SITC cancer immunotherapy resource document: a compass in the land of biomarker discovery

被引:27
作者
Hu-Lieskovan, Siwen [1 ,2 ]
Bhaumik, Srabani [3 ]
Dhodapkar, Kavita [4 ,5 ]
Grivel, Jean-Charles J. B. [6 ]
Gupta, Sumati [1 ]
Hanks, Brent A. [7 ]
Janetzki, Sylvia [8 ]
Kleen, Thomas O. [9 ]
Koguchi, Yoshinobu [10 ]
Lund, Amanda W. [11 ]
Maccalli, Cristina [6 ]
Mahnke, Yolanda D. [12 ]
Novosiadly, Ruslan D. [13 ]
Selvan, Senthamil R. [14 ]
Sims, Tasha [15 ]
Zhao, Yingdong [16 ]
Maecker, Holden T. [17 ]
机构
[1] Huntsman Canc Inst, Salt Lake City, UT USA
[2] Univ Utah, Sch Med, Salt Lake City, UT USA
[3] Roche Tissue Diagnost, Tucson, AZ USA
[4] Emory Univ, Dept Pediat, Atlanta, GA 30322 USA
[5] Childrens Healthcare Atlanta, Aflac Canc & Blood Disorders Ctr, Atlanta, GA USA
[6] Sidra Med, Res Dept, Doha, Qatar
[7] Duke Univ, Med Ctr, Durham, NC USA
[8] ZellNet Consulting Inc, Ft Lee, NJ USA
[9] Immodulon Therapeut Ltd, Uxbridge, Middx, England
[10] Providence Canc Inst, Earle A Chiles Res Inst, Portland, OR USA
[11] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[12] FlowKnowHow LLC, Brooklyn, NY USA
[13] Bristol Myers Squibb, Princeton, NJ USA
[14] BioMarker Strategies LLC, Rockville, MD USA
[15] Regeneron Pharmaceut Inc, 777 Old Saw Mill River Rd, Tarrytown, NY 10591 USA
[16] NCI, Bethesda, MD 20892 USA
[17] Stanford Univ, Med Ctr, Stanford, CA 94305 USA
关键词
immunotherapy; biomarkers; tumor; antigens; computational biology; immunomodulation; CELL LUNG-CANCER; MINIMAL RESIDUAL DISEASE; POSITRON-EMISSION-TOMOGRAPHY; GENE-EXPRESSION DATA; REGULATORY T-CELLS; IMMUNE-CHECKPOINT BLOCKADE; PHASE-III TRIAL; RNA-SEQ DATA; FLOW-CYTOMETRY; MASS CYTOMETRY;
D O I
10.1136/jitc-2020-000705
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since the publication of the Society for Immunotherapy of Cancer's (SITC) original cancer immunotherapy biomarkers resource document, there have been remarkable breakthroughs in cancer immunotherapy, in particular the development and approval of immune checkpoint inhibitors, engineered cellular therapies, and tumor vaccines to unleash antitumor immune activity. The most notable feature of these breakthroughs is the achievement of durable clinical responses in some patients, enabling long-term survival. These durable responses have been noted in tumor types that were not previously considered immunotherapy-sensitive, suggesting that all patients with cancer may have the potential to benefit from immunotherapy. However, a persistent challenge in the field is the fact that only a minority of patients respond to immunotherapy, especially those therapies that rely on endogenous immune activation such as checkpoint inhibitors and vaccination due to the complex and heterogeneous immune escape mechanisms which can develop in each patient. Therefore, the development of robust biomarkers for each immunotherapy strategy, enabling rational patient selection and the design of precise combination therapies, is key for the continued success and improvement of immunotherapy. In this document, we summarize and update established biomarkers, guidelines, and regulatory considerations for clinical immune biomarker development, discuss well-known and novel technologies for biomarker discovery and validation, and provide tools and resources that can be used by the biomarker research community to facilitate the continued development of immuno-oncology and aid in the goal of durable responses in all patients.
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页数:55
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