Sunitinib is one of the first-line standard treatments for metastatic clear cell renal cell carcinoma (ccRCC) with a median time to progression shorter than 1 year. The objective is to discover predictive markers of response to adapt the treatment at diagnosis. Methods: Prospective phase 2 multi-centre trials were conducted in ccRCC patients initiating sunitinib (54 patients) or bevacizumab (45 patients) in the first-line metastatic setting (SUVEGIL and TORAVA trials). The plasmatic level of CXCL7 at baseline was correlated with progression-free survival (PFS). Results: The cut-off value of CXCL7 for PFS was 250 ng ml(-1). Patients with CXCL7 plasmatic levels above the cut-off at baseline (250 ng ml(-1)) had a significantly longer PFS (hazard ratio 0.323 (95% confidence interval 0.147-0.707), P = 0.001). These results were confirmed in a retrospective validation cohort. The levels of CXCL7 did not influence PFS of the bevacizumab-treated patients. Conclusions: CXCL7 may be considered as a predictive marker of sunitinib efficacy for ccRCC patients.

CXCL7 is a predictive marker of sunitinib efficacy in clear cell renal cell carcinomas

Milano G.;Porta C.;
2017-01-01

Abstract

Sunitinib is one of the first-line standard treatments for metastatic clear cell renal cell carcinoma (ccRCC) with a median time to progression shorter than 1 year. The objective is to discover predictive markers of response to adapt the treatment at diagnosis. Methods: Prospective phase 2 multi-centre trials were conducted in ccRCC patients initiating sunitinib (54 patients) or bevacizumab (45 patients) in the first-line metastatic setting (SUVEGIL and TORAVA trials). The plasmatic level of CXCL7 at baseline was correlated with progression-free survival (PFS). Results: The cut-off value of CXCL7 for PFS was 250 ng ml(-1). Patients with CXCL7 plasmatic levels above the cut-off at baseline (250 ng ml(-1)) had a significantly longer PFS (hazard ratio 0.323 (95% confidence interval 0.147-0.707), P = 0.001). These results were confirmed in a retrospective validation cohort. The levels of CXCL7 did not influence PFS of the bevacizumab-treated patients. Conclusions: CXCL7 may be considered as a predictive marker of sunitinib efficacy for ccRCC patients.
2017
Esperti anonimi
Inglese
Internazionale
STAMPA
117
7
947
953
7
ccRCC; CXCL7; plasma; predictive marker; sunitinib; Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Bevacizumab; Biomarkers, Tumor; Carcinoma, Renal Cell; Disease-Free Survival; Female; Humans; Indoles; Kidney Neoplasms; Killer Cells, Natural; Lymphocytes, Tumor-Infiltrating; Macrophages; Male; Mice; Middle Aged; Neoplasm Grading; Neoplasm Transplantation; Nephrectomy; Neutrophils; Prospective Studies; Pyrroles; Retrospective Studies; Sirolimus; Sunitinib; Survival Rate; beta-Thromboglobulin
http://www.nature.com/bjc/index.html
26
info:eu-repo/semantics/article
262
Dufies, M.; Giuliano, S.; Viotti, J.; Borchiellini, D.; Cooley, L. S.; Ambrosetti, D.; Guyot, M.; Ndiaye, P. D.; Parola, J.; Claren, A.; Schiappa, R.;...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1301626
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