Superior Tolerability of Altered Dosing Schedule of Sunitinib with 2-Weeks-on and 1-Week-off in Patients with Metastatic Renal Cell Carcinoma-Comparison to Standard Dosing Schedule of 4-Weeks-on and 2-Weeks-off
被引:66
作者:
Kondo, Tsunenori
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Kondo, Tsunenori
[1
]
Takagi, Toshio
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Takagi, Toshio
[1
]
Kobayashi, Hirohito
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Kobayashi, Hirohito
[1
]
Iizuka, Junpei
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Iizuka, Junpei
[1
]
Nozaki, Taiji
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Nozaki, Taiji
[1
]
Hashimoto, Yasunobu
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Hashimoto, Yasunobu
[1
]
Ikezawa, Eri
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Ikezawa, Eri
[1
]
Yoshida, Kazuhiko
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Yoshida, Kazuhiko
[1
]
Omae, Kenji
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Omae, Kenji
[1
]
Tanabe, Kazunari
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Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, JapanTokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
Tanabe, Kazunari
[1
]
机构:
[1] Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
sunitinib;
renal cell carcinoma;
drug administration schedule;
adverse drug event;
drug tolerances;
TYROSINE KINASE INHIBITOR;
PHASE-II TRIAL;
INTERFERON-ALPHA;
ANTITUMOR-ACTIVITY;
GROWTH-FACTOR;
SU11248;
SAFETY;
SURVIVAL;
EFFICACY;
D O I:
10.1093/jjco/hyt232
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Objective: Poor tolerability to sunitinib with the standard dosing schedule has become an issue. We retrospectively analyzed the treatment efficacy and the profile of adverse events of 2 weeks of sunitinib treatment followed by 1-week-off (Schedule 2/1) and compared the results with the standard dosing schedule with 4 weeks of treatment followed by 2-weeks-off (Schedule 4/2). Methods: From January 2010 until December 2012, 48 patients with metastatic renal cell carcinoma who received at least two cycles of sunitinib as first-line therapy were the subjects of this study. After 2011, we switched to Schedule 2/1 for most patients. Results: Schedule 2/1 included 26 patients and Schedule 4/2 had 22. The incidence of most adverse events was not significantly different between the two groups except for hand-foot syndrome and diarrhoea, which were observed more frequently in Schedule 4/2 and reached statistical significance. A dose interruption due to adverse events in the first three cycles was significantly lower in Schedule 2/1 patients than in those on Schedule 4/2 (27 versus 53% P = 0.04). With respect to treatment efficacy, the objective response rate tended to be higher in Schedule 4/2 than in Schedule 2/1 (50 versus 32%), and median progression-free survival was longer in patients on Schedule 2/1 than those on Schedule 4/2 (18.4 versus 9.1 months). These differences, however, did not reach statistical significance (P = 0.14, P = 0.13). Conclusions: Alteration in dosing schedule of sunitinib with 2-weeks-on and 1-week-off showed a lower incidence of dose interruption and a similar oncological outcome compared with the standard dosing schedule of 4-weeks-on and 2-weeks-off.