were 37 months and 14 months respectively. Patients who continued the same therapy after a locoregional treatment on a site of progression had a significantly longer mPFOPOS compared to patients who changed therapy (39 vs 11 months, p=0.014). An advantage in mPFOPOS was also observed in patients with a Memorial Sloan-Kettering Cancer Center (MSKCC) good risk score compared to patients of the intermediate risk group (39 vs 29 months, p=0.036); patients with bone metastases had a longer mPFOPOS compared to those with visceral metastases (not reached vs 31 months, p=0.045). The only independent predictor of poor prognosis, in terms of PFOPOS at multivariate analysis (p=0.007), proved out to be change of treatment after first progression.
2017
metastatic renal cell carcinoma (mRCC); oligoprogression; pazopanib; sunitinib; targeted therapy
01 Pubblicazione su rivista::01a Articolo in rivista
Outcome of oligoprogressing metastatic renal cell carcinoma patients treated with locoregional therapy. A multicenter retrospective analysis / Santini, D; Ratta, R; Pantano, F; De Lisi, D; Maruzzo, M; Galli, L; Biasco, E; Farnesi, A; Buti, S; Sternberg, Cn; Cerbone, L; Di Lorenzo, G; Spoto, S; Sterpi, M; De Giorgi, U; Berardi, R; Torniai, M; Camerini, A; Massari, F; Procopio, G; Tonini, G. - In: ONCOTARGET. - ISSN 1949-2553. - 8:59(2017), pp. 100708-100716. [10.18632/oncotarget.20022]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1642292
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