One-month relative dose intensity of not less than 50% predicts favourable progression-free survival in sorafenib therapy for advanced renal cell carcinoma in Japanese patients

被引:29
作者
Kawashima, Atsunari [1 ]
Takayama, Hitoshi [1 ]
Arai, Yasuyuki [2 ]
Tanigawa, Go [3 ]
Nin, Mikio [4 ]
Kajikawa, Jiro [5 ]
Imazu, Tetsuo [6 ]
Kinoshita, Tatsuya [7 ]
Yasunaga, Yutaka [8 ]
Inoue, Hitoshi [9 ]
Nishimura, Kenji [10 ]
Takada, Shingo [11 ]
Nishimura, Kazuo [2 ]
Tsujimura, Akira [1 ]
Nonomura, Norio [1 ]
机构
[1] Osaka Univ, Dept Urol, Grad Sch Med, Suita, Osaka 5650871, Japan
[2] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Urol, Osaka, Japan
[3] Osaka Gen Med Ctr Hosp, Dept Urol, Osaka, Japan
[4] Osaka Rosai Hosp, Dept Urol, Osaka, Japan
[5] Sakai Municipal Hosp, Dept Urol, Sakai, Osaka, Japan
[6] Toyonaka City Hosp, Dept Urol, Toyonaka, Osaka, Japan
[7] Sumitomo Hosp, Dept Urol, Osaka, Japan
[8] Osaka Natl Hosp, Natl Hosp Org, Dept Urol, Osaka, Japan
[9] Ikeda Municipal Hosp, Dept Urol, Ikeda, Osaka, Japan
[10] Hyogo Prefectural Nishinomiya Hosp, Dept Urol, Nishinomiya, Hyogo, Japan
[11] Osaka Police Hosp, Dept Urol, Osaka, Japan
关键词
Sorafenib; Renal cell carcinoma; Relative dose intensity; First-line refractory; Progression-free survival; CHOP CHEMOTHERAPY; PHASE-II; EFFICACY; SAFETY; TRIAL;
D O I
10.1016/j.ejca.2011.04.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Sorafenib is a multikinase inhibitor used as a second-line treatment for metastatic renal cell carcinoma (mRCC). However, it is very difficult to estimate sorafenib dosage because it is difficult to maintain stable administration and dosage intervals due to several side-effects. We examined the correlation between relative dose intensity (RDI) and clinical outcome of sorafenib therapy in a multi-institutional study. Methods: A study population of 70 first-line therapy-refractory patients with pathologically confirmed RCC was eligible for this investigation. Clinical outcomes were evaluated according to clinicopathological features and RDI for 1 month (1M-RDI). Results: There was significant difference in progression-free survival (PFS) time but not overall survival (OS) time when the 1M-RDI cut-off value was >= 50%. In 15 patients (21.4%) with 1M-RDI of <50%, median PFS time was 4.1 months (95% I collagen (95% Cl): 2.0-6.2), whereas it was 10.5 months (95% CI: 7.6-13.4) in the patients with 1M-RDI of >= 50% (P = 0.022). Multivariate analysis showed 1M-RDI status to be significantly associated with PFS (HR: 3.838, 95% CI: 1.658-8.883, P = 0.002) but not OS (P = 0.328). Conclusion: Although this study was retrospective, a 1M-RDI cut-off value of 50% for sorafenib may be the first factor to predict PFS but not OS in cytokine pretreated mRCC patients. The data indicate that a dose of 400 mg/day of sorafenib administered successively for the first one month was necessary to prolong disease stabilisation and could be tolerated by Japanese patients. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1521 / 1526
页数:6
相关论文
共 16 条
[1]   Phase II study to investigate the efficacy, safety, and pharmacokinetics of sorafenib in Japanese patients with advanced renal cell carcinoma [J].
Akaza, Hideyuki ;
Tsukamoto, Taiji ;
Murai, Masaru ;
Nakajima, Keiko ;
Naito, Seiji .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2007, 37 (10) :755-762
[2]   Dose-intense chemotherapy every 2 weeks with dose-intense cyclophosphamide, doxorubicin, vincristine, and prednisone may improve survival in intermediate- and high-grade lymphoma: A phase II study of the Southwest Oncology Group (SWOG 9349) [J].
Blayney, DW ;
LeBlanc, ML ;
Grogan, T ;
Gaynor, ER ;
Chapman, RA ;
Spiridonidis, CH ;
Taylor, SA ;
Bearman, SI ;
Miller, TP ;
Fisher, RI .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (13) :2466-2473
[3]   Nephrectomy in metastatic renal cell carcinoma. [J].
Steven C. Campbell ;
Robert C. Flanigan ;
Joseph I. Clark .
Current Treatment Options in Oncology, 2003, 4 (5) :363-372
[4]   Renal-cell carcinoma [J].
Cohen, HT ;
McGovern, FJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (23) :2477-2490
[5]  
EPELBAUM R, 1988, ISRAEL J MED SCI, V24, P533
[6]   Sorafenib in advanced clear-cell renal-cell carcinoma [J].
Escudier, Bernard ;
Eisen, Tim ;
Stadler, Walter M. ;
Szczylik, Cezary ;
Oudard, Stephane ;
Siebels, Michael ;
Negrier, Sylvie ;
Chevreau, Christine ;
Solska, Ewa ;
Desai, Apurva A. ;
Rolland, Frederic ;
Demkow, Tomasz ;
Hutson, Thomas E. ;
Gore, Martin ;
Freeman, Scott ;
Schwartz, Brian ;
Shan, Minghua ;
Simantov, Ronit ;
Bukowski, Ronald M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (02) :125-134
[7]   Sorafenib for Treatment of Renal Cell Carcinoma: Final Efficacy and Safety Results of the Phase III Treatment Approaches in Renal Cancer Global Evaluation Trial [J].
Escudier, Bernard ;
Eisen, Tim ;
Stadler, Walter M. ;
Szczylik, Cezary ;
Oudard, Stephane ;
Staehler, Michael ;
Negrier, Sylvie ;
Chevreau, Christine ;
Desai, Apurva A. ;
Rolland, Frederic ;
Demkow, Tomasz ;
Hutson, Thomas E. ;
Gore, Martin ;
Anderson, Sibyl ;
Hofilena, Gloria ;
Shan, Minghua ;
Pena, Carol ;
Lathia, Chetan ;
Bukowski, Ronald M. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (20) :3312-3318
[8]  
Greene F., 2002, AJCC cancer staging handbook: From the AJCC cancer staging manual, V6th
[9]   Importance of maintaining the relative dose intensity of CHOP-like regimens combined with rituximab in patients with diffuse large B-cell lymphoma [J].
Hirakawa, Tsuneaki ;
Yamaguchi, Hiroki ;
Yokose, Norio ;
Gomi, Seiji ;
Inokuchi, Koiti ;
Dan, Kazuo .
ANNALS OF HEMATOLOGY, 2010, 89 (09) :897-904
[10]   Long-term safety of sorafenib in advanced renal cell carcinoma: Follow-up of patients from phase III TARGET [J].
Hutson, Thomas E. ;
Bellmunt, Joaquim ;
Porta, Camillo ;
Szczylik, Cezary ;
Staehler, Michael ;
Nadel, Andrea ;
Anderson, Sibyl ;
Bukowski, Ronald ;
Eisen, Tim ;
Escudier, Bernard .
EUROPEAN JOURNAL OF CANCER, 2010, 46 (13) :2432-2440