Follow-up
Further Outpatient Care
- The following laboratory results are helpful in the follow-up care of patients with multiple myeloma:
- CBC, chemical profile 7 (especially BUN and serum creatinine), serum calcium, and serum uric acid, and SPEP findings.
- M-component level in the serum and/or urine. (This is an indicator of tumor burden; a reduction with chemotherapy is used as a sign of a treatment response.)
- Serum beta-2-microglobin (B2M). (An elevated level indicates a large malignant cell mass, renal impairment, or both.)
- Serum LDH level. (A high level is predictive of an aggressive lymphomalike course.)
Complications
- Renal failure and insufficiency are seen in 25% of patients with multiple myeloma21 :
- Myeloma kidney syndrome with multiple etiologies
- Amyloidosis with light chains
- Nephrocalcinosis due to hypercalcemia
- Anemia, neutropenia, or thrombocytopenia is due to bone marrow infiltration of plasma cells.
- Bacterial infection is the leading cause of death in patients with myeloma. The highest risk is in the first 2-3 months of chemotherapy.
- Radiculopathy and/or cord compression may occur because of skeletal destruction and nerve compression.
- Bone disease may result in:
- Severe bone pain, pathologic fracture due to lytic lesions
- Increased bone resorption leading to hypercalcemia
- Spinal cord compression
- Purpura, retinal hemorrhage, papilledema, coronary ischemia, seizures, and confusion are due to hyperviscosity syndrome.
- Thrombosis and Raynaud phenomenon due to cryoglobulinemia may be present.
- Hypercalcemia may cause polyuria and polydipsia, muscle cramps, constipation, and a change in the patient's mental status.
Prognosis
- Multiple myeloma (MM) is a heterogeneous disease, with survival ranging from 1 year to more than 10 years.
- The tumor burden and proliferation rate are the 2 key indicators for the prognosis in patients with MM.
- B2M is an expression of tumor burden and is correlated with the Durie and Salmon staging system for assigning a prognosis.
- Poor prognostic factors include the following:
- Tumor mass
- Hypercalcemia
- Bence Jones proteinemia
- Renal failure
- The prognosis by treatment is as follows:
- Conventional therapy: Overall survival is approximately 3 years, and event-free survival is less than 2 years.
- High-dose chemotherapy with stem-cell transplantation: The overall survival rate is greater than 50% at 5 years.
- Serum amyloid P retention: More than 50% of patients have a median survival of approximately 11 months.
- Serum amyloid P retention: Median survival is 24 months.
Patient Education
- What is multiple myeloma (MM), and how does it affect the body? MM is a cancer of bone marrow. People with myeloma have uncontrolled growth of plasma cells and have large numbers of plasma cells in their bone marrow. Plasma cells produce enzymes that stimulate the growth of osteoclasts, which destroy bone (bone resorption). Plasma cells secrete proteins called antibodies, which can potentially be dangerous and cause thickening of the blood (stroke-induced condition).
- What are the causes of myeloma? The etiology is unknown. Fertilizers and insecticides may cause MM. Myeloma usually occurs in people older than 55 years, it occurs more commonly in African Americans than in whites, and it occurs slightly more frequently in men than in women.
- What is the treatment for myeloma? Myeloma is life threatening, but treatment helps patients to live better and longer. Remission can last months to decades. The 2 medicines most often used are prednisone (a steroid) and melphalan.
- What are the adverse effects of medicine? Like most cancer treatments, myeloma treatments generally involved the use of strong drugs to destroy malignant cells; however, these can have adverse effects. Patients undergo blood tests once a month while taking these medicines. Patients will probably lose their hair and have skin rashes, cough, fever, bleeding, and possibly other adverse effects.
- What are some of the complications of MM? Pain and/or fractures may result when myeloma leads to destruction of bone. Orthopedic surgeons have developed improved techniques to treat these pathologic fractures and also to prevent them from occurring. Radiation therapy and newer medications (bisphosphonates) may also be used to effectively treat bone disease.
- Where can additional information be found? For information on MM, visit the International Myeloma Foundation (IMF) or call the IMF at 1-800-452-CURE.
- For excellent patient education resources, visit eMedicine's Blood and Lymphatic System Center. Also, see eMedicine's patient education article Myeloma.
More on Myeloma |
| Overview: Myeloma |
| Differential Diagnoses & Workup: Myeloma |
| Treatment & Medication: Myeloma |
Follow-up: Myeloma |
| References |
| Further Reading |
| « Previous Page |
References
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Further Reading
Related eMedicine topics
Multiple Myeloma (Hematology)
Multiple Myeloma (Radiology)
Monoclonal Gammopathies of Uncertain Origin (Hematology)
Heavy Chain Disease, Gamma (Hematology)
Heavy Chain Disease, Mu (Hematology)
Light-Chain Deposition Disease (Hematology)
Waldenstrom Hypergammaglobulinemia (Hematology)
Clinical guidelines
Guidelines on the diagnosis and management of multiple myeloma 2005.
Bortezomib in multiple myeloma and lymphoma: a clinical practice guideline.
American Society of Clinical Oncology 2007 clinical practice guideline update on the role of bisphosphonates in multiple myeloma.
Clinical trials
Study of MAGE-A3 and NY-ESO-1 Immunotherapy in Combo With DTPACE Chemo and Auto Transplantation in Multiple Myeloma
Dexamethasone and Chemotherapy With or Without Plasma Exchange in Patients With Newly Diagnosed Multiple Myeloma and Acute Kidney Failure
High-Dose Melphalan and a Second Stem Cell Transplant or Low-Dose Cyclophosphamide in Treating Patients With Relapsed Multiple Myeloma After Chemotherapy
Bortezomib, Thalidomide, and Dexamethasone After Melphalan and Stem Cell Transplant in Treating Patients With Stage I, Stage II, or Stage III Multiple Myeloma
Keywords
myeloma, multiple myeloma, MM, plasma cell dyscrasia, plasma cell proliferation, hematologic cancer, plasmacytoid lymphocytes, M proteins
Follow-up: Myeloma