Literature DB >> 24474815

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.

Tsunenori Kondo1, Toshio Takagi, Hirohito Kobayashi, Junpei Iizuka, Taiji Nozaki, Yasunobu Hashimoto, Eri Ikezawa, Kazuhiko Yoshida, Kenji Omae, Kazunari Tanabe.   

Abstract

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.

Entities:  

Keywords:  adverse drug event; drug administration schedule; drug tolerances; renal cell carcinoma; sunitinib

Mesh:

Substances:

Year:  2014        PMID: 24474815     DOI: 10.1093/jjco/hyt232

Source DB:  PubMed          Journal:  Jpn J Clin Oncol        ISSN: 0368-2811            Impact factor:   3.019


  33 in total

1.  Improved health-related quality of life of patients with metastatic renal cell carcinoma treated with a 2 weeks on and 1 week off schedule of sunitinib.

Authors:  Hideaki Miyake; Ken-ichi Harada; Akira Miyazaki; Masato Fujisawa
Journal:  Med Oncol       Date:  2015-02-20       Impact factor: 3.064

Review 2.  Can individualized sunitinib dose and schedule changes optimize outcomes for kidney cancer patients?

Authors:  Georg A Bjarnason
Journal:  Can Urol Assoc J       Date:  2016 Nov-Dec       Impact factor: 1.862

3.  Oncological outcomes classified according to metastatic lesions in the era of molecular targeted drugs for metastatic renal cancer.

Authors:  Yasuomi Shimizu; Taro Iguchi; Satoshi Tamada; Sayaka Yasuda; Minoru Kato; Noriko Ninomiya; Takeshi Yamasaki; Tatsuya Nakatani
Journal:  Mol Clin Oncol       Date:  2018-04-24

4.  Outcome of advanced renal cell carcinoma arising in end-stage renal disease: comparison with sporadic renal cell carcinoma.

Authors:  Hiroki Ishihara; Hironori Fukuda; Hidekazu Tachibana; Kazuhiko Yoshida; Hirohito Kobayashi; Toshio Takagi; Junpei Iizuka; Hideki Ishida; Yoji Nagashima; Tsunenori Kondo; Kazunari Tanabe
Journal:  Clin Exp Nephrol       Date:  2021-02-27       Impact factor: 2.801

Review 5.  Alternate sunitinib schedules in patients with metastatic renal cell carcinoma.

Authors:  S Kalra; B I Rini; E Jonasch
Journal:  Ann Oncol       Date:  2015-01-26       Impact factor: 32.976

6.  Comparison of axitinib and sunitinib as first-line therapies for metastatic renal cell carcinoma: a real-world multicenter analysis.

Authors:  Sakae Konishi; Shingo Hatakeyama; Toshiaki Tanaka; Yoshinori Ikehata; Toshikazu Tanaka; Naoki Fujita; Yusuke Ishibashi; Hayato Yamamoto; Takahiro Yoneyama; Yasuhiro Hashimoto; Kazuaki Yoshikawa; Toshiaki Kawaguchi; Naoya Masumori; Hiroshi Kitamura; Chikara Ohyama
Journal:  Med Oncol       Date:  2018-11-24       Impact factor: 3.064

7.  Evaluation of relative dose intensity during the early phase of first-line sunitinib treatment using a 2-week-on/1-week-off regimen for metastatic renal cell carcinoma.

Authors:  Kana Iwamoto; Hiroki Ishihara; Toshio Takagi; Tsunenori Kondo; Kazuhiko Yoshida; Junpei Iizuka; Kazunari Tanabe
Journal:  Med Oncol       Date:  2018-04-23       Impact factor: 3.064

Review 8.  The Current and Evolving Landscape of First-Line Treatments for Advanced Renal Cell Carcinoma.

Authors:  Emiliano Calvo; Camillio Porta; Viktor Grünwald; Bernard Escudier
Journal:  Oncologist       Date:  2018-08-29

9.  Assessment of efficacy, safety and quality of life of 110 patients treated with sunitinib as first-line therapy for metastatic renal cell carcinoma: experience in real-world clinical practice in Japan.

Authors:  Hideaki Miyake; Akira Miyazaki; Ken-Ichi Harada; Masato Fujisawa
Journal:  Med Oncol       Date:  2014-05-04       Impact factor: 3.064

10.  First-line sunitinib or pazopanib in metastatic renal cell carcinoma: The Canadian experience.

Authors:  Aly-Khan A Lalani; Haocheng Li; Daniel Y C Heng; Lori Wood; Austin Kalirai; Georg A Bjarnason; Hao-Wen Sim; Christian K Kollmannsberger; Anil Kapoor; Sebastien J Hotte; Marie Vanhuyse; Piotr Czaykowski; M Neil Reaume; Denis Soulieres; Peter Venner; Scott North; Naveen S Basappa
Journal:  Can Urol Assoc J       Date:  2017 Mar-Apr       Impact factor: 1.862

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.