TY - JOUR
T1 - Efficacy and safety of axitinib for metastatic renal cell carcinoma
T2 - Real-world data on patients with renal impairment
AU - Japanese Urological Oncology Group
AU - Minami, Keita
AU - Osawa, Takahiro
AU - Kojima, Takahiro
AU - Hara, Tomohiko
AU - Eto, Masatoshi
AU - Takeuchi, Ario
AU - Nakai, Yasutomo
AU - Ueda, Kosuke
AU - Ozawa, Michinobu
AU - Uemura, Motohide
AU - Ohba, Kojiro
AU - Tamura, Keita
AU - Shindo, Tetsuya
AU - Nakagomi, Hiroshi
AU - Takahashi, Atsushi
AU - Anai, Satoshi
AU - Yokomizo, Akira
AU - Morizane, Shuichi
AU - Kimura, Takahiro
AU - Shimazui, Toru
AU - Miyauchi, Yasuyuki
AU - Mitsuzuka, Koji
AU - Hara, Hiroaki
AU - Yoshimura, Koji
AU - Shiina, Hiroaki
AU - Ito, Youichi M.
AU - Murai, Sachiyo
AU - Nishiyama, Hiroyuki
AU - Shinohara, Nobuo
AU - Kitamura, Hiroshi
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023/11
Y1 - 2023/11
N2 - Objectives: Limited information is currently available on the efficacy and safety of axitinib for metastatic renal cell carcinoma (mRCC) patients with renal impairment. Therefore, the present study investigated the efficacy and toxicity of axitinib in patients with chronic kidney disease. Methods: Post-hoc analyses were performed on a Japanese multicenter cohort study of 477 mRCC patients who received axitinib followed by 1 or 2 regimens of systemic antiangiogenic therapy between January 2012 and December 2016. Differences in clinical characteristics and the efficacy and safety of axitinib were assessed based on pretreatment renal function. Results: Patients were categorized into the following 5 renal function groups according to baseline renal function: estimated glomerular filtration rate (eGFR) ≥60 ml/min (n = 133), 45 ml/min ≤eGFR <60 ml/min (n = 153), 30 ml/min ≤eGFR< 45 ml/min (n = 130), eGFR <30 ml/min (n = 45), and dialysis (n = 16). Median progression-free survival (PFS) (95% confidence interval [CI]) in the 5 groups was 11 (8−16), 14 (11−19), 14 (10–19), 12 (8−24), and 6 (3-NR) months, respectively (p = 0.781). After adjustments for treatment-related confounders, the renal function group was not a significant prognostic factor for PFS. Objective response rates in the 5 groups were 22%, 23%, 23%, 18%, 20%, and 38%, respectively (p = 0.468). Regarding adverse events of all grades, hypertension (p = 0.0006) and renal and urinary disorders (p < 0.0001) were more frequently observed in the eGFR <30 ml/min group than in the other groups. Conclusions: Since renal function at the initiation of treatment with axitinib does not adversely affect the efficacy of VEGF-TKI therapy, clinicians do not need to avoid its administration to mRCC patients with impaired renal function in consideration of the risk of progression to end-stage renal disease.
AB - Objectives: Limited information is currently available on the efficacy and safety of axitinib for metastatic renal cell carcinoma (mRCC) patients with renal impairment. Therefore, the present study investigated the efficacy and toxicity of axitinib in patients with chronic kidney disease. Methods: Post-hoc analyses were performed on a Japanese multicenter cohort study of 477 mRCC patients who received axitinib followed by 1 or 2 regimens of systemic antiangiogenic therapy between January 2012 and December 2016. Differences in clinical characteristics and the efficacy and safety of axitinib were assessed based on pretreatment renal function. Results: Patients were categorized into the following 5 renal function groups according to baseline renal function: estimated glomerular filtration rate (eGFR) ≥60 ml/min (n = 133), 45 ml/min ≤eGFR <60 ml/min (n = 153), 30 ml/min ≤eGFR< 45 ml/min (n = 130), eGFR <30 ml/min (n = 45), and dialysis (n = 16). Median progression-free survival (PFS) (95% confidence interval [CI]) in the 5 groups was 11 (8−16), 14 (11−19), 14 (10–19), 12 (8−24), and 6 (3-NR) months, respectively (p = 0.781). After adjustments for treatment-related confounders, the renal function group was not a significant prognostic factor for PFS. Objective response rates in the 5 groups were 22%, 23%, 23%, 18%, 20%, and 38%, respectively (p = 0.468). Regarding adverse events of all grades, hypertension (p = 0.0006) and renal and urinary disorders (p < 0.0001) were more frequently observed in the eGFR <30 ml/min group than in the other groups. Conclusions: Since renal function at the initiation of treatment with axitinib does not adversely affect the efficacy of VEGF-TKI therapy, clinicians do not need to avoid its administration to mRCC patients with impaired renal function in consideration of the risk of progression to end-stage renal disease.
KW - Axitinib
KW - Metastatic
KW - Renal cell carcinoma
KW - Renal impairment
UR - http://www.scopus.com/inward/record.url?scp=85173140804&partnerID=8YFLogxK
U2 - 10.1016/j.urolonc.2023.08.008
DO - 10.1016/j.urolonc.2023.08.008
M3 - 学術論文
C2 - 37798145
AN - SCOPUS:85173140804
SN - 1078-1439
VL - 41
SP - 458.e9-458.e19
JO - Urologic Oncology: Seminars and Original Investigations
JF - Urologic Oncology: Seminars and Original Investigations
IS - 11
ER -