Impact of cabazitaxel on 2-year survival and palliation of tumour-related pain in men with metastatic castration-resistant prostate cancer treated in the TROPIC trial

被引:122
作者
Bahl, A. [1 ]
Oudard, S. [2 ]
Tombal, B. [3 ]
Ozguroglu, M. [4 ]
Hansen, S. [5 ]
Kocak, I. [6 ]
Gravis, G. [7 ]
Devin, J. [8 ]
Shen, L. [8 ]
de Bono, J. S. [9 ,10 ]
Sartor, A. O. [11 ,12 ]
机构
[1] Univ Hosp Bristol NHS Fdn Trust, Bristol Haematol & Oncol Ctr, Bristol, Avon, England
[2] Univ Paris 05, Dept Med Oncol, Hop Europeen Georges Pompidou, Paris, France
[3] Clin Univ St Luc, Div Urol, B-1200 Brussels, Belgium
[4] Istanbul Univ, Cerrahpasa Med Fac, Dept Med Oncol, Istanbul, Turkey
[5] Odense Univ Hosp, Dept Oncol, DK-5000 Odense, Denmark
[6] Masaryk Mem Canc Inst, Clin Comprehens Canc Care, Brno, Czech Republic
[7] Hop Jour, Inst Paoli Calmette, Dept Med Oncol, Marseille, France
[8] Sanofi, Dept Biostat & Programming, Bridgewater, MA USA
[9] Inst Canc Res, Dept Drug Dev, Sutton SM2 5PT, Surrey, England
[10] Royal Marsden NHS Fdn Trust, Sutton, Surrey, England
[11] Tulane Univ, Dept Med, Tulane Canc Ctr, New Orleans, LA 70118 USA
[12] Tulane Univ, Dept Urol, Tulane Canc Ctr, New Orleans, LA 70118 USA
关键词
cabazitaxel; symptom relief; palliative care; prostate cancer; treatment response; quality of life; ABIRATERONE ACETATE; CHEMOTHERAPY; MITOXANTRONE; PREDNISONE; PLACEBO;
D O I
10.1093/annonc/mdt194
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Cabazitaxel significantly improves overall survival (OS) versus mitoxantrone in patients with metastatic castration-resistant prostate cancer after docetaxel failure. We examined patient survival at 2 years and tumour-related pain with cabazitaxel versus mitoxantrone. Updated TROPIC data (cut-off 10 March 2010) were used to compare 2-year survival between treatment groups and assess patient demographics and disease characteristics. Factors prognostic for survival >= 2 years were assessed. Pain and Eastern Cooperative Oncology Group performance status were evaluated in the overall patient population. Median follow-up was 25.5 months. After 2 years, more patients remained alive following cabazitaxel than mitoxantrone [odds ratio 2.11; 95% confidence interval (CI) 1.33-3.33]. Treatment with cabazitaxel was prognostic for survival >= 2 years. Demographics/baseline characteristics were balanced between treatment arms irrespective of survival. Pain at baseline and pain response were comparable between treatment groups. Average daily pain performance index was lower for cabazitaxel versus mitoxantrone (all cycles; 95% CI -0.27 to -0.01; P = 0.035) and analgesic scores were similar. Grade >= 3 peripheral neuropathies were uncommon and comparable between treatment groups. Cabazitaxel prolongs OS at 2 years versus mitoxantrone and has low rates of peripheral neuropathy. Palliation benefits of cabazitaxel were comparable to those of mitoxantrone. The study was registered with (NCT00417079).
引用
收藏
页码:2402 / 2408
页数:7
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