Skip to main content

Advertisement

Log in

Successful treatment with tirabrutinib for relapsed lymphoplasmacytic lymphoma complicated by Bing–Neel syndrome

  • Case Report
  • Published:
International Journal of Hematology Aims and scope Submit manuscript

Abstract

A 53-year-old woman was diagnosed with lymphoplasmacytic lymphoma (LPL)/Waldenström's macroglobulinemia (WM) in 2008. Six courses of R-COP (rituximab, cyclophosphamide, vincristine, and prednisolone) resulted in complete remission, but LPL/WM relapsed in 2015. After six courses of R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisolone), the M-peak disappeared, but the patient presented with muscle weakness and sensory disturbance in the lower extremities. No lesions were apparent in the brain parenchyma, but T2-weighted magnetic resonance imaging (MRI) showed a signal-hyperintense area with contrast enhancement in the spinal cord at the C2–4 and Th2–3 levels, and cerebrospinal fluid (CSF) examination showed only a few mononuclear cells. In 2020, the patient started to require walking assistance, and MRI findings worsened. Neurologically, lower limb muscle strength was reduced (manual muscle test score 3), and sensations of touch and pain were about 30% of normal. Vibratory sensation was absent at the knees and medial malleoli, accompanied by dysuria due to neurogenic bladder. CSF cell count was 15/μl (all mononuclear cells). Bing–Neel syndrome (BNS) was diagnosed and tirabrutinib was started. Within 2 months of treatment, lower extremity muscle strength had normalized and MRI findings had improved. Tirabrutinib may offer a promising therapeutic option for BNS.

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.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Sekiguchi N, Rai S, Munakata W, Suzuki K, Handa H, Shibayama H, et al. A multicenter, open-label, phase II study of tirabrutinib (ONO/GS-4059) in patients with Waldenström’s macroglobulinemia. Cancer Sci. 2020;111:3327–37.

    Article  CAS  Google Scholar 

  2. Narita Y, Nagane M, Mishima K, Terui Y, Arakawa Y, Yonezawa H, et al. Phase I/II study of tirabrutinib, a second-generation Bruton’s tyrosine kinase inhibitor, in relapsed/refractory primary central nervous system lymphoma. Neuro Oncol. 2021;23:122–33.

    Article  Google Scholar 

  3. Malkani RG, Tallman M, Gottardi-Littell N, Karpus W, Marszalek L, Variakojis D, et al. Bing–Neel syndrome: an illustrative case and a comprehensive review of the published literature. J Neurooncol. 2010;96:301–12.

    Article  Google Scholar 

  4. Simon L, Fitsiori A, Lemal R, Dupuis J, Carpentier B, Boudin L, et al. Bing–Neel syndrome, a rare complication of Waldenström macroglobulinemia: analysis of 44 cases and review of the literature. A study on behalf of the French Innovative Leukemia Organization (FILO). Haematologica. 2015;100:1587–94.

    Article  CAS  Google Scholar 

  5. Castillo JJ, D’Sa S, Lunn MP, Minnema MC, Tedeschi A, Lansigan F, et al. Central nervous system involvement by Waldenström macroglobulinaemia (Bing–Neel syndrome): a multi-institutional retrospective study. Br J Haematol. 2016;172:709–15.

    Article  Google Scholar 

  6. Minnema MC, Kimby E, D’Sa S, Fornecker LM, Poulain S, Snijders TJ, et al. Guideline for the diagnosis, treatment and response criteria for Bing–Neel syndrome. Haematologica. 2017;102:43–51.

    Article  CAS  Google Scholar 

  7. Swerdlow SH, Campo E, Pileri SA, Harris NL, Stein H, Siebert R, et al. The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood. 2016;127:2375–90.

    Article  CAS  Google Scholar 

  8. Kulkarni T, Treon SP, Manning RA, Xu L, Rinne M, Lee EQ, et al. Clinical characteristics and treatment outcome of CNS involvement (Bing–Neel syndrome) in Waldenstroms macroglobulinemia. Blood. 2013;122:5090.

    Article  Google Scholar 

  9. Vermeiren K, Lemmerling M, Louagie H, Vantomme M, Petrick M, Bouttens F, et al. Bing–Neel syndrome presenting as gait problems due to spinal cord involvement. Clin Neurol Neurosurg. 2018;167:59–61.

    Article  Google Scholar 

  10. Cabannes-Hamy A, Lemal R, Goldwirt L, Poulain S, Amorim S, Pérignon R, et al. Efficacy of ibrutinib in the treatment of Bing–Neel syndrome. Am J Hematol. 2016;91:E17–9.

    Article  Google Scholar 

  11. Boudin L, Patient M, Roméo E, Bladé JS, de Jauréguiberry JP. Efficacy of ibrutinib as first-line treatment of tumoral Bing–Neel syndrome. Leuk Lymphoma. 2018;59:2746–8.

    Article  Google Scholar 

  12. Mason C, Savona S, Rini JN, Castillo JJ, Xu L, Hunter ZR, et al. Ibrutinib penetrates the blood brain barrier and shows efficacy in the therapy of Bing Neel syndrome. Br J Haematol. 2017;179:339–41.

    Article  CAS  Google Scholar 

  13. Treon SP, Xu L, Yang G, Zhou Y, Liu X, Cao Y, et al. MYD88 L265P somatic mutation in Waldenström’s macroglobulinemia. N Engl J Med. 2012;367:826–33.

    Article  CAS  Google Scholar 

  14. Yang G, Zhou Y, Liu X, Xu L, Cao Y, Manning RJ, et al. A mutation in MYD88 (L265P) supports the survival of lymphoplasmacytic cells by activation of Bruton tyrosine kinase in Waldenström macroglobulinemia. Blood. 2013;122:1222–32.

    Article  CAS  Google Scholar 

  15. Argyropoulos KV, Vogel R, Ziegler C, Altan-Bonnet G, Velardi E, Calafiore M, et al. Clonal B cells in Waldenström’s macroglobulinemia exhibit functional features of chronic active B-cell receptor signaling. Leukemia. 2016;30:1116–25.

    Article  CAS  Google Scholar 

  16. Munshi M, Liu X, Chen JG, Xu L, Tsakmaklis N, Demos MG, et al. SYK is activated by mutated MYD88 and drives pro-survival signaling in MYD88 driven B-cell lymphomas. Blood Cancer J. 2020;10:12.

    Article  Google Scholar 

  17. Treon SP, Tripsas CK, Meid K, Warren D, Varma G, Green R, et al. Ibrutinib in previously treated Waldenström’s macroglobulinemia. N Engl J Med. 2015;372:1430–40.

    Article  CAS  Google Scholar 

  18. Treon SP, Gustine J, Meid K, Yang G, Xu L, Liu X, et al. Ibrutinib monotherapy in symptomatic, treatment-naïve patients with Waldenström macroglobulinemia. J Clin Oncol. 2018;36:2755–61.

    Article  CAS  Google Scholar 

  19. Bernard S, Goldwirt L, Amorim S, Brice P, Brière J, de Kerviler E, et al. Activity of ibrutinib in mantle cell lymphoma patients with central nervous system relapse. Blood. 2015;126:1695–8.

    Article  CAS  Google Scholar 

  20. Tucker DL, Naylor G, Kruger A, Hamilton MS, Follows G, Rule SA. Ibrutinib is a safe and effective therapy for systemic mantle cell lymphoma with central nervous system involvement—a multi-centre case series from the United Kingdom. Br J Haematol. 2017;178:327–9.

    Article  CAS  Google Scholar 

  21. Wanquet A, Birsen R, Lemal R, Hunault M, Leblond V, Aurran-Schleinitz T. Ibrutinib responsive central nervous system involvement in chronic lymphocytic leukemia. Blood. 2016;127:2356–8.

    Article  CAS  Google Scholar 

  22. Wong J, Cher L, Griffiths J, Cohen A, Huang J, Wang L, et al. Efficacy of zanubrutinib in the treatment of Bing–Neel syndrome. Hemasphere. 2018;2:e155.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Masuho Saburi.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Saburi, M., Saburi, Y., Kawano, K. et al. Successful treatment with tirabrutinib for relapsed lymphoplasmacytic lymphoma complicated by Bing–Neel syndrome. Int J Hematol 115, 585–589 (2022). https://doi.org/10.1007/s12185-021-03246-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12185-021-03246-z

Keywords

Navigation