Toward the individualization of lung cancer therapy

被引:17
作者
Anguiano, Ariel [1 ,2 ]
Nevins, Joseph R. [1 ,3 ]
Potti, Anil [1 ,2 ]
机构
[1] Duke Univ, Duke Inst Genome Sci & Policy, Med Ctr, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
关键词
expression signature; improved prognosis; chemotherapy prediction; pathway prediction;
D O I
10.1002/cncr.23644
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The goal of personalized cancer medicine is to effectively match the right treatment strategy with the patient. This includes an improvement of prognosis to identify which patients should be treated as well as the ability to predict which therapy will be most effective for the individual patient. Recent advances in the use of genomic technologies, primarily gene expression profiling with DNA microarrays, has provided mechanisms to address each of these questions. The prognosis of early-stage lung cancer patients (stage IA) is clearly imprecise because nearly 30% of these patients will develop disease recurrence (determined according to the TNM staging system). Gene expression profiles have been developed that can accurately predict recurrence and, when applied to the population of patients with stage IA disease, demonstrate a capacity to potentially identify those individuals likely to have been misclassified as low risk. In addition, gene expression information has also demonstrated an ability to predict who will respond to a particular chemotherapy regimen, providing a further opportunity to more effectively guide the selection of available therapies that best match the individual patient. Finally, other strategies offer the hope of better using the newly developed, experimental therapies that target specific components of the oncogenic process. Taken together, these new genomic tools provide the opportunity to develop rational strategies for treating the individual long cancer patient.
引用
收藏
页码:1760 / 1767
页数:8
相关论文
共 65 条
  • [1] Genetic regulators of large-scale transcriptional signatures in cancer
    Adler, AS
    Lin, MH
    Horlings, H
    Nuyten, DSA
    van de Vijver, MJ
    Chang, HY
    [J]. NATURE GENETICS, 2006, 38 (04) : 421 - 430
  • [2] Intrinsic chemoresistance to gemcitabine is associated with decreased expression of BNIP3 in pancreatic cancer
    Akada, M
    Crnogorac-Jurcevic, T
    Lattimore, S
    Mahon, P
    Lopes, R
    Sunamura, M
    Matsuno, S
    Lemoine, NR
    [J]. CLINICAL CANCER RESEARCH, 2005, 11 (08) : 3094 - 3101
  • [3] Gene expression profiles predict complete pathologic response to neoadjuvant paclitaxel and fluorouracil, doxorubicin, and cyclophosphamide chemotherapy in breast cancer
    Ayers, M
    Symmans, WF
    Stec, J
    Damokosh, AI
    Clark, E
    Hess, K
    Lecocke, M
    Metivier, J
    Booser, D
    Ibrahim, N
    Valero, V
    Royce, M
    Arun, B
    Whitman, G
    Ross, J
    Sneige, N
    Hortobagyi, GN
    Pusztai, L
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (12) : 2284 - 2293
  • [4] Bachvarov D, 2006, INT J ONCOL, V29, P919
  • [5] Gene-expression profiles predict survival of patients with lung adenocarcinoma
    Beer, DG
    Kardia, SLR
    Huang, CC
    Giordano, TJ
    Levin, AM
    Misek, DE
    Lin, L
    Chen, GA
    Gharib, TG
    Thomas, DG
    Lizyness, ML
    Kuick, R
    Hayasaka, S
    Taylor, JMG
    Iannettoni, MD
    Orringer, MB
    Hanash, S
    [J]. NATURE MEDICINE, 2002, 8 (08) : 816 - 824
  • [6] The gene expression signature of relapse in paediatric acute lymphoblastic leukaemia: implications for mechanisms of therapy failure
    Beesley, AH
    Cummings, AJ
    Freitas, JR
    Hoffmann, K
    Firth, MJ
    Ford, J
    Klerk, NH
    Kees, UR
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2005, 131 (04) : 447 - 456
  • [7] Survival trees for analyzing clinical outcome in lung adenocarcinomas based on gene expression profiles:: Identification of neogenin and diacylglycerol kinase α expression as critical factors
    Berrar, D
    Sturgeon, B
    Bradbury, I
    Downes, CS
    Dubitzky, W
    [J]. JOURNAL OF COMPUTATIONAL BIOLOGY, 2005, 12 (05) : 534 - 544
  • [8] Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses
    Bhattacharjee, A
    Richards, WG
    Staunton, J
    Li, C
    Monti, S
    Vasa, P
    Ladd, C
    Beheshti, J
    Bueno, R
    Gillette, M
    Loda, M
    Weber, G
    Mark, EJ
    Lander, ES
    Wong, W
    Johnson, BE
    Golub, TR
    Sugarbaker, DJ
    Meyerson, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) : 13790 - 13795
  • [9] Oncogenic pathway signatures in human cancers as a guide to targeted therapies
    Bild, AH
    Yao, G
    Chang, JT
    Wang, QL
    Potti, A
    Chasse, D
    Joshi, MB
    Harpole, D
    Lancaster, JM
    Berchuck, A
    Olson, JA
    Marks, JR
    Dressman, HK
    West, M
    Nevins, JR
    [J]. NATURE, 2006, 439 (7074) : 353 - 357
  • [10] Gene signature evaluation as a prognostic tool: challenges in the design of the MINDACT trial
    Bogaerts, Jan
    Cardoso, Fatima
    Buyse, Marc
    Braga, Sofia
    Loi, Sherene
    Harrison, Jillian A.
    Bines, Jacques
    Mook, Stella
    Decker, Nuria
    Ravdin, Peter
    Therasse, Patrick
    Rutgers, Emiel
    van't Veer, Laura J.
    Piccart, Martine
    [J]. NATURE CLINICAL PRACTICE ONCOLOGY, 2006, 3 (10): : 540 - 551