PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
January 18, 2016Journal for ImmunoTherapy of Cancer229 citationsOpen Access

Novel technologies and emerging biomarkers for personalized cancer immunotherapy

View Full Paper
JYJianda YuanPHPriti S. HegdeRCRaphael Clynes

Key Points

Key points are not available for this paper at this time.

Abstract

The culmination of over a century's work to understand the role of the immune system in tumor control has led to the recent advances in cancer immunotherapies that have resulted in durable clinical responses in patients with a variety of malignancies. Cancer immunotherapies are rapidly changing traditional treatment paradigms and expanding the therapeutic landscape for cancer patients. However, despite the current success of these therapies, not all patients respond to immunotherapy and even those that do often experience toxicities. Thus, there is a growing need to identify predictive and prognostic biomarkers that enhance our understanding of the mechanisms underlying the complex interactions between the immune system and cancer. Therefore, the Society for Immunotherapy of Cancer (SITC) reconvened an Immune Biomarkers Task Force to review state of the art technologies, identify current hurdlers, and make recommendations for the field. As a product of this task force, Working Group 2 (WG2), consisting of international experts from academia and industry, assembled to identify and discuss promising technologies for biomarker discovery and validation. Thus, this WG2 consensus paper will focus on the current status of emerging biomarkers for immune checkpoint blockade therapy and discuss novel technologies as well as high dimensional data analysis platforms that will be pivotal for future biomarker research. In addition, this paper will include a brief overview of the current challenges with recommendations for future biomarker discovery.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Yuan et al. (2016) studied this question.

synapsesocial.com/papers/69d96f7be6ab964fb0835d67https://doi.org/10.1186/s40425-016-0107-3
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Association of peripheral blood absolute lymphocyte count (ALC) and clinical activity in patients (pts) with advanced melanoma treated with ipilimumab2009 · 62 citations
  2. 2KLF2 is a rate-limiting transcription factor that can be targeted to enhance regulatory T-cell production2014 · 62 citations
  3. 3B7-H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin-10 secretion1999 · 2,503 citations
  4. 4Pembrolizumab for the Treatment of Non–Small-Cell Lung Cancer2015 · 6,293 citations
  5. 5Pretreatment Serum VEGF Is Associated with Clinical Response and Overall Survival in Advanced Melanoma Patients Treated with Ipilimumab2014 · 141 citations