From Famine to Feast: Developing Early-Phase Combination Immunotherapy Trials Wisely

被引:12
作者
Day, Daphne [1 ,2 ,3 ]
Monjazeb, Arta M. [4 ]
Sharon, Elad [5 ]
Ivy, S. Percy [5 ]
Rubin, Eric H. [6 ]
Rosner, Gary L. [7 ]
Butler, Marcus O. [1 ,2 ]
机构
[1] Princess Margaret Canc Ctr, Drug Dev Program, Div Med Oncol & Hematol, Toronto, ON, Canada
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] Ontario Inst Canc Res, Toronto, ON, Canada
[4] UC Davis Comprehens Canc Ctr, Dept Radiat Oncol, Sacramento, CA USA
[5] NCI, Canc Therapy Evaluat Program, Bethesda, MD 20892 USA
[6] Merck & Co Inc, Merck Res Labs, Kenilworth, NJ USA
[7] Johns Hopkins, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
关键词
CELL LUNG-CANCER; NIVOLUMAB PLUS IPILIMUMAB; RESISTANT PROSTATE-CANCER; DESIGN TASK-FORCE; QUALITY-OF-LIFE; OPEN-LABEL; PD-1; BLOCKADE; CLINICAL-TRIALS; 1ST-LINE TREATMENT; CTLA-4;
D O I
10.1158/1078-0432.CCR-16-3064
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Not until the turn of this century has immunotherapy become a fundamental component of cancer treatment. While monotherapy with immune modulators, such as immune checkpoint inhibitors, provides a subset of patients with durable clinical benefit and possible cure, combination therapy offers the potential for antitumor activity in a greater number of patients. The field of immunology has provided us with a plethora of potential molecules and pathways to target. This abundance makes it impractical to empirically test all possible combinations efficiently. We recommend that potential immunotherapy combinations be chosen based on sound rationale and available data to address the mechanisms of primary and acquired immune resistance. Novel trial designs may increase the proportion of patients receiving potentially efficacious treatments and, at the same time, better define the balance of clinical activity and safety. We believe that implementing a strategic approach in the early development of immunotherapy combinations will expedite the delivery of more effective therapies with improved safety and durable outcomes. (C) 2017 AACR.
引用
收藏
页码:4980 / 4991
页数:12
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