Evidence map›Paper›PMID 27669655›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2016

Robust Oncolytic Virotherapy Induces Tumor Lysis Syndrome and Associated Toxicities in the MPC-11 Plasmacytoma Model.

Lianwen Zhang, Michael B Steele, Nathan Jenks, Jacquelyn Grell, Marshall Behrens, Rebecca Nace, Shruthi Naik, Mark J Federspiel, Stephen J Russell, Kah-Whye Peng

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Lianwen ZhangDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Michael B SteeleDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Nathan JenksDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Jacquelyn GrellDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Marshall BehrensDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Rebecca NaceDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Shruthi NaikDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Mark J FederspielDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Stephen J RussellDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Kah-Whye PengDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Mayo Clinic · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Rafael Fonseca · 2015 to 2026
$25.5M
Intravenous Administration of Vesicular Stomatitis VectorsR01CA175795 · NCI · MAYO CLINIC ROCHESTER · PI PENG, KAH-WHYE · 2014 to 2017
$1.5M
NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA175795
6 · The paper itself

Abstract

Tumor-selective oncolytic vesicular stomatitis viruses (VSVs) are being evaluated in clinical trials. Here, we report that the MPC-11 murine plasmacytoma model is so extraordinarily susceptible to oncolytic VSVs that a low dose of virus leads to extensive intratumoral viral replication, sustained viremia, intravascular coagulation, and a rapidly fatal tumor lysis syndrome (TLS). Rapid softening, shrinkage and hemorrhagic necrosis of flank tumors was noted within 1-2 days after virus administration, leading to hyperkalemia, hyperphosphatemia, hypocalcemia, hyperuricemia, increase in plasma cell free DNA, lymphopenia, consumptive coagulopathy, increase in fibrinogen degradation products, decreased liver function tests, dehydration, weight loss, and euthanasia or death after 5-8 days. Secondary viremia was observed but viral replication in normal host tissues was not detected. Toxicity could be mitigated by using VSVs with slowed replication kinetics, and was less marked in animals with smaller flank tumors. The MPC-11 tumor represents an interesting model to further study the complex interplay of robust intratumoral viral replication, tumor lysis, and associated toxicities in cases where tumors are highly responsive to oncolytic virotherapy.

Indexed as

AnimalsCell Line, TumorHumansMiceNeoplasm TransplantationOncolytic VirotherapyOncolytic VirusesPlasmacytomaTreatment OutcomeTumor Lysis SyndromeVesicular stomatitis Indiana virus

Identifiers

PMID27669655
PMCPMC5167781
OpenAlexW2527126502

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.