Targeted therapies and the treatment of non-clear cell renal cell carcinoma

被引:47
作者
Bellmunt, J. [1 ]
Dutcher, J. [2 ]
机构
[1] Univ Hosp del Mar IMIM, Solid Tumor Oncol GU & GI, Med Oncol Serv, Barcelona 08003, Spain
[2] St Lukes Roosevelt Hosp, Beth Israel Med Ctr, Continuum Canc Ctr, New York, NY USA
关键词
chromophobe renal cell carcinoma; non-clear cell RCC; papillary RCC; sarcomatoid features; targeted therapies; Xp11 translocated RCC; INTERFERON-ALPHA; HISTOLOGIC SUBTYPES; EXPANDED-ACCESS; C-MET; SARCOMATOID DIFFERENTIATION; RADIOFREQUENCY ABLATION; ONCOLOGICAL OUTCOMES; CYTOGENETIC FEATURES; PROGNOSTIC-FACTORS; MTOR PATHWAY;
D O I
10.1093/annonc/mdt152
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Targeted therapies have shown profound effects on the outcome of patients with advanced renal cell carcinoma (RCC). However, the optimal treatment for RCC of non-clear cell histology (nccRCC)-typically excluded from trials of targeted agents-remains uncertain. Materials and methods: By carrying out extensive searches of PubMed and ASCO databases, we identified and summarised research into the biological characteristics, clinical behaviour and treatment of different histological subtypes of nccRCC, focusing on targeted therapy. Results: The available data suggest that treatments currently approved for RCC are active in ncc subtypes, although the overall clinical benefit may be less than for clear cell RCC. Temsirolimus has proven benefit over interferon-alfa (IFN-alpha) in patients with nccRCC, based on phase Ill data, while everolimus, sunitinib and sorafenib have all demonstrated some degree of activity in nccRCC in expanded-access trials. No clear picture has emerged of whether individual histological subtypes are particularly responsive to any individual treatment. Conclusions: Further molecular studies into the pathogenesis of RCC histological subtypes will help direct the development of novel, appropriate targeted agents. Clinical trials specifically designed to evaluate the role of targeted agents in nccRCC are ongoing, and data from trials with sunitinib and everolimus will be reported soon.
引用
收藏
页码:1730 / 1740
页数:11
相关论文
共 113 条
[1]  
Albiges L., 2010, 5 EUR INT KIDN CANC
[2]   Chromophobe Renal Cell Carcinoma: Histomorphologic Characteristics and Evaluation of Conventional Pathologic Prognostic Parameters in 145 Cases [J].
Amin, Mahul B. ;
Paner, Gladell P. ;
Alvarado-Cabrero, Isabel ;
Young, Andrew N. ;
Stricker, Hans J. ;
Lyles, Robert H. ;
Moch, Holger .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2008, 32 (12) :1822-1834
[3]  
[Anonymous], 35 EUR SOC MED ONC C
[4]  
[Anonymous], 2012, NCCN clinical practice guidelines in oncology: Breast cancer
[5]  
[Anonymous], J CLIN ONCOL S5
[6]   Cytogenetic features, clinical significance and prognostic impact of type 1 and type 2 papillary renal cell carcinoma [J].
Antonelli, Alessandro ;
Tardanico, Regina ;
Balzarini, Piera ;
Arrighi, Nicola ;
Perucchini, Laura ;
Zanotelli, Tiziano ;
Cozzoli, Alberto ;
Zani, Danilo ;
Cunico, Sergio Cosciani ;
Simeone, Claudio .
CANCER GENETICS AND CYTOGENETICS, 2010, 199 (02) :128-133
[7]   Xp11 translocation renal cell carcinoma in adults: Expanded clinical, pathologic, and genetic spectrum [J].
Argani, Pedram ;
Olgac, Semra ;
Tickoo, Satish K. ;
Goldfischer, Michael ;
Moch, Holger ;
Chan, David Y. ;
Eble, John N. ;
Bonsib, Stephen M. ;
Jimeno, Mireya ;
Lloreta, Josep ;
Billis, Athanase ;
Hicks, Jessica ;
De Marzo, Angelo M. ;
Reuter, Victor E. ;
Ladanyi, Marc .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2007, 31 (08) :1149-1160
[8]  
Atkins MB, ED LECT ASCO GEN CAN
[9]   Genetic and epigenetic analysis of von Hippel-Lindau (VHL) gene alterations and relationship with clinical variables in sporadic renal cancer [J].
Banks, RE ;
Tirukonda, P ;
Taylor, C ;
Hornigold, N ;
Astuti, D ;
Cohen, D ;
Maher, ER ;
Stanley, AJ ;
Harnden, P ;
Joyce, A ;
Knowles, M ;
Selby, PJ .
CANCER RESEARCH, 2006, 66 (04) :2000-2011
[10]   Final results of the European Advanced Renal Cell Carcinoma Sorafenib (EU-ARCCS) expanded-access study: a large open-label study in diverse community settings [J].
Beck, J. ;
Procopio, G. ;
Bajetta, E. ;
Keilholz, U. ;
Negrier, S. ;
Szczylik, C. ;
Bokemeyer, C. ;
Bracarda, S. ;
Richel, D. J. ;
Staehler, M. ;
Strauss, U. P. ;
Mersmann, S. ;
Burock, K. ;
Escudier, B. .
ANNALS OF ONCOLOGY, 2011, 22 (08) :1812-1823