![]() Epidemiology
Pathophysiology
Multiple myeloma is a plasma cell neoplasm characterized by skeletal destruction, renal failure, anemia, and hypercalcemia. The disease is incurable. Myeloma develops with the emergence of clonal plasma cells, clinically known as monoclonal gammopathy of undetermined significance (MGUS). At this stage, patients do not show signs of end-organ damage; however, there is a 1% annual risk of progression to myeloma or a related malignant disease. As the disease progresses, complex genetic events occur in the bone marrow microenvironment. The interactions of myeloma cells, bone marrow cells, and microvessels lead to a progression of the tumor and a resistance to drugs. The development of bone lesions is a result of changes in bone turnover.1 Incidence
Multiple myeloma is the second most prevalent blood cancer after non-Hodgkin's lymphoma. It represents approximately 1% of all cancers and 2% of all cancer deaths.2,3
The median age at diagnosis is about 71 years; only 2% of cases are diagnosed in individuals younger than age 45. An estimated 50,000 Americans currently have myeloma. According to the American Cancer Society, approximately 15,270 new cases of myeloma will be diagnosed during 2004.2,3 Multiple myeloma affects slightly more men than women (of the estimated 15,270 new cases referenced above, 8090 are expected to occur in men versus 7180 in women). African Americans and Native Pacific Islanders have the highest reported incidence of this disease, and Asians, the lowest. A recent study found the incidence of myeloma to be 9.5 cases per 100,000 African Americans and 4.1 cases per 100,000 Caucasian Americans. Among African Americans, myeloma is one of the leading causes of cancer death.2,3 Etiology
Little is known about the etiology of multiple myeloma. However, there are some factors that appear to make a person more likely to develop multiple myeloma. These factors are discussed below.4
Because the majority of diagnoses occurs among older adults, it is thought that susceptibility to the disease may increase with the aging process and the consequent reduction in immune surveillance of evolving cancer. Another hypothesis is that myeloma may result from a lifelong accumulation of toxic insults or antigenic challenges.2 References
|