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Author Spotlight: Unlocking Insights into the Immune Cell Landscape of Tumors
Published on: August 18, 2023
Insights into immuno-oncology drug development landscape with focus on bone metastasis
Tiina E Kähkönen1, Jussi M Halleen1, Gary MacRitchie2
1OncoBone Ltd, Oulu, Finland.
Abstract:
Bone is among the main sites of metastasis in breast, prostate and other major cancers. Bone metastases remain incurable causing high mortality, severe skeletal-related effects and decreased quality of life. Despite the success of immunotherapies in oncology, no immunotherapies are approved for bone metastasis and no clear benefit has been observed with approved immunotherapies in treatment of bone metastatic disease. Therefore, it is crucial to consider unique features of tumor microenvironment in bone metastasis when developing novel therapies. The vicious cycle of bone metastasis, referring to crosstalk between tumor and bone cells that enables the tumor cells to grow in the bone microenvironment, is a well-established concept. Very recently, a novel osteoimmuno-oncology (OIO) concept was introduced to the scientific community. OIO emphasizes the significance of interactions between tumor, immune and bone cells in promoting tumor growth in bone metastasis, and it can be used to reveal the most promising targets for bone metastasis. In order to provide an insight into the current immuno-oncology drug development landscape, we used 1stOncology database, a cancer drug development resource to identify novel immunotherapies in preclinical or clinical development for breast and prostate cancer bone metastasis. Based on the database search, 24 immunotherapies were identified in preclinical or clinical development that included evaluation of effects on bone metastasis. This review provides an insight to novel immuno-oncology drug development in the context of bone metastasis. Bone metastases can be approached using different modalities, and tumor microenvironment in bone provides many potential targets for bone metastasis. Noting current increasing interest in the field of OIO, more therapeutic opportunities that primarily target bone metastasis are expected in the future.
Insights
Novel immunotherapies targeting bone metastasis are emerging, focusing on the tumor microenvironment and osteoimmuno-oncology (OIO). Research identified 24 immunotherapies in development for breast and prostate cancer bone metastasis.
Area of Science:
- Oncology
- Immunology
- Bone Biology
Background:
- Bone metastases are a significant challenge in breast, prostate, and other cancers, leading to high mortality and poor quality of life.
- Current immunotherapies show limited efficacy against bone metastasis, highlighting the need for novel therapeutic strategies.
- The tumor microenvironment in bone plays a critical role in the progression of bone metastasis, involving complex interactions between tumor cells, immune cells, and bone cells.
Purpose of the Study:
- To review the current landscape of immuno-oncology drug development for bone metastasis.
- To identify novel immunotherapies targeting the unique bone tumor microenvironment.
- To explore the emerging field of osteoimmuno-oncology (OIO) for therapeutic opportunities.
Main Methods:
- Utilized the 1stOncology database, a cancer drug development resource.
- Identified immunotherapies in preclinical or clinical development for breast and prostate cancer bone metastasis.
- Focused on therapies evaluating effects on bone metastasis.
Main Results:
- Identified 24 immunotherapies in preclinical or clinical development for bone metastasis.
- These therapies target various aspects of the bone tumor microenvironment.
- The study highlights the growing interest and development in osteoimmuno-oncology.
Conclusions:
- The bone tumor microenvironment offers numerous potential therapeutic targets for bone metastasis.
- The novel osteoimmuno-oncology (OIO) concept provides a framework for understanding and targeting these interactions.
- Further development of OIO-based therapies is expected to yield new treatment opportunities for bone metastasis.
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