Summary statement - Novel Agents in the Treatment of Lung Cancer: Fifth Cambridge Conference assessing opportunities for combination therapy

被引:27
|
作者
Lynch, Thomas J., Jr. [1 ]
Blumenschein, George R., Jr. [2 ]
Engelman, Jeffrey A. [1 ]
Espinoza-Delgado, Igor [3 ]
Govindan, Ramaswamy [4 ]
Hanke, Jeff [5 ]
Hanna, Nasser H. [6 ]
Heymach, John V. [2 ]
Hirsch, Fred R. [7 ]
Janne, Pasi A. [8 ]
Lilenbaum, Rogerio C. [9 ]
Natale, Ronald B. [10 ]
Riely, Gregory J. [11 ]
Sequist, Lecia V. [1 ]
Shapiro, Geoffrey T. [8 ]
Shaw, Alice [12 ]
Shepherd, Frances A. [13 ]
Socinski, Mark [14 ]
Sorensen, A. Gregory [15 ]
Wakelee, Heather A. [16 ]
Weitzman, Aaron [17 ]
机构
[1] Massachusetts Gen Hosp, Ctr Canc, Boston, MA 02114 USA
[2] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] NCI, Bethesda, MD 20892 USA
[4] Washington Univ, Sch Med, St Louis, MO USA
[5] AstraZeneca, Waltham, MA USA
[6] Indiana Univ, Sch Med, Indianapolis, IN USA
[7] Univ Colorado, Ctr Canc, Denver, CO 80262 USA
[8] Dana Farber Canc Inst, Boston, MA 02115 USA
[9] Mt Sinai Comprehens Canc Ctr, Miami Beach, FL USA
[10] Cedars Sinai Outpatient Canc Ctr, Los Angeles, CA USA
[11] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[12] MIT, Ctr Canc Res, Cambridge, MA 02139 USA
[13] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[14] Univ N Carolina, Chapel Hill, NC USA
[15] Massachusetts Gen Hosp, MGH HST AA Martinos Ctr Biomed Imaging, Charlestown, MA USA
[16] Stanford Univ, Ctr Canc, Stanford, CA 94305 USA
[17] Genentech Inc, San Francisco, CA 94080 USA
关键词
lung cancer; profiling; biopsies; EGFR; VEGF; novel targets;
D O I
10.1097/JTO.0b013e318174e9d3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The promise of effective targeted therapy for lung cancer requires rigorous identification of potential targets combined with intensive discovery and development efforts aimed at developing effective "drugs" for these targets. We now recognize that getting the right drug to the right target in the right patient is more complicated than one could have imagined a decade ago. As knowledge of targets and development of agents have proliferated and advanced, so too have data demonstrating the biologic heterogeneity of tumors. The finding that lung cancers are genetically diverse and can exhibit several pathways of resistance in response to targeted agents makes the prospect for curative therapy more daunting. It is becoming increasingly clear that single-agent treatment will be the exception rather than the rule. This information raises important new questions about the development and assessment of novel agents in lung cancer treatment: (1) How do we identify the most important drug targets for tumor initiation and maintenance? (2) What is the best way to assess drug candidates that may only be relevant in a small fraction of patients? (3) What models do we use to predict clinical response and identify effective combinations? And (4) how do we bring combination regimens to the clinic, particularly when the agents are not yet approved individually and may be under development from different companies? The Fifth Cambridge Conference on Novel Agents in the Treatment of Lung Cancer was held in Cambridge, Massachusetts, on October 1-2, 2007, to discuss these questions by reviewing recent progress in the field and advancing recommendations for research and patient care. New information, conclusions, and recommendations considered significant for the field by the program faculty are summarized here and presented at greater length in the individual articles and accompanying discussions that comprise the full conference proceedings. A CME activity based on this summary is also available at www.informedicalcme.com/cme.
引用
收藏
页码:S107 / S112
页数:6
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