Multiple myeloma (myeloma) is a complex cancer that can be difficult to diagnose and challenging to treat.
Every case of myeloma is unique in terms of disease characteristics, including genetic mutations.
Over more than 25 years of focusing exclusively on myeloma and related diseases, we have learned that targeting treatment to each individual’s disease holds the most promise for cure.
Advanced diagnostics at the Myeloma Center enable us to identify the specifics of each person’s disease and personalize a course of treatment for the best possible results.
Not only do we conduct advanced diagnostic testing, but we also have the expertise to interpret test results and understand their scientific basis and significance.
The ability to develop and utilize advanced diagnostic tools and fine-tune treatment accordingly is unique to the Myeloma Center.
Multiple myeloma is a cancer of plasma cells, a type of white blood cell.
Blood cells develop from blood-forming stem cells in the bone marrow. These stem cells mature into different types of blood cells – white blood cells, red blood cells and platelets. Plasma cells are white blood cells that make antibodies to help protect the body from germs and other harmful substances.
Molecular genetics & diagnostics
“Molecular genetics” refers to the study of the molecular processes underlying gene structure and function.
“Molecular diagnostics” refers to the application of molecular biology techniques and knowledge of the molecular mechanisms of disease to determine diagnosis, prognosis and treatment of disease.
Like other cancers, myeloma is characterized by genetic abnormalities, or mutations, that result from damage to normal cells. In particular, the biologic mechanisms that control normal cell growth are affected. This wreaks havoc with the function of the cells through altered patterns of gene activity, known as gene expression.
The unique characteristics of each individual’s genetic make-up and the genetic changes that give rise to cancer result in a truly unique profile of behavior for each person’s disease. Thus, no two cancers are absolutely identical. The same type of cancer (for example, myeloma or leukemia) is different for each individual.
Therefore, in order to determine the most effective treatment for an individual patient, it is very important to identify the unique characteristics of each person’s disease, including mutations and patterns of gene expression.
At the Myeloma Center we utilize a full array of standard diagnostic tools, such as blood profiling, Magnetic Resonance Imaging (MRI), skeletal survey, bone densitometry, Positron Emission Tomography-Computed Tomography (CT/PET), bone marrow biopsy and more.
In addition, we utilize genetic testing at the molecular level to reveal information about gene expression patterns and disease nuances. This helps us predict how myeloma cells are likely to respond to different therapeutic agents and strategies.
Gene Expression Profiling
The Myeloma Center pioneered the routine use of gene expression profiling (GEP) to uncover important information about myeloma biology.
Based on GEP studies of more than 1,300 newly diagnosed patients, our researchers
- Identified a set of four genes that allows us to predict with high probability which patients are likely to progress from MGUS (monoclonal gammopathy of undetermined significance, a precursor condition) to myeloma
- Developed a 70-gene test (GEP70) that identifies patients with high risk for short progression-free survival.
- Identified seven distinct molecular subtypes of myeloma.
- Identified mutations that affect response to therapy.
GEP studies are conducted at time of diagnosis and at various points throughout treatment.
Information gleaned from GEP studies is used to fine-tune and direct individualized therapies.
This is particularly important for patients with high-risk disease.
Predicting Response to Therapy
Gene expression profiling makes it possible to predict with significant accuracy how a patient will respond to treatment. Myeloma Center physicians select treatment plans with the best potential for curative outcome, based on the individual’s genetic profile.
Genomics refers to the study of genes and their functions. While genetics scrutinizes the functioning and composition of the single gene, genomics addresses all genes and their inter-relationships in order to identify their combined influence on the growth and development of cells.
Through advances in genomics, the Myeloma Center conducts studies that reveal high-level information for fine-tuning diagnosis and developing “precision medicine” treatments.
Specifically, we use DNA and RNA sequencing methods to look for a range of mutations that can help us target treatment. The data can inform us of treatment strategies and can help us identify approaches for cure. We also use Methylation Analysis to guide treatments that target tumor suppressor genes.
DNA sequencing is the process of determining the precise order of nucleotides within a DNA molecule. It includes any method or technology that is used to determine the order of the four bases—adenine, guanine, cytosine and thymine – in a strand of DNA. The development of rapid DNA sequencing methods has greatly accelerated biological and medical research and discovery.
The first DNA sequences were obtained in the early 1970s through laborious methods based on two-dimensional chromatography. Following the development of fluorescence-based sequencing methods with automated analysis, DNA sequencing has become much easier and faster.
Next-generation sequencing, via high-throughput technology, enables sequencing of multiple genes and samples at one time. The technologies parallelize the sequencing process, producing thousands or millions of sequences concurrently.
RNA Sequencing is a technology that uses the capabilities of next-generation sequencing to reveal the mutations causing myeloma that can be targeted with specific therapies. It can also be used to understand the level at which a gene is turned into a protein.
Genomic-based Sequencing Studies at the Myeloma Center include
- Targeted Sequencing
- Whole Exome Sequencing
- RNA Sequencing
- Whole Genome Sequencing
DNA methylation is a chemical reaction that places a methyl group (combination of carbon and hydrogen atoms) at a particular spot on DNA. It can cause tumor suppressor genes that keep cell behavior normal to be switched off during myeloma progression.
Methylation Analysis provides insight for switching the tumor suppressor genes back on through the use of epigenetic treatments in order to normalize DNA packing and cell behavior.
Epigenetics refers to the way DNA is packed and wound into chromosomes and modifications to the genome that influence when and how often a gene is active.
Benefits of Advanced Diagnostics
Information obtained from advanced diagnostic testing, including Gene Expression Profiling and DNA and RNA sequencing, allows us to develop precision medicine approaches based on incorporating targeted therapies that are individualized for each patient.
The information supports development of prevention and early intervention strategies.
Understanding this information enables us to:
- Design methods for normalizing cell biology that has gone astray and preventing disease progression.
- Design treatment regimens based on altering the cell’s behavior to prevent resistance to therapy and disease relapse.
- Design treatment strategies aimed at switching off the genetic signals that lead to myeloma development.
- Identify additional mutations that could initiate cancerous activity in cells.
Cure more patients with less toxic treatments.
Prognosis: Cure is Achievable
With our robust diagnostic capabilities and a state-of-the-art laboratory dedicated to molecular diagnostics discovery, we are well equipped to define the nuances of each patient’s disease. This, in turn, allows us to develop individualized treatment regimens for optimal effectiveness and, ultimately, cure for patients with myeloma and related diseases.