Inclusion Criteria:

          -  A diagnosis of Essential Thrombocythemia (ET) or Polycythemia Vera (PV) shall be made
             in accordance with the WHO (2008)criteria (Swerdlow 2008) as shown below.

          -  Diagnosis < 5 years prior to entry.

          -  Polycythemia Vera (2 major criteria required)

               1. Hb >18.5g/dl (♂) or 16.5g/dl (♀) or HCT >99 percentile reference range or
                  Elevated red cell mass (>25% above mean predicted value) or Hb >17g/dl (♂) or
                  15g/dl (♀) if associated with a sustained rise from baseline with no apparent
                  cause (e.g. treated iron deficiency).

               2. Presence of JAK2V617F

                    -  If source documentation of diagnostic criterion #1 cannot be obtained, then
                       diagnosis can be made with (1) the addition of an erythropoietin level below
                       the reference range of normal AND (2) bone marrow biopsy showing
                       hypercellularity for age with trilineage (panmyelosis) with prominent
                       erythroid, granulocytic, and megakaryocytic proliferation.

          -  Essential Thrombocythemia (all 6 criteria required)

               1. Platelets count ≥ 450 x 10 to 9/L

               2. Megakaryocyte proliferation with large and mature morphology. No significant
                  increase or left shift of neutrophil granulopoiesis or erythropoiesis. Patients
                  may have up to and including 2+ marrow reticulin fibrosis (0, 1 or 2 on scale 0
                  -4).

               3. Not meeting WHO criteria for CML, PV, MDS, PMF or other myeloid neoplasm

               4. Demonstration of clonal cytogenetic marker or no evidence of reactive
                  thrombocytosis.

               5. Absence of a leukoerythroblastic blood picture.

               6. May participate in study without presence of JAK2V617F.

                  Patients must have high risk disease as defined below:

                  High risk PV ANY ONE of the following:

                    -  Age ≥ 60 years

                    -  Previous documented thrombosis, erythromelalgia or migraine (severe,
                       recurrent, requiring medications, and felt to be secondary to the MPN)
                       either after diagnosis or within 10 years before diagnosis and considered to
                       be disease related

                    -  Significant splenomegaly (> 5cm below the left costal margin on palpitation)
                       or symptomatic splenomegaly (splenic infarcts or requiring analgesia)

                    -  Platelets ≥ 1000 x 10 to 9/L

                    -  Diabetes or hypertension requiring pharmacological therapy for > 6 months

                  High risk ET ANY ONE of the following:

                    -  Age ≥ 60 years

                    -  Platelet count ≥ 1500 x 10 to 9/L

                    -  Previous documented thrombosis, erythromelalgia or migraine headaches
                       (severe, recurrent, requiring medications, and felt to be secondary to the
                       MPN) either after diagnosis or within 10 years before diagnosis and
                       considered to be disease related

                    -  Previous hemorrhage related to ET

                    -  Diabetes or hypertension requiring pharmacological therapy for > 6 months

                  Other Inclusion criteria (Both Strata)

                    -  Diagnosed less than 5 years prior to entry on trial

                    -  Never treated with cytoreductive drugs except hydroxyurea for up to 3 months
                       maximum (phlebotomy, aspirin allowed, anagrelide allowed)

                    -  Age: ≥ 18 years (no upper limit)

                    -  Ability and willingness to comply with all study requirements

                    -  Signed informed consent to participate in this study.

                    -  Willing to participate in associated correlative science biomarker study

                    -  Serum creatinine ≤ 1.5 x upper limit of normal

                    -  ST and ALT ≤ 2 x upper limit of normal

                    -  No known PNH (paroxysmal nocturnal hemoglobinuria) clone

                    -  No concurrent hormonal oral contraceptive use

                  Exclusion Criteria:

                  (ANY of the following, both strata)

                    -  Known to meet the criteria for primary myelofibrosis (as opposed to ET) by
                       WHO 2008

                    -  Patients with a prior malignancy within the last 5 years (except for basal
                       or squamous cell carcinoma, or in situ cancer of the cervix)

                    -  Any contraindications to pegylated interferon or hydroxyurea

                    -  Presence of any life-threatening co-morbidity

                    -  History of active substance or alcohol abuse within the last year

                    -  Subjects who are pregnant, lactating or of reproductive potential and not
                       practicing an effective means of contraception

                    -  History of psychiatric disorder (e.g. depression) Subjects with a history of
                       mild depression may be considered for entry into this study, provided that a
                       pretreatment assessment of the subject's affective status supports that the
                       subject is clinically stable based on the investigator's normal practice for
                       such subject.

                    -  History of autoimmune disorder (e.g. hepatitis)

                    -  Hypersensitivity to interferon alfa

                    -  Hepatitis B or C infection (HBV), or untreated systemic infection

                    -  Known HIV disease

                    -  Evidence of severe retinopathy (e.g. CMV retinitis, macular degeneration) or
                       clinically relevant ophthalmological disorder (e.g. due to diabetes mellitus
                       or hypertension)

                    -  History or other evidence of decompensated liver disease

                    -  History or other evidence of chronic pulmonary disease associated with
                       functional limitation

                    -  Thyroid dysfunction not adequately controlled

                    -  Neutrophil count <1.5 x 10 to 9/L

                    -  JAK2 exon 12 mutation: PV that lacks the JAK2V617F mutation but is
                       characterized by the exon 12 mutation.

                    -  Meets criteria for post PV or post ET-MF

                    -  Subjects with any other medical condition, which in the opinion of the
                       investigator would compromise the results of the study by deleterious
                       effects of treatment.

                    -  Previous exposure to any formulation of pegylated interferon

                    -  History of major organ transplantation

                    -  History of uncontrolled severe seizure disorder

                    -  Inability to give informed written consent

                    -  Total bilirubin >1.5 x ULN (patients that have an isolated indirect
                       bilirubin that causes total bilirubin to be elevated beyond 1.5 x ULN due to
                       documented Gilbert's syndrome or hemolysis may be included). No detectable
                       PNH (paroxysmal nocturnal hemoglobinuria) clone where tested