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 [1 ]
Takagi, Toshio [1 ]
Kobayashi, Hirohito [1 ]
Iizuka, Junpei [1 ]
Nozaki, Taiji [1 ]
Hashimoto, Yasunobu [1 ]
Ikezawa, Eri [1 ]
Yoshida, Kazuhiko [1 ]
Omae, Kenji [1 ]
Tanabe, Kazunari [1 ]
机构
[1] Tokyo Womens Med Univ, Dept Urol, Tokyo 1628666, Japan
关键词
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.
引用
收藏
页码:270 / 277
页数:8
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