"Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it is the only thing that ever has."

Margaret Mead
Case report
peer-reviewed

Simultaneous Presentation of Waldenström's Macroglobulinemia and MYD88 Gene Mutation with Multiple Myeloma



Abstract

Waldenström's macroglobulinemia (WM) and multiple myeloma (MM) are two distinct forms of mature hematologic B-cell malignancies. A missense somatic mutation in MYD88 gene (MYD88L265P) has been found in hematologic B-cell malignancies. The simultaneous presentation of Waldenström's macroglobulinemia and MYD88 mutation with multiple myeloma in the same patient is very rare and only a few cases have been reported in the literature.

Introduction

Waldenström's macroglobulinemia (WM) is a rare, indolent B-cell lymphoproliferative disorder characterized by a lymphoplasmacytic infiltration in the bone marrow or lymphatic tissue and a monoclonal immunoglobulin M (IgM) protein in the serum [1-2]. It demonstrates features of both plasma cells and B lymphocytes and therefore classified as lymphoplasmacytic lymphoma. On the other hand, multiple myeloma (MM) is a multi-focal plasma-cell neoplasm characterized by serum monoclonal gammopathy in addition to other constitutional symptoms including bone lytic lesions, renal failure, anemia and/or hypercalcemia [3]. It is crucially important to distinguish between both conditions as the clinical approach and treatment to each is different.

Case Presentation

A 67-year-old male with a past medical history significant for diverticulitis and hypertension presented to the emergency department for a complaint of back pain that started two days prior to admission. The patient described the pain as severe, sharp in nature and aggravates with movement. A skeletal survey reported multiple small lytic lesions. A computed tomography (CT) scan without contrast of thoracic spine showed multiple myelomatous involvements of the T6 and T7 vertebra including compression deformity and ventral epidural extension at the T6 level (Figure 1). Magnetic resonance imaging (MRI) of the thoracic and lumbar spine showed destructive osseous lesions in T6 and the transverse process on the left of the T7 vertebral body (Figure 2). CT-guided biopsy reported plasmacytoma with a negative MYD88 L265P status. M-protein concentration (1.88 mg/dL) and IgM (2,570 mg/dL) level were elevated. Serum lambda was normal (174 mg/dL), while both kappa (3,130 mg/dL) and kappa/lambda ratio (17.99) were increased. Interpretation of serum protein immunofixation electrophoresis showed biclonal gammopathy with IgM and IgG kappa light chain restriction. Flow cytometry showed no immunophenotypic evidence of involvement by a B-cell non-Hodgkin lymphoma (NHL). A subsequent bone marrow biopsy showed B-cell NHLs with plasmacytic differentiation and positive MYD88 L265P mutation. The immunostains in the core biopsy demonstrated kappa monotypic plasma cells involving approximately 5% of the marrow cellularity. Palliative radiation to T5-T9 helped improve bone lesions and pain. The patient received dexamethasone during hospitalization and was then started on a combined bendamustine and rituximab therapy. The therapy was later discontinued after a total of five cycles due to the progression of his M protein and lack of response. He was then switched to Revlimid, Velcade and dexamethasone. Consequently, his M-protein concentration started to decrease (Figure 3).

 
 
 

Discussion

Interestingly, genomic data has led to the identification of a common missense somatic mutation within the MYD88 gene (MYD88L265P) found in hematologic B-cell malignancies. Subsequent investigations confirmed MYD88 mutation occurrence at high frequencies in many NHLs including the rare lymphoplasmacytic lymphoma and WM [4]. In fact, MYD88 hits were uniquely high in prevalence in WM (90% to 100% of cases) [5-7], and consequently, it facilitated as a diagnostic tool to discriminate WM from other IgM‐secreting B‐cell malignancies [8]. The MYD88 L265P is not exclusive to WM/LPL, but can also be identified, with lower prevalence, in a subset of diffuse large B‐cell lymphomas (DLBCL) of the activated B‐cell type, including splenic marginal zone lymphomas (SMZL) (4% to 13%), mucosa‐associated lymphoid tissue (MALT) lymphomas (7% to 9%) [9] and rare cases of chronic lymphocytic leukemia (CLL) [10]. However, this mutation is absent in nodal MZLs and MM [9,11].

Indeed, in our presented case, mutation detection has influenced the diagnosis of WM and the treatment initiation of bendamustine and rituximab therapy. The patient, however, did not endorse any improvement of his M-protein concentration post five cycles (Figure 3). This result has led to changing the therapy. As we started him on a new treatment with Revlimid, Velcade and dexamethasone, his M-protein concentration significantly improved (Figure 3). The latter treatment is routinely used for MM. Hence, the patient's successful response to it suggested a concurrent presentation of WM and MM that is contributing to his underlying pathology.

The simultaneous occurrence of WM and MM was present in this case. In fact, this presentation is very rare in clinical settings. Furthermore, MYD88 L265P mutation, which has been recognized as a molecular marker for WM, is not usually found in the presence of MM.

Conclusions

Our case shows that this rare co-existence of WM and MM may occur; and molecular investigation for MYD88 mutation, on top of the clinical findings, can facilitate the recognition of such infrequent association. We, therefore, suggest that further research investigations should study this phenomenon and clarify the significance of molecular data in determining the simultaneous presentation of both diseases.


References

  1. Owen RG, Treon SP, Al-Katib A, et al.: Clinicopathological definition of Waldenstrom's macroglobulinemia: consensus panel recommendations from the Second International Workshop on Waldenström's Macroglobulinemia. Semin Oncol. 2003, 30:110-115. 10.1053/sonc.2003.50082
  2. Dimopoulos MA, Kyle RA, Anagnostopoulos A, Treon SP: Diagnosis and management of Waldenström's macroglobulinemia. J Clin Oncol. 2005, 23:1564-1577.
  3. Carrasco DR, K Sukhdeo, M Protopopova, et al.: The differentiation and stress response factor XBP-1 drives multiple myeloma pathogenesis. Cancer Cell. 2007, 11:349-360. 10.1016/j.ccr.2007.02.015
  4. Treon SP, Xu L, Yang G, et al.: MYD88 L265P somatic mutation in Waldenstrom's macroglobulinemia. N Engl J Med. 2012, 367:826-833. 10.1056/NEJMoa1200710
  5. Poulain S, Roumier C, Decambron A, et al.: MYD88 L265P mutation in Waldenstrom macroglobulinemia. Blood. 2013, 121:4504-4511.
  6. Schmidt J, Federmann B, Schindler N, Steinhilber J, Bonzheim I, Fend F, Quintanilla‐Martinez L: MYD88 L265P and CXCR4 mutations in lymphoplasmacytic lymphoma identify cases with high disease activity. Br J Haematol. 2015, 795-803. 10.1111/bjh.13361
  7. Hunter ZR, Xu L, Yang G, et al.: The genomic landscape of Waldenstrom macroglobulinemia is characterized by highly recurring MYD88 and WHIM‐like CXCR4 mutations, and small somatic deletions associated with B‐cell lymphomagenesis. Blood. 2014, 123:1637-1646. 10.1182/blood-2013-09-525808
  8. Treon SP, Gustine J, Xu L, et al.: MYD88 wild‐type Waldenstrom macroglobulinaemia: differential diagnosis, risk of histological transformation, and overall survival. Br J Haematol. 2018, 88:374-380. 10.1111/bjh.15049
  9. Gachard N, Parrens M, Soubeyran I, et al.: IGHV gene features and MYD88 L265P mutation separate the three marginal zone lymphoma entities and Waldenstrom macroglobulinemia/lymphoplasmacytic lymphomas. Leukemia. 2013. 27:183-189. 10.1038/leu.2012.257
  10. Martinez‐Trillos A, Pinyol M, Navarro A, et al.: Mutations in the toll‐like receptor/MYD88 pathway in chronic lymphocytic leukemia identify a subset of young patients with favorable outcome. Blood. 2014, 123:3790-3796. 10.1182/blood-2013-12-543306
  11. Je EM, Yoo N, Lee SH: Absence of MYD88 gene mutation in acute leukemias and multiple myelomas. Eur J Haematol. 2012, 88:273-274. 10.1111/j.1600-0609.2011.01720.x
Case report
peer-reviewed

Simultaneous Presentation of Waldenström's Macroglobulinemia and MYD88 Gene Mutation with Multiple Myeloma


Author Information

Hassan Awada Corresponding Author

Translational Hematology and Oncology Research, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA

Tariq Kewan

Internal Medicine, Cleveland Clinic, Cleveland, OH, USA

Fahrettin Covut

Internal Medicine, Cleveland Clinic - Fairview Hospital, Rocky River, OH, USA

Internal Medicine, Cleveland Clinic, Rocky River, OH, USA

Hamed Daw

Hematology and Oncology, Cleveland Clinic - Fairview Hospital, Cleveland, OH, USA

Abdo Haddad

Hematology and Oncology, Cleveland Clinic Foundation, Cleveland, OH, USA


Ethics Statement and Conflict of Interest Disclosures

Human subjects: Consent was obtained by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.


Case report
peer-reviewed

Simultaneous Presentation of Waldenström's Macroglobulinemia and MYD88 Gene Mutation with Multiple Myeloma


Figures etc.

PDF Print Share