Abstract
The tremendous clinical success of checkpoint blockers illustrates the potential of reestablishing latent immunosurveillance for cancer therapy. Although largely neglected in the clinical practice, accumulating evidence indicates that the efficacy of conventional and targeted anticancer agents does not only involve direct cytostatic/cytotoxic effects, but also relies on the (re)activation of tumor-targeting immune responses. Chemotherapy can promote such responses by increasing the immunogenicity of malignant cells, or by inhibiting immunosuppressive circuitries that are established by developing neoplasms. These immunological "side" effects of chemotherapy are desirable, and their in-depth comprehension will facilitate the design of novel combinatorial regimens with improved clinical efficacy.
| Original language | English |
|---|---|
| Pages (from-to) | 690-714 |
| Number of pages | 25 |
| Journal | Cancer Cell |
| Volume | 28 |
| Issue number | 6 |
| DOIs | |
| State | Published - Dec 14 2015 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Checkpoint blockade
- Immune contexture
- Immunogenic cell death
- Natural killer cells
- Tumor-associated macrophages
- Tumor-infiltrating lymphocytes
- Humans
- Neoplasms/drug therapy
- Tumor Microenvironment
- Treatment Outcome
- Molecular Targeted Therapy
- Signal Transduction/drug effects
- Immunologic Factors/adverse effects
- Animals
- Antineoplastic Agents/adverse effects
- Lymphocytes, Tumor-Infiltrating/drug effects
- Tumor Escape/drug effects
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