A randomised, phase II study of repeated rhenium-188-HEDP combined with docetaxel and prednisone versus docetaxel and prednisone alone in castration-resistant prostate cancer (CRPC) metastatic to bone; the Taxium II trial

被引:15
|
作者
van Dodewaard-de Jong, Joyce M. [1 ,2 ]
de Klerk, John M. H. [3 ]
Bloemendal, Haiko J. [2 ,4 ]
Oprea-Lager, Daniela E. [5 ]
Hoekstra, Otto S. [5 ]
van den Berg, H. Pieter [6 ]
Los, Maartje [7 ]
Beeker, Aart [8 ]
Jonker, Marianne A. [9 ]
O'Sullivan, Joe M. [10 ]
Verheul, Henk M. W. [1 ]
van den Eertwegh, Alfons J. M. [1 ]
机构
[1] Vrije Univ Amsterdam, Dept Med Oncol, Med Ctr, De Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
[2] Meander Med Ctr, Dept Med Oncol, Maatweg 3, NL-3813 TZ Amersfoort, Netherlands
[3] Meander Med Ctr, Dept Nucl Med, Maatweg 3, NL-3813 TZ Amersfoort, Netherlands
[4] Univ Med Ctr Utrecht, Dept Med Oncol, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[5] Vrije Univ Amsterdam, Med Ctr, Dept Radiol & Nucl Med, De Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
[6] Tergooi Med Hosp, Dept Med Oncol, Van Riebeeckweg 212, NL-1213 XZ Hilversum, Netherlands
[7] St Antonius Hosp, Dept Med Oncol, Soestwetering 1, NL-3543 AZ Utrecht, Netherlands
[8] Spaarne Gasthuis, Dept Med Oncol, Spaarnepoort 1, NL-2134 TM Hoofddorp, Netherlands
[9] Vrije Univ Amsterdam, Med Ctr, Dept Epidemiol & Biostat, De Boelelaan 1089a, NL-1081 HV Amsterdam, Netherlands
[10] Queens Univ Belfast, Ctr Canc Res & Cell Biol, Lisburn Rd, Belfast BT9 7AB, Antrim, North Ireland
关键词
Prostate cancer; Chemotherapy; Radiopharmaceutical; Rhenium-188-HEDP; Docetaxel; Bone metastases; DOUBLE-BLIND; TARGETED THERAPY; PLACEBO; CARCINOMA; MEN; MITOXANTRONE; COMBINATION;
D O I
10.1007/s00259-017-3673-9
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Rhenium-188-HEDP is a beta-emitting radiopharmaceutical used for palliation of metastatic bone pain. We investigated whether the addition of rhenium-188-HEDP to docetaxel/prednisone improved efficacy of chemotherapy in patients with CRPC. Patients with progressive CRPC and osteoblastic bone metastases were randomised for first-line docetaxel 75 mg/m(2) 3-weekly plus prednisone with or without 2 injections of rhenium-188-HEDP after the third (40 MBq/kg) and after the sixth (20 MBq/kg) cycle of docetaxel. Primary endpoint was progression-free survival (PFS), defined as either PSA, radiographic or clinical progression. Patients were stratified by extent of bone metastases and hospital. Forty-two patients were randomised for standard treatment and 46 patients for combination therapy. Median number of cycles of docetaxel was 9 in the control group and 8 in the experimental group. Median follow-up was 18.4 months. Two patients from the experimental group did not start treatment after randomisation. In the intention to treat analysis no differences in PFS, survival and PSA became apparent between the two groups. In an exploratory per-protocol analysis median overall survival was significantly longer in the experimental group (33.8 months (95%CI 31.75-35.85)) than in the control group (21.0 months (95%CI 13.61-28.39); p 0.012). Also median PFS in patients with a baseline phosphatase > 220U/L was significantly better with combination treatment (9.0 months (95%CI 3.92-14.08) versus 6.2 months (95%CI 3.08-9.32); log rank p 0.005). As expected, thrombocytopenia (grade I/II) was reported more frequently in the experimental group (25% versus 0%). Combined treatment with rhenium-188-HEDP and docetaxel did not prolong PFS in patients with CRPC. The observed survival benefit in the per-protocol analysis warrants further studies in the combined treatment of chemotherapy and radiopharmaceuticals.
引用
收藏
页码:1319 / 1327
页数:9
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