Success of cancer immunotherapy is limited by the ability of solid tumors to evade local and systemic antitumoral immune responses. Several mechanisms of tumor immune evasion have been identified, including low intratumor expression of antigens and elevated expression of inhibitory co-regulatory molecules. An effective immunotherapy is one which would induce necrotic cell death and accompanying proinflammatory cytokine induction. Stereotactic Body Radiotherapy (SBRT) or Intensity Modulated Radiotherapy (IMRT) or brachytherapy, which is capable of delivering high, conformal radiation doses (\>8 Gy) of tumor ablative radiation may be an effective means of conditioning a tumor bed to a state favorable to the initiation of robust antitumoral immune responses.
Study Type
OBSERVATIONAL
Enrollment
98
Mayo Clinic in Rochester
Rochester, Minnesota, United States
Change in immune biomarkers from baseline and after radiation treatments for breast, prostate, and lung cancers.
Changes in baseline circulating tumor reactive immune markers after radiotherapy.
Time frame: Before and after SBRT, IMRT, or brachytherapy
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