Lung-MAP-framework, overview, and design principles

被引:31
作者
Ferrarotto, Renata [1 ]
Redman, Mary W. [2 ]
Gandara, David R. [3 ]
Herbst, Roy S. [4 ]
Papadimitrakopoulou, Vassiliki A. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Thorac & Head & Neck Med Oncol, Houston, TX 77030 USA
[2] Fred Hutchinson Canc Ctr, Clin Stat, Clin Res Div, Seattle, WA USA
[3] Univ Calif Davis, Canc Ctr, Sacramento, CA 95817 USA
[4] Yale Sch Med, Yale Canc Ctr, New Haven, CT USA
关键词
Clinical trial; lung cancer; master protocol; squamous cell carcinoma (SCC);
D O I
10.3978/j.issn.2304-3865.2015.09.02
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastatic lung squamous cell carcinoma (SCC) is a common disease with limited therapeutic options and poor patient outcomes. Standard "all comers" clinical trial designs usually benefit only a small population sub-group. Targeted-therapy matched clinical trials have a higher potential to achieve better results, however, given the low frequency of driver genetic alterations, they are associated with a large number of screen-failures, are not cost-effective, and frequently not feasible. Lung-MAP is an umbrella master protocol for recurrent or metastatic lung SCC patients that uses a central genomic profiling screening platform to allocate patients to phase II/III biomarker-matched target therapy clinical trials or to a "non-match" treatment arm; therefore, all eligible patients screened can be treated under the protocol. If evidence of efficacy is seen in the phase II trial portion for a particular treatment/marker combination, that sub-study moves directly to phase III and incorporates the patients treated in phase II. Lung-MAP has an efficient and adaptable structure that allows for sub-studies to open and close based on changes in an evolving cancer research field. It also provides a path for FDA-approval in order to bring promising agents to clinic in a time efficient manner, with the ultimate goal of significantly improving lung SCC patient's quality and length of life.
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页数:6
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