CP-221 Clinical experience with intrathecal rituximab for treatment of progressive multiple sclerosis

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Abstract

Background

Inaccessibility of inflammation compartmentalised to the CNS may underlie the lack of effectiveness of immunomodulatory treatments in progressive multiple sclerosis (PMS), turning its treatment into a challenge for researches. Intrathecal rituximab (IT-RTX) is a new treatment option which has shown promising results in clinical trials but clinical experience is limited.1

Purpose

Case report of the use and outcomes in 3 patients with PMS treated with IT-RTX in a tertiary hospital.

Material and methods

3 cases of PMS are reported: patient A (man), patient B (man) and patient C (woman) aged 44, 48 and 42 years, respectively. All patients were treated with IT-RTX. Effectiveness and safety of IT-RTX were evaluated. Demographic and clinical data were collected from patients’ electronic medical records. All patients started IT-RTX treatment following a compassionate use clinical study protocol, after hospital approval and informed consent was obtained.

Results

All patients received weekly 25 mg doses of IT-RTX, over a 3 week period. Patient B also received a fourth dose of 25 mg 8 months after the first dose. Flow cytometry was performed on peripheral blood (table), revealing a remarkable effect on peripheral B lymphocytes CD45 and CD19, with undetectable levels of CD19. Similar depletion was observed with peripheral B lymphocytes CD3, CD4, CD8 and CD16+CD56. This effect was maintained over time, rising again after several months without treatment.

Results

No changes in the Expanded Disability Status Scale (EDSS) were observed (table), except for patient B, who developed a slight improvement. The treatment was well tolerated, although patient B suffered a fever episode after the first dose and patient C died from massive pulmonary embolism, a rare RTX related complication, 5 months after finishing treatment.

Conclusion

In our patients, IT-RTX showed limited effectiveness, with disease stabilisation (similar EDSS) and depletion of peripheral B lymphocytes (especially CD19). Although the treatment was well tolerated, a rare and severe adverse event was reported.

References and/or acknowledgements

1. Svenningsson. Neurol Neuroimmunol Neuroinflamm2015;2:e79.

References and/or acknowledgements

No conflict of interest

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