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Background
Multiple
myeloma is a malignancy caused by the unregulated proliferation
of a population of plasma cells in the bone marrow. Plasma
cells are part of the normal immune system. Their primary
purpose is the production of normal immunoglobulins or antibodies
which are produced in response to infections, inflammation,
and even malignancies. These plasma cells are normally
well regulated and can be thought of as small factories
for immunoglobulins. The typical signs and symptoms of
multiple myeloma relate to the loss of normal bone marrow
function and weakening of the bone itself.
Epidemiology
Multiple
myeloma represents approximately 1% of all new cases of
cancer identified annually. It does account for approximately
13% of all blood related malignant disorders in the United
States. There is a slightly higher incidence rate in African-Americans
and in males. The average age of patients presenting at
diagnosis is 63 years. There is a slight increased incidence
as age increases. Studies have shown an increased prevalence
in patients who have been exposed to fuel oil products,
agricultural workers, miners and sheet metal workers. The
specific etiologic factors regarding multiple myeloma are
unknown.
Signs and Symptoms
The
most common presenting complaint in multiple myeloma is
bone pain relating to the destruction of the bone by the
myeloma plasma cells. Other common symptoms include: fatigue,
increased incidence of infection and bruising or easy bleeding.
Signs of the disease include: anemia, abnormal bone x-rays,
abnormal findings of protein in the blood or urine, and
kidney dysfunction.
Diagnostic tests
Studies
which are indicated in patients who have multiple myeloma
should include: Complete blood counts, blood chemistry studies,
uinalysis, specific immunoelectrophoretic studies of blood
and urine, x-rays of the spine, skull and long bones, and
a bone marrow aspirate and biopsy examination. Other studies
may be taken from the bone marrow which may be used to help
identify certain prognostic categories in myeloma patients.
Further imaging studies such as MRI or CT scans may be indicated
to identify causes of atypical pain or neurologic symptoms.
Staging of multiple myeloma
Although
staging malignancies is an important part of developing
therapeutic strategies for many malignancies, staging has
not been as significant in determining therapy for multiple
myeloma. Localized myeloma (solitary plasmacytomas) are
most typically treated with radiation therapy alone and
followed carefully. However, in true multiple myeloma staging
has been used to help in determining prognosis and at times
the aggressiveness of therapy. The most typical staging
system utilized is called the Durie-Salmon staging system.
Different signs of disease such as anemia, calcium level,
kidney function and degree of bone disease are used to determine
the stage at presentation or at original diagnosis. The
staging for multiple myeloma can be developed from the basic
studies performed during the diagnostic evaluation.
Treatment alternatives
Unlike
certain malignancies the rationale for therapy of multiple
myeloma is based upon the signs, symptoms and laboratory
results found at the time of diagnosis more so than simply
making the diagnosis. Although timing of treatment for
multiple myeloma may be variable, and dependent upon the
strategy agreed upon between the patient and treating physicians,
the principal form of therapy utilized in this disease is
chemotherapy. As in most malignancies there have been a
variety of treatment programs which have been utilized and
studied in attempts to improve the overall response and
survival in this disease process. The determination of
treatment is usually based upon age, underlying health,
specific laboratory results and symptoms. The treatment
may include what one could consider standard oral treatment
with Melphalan and Prednisone, or move to an aggressive
form of therapy such as/or including bone marrow transplantation.
A number of cooperative cancer study groups throughout the
world are continuing to try to develop improved treatment
programs.
When
determining the appropriate treatment for multiple myeloma
your hematologist/oncologist will likely have reviewed the
concerns regarding treatment of smoldering myeloma, indolent
myeloma versus active disease. By close monitoring of the
disease process appropriate therapy can be determined and
initiated at the proper time. As one would expect different
drug regimens may have different side effects or concerns
and are better reviewed in a more specific drug related
discussion.
Radiation
therapy can be an important part of the treatment program
available for multiple myeloma patients. The role of radiation
therapy may include those instances of solitary plasmacytoma
of bone, osteosclerotic myeloma, relief of spinal cord or
nerve root compression, prevention of pathologic fractures,
and palliation of pain due to localized tumor growth. In
each of these instances radiation can be provided in such
a way as to effectively eradicate the disease at the site
of radiation, but may not have significant impact upon the
systemic process requiring chemotherapy. In treatment programs
utilizing aggressive types of therapy such as stem cell
treatment or bone marrow transplantation more sophisticated
and systemic radiation therapy may be utilized. Side effects
of the radiation tend to be limited, especially because
of the localized nature of most of the therapeutic programs.
Blood counts may be affected in patients receiving radiation
therapy, even if they are not receiving chemotherapy at
the same time. Close observation may be indicated depending
upon the circumstances of therapy.
Summary
Multiple
myeloma is a relatively rare malignancy which results in
systemic symptoms and frequently local bone disease. As
a general statement, active multiple myeloma is best treated
with systemic chemotherapy programs but may be benefitted
by the addition of radiation therapy in circumstances as
noted above. Your hematologist/oncologist or radiation
oncologist will be able to give more specific information
in regard to treatment programs, side effects and response.
John Garton, MD
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