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Updated: Aug 9, 2026

Orthotopic Implantation and Peripheral Immune Cell Monitoring in the II-45 Syngeneic Rat Mesothelioma Model
Published on: October 2, 2015
Ranpirnase--an antitumour ribonuclease: its potential role in malignant mesothelioma
Nick Pavlakis1, Nicholas J Vogelzang
1Royal North Shore Hospital, Department of Medical Oncology, St Leonards, NSW 2065, Australia. pavlakis@med.usyd.edu.au
Abstract:
Ranpirnase (Onconase) is a novel cytotoxic ribonuclease. In clinical development as a single agent in patients with malignant mesothelioma (MM), at 480 microg/m2 intravenously weekly, analysis of survival indicated prolonged periods of stable disease in Phase II trials and a potential survival benefit, compared with doxorubicin, in a small unpublished Phase III trial. In all clinical studies it has generally demonstrated a favourable safety profile except for easily controlled allergic reactions and dose modifications for renal impairment. Standard first-line treatment for MM has recently been established with an antifolate and cisplatin. At present, a Phase III trial of doxorubicin with or without ranpirnase is nearing completion in MM patients without prior chemotherapy or one prior chemotherapy regimen.
Insights
Ranpirnase (Onconase) shows promise in treating malignant mesothelioma (MM). Clinical trials suggest it may prolong stable disease and offer survival benefits, with a generally favorable safety profile.
Area of Science:
- Oncology
- Biochemistry
Background:
- Malignant mesothelioma (MM) is a rare and aggressive cancer.
- Standard first-line treatments for MM have recently been established.
- Ranpirnase (Onconase) is a novel cytotoxic ribonuclease under clinical investigation.
Purpose of the Study:
- To evaluate the efficacy and safety of ranpirnase as a single agent for malignant mesothelioma.
- To compare ranpirnase with doxorubicin in MM patients.
Main Methods:
- Phase II and III clinical trials were conducted.
- Ranpirnase was administered intravenously at 480 microg/m2 weekly.
- Survival data and safety profiles were analyzed.
Main Results:
- Phase II trials indicated prolonged periods of stable disease.
- A potential survival benefit was observed compared to doxorubicin in a Phase III trial.
- Ranpirnase demonstrated a favorable safety profile, with manageable allergic reactions and dose modifications for renal impairment.
Conclusions:
- Ranpirnase shows potential as a therapeutic agent for malignant mesothelioma.
- Further investigation in ongoing Phase III trials will clarify its role in combination therapy.
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