好色先生

好色先生

Explore the latest content from across our publications

Log In

Forgot Password?
Create New Account

Loading... please wait

Abstract Details

Longitudinal Extensive Transverse Myelitis: rare immunotherapy related adverse effect vs COVID-19-related immunization complication
Multiple Sclerosis
P1 - Poster Session 1 (9:00 AM-5:00 PM)
315
To report an acute presentation of long extensive transverse myelitis (LETM) in the setting of Atezolizumab monotherapy and COVID-19 mRNA immunization

Patients being treated with immune checkpoint inhibitors (ICI) for advanced malignancy have an increased propensity of developing neuro-immune complications. With the advent of the COVID-19 pandemic there have been reported cases of TM following COVID-19 immunization. The reported infrequency of TM with both aforementioned causes makes delineating the etiology challenging.

A 58-year-old male with metastatic SCLC completed 4 cycles of Atezolizumab, Carboplatin and Etoposide and was transitioned to Atezolizumab maintenance. He previously underwent Atezolizumab infusion and was administered the second dose of COVID-19 mRNA vaccine one day prior to developing acute lower extremity paralysis, sensory loss from chest down and overflow incontinence. MRI spine illustrated centromedullary enhancing lesions from C7-T7.  CSF analysis showed 25 WBC, 116/uL RBC, 94 mg/dL protein, normal glucose, negative oligoclonal bands and normal IgG index. CSF bacterial and virology studies were negative. Additionally, serum anti-myelin oligodendrocyte glycoprotein (MOG) and anti-aquaporin receptor 4 (AQP4) antibodies were unremarkable. 

5-day course of pulsed methylprednisolone followed by three therapeutic plasma exchanges produced minimal improvement in lower extremities strength and sensory level.

This case demonstrates the complication and symptomatology of TM in the setting of anti-PD-L1 monoclonal antibody with the co-incidental COVID-19 mRNA vaccine administration. The causal relationship between the vaccine and TM is difficult to establish due to limited data and the presence of a known inciting factor but hints at a possible exaggeration of the existing neuroinflammatory process.  Currently, CDC recommends that individuals who are moderately to severely immunocompromised receive an additional dose of an mRNA COVID-19 Vaccine (Pfizer-BioNTech or Moderna) at least 28 days after the completion of the initial mRNA COVID-19 vaccine series. Caution should be given for those patients who are on ICI therapy.

Authors/Disclosures
Aimalohi Esechie, MD, PhD (SLUH)
PRESENTER
Dr. Esechie has nothing to disclose.
Xiang Fang, MD, PhD, FAAN (University of Texas Medical Branch) Dr. Fang has nothing to disclose.
Pankhuri Banerjee, MBBS Dr. Banerjee has nothing to disclose.
Prashant K. Rai, MD (University of Texas Medical Branch Hospital) Dr. Rai has nothing to disclose.
Neeharika Thottempudi, MD Dr. Thottempudi has nothing to disclose.