Frontiers in Oncology (Apr 2024)

Successful treatment with fludarabine and cyclophosphamide in a VEXAS syndrome patient with associated myelodysplastic syndrome: a case report and systematic review

  • Polina Bellman,
  • Jesus D. Gonzalez-Lugo,
  • Moazzam Shahzad,
  • Moazzam Shahzad,
  • Muhammad Kashif Amin,
  • Muhammad Fareed Khalid,
  • Nahid Suleman,
  • Nausheen Ahmed,
  • Anurag K. Singh,
  • Abdulraheem Yacoub,
  • Da Zhang,
  • Joseph P. McGuirk,
  • Muhammad Umair Mushtaq

DOI
https://doi.org/10.3389/fonc.2024.1383730
Journal volume & issue
Vol. 14

Abstract

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Vacuoles, E1 syndrome, X-linked, autoinflammatory, somatic (VEXAS) syndrome is a chronic inflammatory disorder that affects various organ systems. It is associated with hematologic malignancies and is generally refractory to therapies. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) may be considered for selected patients. We report a case wherein systemic and hematological manifestations completely resolved in a patient with VEXAS and associated myelodysplastic syndrome (MDS), following the administration of fludarabine and cyclophosphamide as part of the preparation for allo-HSCT. We conducted a systematic literature review and included 86 patients with VEXAS syndrome and associated MDS. Most cases presented with musculoskeletal involvement (71%) and anemia (72%) with lower-risk MDS. Most patients responded to corticosteroids (CS) but had a recurrence of symptoms with CS taper and were refractory to other immunosuppressive agents. Hypomethylating agents and Janus kinase inhibitors achieved a complete response in some cases. Further research is needed to develop more effective treatment strategies.

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