Besremi (ropeginterferon alfa-2b-njft)
Indications for Prior Authorization
Besremi (ropeginterferon alfa-2b-njft)
-
For diagnosis of Polycythemia Vera
Indicated for the treatment of adults with polycythemia vera.
Criteria
Besremi
Prior Authorization (Initial Authorization)
Length of Approval: 12 Month(s)
- Diagnosis of polycythemia vera as confirmed by all of the following [A]:
- One of the following:
- Hemoglobin greater than 16.5 g/dL for men or hemoglobin greater than 16.0 g/dL for women
- Hematocrit greater than 49% for men or hematocrit greater than 48% for women
- Increased red cell mass
- Bone marrow biopsy showing age-adjusted hypercellularity with trilineage proliferation (panmyelosis) including prominent erythroid, granulocytic, and increase in pleomorphic, mature megakaryocytes without atypia AND
- One of the following:
- Presence of JAK2 V617F or JAK2 exon 12 mutation
- Subnormal serum erythropoietin level
Besremi
Prior Authorization (Reauthorization)
Length of Approval: 12 Month(s)
- Patient demonstrates positive clinical response to therapy (e.g., improvement in hematological response, resolution of splenomegaly, absence of thromboembolic events) [2]
P & T Revisions
2025-02-06, 2024-12-04, 2024-09-04, 2024-03-07, 2023-08-22, 2023-07-03, 2023-01-04, 2022-07-28, 2022-01-28, 2022-01-05
References
- BESREMi (ropeginterferon alfa-2b-njft) [Prescribing Information]. Taipei, Taiwan. PharmaEssentia Corporation. November 2021.
- Vannucchi A, Barbui T, Cervantes F et al. Philadelphia chromosome-negative chronic myeloproliferative neoplasms: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Annals of Oncology. 2015;26:v85-v99.
- Barbui T, Thiele J, Gisslinger H et al. The 2016 WHO classification and diagnostic criteria for myeloproliferative neoplasms: document summary and in-depth discussion. Blood Cancer J. 2018;8(2)
- Abu-Zeinah, G., Krichevsky, S., Cruz, T. et al. Interferon-alpha for treating polycythemia vera yields improved myelofibrosis-free and overall survival. Leukemia 35, 2592–2601 (2021).
- National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines in Oncology. Myeloproliferative Neoplasms v2.2024. Available by subscription at: https://www.nccn.org/professionals/physician_gls/pdf/mpn.pdf. Accessed January 23, 2025.
- Thiele J, Kvasnicka HM, Orazi A, et al. The international consensus classification of myeloid neoplasms and acute Leukemias: myeloproliferative neoplasms. Am J Hematol. 2023; 98(1): 166-179.
End Notes
- According to The International Consensus Classification of myeloid neoplasms and acute Leukemias, diagnosis of polycythemia vera requires meeting either all three major criteria or the first two major criteria and one minor criterion. The three major criteria are as follows: 1) Hemoglobin > 16.5 g/dL for men or hemoglobin > 16.0 g/dL for women, or Hematocrit > 49% for men or Hematocrit > 48% for women, or increased red cell mass; 2) Bone marrow biopsy showing age-adjusted hypercellularity with trilineage proliferation (panmyelosis) including prominent erythroid, granulocytic, and increase in pleomorphic, mature megakaryocytes without atypia; 3) Presence of JAK2 V617F or JAK2 exon 12 mutation. The minor criterion is subnormal serum erythropoietin level. [5,6]
Revision History
- 2025-02-06: 2025 Annual Review. Updated language in diagnostic criteria to align with diagnostic criteria in NCCN guideline. Background updates.
- 2024-12-04: Removed hydroxyurea trial requirement and removed NF criteria section.
- 2024-09-04: Added continuation of therapy bypass for hydroxyurea trial requirement.
- 2024-03-07: 2024 Annual Review. Updated criteria to reflect latest NCCN guidelines (v1.2024). Updated references.
- 2023-08-22: Program update to standard reauthorization language. No changes to clinical intent.
- 2023-07-03: July P&T Oncology Updates
- 2023-01-04: Annual review: No criteria changes. Updated references.
- 2022-07-28: Removed submission of medical records or paid claims verbiage from PA criteria. Added NF criteria.
- 2022-01-28: Updated interferon therapy trial and failure requirement to account for projected Intron A discontinuation.
- 2022-01-05: New program.