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Tuberculosis Peritonitis During Treatment of Polycythemia Vera with Ruxolitinib
Emiko Sakiyama1, Yoshiaki Chinen1, Taku Tsukamoto1
1Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Abstract:
Ruxolitinib is a selective JAK1/2 inhibitor that is widely used for the treatment of myeloproliferative neoplasms (MPNs), including myelofibrosis and polycythemia vera (PV). Despite its clinical efficacy for MPNs, ruxolitinib possesses immunosuppressive properties that potentially increase the risks for opportunistic infection, such as mycobacterium tuberculosis (MTB) infection, and reactivation of occult viral infection. Herein, we report the case of a 76-year-old male with PV who developed tuberculosis peritonitis under ruxolitinib therapy for 28 weeks. While previous studies and case reports have suggested an increased risk of MTB infection of various organs during ruxolitinib treatment of MPNs, this case is apparently the first of tuberculosis peritonitis in a patient with MPN treated with ruxolitinib. A review of previous case reports suggests the need for careful observation for MTB from the relatively early phase of ruxolitinib treatment, given that the median duration from the start of ruxolitinib treatment to the emergence of MTB was 20 weeks (range: 3-88 weeks). Clinicians should consider tuberculosis peritonitis as a differential diagnosis when patients with MPN treated with ruxolitinib develop infectious abdominal symptoms.
Insights
Ruxolitinib treats myeloproliferative neoplasms but can increase infection risk. This case highlights tuberculosis peritonitis as a rare but serious complication in polycythemia vera patients on ruxolitinib therapy.
Area of Science:
- Oncology
- Immunology
- Infectious Diseases
Background:
- Ruxolitinib is a Janus kinase (JAK) 1/2 inhibitor approved for myeloproliferative neoplasms (MPNs).
- MPNs include myelofibrosis and polycythemia vera (PV).
- Ruxolitinib's immunosuppressive effects may elevate opportunistic infection risks, including Mycobacterium tuberculosis (MTB).
Observation:
- A 76-year-old male with PV developed tuberculosis peritonitis.
- The patient was undergoing ruxolitinib therapy for 28 weeks.
- This is the first reported case of tuberculosis peritonitis in an MPN patient treated with ruxolitinib.
Findings:
- Previous reports indicate an increased risk of MTB infections in various organs during ruxolitinib treatment for MPNs.
- The median time from ruxolitinib initiation to MTB emergence is 20 weeks (range: 3-88 weeks).
- Tuberculosis peritonitis should be considered in MPN patients on ruxolitinib presenting with abdominal infectious symptoms.
Implications:
- Clinicians should maintain vigilance for MTB infections, including tuberculosis peritonitis, early in ruxolitinib treatment.
- Early diagnosis and management are crucial for patients with MPN receiving ruxolitinib.
- This case underscores the importance of monitoring for opportunistic infections during targeted cancer therapies.
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