Papillary Renal Cell Carcinoma: Current Progress and Future Directions

被引:21
作者
Twardowski, Przemyslaw W. [1 ,2 ]
Mack, Philip C. [2 ,3 ]
Lara, Primo N., Jr. [2 ,3 ]
机构
[1] City Hope Natl Med Ctr, Dept Med Oncol, Duarte, CA 91010 USA
[2] SW Oncol Grp, Portland, OR USA
[3] Univ Calif Davis, Ctr Comprehens Canc, Div Hematol Oncol, Sacramento, CA 95817 USA
关键词
ARQ197; EGFR pathway; Erlotinib; MET pathway; Tivantinib; MET PROTOONCOGENE; INTERFERON-ALPHA; LUNG-CANCER; MUTATIONS; SORAFENIB; SUNITINIB; EFFICACY; DOMAIN;
D O I
10.1016/j.clgc.2013.11.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Papillary renal cell carcinoma (pRCC) represents the second most common histologic variant of kidney cancer. It exhibits a different molecular signature than clear-cell carcinoma and is typically not associated with mutations in the VHL (von Hippel-Lindau) tumor suppressor gene. pRCC is less responsive to modern drugs introduced in the management of kidney cancer in the past decade. In this article, the heredity and biology of 2 main variants of pRCC are outlined. New targets that are being explored in the treatment of this disease are discussed, with particular emphasis on inhibition of mesenchymal epithelial transition (MET) and epidermal growth factor receptor (EGFR) pathways. We discuss preclinical data providing rationale for the combination of MET and EGFR inhibitors and review recently completed and ongoing clinical trials that attempt to expand our therapeutic options for this important subset of kidney cancer. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:74 / 79
页数:6
相关论文
共 30 条
  • [1] C-met inhibitors with novel binding mode show activity against several hereditary papillary renal cell carcinoma-related mutations
    Bellon, Steven F.
    Kaplan-Lefko, Paula
    Yang, Yajing
    Zhang, Yihong
    Moriguchi, Jodi
    Rex, Karen
    Johnson, Carol W.
    Rose, Paul E.
    Long, Alexander M.
    O'Connor, Anne B.
    Gu, Yan
    Coxon, Angela
    Kim, Tae-Seong
    Tasker, Andrew
    Burgess, Teresa L.
    Dussault, Isabelle
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (05) : 2675 - 2683
  • [2] Blank CU, 2012, J CLIN ONCOL S5, V30
  • [3] Choueiri TK, 2008, J CLIN ONCOL, V26, P127, DOI 10.1200/JCO.2007.13.3223
  • [4] Phase II and Biomarker Study of the Dual MET/VEGFR2 Inhibitor Foretinib in Patients With Papillary Renal Cell Carcinoma
    Choueiri, Toni K.
    Vaishampayan, Ulka
    Rosenberg, Jonathan E.
    Logan, Theodore F.
    Harzstark, Andrea L.
    Bukowski, Ronald M.
    Rini, Brian I.
    Srinivas, Sandy
    Stein, Mark N.
    Adams, Laurel M.
    Ottesen, Lone H.
    Laubscher, Kevin H.
    Sherman, Laurie
    McDermott, David F.
    Haas, Naomi B.
    Flaherty, Keith T.
    Ross, Robert
    Eisenberg, Peter
    Meltzer, Paul S.
    Merino, Maria J.
    Bottaro, Donald P.
    Linehan, W. Marston
    Srinivasan, Ramaprasad
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (02) : 181 - 186
  • [5] Molecular genetics of familial renal cell carcinoma syndromes
    Cohen, D
    Zhou, M
    [J]. CLINICS IN LABORATORY MEDICINE, 2005, 25 (02) : 259 - +
  • [6] Delahunt B, 1997, MODERN PATHOL, V10, P537
  • [7] MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling
    Engelman, Jeffrey A.
    Zejnullahu, Kreshnik
    Mitsudomi, Tetsuya
    Song, Youngchul
    Hyland, Courtney
    Park, Joon Oh
    Lindeman, Neal
    Gale, Christopher-Michael
    Zhao, Xiaojun
    Christensen, James
    Kosaka, Takayuki
    Holmes, Alison J.
    Rogers, Andrew M.
    Cappuzzo, Federico
    Mok, Tony
    Lee, Charles
    Johnson, Bruce E.
    Cantley, Lewis C.
    Janne, Pasi A.
    [J]. SCIENCE, 2007, 316 (5827) : 1039 - 1043
  • [8] Escudier B, 2013, EUROPEAN CANC C
  • [9] Escudier BJ, 2008, ASCO M, V26, P5025
  • [10] Garcia A, 2007, J CLIN ONCOL, V25