Consensus Report of a Joint NCI Thoracic Malignancies Steering Committee: FDA Workshop on Strategies for Integrating Biomarkers into Clinical Development of New Therapies for Lung Cancer Leading to the Inception of "Master Protocols" in Lung Cancer

被引:18
作者
Malik, Shakun M. [1 ]
Pazdur, Richard [2 ,3 ]
Abrams, Jeffrey S. [1 ]
Socinski, Mark A. [4 ]
Sause, William T. [5 ]
Harpole, David H., Jr. [6 ]
Welch, John J. [1 ]
Korn, Edward L. [7 ]
Ullmann, Claudio Dansky [1 ]
Hirsch, Fred R. [8 ]
机构
[1] NCI, Clin Invest Branch, Canc Therapy Evaluat Program, NIH, Bethesda, MD 20850 USA
[2] US FDA, Off Hematol Prod, Ctr Drug Evaluat & Res, Silver Spring, MD USA
[3] US FDA, Off Oncol Prod, Ctr Drug Evaluat & Res, Silver Spring, MD USA
[4] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[5] Univ Utah, Salt Lake City, UT USA
[6] Duke Univ, Med Ctr, Durham, NC USA
[7] NCI, Biometr Res Branch, Canc Therapy Evaluat Program, NIH, Bethesda, MD 20850 USA
[8] Univ Colorado, Sch Med, Denver, CO USA
关键词
NCI/FDA workshop leading to the Inception of "Master; Protocols" in Lung Cancer; GROWTH-FACTOR RECEPTOR; PHASE-III TRIAL; PREDICTIVE BIOMARKERS; GEFITINIB; ERLOTINIB; DESIGN; CHEMOTHERAPY; MUTATIONS; SURVIVAL; MULTICENTER;
D O I
10.1097/JTO.0000000000000314
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
On February 2, 2012, the National Cancer Institute (NCI) sponsored a 2-day workshop with the NCI Thoracic Malignancies Steering Committee and the Food and Drug Administration to bring together leading academicians, clinicians, industry and government representatives to identify challenges and potential solutions in the clinical development of novel targeted therapies for lung cancer. Measures of success are rapidly evolving from a scientific and regulatory perspective and the objectives of this workshop were to achieve initial consensus on a high priority biomarker-driven clinical trial designed to rapidly assess the activity of targeted agents in molecularly defined lung cancer subsets and to facilitate generation of data leading to approval of these new therapies. Additionally, the meeting focused on identification of the barriers to conduct such a trial and the development of strategies to overcome those barriers. The "Lung Master Protocols" recently launched by NCI were the direct outcome of this workshop.
引用
收藏
页码:1443 / 1448
页数:6
相关论文
共 32 条
  • [1] [Anonymous], SEER CANC STAT REV 1
  • [2] I-SPY 2: An Adaptive Breast Cancer Trial Design in the Setting of Neoadjuvant Chemotherapy
    Barker, A. D.
    Sigman, C. C.
    Kelloff, G. J.
    Hylton, N. M.
    Berry, D. A.
    Esserman, L. J.
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2009, 86 (01) : 97 - 100
  • [3] Customizing cisplatin based on quantitative excision repair cross-complementing 1 mRNA expression:: A phase III trial in non-small-cell lung cancer
    Cobo, Manuel
    Isla, Dolores
    Massuti, Bartomeu
    Montes, Ana
    Miguel Sanchez, Jose
    Provencio, Mariano
    Vinolas, Nuria
    Paz-Ares, Luis
    Lopez-Vivanco, Guillermo
    Angel Munoz, Miguel
    Felip, Enriqueta
    Alberola, Vicente
    Camps, Carlos
    Domine, Manuel
    Sanchez, Jose Javier
    Sanchez-Ronco, Maria
    Danenberg, Kathleen
    Taron, Miquel
    Gandara, David
    Rosell, Rafael
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (19) : 2747 - 2754
  • [4] Rapidly rising clinical trial costs worry researchers
    Collier, Roger
    [J]. CANADIAN MEDICAL ASSOCIATION JOURNAL, 2009, 180 (03) : 277 - 278
  • [5] Rationale for Treatment and Study Design of TAILOR: A Randomized Phase III Trial of Second-line Erlotinib Versus Docetaxel in the Treatment of Patients Affected by Advanced Non-Small-Cell Lung Cancer With the Absence of Epidermal Growth Factor Receptor Mutations
    Farina, Gabriella
    Longo, Flavia
    Martelli, Olga
    Pavese, Ida
    Mancuso, Andrea
    Moscetti, Luca
    Labianca, Roberto
    Bertolini, Alessandro
    Cortesi, Enrico
    Farris, Antonio
    Fagnani, Daniele
    Locatelli, Maria Cristina
    Valmadre, Giuseppe
    Ardizzoia, Antonio
    Tomirotti, Maurizio
    Rulli, Eliana
    Garassino, Marina Chiara
    Scanni, Alberto
    [J]. CLINICAL LUNG CANCER, 2011, 12 (02) : 138 - 141
  • [6] Biomarker enrichment strategies: matching trial design to biomarker credentials
    Freidlin, Boris
    Korn, Edward L.
    [J]. NATURE REVIEWS CLINICAL ONCOLOGY, 2014, 11 (02) : 81 - 90
  • [7] The Cross-Validated Adaptive Signature Design
    Freidlin, Boris
    Jiang, Wenyu
    Simon, Richard
    [J]. CLINICAL CANCER RESEARCH, 2010, 16 (02) : 691 - 698
  • [8] Randomized Clinical Trials With Biomarkers: Design Issues
    Freidlin, Boris
    McShane, Lisa M.
    Korn, Edward L.
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2010, 102 (03) : 152 - 160
  • [9] George SL, 2012, APPL BIOINF BIOSTAT, P157, DOI 10.1007/978-1-4614-0140-7_7
  • [10] Randomized phase III clinical trial designs for targeted agents
    Hoering, Antje
    LeBlanc, Mike
    Crowley, John J.
    [J]. CLINICAL CANCER RESEARCH, 2008, 14 (14) : 4358 - 4367