Temsirolimus for advanced renal cell carcinoma

被引:31
作者
Bergmann, Lothar [1 ]
Maute, Luise [1 ]
Guschmann, Michael [2 ]
机构
[1] Goethe Univ Frankfurt, Med Klin 2, D-60590 Frankfurt, Germany
[2] Inst Pharmakol & Pravent Med, D-15831 Mahlow, Germany
关键词
carcinoma; mTOR targeting therapy; renal; temsirolimus; CLINICAL-PRACTICE GUIDELINES; ADVERSE EVENT MANAGEMENT; INTERFERON-ALPHA; MTOR INHIBITOR; MAMMALIAN TARGET; INTRAVENOUS-INFUSION; HISTOLOGIC SUBTYPES; KINASE INHIBITOR; RISING INCIDENCE; TUMOR-GROWTH;
D O I
10.1586/14737140.2014.864562
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Renal cell carcinomas (RCCs) represent one of the ten leading cancer entities with an increasing incidence especially in the western world. Unfortunately, about 25% of the patients develop metastatic RCC (mRCC) associated with a most unfavorable prognosis. In the recent years, various new agents targeting VEGF or VEGF receptor (VEGFR) or the mTOR pathway have been approved for the treatment of mRCC with significant prolongation of progression-free survival and, in part, of overall survival (OS). Targeting the mTOR kinase is an interesting option for mRCC. Temsirolimus, one of the available mTOR inhibitors, has been approved as a single agent in poor-risk mRCC patients based on the pivotal Phase III trial showing a significant superiority in OS versus IFN-alpha or temsirolimus + IFN-alpha, which has been verified by a pivotal Phase III trial. The benefit has been shown for clear cell carcinoma and papillary RCC as well. For poor prognosis patients, temsirolimus improves median survival by 3.6 months. In second-line treatment compared with sorafenib following first-line treatment with sunitinib temsirolimus showed a relative progression-free survival benefit for patients with nonclear cell RCC with temsirolimus. The median OS for the temsirolimus group was 12.27 and 16.64 months for the sorafenib group. In 2007, the US FDA granted approval for temsirolimus for the treatment of advanced RCC.
引用
收藏
页码:9 / 21
页数:13
相关论文
共 93 条
[1]
Non-Clear Cell Renal Cell Carcinoma: Does the Mammalian Target of Rapamycin Represent a Rational Therapeutic Target? [J].
Albiges, Laurence ;
Molinie, Vincent ;
Escudier, Bernard .
ONCOLOGIST, 2012, 17 (08) :1051-1062
[2]
A Phase 2 Study With a Daily Regimen of the Oral mTOR Inhibitor RAD001 (Everolimus) in Patients With Metastatic Clear Cell Renal Cell Cancer [J].
Amato, Robert J. ;
Jac, Jaroslaw ;
Giessinger, Sarah ;
Saxena, Somyata ;
Willis, James P. .
CANCER, 2009, 115 (11) :2438-2446
[3]
[Anonymous], 2019, CLIN PRACTICE GUIDEL
[4]
Randomized phase II study of multiple dose levels of CCI-779, a novel mammalian target of rapamycin kinase inhibitor, in patients with advanced refractory renal cell carcinoma [J].
Atkins, MB ;
Hidalgo, M ;
Stadler, WM ;
Logan, TF ;
Dutcher, JP ;
Hudes, GR ;
Park, Y ;
Lion, SH ;
Marshall, B ;
Boni, JP ;
Dukart, G ;
Sherman, ML .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (05) :909-918
[5]
Temsirolimus safety profile and management of toxic effects in patients with advanced renal cell carcinoma and poor prognostic features [J].
Bellmunt, J. ;
Szczylik, C. ;
Feingold, J. ;
Strahs, A. ;
Berkenblit, A. .
ANNALS OF ONCOLOGY, 2008, 19 (08) :1387-1392
[6]
Everolimus in Metastatic Renal Cell Carcinoma after Failure of Initial Vascular Endothelial Growth Factor Receptor-Tyrosine Kinase Inhibitor (VEGFr-TKI) Therapy: Results of an Interim Analysis of a Non-Interventional Study [J].
Bergmann, Lothar ;
Goebell, Peter J. ;
Kube, Ulrich ;
Kindler, Manfred ;
Herrmann, Edwin ;
Janssen, Jan ;
Schmitz, Joerg ;
Weikert, Steffen ;
Steiner, Gabriel ;
Jakob, Andreas ;
Staehler, Michael D. ;
Steiner, Thomas ;
Overkamp, Friedrich ;
Albrecht, Michael ;
Guderian, Gernot ;
Doehn, Christian .
ONKOLOGIE, 2013, 36 (03) :95-100
[7]
The mTOR inhibitor RAD001 sensitizes tumor cells to DNA-damaged induced apoptosis through inhibition of p21 translation [J].
Beuvink, I ;
Boulay, A ;
Fumagalli, S ;
Zilbermann, F ;
Ruetz, S ;
O'Reilly, T ;
Natt, F ;
Hall, J ;
Lane, HA ;
Thomas, G .
CELL, 2005, 120 (06) :747-759
[8]
Temsirolimus for advanced renal cell carcinoma (RCC): Compassionate versus commercial use [J].
Bojanapally, P. R. ;
Graham, S. ;
Rustine, A. L. ;
Sacris, L. A. ;
Dutcher, J. P. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (15)
[9]
Differential effects of ketoconazole on exposure to temsirolimus following intravenous infusion of temsirolimus [J].
Boni, J. P. ;
Leister, C. ;
Burns, J. ;
Hug, B. .
BRITISH JOURNAL OF CANCER, 2008, 98 (11) :1797-1802
[10]
Disposition of desipramine, a sensitive cytochrome P450 2D6 substrate, when coadministered with intravenous temsirolimus [J].
Boni, Joseph ;
Abbas, Richat ;
Leister, Cathie ;
Burns, Jaime ;
Jordan, Ronald ;
Hoffmann, Matthew ;
DeMaio, William ;
Hug, Bruce .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2009, 64 (02) :263-270