Current View on Diagnosis and Treatment of Classical Ph-Negative Myeloproliferative Neoplasms

AL Melikyan1, IN Subortseva1, VA Shuvaev2,3, EG Lomaia4, EV Morozova5, LA Kuzmina1, OYu Vinogradova6,7,8, AYu Zaritskey4

1 National Research Center for Hematology, 4 Novyi Zykovskii pr-d, Moscow, Russian Federation, 125167

2 Russian Research Institute of Hematology and Transfusiology, 16 2-ya Sovetskaya str., Saint Petersburg, Russian Federation, 191024

3 VV Veresaev Municipal Clinical Hospital, 10 Lobnenskaya str., Moscow, Russian Federation, 127644

4 VA Almazov National Medical Research Center, 2 Akkuratova str., Saint Petersburg, Russian Federation, 197341

5 RM Gorbacheva Scientific Research Institute of Pediatric Oncology, Hematology and Transplantation; IP Pavlov First Saint Petersburg State Medical University, 6/8 L’va Tolstogo str., Saint Petersburg, Russian Federation, 197022

6 SP Botkin Municipal Clinical Hospital, 5 2-i Botkinskii pr-d, Moscow, Russian Federation, 125284

7 Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology, 1 Samory Mashela str., Moscow, Russian Federation, 117997

8 NI Pirogov Russian National Research Medical University, 1 Ostrovityanova str., Moscow, Russian Federation, 117997

For correspondence: Anait Levonovna Melikyan, MD, PhD, 4 Novyi Zykovskii pr-d, Moscow, Russian Federation, 125167; e-mail: anoblood@mail.ru

For citation: Melikyan AL, Subortseva IN, Shuvaev VA, et al. Current View on Diagnosis and Treatment of Classical Ph-Negative Myeloproliferative Neoplasms. Clinical oncohematology. 2021;14(1):129–37. (In Russ).

DOI: 10.21320/2500-2139-2021-14-1-129-137


ABSTRACT

Classical Ph-negative myeloproliferative neoplasms (MPN) constitute a group of diseases including polycythemia vera, essential thrombocythemia, and primary myelofibrosis. Over the past decade, the approaches to understanding of MPN pathogenesis and therapy have considerably changed. At the same time, etiological factors and pathophysiological mechanisms of disease progress are being thoroughly studied. The improvement of diagnosis methods and new approaches to therapy can reduce complications and mortality risks. The review outlines the current diagnosis methods, such as the molecular genetic one, and provides prognostic scores. Different methods of conservative therapy are assessed. Special attention is paid to quality of life measurement and targeted treatment of patients.

Keywords: myeloproliferative neoplasms, polycythemia vera, essential thrombocythemia, primary myelofibrosis, JAK2V617F, CALR, MPL, prognosis, constitutional symptoms, MPN10, ruxolitinib.

Received: September 1, 2020

Accepted: December 10, 2020

Read in PDF

Статистика Plumx английский

REFERENCES

  1. Меликян А.Л., Туркина А.Г., Абдулкадыров К.М. и др. Клинические рекомендации по диагностике и терапии Ph-негативных миелопролиферативных заболеваний (истинная полицитемия, эссенциальная тромбоцитемия, первичный миелофиброз). Гематология и трансфузиология. 2014;59:31–56.
    [Melikyan AL, Turkina AG, Abdulkadyrov KM, et al. Clinical guidelines on diagnosis and therapy of Ph-negative myeloproliferative neoplasms (polycythemia vera, essential thrombocythemia, primary myelofibrosis). Gematologiya i transfuziologiya. 2014;59:31–56. (In Russ)]
  2. Меликян А.Л., Ковригина А.М., Суборцева И.Н. и др. Национальные клинические рекомендации по диагностике и терапии Ph-негативных миелопролиферативных заболеваний (истинная полицитемия, эссенциальная тромбоцитемия, первичный миелофиброз) (редакция 2018 г.) Гематология и трансфузиология. 2018;63(3):275–315.
    [Melikyan AL, Kovrigina AM, Subortseva IN, et al. National clinical guidelines on diagnosis and therapy of Ph-negative myeloproliferative neoplasms (polycythemia vera, essential thrombocythemia, primary myelofibrosis) (edition 2018). Gematologiya i transfuziologiya. 2018;63(3):275–315. (In Russ)]
  3. Абрамова А.В., Абдуллаев А.О., Азимова М.Х. и др. Алгоритмы диагностики и протоколы лечения заболеваний системы крови. В 2 томах. М.: Практика, 2018. Том 2.
    [Abramova AV, Abdullaev AO, Azimova MKh, et al. Algoritmy diagnostiki i protokoly lecheniya zabolevanii sistemy krovi. V 2 tomakh. (Diagnostic algorithms and treatment protocols in hematological diseases. 2 volumes.) Moscow: Praktika Publ.; 2018. 2. (In Russ)]
  4. Меликян А.Л., Суборцева И.Н., Галстян Г.М. Протокол дифференцированного посиндромного лечения больных первичным миелофиброзом. В кн.: Алгоритмы диагностики и протоколы лечения заболеваний системы крови. По ред. А.В. Абрамовой, А.О. Абдуллаева и др. В 2 томах. М.: Практика, 2018. Том 2. С. 777–802.
    [Melikyan AL, Subortseva IN, Galstyan GM. Protocol of differentiated syndromic treatment of patients with primary myelofibrosis. In: Abramova AV, Abdullaev AO, et al., eds. Algoritmy diagnostiki i protokoly lecheniya zabolevanii sistemy krovi. V 2 tomakh. (Diagnostic algorithms and treatment protocols in hematological diseases. 2 volumes.) Moscow: Praktika Publ.; 2018. Vol. 2. pр. 777–802. (In Russ)]
  5. Geyer H, Scherber R, Kosiorek H, et al. Symptomatic Profiles of Patients With Polycythemia Vera: Implications of Inadequately Controlled Disease. J Clin Oncol. 2016. 34(2):151–9. doi: 10.1200/JCO.2015.62.9337.
  6. Ионова Т.И., Анчукова Л.В., Виноградова О.Ю. и др. Качество жизни и спектр симптомов у больных миелофиброзом на фоне терапии: данные клинической практики. Гематология и трансфузиология. 2016;61(1):17–25. doi: 10.18821/0234-5730-2016-61-1-17-25.
    [Ionova TI, Anchukova LV, Vinogradova OYu, et al. Quality of life and symptom profile in patients with myelofibrosis undergoing treatment: Data of clinical practice. Gematologiya i transfuziologiya. 2016;61(1):17–25. doi: 10.18821/0234-5730-2016-61-1-17-25. (In Russ)]
  7. Xiao Z, Chang C-S, Morozova E, et al. Impact of myeloproliferative neoplasms (MPNS) and perceptions of treatment goals amongst physicians and patients in 6 countries: an expansion of the MPN landmark survey. 2019;3(s1):294–5. doi: 10.1097/01.hs9.0000561008.75001.e7.
  8. Cervantes F, Dupriez B, Pereira A, et al. New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment. 2009;113(13):2895–901. doi: 10.1182/blood-2008-07-170449.
  9. Passamonti F, Cervantes F, Vannucchi AM, et al. Dynamic International Prognostic Scoring System (DIPSS) predicts progression to acute myeloid leukemia in primary myelofibrosis. 2010;116(15):2857–8. doi: 10.1182/blood-2010-06-293415.
  10. Gangat N, Caramazza D, Vaidya R, et al. DIPSS plus: a refined Dynamic International Prognostic Scoring System for primary myelofibrosis that incorporates prognostic information from karyotype, platelet count, and transfusion status. J Clin Oncol. 2011;29(4):392–7. doi: 10.1200/JCO.2010.32.2446.
  11. Vannucchi AM, Guglielmelli P, Rotunno G, et al. Mutation-Enhanced International Prognostic Scoring System (MIPSS) for primary myelofibrosis: an AGIMM & IWG-MRT project. 2014;124(21):405. doi: 10.1182/blood.v124.21.405.405.
  12. Guglielmelli P, Lasho TL, Rotunno G, et al. MIPSS70: Mutation-Enhanced International Prognostic Score System for transplantation-age patients with primary myelofibrosis. J Clin Oncol. 2018;36(4):310–8. doi: 10.1200/JCO.2017.76.4886.
  13. Passamonti F, Giorgino T, Mora B, et al. A clinical-molecular prognostic model to predict survival in patients with post polycythemia vera and post essential thrombocythemia myelofibrosis. 2017;31(12):2726–31. doi: 10.1038/leu.2017.169.
  14. Robin M, de Wreede LC, Wolschke C, et al. Long-term outcome after allogeneic hematopoietic cell transplantation for myelofibrosis. 2019;104(9):1782–8. doi: 10.3324/haematol.2018.205211.
  15. Барабанщикова М.В., Морозова Е.В., Байков В.В. и др. Аллогенная трансплантация гемопоэтических стволовых клеток при миелофиброзе. Клиническая онкогематология. 2016;9(3):279–86. doi: 10.21320/2500-2139-2016-9-3-279-286.
    [Barabanshchikova MV, Morozova EV, Baykov VV, et al. Allogeneic Hematopoietic Stem Cell Transplantation in Myelofibrosis. Clinical oncohematology. 2016;9(3):279–86. doi: 10.21320/2500-2139-2016-9-3-279-286. (In Russ)]
  16. Виноградова О.Ю., Шуваев В.А., Мартынкевич И.С. и др. Таргетная терапия миелофиброза. Клиническая онкогематология. 2017;10(4):471–8. doi: 10.21320/2500-2139-2017-10-4-471-478.
    [Vinogradova OYu, Shuvaev VA, Martynkevich IS, et al. Targeted Therapy of Myelofibrosis. Clinical oncohematology. 2017;10(4):471–8. doi: 10.21320/2500-2139-2017-10-4-471-478. (In Russ)]
  17. Руксолитиниб (инструкция по медицинскому применению). Доступно по: https://www.vidal.ru/drugs/molecule/2304. Ссылка активна на 22.10.2020.
    [Ruxolitinib (package insert). Available from: https://www.vidal.ru/drugs/molecule/2304. (accessed 22.10.2020) (In Russ)]
  18. Tefferi A, Cervantes F, Mesa R, et al. Revised response criteria for myelofibrosis: International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) and European Leukemia Net (ELN) consensus report. 2013;122(8):1395–8. doi: 10.1182/blood-2013-03-488098.
  19. Ломаиа Е.Г., Сиордия Н.Т., Сендерова О.М. и др. Ранний ответ и отдаленные результаты терапии миелофиброза руксолитинибом: многоцентровое ретроспективное исследование в 10 центрах Российской Федерации. Клиническая онкогематология. 2020;13(3):335–45. doi: 10.21320/2500-2139-2020-13-3-335-345.
    [Lomaia EG, Siordiya NT, Senderova OM, et al. Early Response and Long-Term Outcomes of Ruxolitinib Therapy in Myelofibrosis: Multicenter Retrospective Study in 10 Centers of the Russian Federation. Clinical oncohematology. 2020;13(3):335–45. doi: 10.21320/2500-2139-2020-13-3-335-345. (In Russ)]
  20. Lomaia E, Siordiya N, Dimov G, et al. Early spleen response is a good prognostic factor of ruxolinib outcome in patients with myelofibrosis. 2019;3(S1):989. doi: 10.1097/01.hs9.0000567308.09016.52.