Polycythemia Vera Health Article

Laboratory testing

BLOOD TESTS. The diagnosis of PV depends on a set of findings from blood tests. The most important single measurement is the patient's red blood cell mass as a proportion of the total blood volume. This measurement is made by tagging RBCs with radioactive chromium (⁵¹Cr) in order to determine the patient's RBC volume. While a few patients with PV may have a red cell mass level within the normal range if they have had recent heavy bleeding, a high score may eliminate the need for some other tests. A score higher than 36 mL/kg for males and 32 mL/kg for females on the ⁵¹Cr test suggests PV. Measurements of the oxygen level in the patient's arterial blood, of the concentration of vitamin B₁₂ in the blood serum, and of leukocyte alkaline phosphatase (LAP) staining can be used to distinguish PV from certain types of leukemia or from other types of polycythemia. LAP staining measures the intensity of enzyme activity in a type of white blood cell called a neutrophil. In PV, the LAP score is higher than normal whereas in leukemia it is below normal.

BONE MARROW TESTS. Bone marrow testing can be used as part of the diagnostic process. A sample of marrow can be cultured to see if red blood cell colonies develop without the addition of a hormone that stimulates RBC production. The growth of a cell colony without added hormone indicates PV. Bone marrow testing is also important in monitoring the progress of the disease, particularly during the spent phase.

GENETIC TESTING. Genetic testing can be used to rule out the possibility of chronic myeloid leukemia. Patients with this disease have a characteristic chromosomal abnormality called the Philadelphia chromosome. The Philadelphia chromosome does not occur in patients with PV.

Imaging studies

Imaging studies are not necessary to make the diagnosis of PV. In some cases, however, imaging studies can detect enlargement of the spleen that the doctor may not be able to feel during the physical examination.

Treatment

Treatment of PV is tailored to the individual patient according to his or her age, the severity of the symptoms and complications, and the stage of the disease.

Phlebotomy

Phlebotomy is the withdrawal of blood from a vein. It is the first line of treatment for patients with PV. Phlebotomy is used to bring down the ratio of red blood cells to fluid volume (the hematocrit) in the patient's blood to a level below 45%. In most cases the doctor will withdraw about 500 mL of blood (about 15 fluid ounces) once or twice a week until the hematocrit is low enough. Phlebotomy is considered the best course of treatment for patients younger than 60 and for women of childbearing age. Its drawback is that patients remain at some risk for either thrombosis or hemorrhage.

Myelosuppression

Myelosuppressive therapies are used to slow down the body's production of blood cells. They are given to patients who are older than 60 and at high risk for thrombosis. These therapies, however, increase the patient's risk of developing leukemia. The substances most frequently used as of 1998 include hydroxyurea (Hydrea), interferon alfa (Intron), or radioactive phosphorus (³²P). ³²P is used only in elderly patients with life expectancies of less than five years because it causes leukemia in about 10% of patients. Interferon alfa is expensive and causes side effects resembling the symptoms of influenza but is an option for some younger PV patients.

Investigational treatment

The Food and Drug Administration (FDA) has approved the use of anagrelide, an orphan drug, for investigational use in the treatment of PV. Anagrelide has moderate side effects and controls the platelet level in over 90% of patients.

Treatment of complications

The itching caused by PV is often difficult to control. Patients with pruritus are given diphenhydramine (Benadryl) or another antihistamine. Patients with high levels of uric acid are usually given allopurinol (Lopurin, Zyloprim) by mouth. Supportive care includes advice about diet—splenomegaly often makes patients feel full after eating only a little food. This problem can be minimized by advising patients to eat small meals followed by rest periods.

Because of the clotting problems related to PV, patients should not undergo surgery until their blood counts are close to normal levels. Female patients of childbearing age should be warned about the dangers of pregnancy related to their clotting abnormalities.

Prognosis

The prognosis for untreated polycythemia vera is poor; 50% of patients die within 18 months after diagnosis. Death usually results from heart failure, leukemia, or hemorrhage. Patients being treated for PV can expect to live between 11 and 15 years on average after diagnosis.