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CAR T and CAR NK cells in multiple myeloma: Expanding the targets
Urvi A Shah1, Sham Mailankody1
1Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA.
Abstract:
Multiple myeloma (MM) is a haematologic malignancy with significant improvements in the overall survival over the last decade. However, patients still relapse and die due to a lack of treatment options. Ultimately, novel therapies with the potential for long term remissions are needed for patients with advanced MM. Research efforts for such immune therapies were not successful until recently when the first immunotherapies for MM were approved in 2015 and many more are under development. In this review, we focus on adoptive cell therapies including CAR T-cell and CAR NK-cell therapies for patients with MM. We will provide an update on clinical and translational advances with a focus on results from ongoing clinical trials with BCMA targeted cellular therapies and the development of other novel targets, changes in the manufacturing process, trials focusing on earlier lines of therapy and combinations with other therapies as well as off the shelf products.
Insights
Adoptive cell therapies, like CAR T-cell and CAR NK-cell therapies, show promise for treating advanced multiple myeloma (MM). Ongoing research focuses on novel targets and combination strategies to improve long-term remissions for MM patients.
Area of Science:
- Hematology
- Immunotherapy
- Oncology
Background:
- Multiple myeloma (MM) is a blood cancer with improved survival, but relapse remains a challenge.
- Novel treatments are crucial for advanced MM, necessitating research into effective immunotherapies.
- Recent approvals and ongoing development mark a new era for immunotherapy in MM treatment.
Purpose of the Study:
- To review advancements in adoptive cell therapies for multiple myeloma.
- To highlight clinical and translational progress in CAR T-cell and CAR NK-cell therapies.
- To discuss emerging targets, manufacturing improvements, and combination strategies for MM treatment.
Main Methods:
- Review of clinical trials and translational research in adoptive cell therapy for MM.
- Focus on B-cell maturation antigen (BCMA) targeted therapies.
- Analysis of manufacturing process changes and combination therapy trials.
Main Results:
- First immunotherapies for MM approved in 2015, with many more in development.
- Clinical trials are evaluating BCMA-targeted cellular therapies.
- Research is exploring novel targets, earlier treatment lines, and combination approaches.
Conclusions:
- Adoptive cell therapies, including CAR T-cell and CAR NK-cell therapies, represent a significant advancement in MM treatment.
- Further research into novel targets, manufacturing, and combination therapies is essential for improving patient outcomes.
- The development of off-the-shelf products could broaden accessibility to these innovative treatments.
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