Abstract |
The Eastern Cooperative Oncology Group (ECOG) conducted a phase II trial of interleukin-12 (IL-12) for plateau phase multiple myeloma. Patients were initially treated with IL-12 250 ng/kg I.V. daily for 5 days every 3 weeks. The trial was modified due to toxicity after the first 16 patients. IL-12 was given 300 ng/kg subcutaneously twice weekly for 24 weeks. Of 48 eligible patients, there were 4 objective responses (8.3%), all CR. The median survival and progression-free survival were 42.8 and 11.4 months. Unacceptable grade 3 or 4 non-hematologic toxicity (31% with IL-12 subcutaneously and 63% with IL-12 intravenously) was observed.
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Authors | Martha Q Lacy, Susanna Jacobus, Emily A Blood, Neil E Kay, S Vincent Rajkumar, Philip R Greipp |
Journal | Leukemia research
(Leuk Res)
Vol. 33
Issue 11
Pg. 1485-9
(Nov 2009)
ISSN: 1873-5835 [Electronic] England |
PMID | 19243818
(Publication Type: Clinical Trial, Phase II, Journal Article, Randomized Controlled Trial, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Adult
- Aged
- CD4 Lymphocyte Count
- Female
- Humans
- Interleukin-12
(adverse effects, therapeutic use)
- Male
- Middle Aged
- Multiple Myeloma
(drug therapy, immunology)
- Survival Analysis
- T-Lymphocyte Subsets
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