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Monoclonal antibodies in clinical oncology
S Dalle1, C Thieblemont, L Thomas
1Hospices Civils de Lyon, Lyon, France. stephane.dalle@chu-lyon.fr
Abstract:
Monoclonal antibodies have yet considerably modified the field of clinical oncology. The growing knowledge of key cellular pathways in tumor induction and progression, targeted therapies represent an increasing proportion of new drugs entering clinical trials. Some molecules such as trastuzumab, rituximab, alemtuzumab, cetuximab are now widely used in clinical practice. These antibodies are now tested in different indications alone or in combination with standard chemotherapy. They are also developed for the treatment of inflammatory diseases (rituximab). Numerous others antibodies are currently in pre-clinical and clinical development phases for several malignancies including renal carcinoma, melanoma, lymphomas, leukaemia, breast, ovarian and colorectal cancer. An alternative approach is to conjugate the monoclonal antibody to a toxin, a cytotoxic agent, or a radioisotope. In other cases these antibodies aim to modify the tumour microenvironment through inhibition of angiogenesis or enhancing host immune response against cancer. If the molecule targeted by the antibodies is clearly identified, most often the precise mechanism of action of these immunoglobulins is not fully understood. They can have direct effects in inducing apoptosis or programmed cell death. They can block growth factor receptors, efficiently arresting proliferation of tumor cells. Indirect effects include recruiting cells that exert cytotoxicity, such as monocytes and macrophages (ADCC). Monoclonal antibodies also bind complement, leading to toxicity known as complement dependent cytotoxicity (CDC). The side effects associated with these new treatments were in part foreseeable depending on the affected cell or function. But new or surprising side effects emerged from clinical studies. We present an overview of the monoclonal antibodies used in clinical oncology or currently in development phases. We particularly focus on recent development including new indications, clinical trial results and specific side effects of monoclonal antibodies used in the treatment of cancer.
Insights
Monoclonal antibodies have revolutionized cancer treatment, with many now in clinical use or development. This review covers their mechanisms, applications, and emerging side effects in oncology.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Monoclonal antibodies (mAbs) have significantly advanced clinical oncology.
- Targeted therapies, including mAbs, represent a growing segment of new cancer drugs.
- mAbs are increasingly used in various cancer types, alone or with chemotherapy, and for inflammatory diseases.
Purpose of the Study:
- To provide an overview of monoclonal antibodies in clinical oncology and development.
- To highlight recent advancements, including new indications and clinical trial outcomes.
- To focus on specific side effects associated with monoclonal antibody cancer therapies.
Main Methods:
- Review of current literature on monoclonal antibodies in oncology.
- Analysis of clinical trial data for monoclonal antibody therapies.
- Examination of proposed mechanisms of action and observed side effects.
Main Results:
- Several monoclonal antibodies (e.g., trastuzumab, rituximab) are established in clinical practice.
- Numerous mAbs are in preclinical and clinical development for various malignancies.
- Mechanisms of action include direct apoptosis induction, growth factor receptor blockade, antibody-dependent cell-mediated cytotoxicity (ADCC), and complement-dependent cytotoxicity (CDC).
- While some side effects are predictable, novel and unexpected adverse events have emerged.
Conclusions:
- Monoclonal antibodies are a cornerstone of modern cancer therapy, with ongoing expansion in their applications.
- Understanding their diverse mechanisms and potential side effects is crucial for effective clinical management.
- Continued research into mAb development and application promises further improvements in cancer treatment outcomes.
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