Anti-cancer immune response mechanisms in neoadjuvant and targeted therapy
Carsten Denkert1, Silvia Darb-Esfahani, Sibylle Loibl
1Institute of Pathology, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany. carsten.denkert@charite.de
Abstract:
Several studies suggest that the progression of malignant tumors as well as the response to chemotherapy and targeted therapy is critically dependent on the immunological parameters that are derived from the host immune system as well as a modulation of the immune system by therapeutic antibodies. It has been shown for many tumor types that the presence of a lymphocytic infiltrate in different types of cancers is a positive factor for clinical outcome and that the response to neoadjuvant chemotherapy is increased in a tumor with a prominent pretherapeutic infiltrate. Furthermore, new targeted therapies in breast cancer, such as trastuzumab, as well as in hematological malignancies, such as rituximab and alemtuzumab, have been shown to interact with immunological pathways, and this interaction is critical for response and clinical outcome. In neoplasms of lymphoid and hematopoietic tissues, targeted therapies not only reduce toxic effects on normal tissues but also lead to modulations of the immune system depending on the target molecule, its physiological function and cellular distribution. This review gives an overview on clinical data on response to classical chemotherapy as well as molecular targeted therapy and its interaction with the immune system.
Insights
Tumor progression and treatment response depend on the host immune system and therapeutic antibodies. Understanding these immunological parameters is key for improving cancer therapies and clinical outcomes.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Malignant tumor progression is influenced by host immunological parameters.
- Lymphocytic infiltration in tumors correlates with improved clinical outcomes.
- Therapeutic antibodies modulate immune responses, impacting cancer treatment efficacy.
Purpose of the Study:
- To review clinical data on the interaction between cancer therapies and the immune system.
- To explore the role of immunological parameters in chemotherapy and targeted therapy response.
- To provide an overview of immune system modulation by targeted therapies.
Main Methods:
- Review of existing clinical data.
- Analysis of studies on chemotherapy and targeted therapy response.
- Examination of immunological pathways affected by therapeutic antibodies.
Main Results:
- Lymphocytic infiltrate is a positive prognostic factor in various cancers.
- Pre-therapeutic lymphocytic infiltrate enhances response to neoadjuvant chemotherapy.
- Targeted therapies like trastuzumab, rituximab, and alemtuzumab interact with immune pathways, crucial for outcomes.
Conclusions:
- Immune system modulation is critical for the efficacy of both classical chemotherapy and targeted therapies.
- Understanding host immune parameters can optimize cancer treatment strategies.
- Targeted therapies can modulate the immune system, influencing treatment effectiveness and toxicity.
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