TY - JOUR
T1 - Evaluation of axitinib to downstage cT2a renal tumours and allow partial nephrectomy
T2 - a phase II study
AU - Lebacle, Cedric
AU - Bensalah, Karim
AU - Bernhard, Jean Christophe
AU - Albiges, Laurence
AU - Laguerre, Brigitte
AU - Gross-Goupil, Marine
AU - Baumert, Herve
AU - Lang, Herve
AU - Tricard, Thibault
AU - Duclos, Brigitte
AU - Arnoux, Armelle
AU - Piedvache, Celine
AU - Patard, Jean Jacques
AU - Escudier, Bernard
N1 - Publisher Copyright:
© 2018 The Authors BJU International © 2018 BJU International Published by John Wiley & Sons Ltd
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Objective: To evaluate the ability of neoadjuvant axitinib to reduce the size of T2 renal cell carcinoma (RCC) for shifting from a radical nephrectomy (RN) to a partial nephrectomy (PN) indication, offering preservation of renal function. Patients and Methods: Patients with cT2aN0NxM0 clear-cell RCC, considered not suitable for PN, were enrolled in a prospective, multicentre, phase II trial (AXIPAN). Axitinib 5 mg, and up to 7–10 mg, was administered twice daily, for 2–6 months before surgery, depending on the radiological response. The primary outcome was the number of patients receiving PN for a tumour <7 cm in size after neoadjuvant axitinib. Results: Eighteen patients were enrolled. The median (range) tumour size and RENAL nephrometry score were 76.5 (70–98) mm and 11 (7–11), respectively. After axitinib neoadjuvant treatment, 16 tumours decreased in diameter, with a median size reduction of 17% (64.0 vs 76.5 mm; P < 0.001). The primary outcome was considered achieved in 12 patients who underwent PN for tumours <7 cm. Sixteen patients underwent PN. Axitinib was tolerated in the present study, as has been previously shown in the metastatic setting. Five patients had grade 3 adverse events. Five patients experienced Clavien III–V post-surgery complications. At 2-year follow-up, six patients had metastatic progression, and two had a recurrence. Conclusion: Neoadjuvant axitinib in cT2 ccRCC is feasible and, even with a modest decrease in size, allowed a tumour shrinkage <7 cm in 12 cases; however, PN procedures remained complex, requiring surgical expertise with possible morbidity.
AB - Objective: To evaluate the ability of neoadjuvant axitinib to reduce the size of T2 renal cell carcinoma (RCC) for shifting from a radical nephrectomy (RN) to a partial nephrectomy (PN) indication, offering preservation of renal function. Patients and Methods: Patients with cT2aN0NxM0 clear-cell RCC, considered not suitable for PN, were enrolled in a prospective, multicentre, phase II trial (AXIPAN). Axitinib 5 mg, and up to 7–10 mg, was administered twice daily, for 2–6 months before surgery, depending on the radiological response. The primary outcome was the number of patients receiving PN for a tumour <7 cm in size after neoadjuvant axitinib. Results: Eighteen patients were enrolled. The median (range) tumour size and RENAL nephrometry score were 76.5 (70–98) mm and 11 (7–11), respectively. After axitinib neoadjuvant treatment, 16 tumours decreased in diameter, with a median size reduction of 17% (64.0 vs 76.5 mm; P < 0.001). The primary outcome was considered achieved in 12 patients who underwent PN for tumours <7 cm. Sixteen patients underwent PN. Axitinib was tolerated in the present study, as has been previously shown in the metastatic setting. Five patients had grade 3 adverse events. Five patients experienced Clavien III–V post-surgery complications. At 2-year follow-up, six patients had metastatic progression, and two had a recurrence. Conclusion: Neoadjuvant axitinib in cT2 ccRCC is feasible and, even with a modest decrease in size, allowed a tumour shrinkage <7 cm in 12 cases; however, PN procedures remained complex, requiring surgical expertise with possible morbidity.
KW - #uroonc
KW - neoadjuvant
KW - partial nephrectomy
KW - renal cell carcinoma
KW - targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=85056753702&partnerID=8YFLogxK
U2 - 10.1111/bju.14581
DO - 10.1111/bju.14581
M3 - Article
C2 - 30288884
AN - SCOPUS:85056753702
SN - 1464-4096
VL - 123
SP - 804
EP - 810
JO - BJU International
JF - BJU International
IS - 5
ER -