A Randomized Phase IIa Trial with Temsirolimus versus Sunitinib in Advanced Non-Clear Cell Renal Cell Carcinoma: An Intergroup Study of the CESAR Central European Society for Anticancer Drug Research-EWIV and the Interdisciplinary Working Group on Renal Cell Cancer (IAGN) of the German Cancer Society

被引:24
作者
Bergmann, Lothar [1 ]
Gruenwald, Viktor [2 ]
Maute, Luise [1 ]
Grimm, Marc-Oliver [3 ]
Weikert, Steffen [4 ]
Schleicher, Jan [5 ]
Klotz, Theodor [6 ]
Greiner, Jochen [7 ]
Florcken, Anne [8 ,9 ,10 ,11 ]
Hartmann, Arndt [12 ]
Gauler, Thomas [13 ]
机构
[1] Goethe Univ Frankfurt, Med Clin 2, Frankfurt, Germany
[2] Hannover Med Sch, Hematol & Med Oncol, Hannover, Germany
[3] Friedrich Schiller Univ, Clin Urol, Jena, Germany
[4] Vivantes Humboldt Klinikum, Clin Urol, Berlin, Germany
[5] Klinikum Stuttgart, Clin Hematol & Oncol, Stuttgart, Germany
[6] Klin Nordoberpfalz AG, Clin Urol & Androl, Weiden, Germany
[7] Diakonie Klinikum, Clin Hematol & Oncol, Stuttgart, Germany
[8] Charite Univ Med Berlin, Dept Hematol Oncol & Tumor Immunol, Campus Virchow Klinikum, Berlin, Germany
[9] Free Univ Berlin, Campus Virchow Klinikum, Berlin, Germany
[10] Humboldt Univ, Campus Virchow Klinikum, Berlin, Germany
[11] Berlin Inst Hlth, Campus Virchow Klinikum, Berlin, Germany
[12] Univ Hosp, Inst Pathol, Erlangen, Germany
[13] Univ Duisburg Essen, Dept Med Oncol, Univ Hosp Essen, West German Canc Ctr, Essen, Germany
关键词
Non-clear cell renal cell cancer; Sunitinib; Temsirolimus; Randomized trial; Phase II trial; OPEN-LABEL; EVEROLIMUS; METAANALYSIS; INHIBITION; GUIDELINES;
D O I
10.1159/000508450
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background:Non-clear cell renal cell cancers (nccRCC) are rare entities, and the optimal therapy in metastatic disease has still to be defined.Methods:In this small prospectively randomized phase IIa multicenter trial, we investigated temsirolimus (TEM) versus sunitinib (SUN) as first-line therapy in patients with metastatic nccRCC. The patients were randomized 1:1 to either TEM in a dose of 25 mg i.v. once a week or SUN with 50 mg p.o. daily for 4 weeks on and 2 weeks off. Primary endpoint was progression-free survival (PFS). In total, 22 patients were included with predominantly papillary RCC (16/22) followed by chromophobe RCC and others.Results:The male to female ratio was 16:6. The tumor control rate (CR + PR + SD) was 58% for TEM and 90% for SUN-treated patients. There was also a trend for improved PFS with 9.3 versus 13.2 months (HR 1.64; 95% CI 0.65-4.18) in favor of SUN. There was no trend for overall survival.Conclusions:Despite this trial had to be terminated earlier due to low recruitment, the results match the other studies published so far with the mTOR inhibitor everolimus and SUN, which show a trend in favor of SUN for ORR and PFS.
引用
收藏
页码:333 / 338
页数:6
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