Prefibrotic primary myelofibrosis

Prefibrotic primary myelofibrosis
Other names: Pre-PMF, Early stage myelofibrosis
H&E of bone marrow in grade 0 Prefibrotic PMF
SpecialtyHematology and oncology

Prefibrotic primary myelofibrosis (Pre-PMF) is a rare blood cancer, classified by the World Health Organization as a distinct type of myeloproliferative neoplasm in 2016.[1] The disease is progressive to overt primary myelofibrosis, though the rate of progression is variable and not all patients progress.Symptoms and presentation can mimic essential thrombocythemia, with the main differentiator for pre-PMF being the presence of fibrosis in the bone marrow.

Signs and symptoms

Symptoms are similar to essential thrombocythemia, with the main differentiator for pre-PMF being the presence of fibrosis in bone marrow.

Diagnosis

A bone marrow examination is required for diagnosis.

Major Criteria

The bone marrow histology should demonstrate the following:[2]

Minor Criteria

According to the WHO, at least one of these minor criteria should be present:[1]

  • Anemia which is not attributable to another condition
  • High white blood cell count (leukocytosis)
  • An enlarged spleen (splenomegaly)
  • LDH levels above the upper limit of the reference range.

Comparison with primary myleofibrosis

Reticulin or collagen fibrosis grade 2 or 3 is a diagnostic criteria for primary myelofibrosis.

Comparison with Essential Thrombocythemia

Both pre-PMF and Essential thrombocythemia can share diagnostic similarities, such as a proliferation of megakaryocytes and a presence of a mutation. The presence of Reticulin fibrosis in pre-PMF provides the clearest distinction between the two.

Treatment

Patients considered low risk for thrombosis or major bleeding should be observed only. Low-dose aspirin is recommended for patients without a history of thrombosis. For intermediate risk patients, symptom driven therapy for anaemia or constitutional symptoms.

For high risk patients with a history of thrombosis, oral anticoagulants and cytoreductive drugs such as hydroxycarbamide are recommended, and the patient should be treated as in primary myelofibrosis.[1][3]

Prognosis

Prognosis of pre-PMF currently suffers from a lack of multi-center data, with several biases resulting from the disease being newly distinct in WHO's 2016 reclassification. The 10 year cumulative incidence of progression to overt PMF is between 9.7 and 31.5%. The 10 year incidence of transformation into acute myeloid leukemia ranges from 5.8% to 12%.[4]

A prognostic scoring model designed specifically for pre-PMF does not yet exist, but the International Prognostic Scoring System can be used to predict survival in pre-PMF patients.[5] A multi-center study on reclassified PMF patients showed median survival of pre-PMF patients at 17.6 years compared with 7.2 years for overt PMF patients.[1] However, another study showed 98% of pre-PMF patients were alive after 10 years from diagnosis and while overt PMF patients showed a median survival of 16.6 years, pre-PMF median survival was not able to be calculated as more than 50% of patients were still alive at the time of publication.[6]

History

First described in 1976, pre-PMF was not introduced into the WHO's classification of tumors until 2001, and not formally classified as a distinct entity until the 2016 revision.[1]

References

  1. 1 2 3 4 5 Finazzi, Guido; Vannucchi, Alessandro M.; Barbui, Tiziano (2018-11-07). "Prefibrotic myelofibrosis: treatment algorithm 2018". Blood Cancer Journal. 8 (11): 104. doi:10.1038/s41408-018-0142-z. ISSN 2044-5385. PMC 6221891. PMID 30405096.
  2. ↑ Arber, Daniel A.; Orazi, Attilio; Hasserjian, Robert; Thiele, Jürgen; Borowitz, Michael J.; Le Beau, Michelle M.; Bloomfield, Clara D.; Cazzola, Mario; Vardiman, James W. (2016-05-19). "The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia". Blood. 127 (20): 2391–2405. doi:10.1182/blood-2016-03-643544. ISSN 0006-4971. PMID 27069254. Archived from the original on 2022-06-05. Retrieved 2021-12-19.
  3. ↑ Barbui, Tiziano; Thiele, Juergen; Gisslinger, Heinz; Orazi, Attilio; Vannucchi, Alessandro M.; Gianelli, Umberto; Beham‐Schmid, Christine; Tefferi, Ayalew (2019). "Comments on pre-fibrotic myelofibrosis and how should it be managed". British Journal of Haematology. 186 (2): 358–360. doi:10.1111/bjh.15840. ISSN 1365-2141. PMID 30847907.
  4. ↑ Barbui, Tiziano; Thiele, Juergen; Gisslinger, Heinz; Orazi, Attilio; Vannucchi, Alessandro M.; Gianelli, Umberto; Beham‐Schmid, Christine; Tefferi, Ayalew (2019). "Comments on pre-fibrotic myelofibrosis and how should it be managed". British Journal of Haematology. 186 (2): 358–360. doi:10.1111/bjh.15840. ISSN 1365-2141. PMID 30847907.
  5. ↑ Rumi, Elisa; Sant’Antonio, Emanuela; Boveri, Emanuela; Pietra, Daniela; Cavalloni, Chiara; Roncoroni, Elisa; Astori, Cesare; Arcaini, Luca (2018-07-03). "Diagnosis and management of prefibrotic myelofibrosis". Expert Review of Hematology. 11 (7): 537–545. doi:10.1080/17474086.2018.1484280. ISSN 1747-4086. PMID 29862872. S2CID 44097453.
  6. ↑ Barosi, Giovanni; Rosti, Vittorio; Bonetti, Elisa; Campanelli, Rita; Carolei, Adriana; Catarsi, Paolo; Isgrò, Antonina M.; Lupo, Letizia; Massa, Margherita; Poletto, Valentina; Viarengo, Gianluca (2012-04-20). "Evidence that Prefibrotic Myelofibrosis Is Aligned along a Clinical and Biological Continuum Featuring Primary Myelofibrosis". PLOS ONE. 7 (4): e35631. Bibcode:2012PLoSO...735631B. doi:10.1371/journal.pone.0035631. ISSN 1932-6203. PMC 3334973. PMID 22536419.
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