Related Experiment Videos
A phase II study of menogaril in low-grade non-Hodgkin's lymphoma. An NCI Canada Clinical Trials Group study
J Skillings1, C Cripps, E Eisenhauer
1London Regional Cancer Centre, Ontario, Canada.
Abstract:
The NCI Canada Clinical Trials Group conducted a phase II study of menogaril given intravenously every 4 weeks in low-grade non-Hodgkin's lymphoma. Fifteen of 26 eligible patients had had no prior therapy. Partial responses were seen in 9 patients (35%). Toxicity was moderate including myelosuppression, nausea, phlebitis, alopecia, and lethargy. This drug has only modest activity in this potentially responsive group of patients.
Insights
Menogaril showed modest activity in treating low-grade non-Hodgkin's lymphoma, with partial responses in 35% of patients. Toxicity was moderate, including myelosuppression and nausea.
Area of Science:
- Oncology
- Clinical Pharmacology
Background:
- Low-grade non-Hodgkin's lymphoma (NHL) requires effective treatment options.
- Novel chemotherapeutic agents are continually investigated for NHL.
- Menogaril is an anthracycline antibiotic with potential antineoplastic activity.
Purpose of the Study:
- To evaluate the efficacy and toxicity of menogaril in patients with low-grade non-Hodgkin's lymphoma.
- To determine the response rate of menogaril in a previously untreated patient cohort.
Main Methods:
- A phase II clinical trial was conducted by the NCI Canada Clinical Trials Group.
- Menogaril was administered intravenously every 4 weeks.
- Twenty-six eligible patients with low-grade non-Hodgkin's lymphoma were enrolled.
Main Results:
- Partial responses were observed in 9 out of 26 eligible patients (35% response rate).
- Fifteen patients had not received prior therapy.
- Moderate toxicities were reported, including myelosuppression, nausea, phlebitis, alopecia, and lethargy.
Conclusions:
- Menogaril demonstrated modest activity in the treatment of low-grade non-Hodgkin's lymphoma.
- The observed toxicity profile suggests a need for careful patient monitoring.
- Further investigation may be warranted for specific patient subgroups or combination therapies.