Mechanisms of Resistance in Multiple Myeloma
Athanasios Papadas1,2, Fotis Asimakopoulos3,4
1Division of Hematology and Oncology, Department of Medicine, University of Wisconsin-Madison, Madison, WI, 53705, USA. apapadas@medicine.wisc.edu.
Abstract:
Multiple myeloma (MM) is an incurable hematopoietic cancer that is characterized by malignant plasma cell infiltration of the bone marrow and/or extramedullary sites. Multi-modality approaches including "novel agents," traditional chemotherapy, and/or stem cell transplantation are used in MM therapy. Drug resistance, however, ultimately develops and the disease remains incurable for the vast majority of patients. In this chapter, we review both tumor cell-autonomous and non-autonomous (microenvironment-dependent) mechanisms of drug resistance. MM provides an attractive paradigm highlighting a number of current concepts and challenges in oncology. Firstly, identification of MM cancer stem cells and their unique drug resistance attributes may provide rational avenues towards MM eradication and cure. Secondly, the oligoclonal evolution of MM and alternation of "clonal tides" upon therapy challenge our current understanding of treatment responses. Thirdly, the success of MM "novel agents" provides exemplary evidence for the impact of therapies that target the immune and non-immune microenvironment. Fourthly, the rapid pace of drug approvals for MM creates an impetus for development of precision medicine strategies and biomarkers that promote efficacy and mitigate toxicity and cost. While routine cure of the disease remains the ultimate and yet unattainable prize, MM advances in the last 10-15 years have provided an astounding paradigm for the treatment of blood cancers in the modern era and have radically transformed patient outcomes.
Insights
Multiple myeloma (MM) is an incurable blood cancer. Research reviews drug resistance mechanisms and highlights advances in novel agents and microenvironment targeting for improved patient outcomes.
Area of Science:
- Hematology
- Oncology
- Cancer Biology
Background:
- Multiple myeloma (MM) is a fatal plasma cell malignancy.
- Current therapies include novel agents, chemotherapy, and stem cell transplantation.
- Drug resistance remains a significant challenge, limiting curative potential.
Purpose of the Study:
- To review tumor-intrinsic and microenvironment-dependent mechanisms of drug resistance in MM.
- To discuss current concepts and challenges in MM oncology.
- To highlight recent therapeutic advances and future directions.
Main Methods:
- Literature review of tumor cell-autonomous and microenvironment-dependent drug resistance mechanisms in MM.
- Analysis of MM evolution, cancer stem cells, and novel therapeutic strategies.
- Discussion of precision medicine and biomarker development in MM treatment.
Main Results:
- MM drug resistance involves both cancer cell-intrinsic factors and the tumor microenvironment.
- MM cancer stem cells may offer targets for eradication.
- Oligoclonal evolution and clonal dynamics complicate treatment responses.
- Targeting the immune and non-immune microenvironment shows therapeutic promise.
- Rapid drug approvals necessitate precision medicine approaches.
Conclusions:
- Advances in MM treatment have significantly improved patient outcomes.
- Understanding drug resistance mechanisms is crucial for developing curative strategies.
- Precision medicine and microenvironment-targeted therapies represent future directions for MM treatment.
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