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Updated: Apr 29, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Remission of disseminated cancer after systemic oncolytic virotherapy
Stephen J Russell1, Mark J Federspiel2, Kah-Whye Peng2
1Department of Molecular Medicine, Mayo Clinic, Rochester, MN; Division of Hematology, Mayo Clinic, Rochester, MN.
Abstract:
MV-NIS is an engineered measles virus that is selectively destructive to myeloma plasma cells and can be monitored by noninvasive radioiodine imaging of NIS gene expression. Two measles-seronegative patients with relapsing drug-refractory myeloma and multiple glucose-avid plasmacytomas were treated by intravenous infusion of 10(11) TCID50 (50% tissue culture infectious dose) infectious units of MV-NIS. Both patients responded to therapy with M protein reduction and resolution of bone marrow plasmacytosis. Further, one patient experienced durable complete remission at all disease sites. Tumor targeting was clearly documented by NIS-mediated radioiodine uptake in virus-infected plasmacytomas. Toxicities resolved within the first week after therapy. Oncolytic viruses offer a promising new modality for the targeted infection and destruction of disseminated cancer.
Insights
Engineered measles virus (MV-NIS) shows promise in treating drug-refractory myeloma by selectively destroying cancer cells. Patients experienced tumor reduction and one achieved durable remission, with therapy monitored by radioiodine imaging.
Area of Science:
- Oncology
- Virology
- Immunotherapy
Background:
- Multiple myeloma is a cancer of plasma cells.
- Relapsed or refractory myeloma presents significant treatment challenges.
- Oncolytic viruses are being explored as targeted cancer therapies.
Observation:
- Two patients with relapsing, drug-refractory myeloma and plasmacytomas received MV-NIS therapy.
- MV-NIS is an engineered measles virus designed for myeloma cell destruction.
- Noninvasive radioiodine imaging monitors NIS gene expression, indicating virus activity.
Findings:
- Both patients showed positive responses, including reduced M protein and bone marrow plasmacytosis.
- One patient achieved a durable complete remission across all disease sites.
- Tumor targeting was confirmed by NIS-mediated radioiodine uptake in plasmacytomas.
- Observed toxicities were transient and resolved within a week.
Implications:
- MV-NIS demonstrates potential as a targeted oncolytic virotherapy for multiple myeloma.
- Radioiodine imaging provides a method for monitoring therapeutic efficacy.
- Oncolytic viruses represent a promising avenue for treating disseminated cancers.
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