Skip to main content

Advertisement

Log in

Phase II open label trial of imatinib in polycythemia rubra vera

  • Original Article
  • Published:
International Journal of Hematology Aims and scope Submit manuscript

Abstract

Polycythemia rubra vera is a chronic myeloproliferative disorder characterized by panmyelosis with the resultant potential for thrombosis, myelofibrosis, and acute leukemia. Treatment has rested on phlebotomy and hydroxyurea. In 2002, we reported two patients who were unable to tolerate hydroxyurea but responded to imatinib mesylate (Gleevec). These patients have remained in complete hematologic remission on imatinib since 1999. As a result we began a phase II, open label trial of imatinib in patients with polycythemia vera. Patients meeting the Polycythemia Vera Study group criteria for the diagnosis of polycythemia vera, either naïve or intolerant to prior treatment were allowed to enroll. Initial therapy was begun with imatinib mesylate at 400 mg a day and two dose escalations, one to 600 and second to 800 mg a day, were allowed for patients not achieving a target hematocrit of 44 or less; or a platelet count of less than 600,000/mm3. Twenty patients were enrolled, 15 achieved complete hematologic remission within 12 weeks and ten remain on study. Six patients remain in remission on 400 mg a day and four on 500 mg a day. Gastrointestinal or cutaneous toxicities were primarily grade I or II. All patients were negative for bcr/abl. Imatinib mesylate is capable of producing hematologic remission in the majority of patients with polycythemia vera and provides another option for patient management, particularly in those intolerant to hydroxyurea.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Dai CH, Krantz SB, Green WF, et al. Polycythemia vera. III. Burst-forming units-erythroid (BFU-E) response to stem cell factor and c-kit receptor expression. Br J Haematol. 1994;86:12–21. doi:10.1111/j.1365-2141.1994.tb03246.x.

    Article  CAS  PubMed  Google Scholar 

  2. Dai CH, Krantz SB, Koury ST, et al. Polycythemia vera. IV. Specific binding of stem cell factor to normal and polycythemia vera highly purified erythroid progenitor cells. Br J Haematol. 1994;88:497–505. doi:10.1111/j.1365-2141.1994.tb05065.x.

    Article  CAS  PubMed  Google Scholar 

  3. Dai CH, Krantz SB, Sawyer ST. Polycythemia vera. V. Enhanced proliferation and phosphorylation due to vanadate are diminished in polycythemia vera erythroid progenitor cells; a possible defect of phosphatase activity in polycythemia vera. Blood. 1997;89:3574–81.

    CAS  PubMed  Google Scholar 

  4. James C, Ugo V, Le Couedic JP, Staerk J, Delhommeau F, Lacout C, et al. A unique clonal JAK2–V617F2 mutation leading to constitutive signaling causes polycythemia vera. Nature. 2005;434:1144–8. doi:10.1038/nature03546.

    Article  CAS  PubMed  Google Scholar 

  5. Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S, et al. Cancer Genome Project. Acquired mutation of the tyrosine kinase JAK2–V617F2 in human myeloproliferative disorders. Lancet. 2005;365:1054–61.

    Article  CAS  PubMed  Google Scholar 

  6. Levine RL, Wadleigh M, Cools J, Ebert BL, Wernig G, Huntly BJ, et al. Activating mutation in the tyrosine kinase JAK2–V617F2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell. 2005;7:387–97. doi:10.1016/j.ccr.2005.03.023.

    Article  CAS  PubMed  Google Scholar 

  7. Zhao R, Xing S, Li Z, Fu X, Li Q, Krantz SB, et al. Identification of an acquired JAK2–V617F2 mutation in polycythemia vera. J Biol Chem. 2005;280:22788–92. doi:10.1074/jbc.C500138200.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Novartis STI571. Investigator’s brochure, imatinib mesylate, 8th edn, June 20, 2006.

  9. Oehler l, Jaeger E, Eser A, Sillaber C, Gisslinger H, Geissler K. Imatinib mesylate inhibits autonomous erythropoiesis in patients with polycythemia in vitro. Blood. 2003;15:2240–2.

    Article  Google Scholar 

  10. Siitonen T, Savolainen ER, Koistinen P. Expression of the c-kit proto-oncogene in myeloproliferative disorders and myelodysplastic syndromes. Leukemia. 1994;8:631–7.

    CAS  PubMed  Google Scholar 

  11. Ratajczak MZ, Luger SM, DeRiel K, et al. Role of the KIT proto-oncogene in normal and malignant human hematopoiesis. Proc Natl Acad Sci USA 1992;89:1710–4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Maeda H, Hitomi Y, Hirata R, Tohyama J, Suwata J, Kamata S, et al. The effect of phlebotomy on serum erythropoietin levels in normal healthy subjects. Int J Hematol. 1992;55(2):111–5.

    CAS  PubMed  Google Scholar 

  13. Nussenzvieg RH, Swierczek SI, Jelinek J, Gaikwad A, et al. Polycythemia vera is not initiated by the JAK2V617F mutation. Exp Hematol. 2007;35:32–9.

    Google Scholar 

  14. Gaikwad A, Verstovsek S, Yoon D, Chang KT, Manshouri T, et al. Exp Hematol. 2007;35:931–9. doi:10.1016/j.exphem.2007.03.012.

    Article  CAS  PubMed  Google Scholar 

  15. Jacobs-Helbert SM, Penta K, Sun Z, Lawson A, Sawyer S. Distinct signaling from stem cell factor and erythropoietin in HCD57 cells. J Biol Chem. 1997;272(11):6850–3. doi:10.1074/jbc.272.11.6850.

    Article  Google Scholar 

  16. DeBerry C, Mou S, Linnekin D. Stat1 associates with c-kit and is activated in response to stem cell factor. Biochem J. 1997;327:73–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Jones CM, Dickinson TM. Polycythemia vera responds to imatinib mesylate. Am J Med Sci. 2003;325:149–52. doi:10.1097/00000441-200303000-00007.

    Article  PubMed  Google Scholar 

  18. Silver RT. Imatinib mesylate (GleevecTM) reduces phlebotomy requirements in polycythemia vera. Leukemia. 2003;17:1186–7. doi:10.1038/sj.leu.2402938.

    Article  CAS  PubMed  Google Scholar 

  19. Bent S, Padula A, Avins A. Brief communication: better ways to question patients about adverse medical events. Ann Intern Med. 2006;144:257–61.

    Article  PubMed  Google Scholar 

  20. Berk PD, Goldberg JD, Donovan PB, Fruchtman SM, Berlin NI, Wasserman LR. Therapeutic recommendations in polycythemia vera based on Polycythemia Vera Study Group protocols. Semin Hematol. 1986;23:132–43.

    CAS  PubMed  Google Scholar 

  21. Valeri CR, MacGregor H, Giorgio A, Srey R, Ragno G. Comparison of radioisotope methods and a nonradioisotope method to measure the RBC volume and RBC survival in the baboon. Transfusion. 2003;43:1366–73. doi:10.1046/j.1537-2995.2003.00528.x.

    Article  PubMed  Google Scholar 

  22. Fairbanks V. Polycythemia vera: the packed cell volume and the curious logic of the red cell mass. Hematology. 2000;4:381–95.

    Article  PubMed  Google Scholar 

  23. Parise RA, Ramanathan RK, Hayes MJ, Egorin MJ. Liquid chromatographic-mass spectrometric assay for quantitation of imatinib and its main metabolite (CGP 74588) in plasma. J Chromatogr B Analyt Technol Biomed Life Sci. 2003;791:39–44. doi:10.1016/S1570-0232(03)00206-X.

    Article  CAS  PubMed  Google Scholar 

  24. Donovan PB, Kaplan ME, Goldberg JD, Taarsky I, et al. Treatment of polycythemia vera with hydroxyurea. Am J Hematol. 1984;17:329–34. doi:10.1002/ajh.2830170402.

    Article  CAS  PubMed  Google Scholar 

  25. Najean Y, Rain JD. Treatment of polycythemia vera: the use of hydroxyurea and pipobroman in 292 patients under the age of 65 years. Blood. 1997;90:3370–7.

    CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We thank Dr. Sanford Krantz and Dr. Merrill Egorin for their continued interest and support of this project. We thank Charlena White for her excellent assistance in the preparation of this manuscript. We also wish to thanks Dr. Grant Somes, Chairman of Department of Preventive Medicine, University of Tennessee Health Science Center for his assistance with the design and statistical analysis of this trial.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to C. Michael Jones, Tina M. Dickinson or August Salvado.

Additional information

The study was performed at the Jones Clinic and the University of Pittsburg, Pittsburg Cancer Institute. We would like to thank Novartis Pharmaceuticals for providing study medications for use in this trial.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Hematological parameters (PPT 38 kb)

About this article

Cite this article

Jones, C.M., Dickinson, T.M. & Salvado, A. Phase II open label trial of imatinib in polycythemia rubra vera. Int J Hematol 88, 489–494 (2008). https://doi.org/10.1007/s12185-008-0193-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12185-008-0193-1

Keywords

Navigation