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Phase I, open-label, dose-escalating study of a genetically engineered herpes simplex virus, NV1020, in subjects with metastatic colorectal carcinoma to the liver.
- Source :
-
Human gene therapy [Hum Gene Ther] 2006 Dec; Vol. 17 (12), pp. 1214-24. - Publication Year :
- 2006
-
Abstract
- Current regimens of systemic chemotherapy result in only modest lengthening of survival in patients with advanced stage, liver-dominant, metastatic colorectal cancer who have failed first-line chemotherapy. The objective of this study was to investigate the safety and tolerability of NV1020, a replication-competent, attenuated, genetically engineered herpes simplex virus type 1 (HSV-1), in patients with hepatic colorectal metastases refractory to first-line chemotherapy. A phase I, open-label, dose-escalating study of a single 10-min hepatic arterial infusion of NV1020 in four cohorts. Three patients in each cohort received doses of 3 x 10(6), 1 x 10(7), 3 x 10(7), and 1 x 10(8) plaque-forming units. Adverse events were either mild or moderate in severity, and self-limiting. Only three serious adverse events (one transient rise in serum y-glutamyltransferase, one diarrhea, and one leukocytosis) experienced by three patients were considered to be possibly or probably related to NV1020. There were no deaths during the study, and there was no evidence of disseminated herpes infection. Viral presence was detected in only one saliva sample and two serum samples from one asymptomatic patient in the highest dose cohort. In the first week after viral administration only rare and minor increases were noted for tumor necrosis factor-alpha (six samples; three patients; peak, 40 pg/ml), interleukin (IL)-1 (two samples; two patients; peak, 28 pg/ml), and interferon-y (four samples; two subjects; peak, 54 pg/ml). No IL-2 was detected. Mild liver enzyme elevations were self-limiting and not associated with clinical symptoms. We conclude that NV1020, a genetically engineered but replication-competent HSV-1 oncolytic virus, can be safely administered into the hepatic artery without significant effects on normal liver function.
- Subjects :
- Adult
Aged
Antibodies, Viral blood
Base Sequence
Cohort Studies
Colorectal Neoplasms immunology
DNA Primers genetics
Female
Genetic Engineering
Genetic Therapy adverse effects
Hepatic Artery
Herpesvirus 1, Human immunology
Humans
Infusions, Intra-Arterial
Liver Neoplasms immunology
Male
Middle Aged
Colorectal Neoplasms therapy
Genetic Therapy methods
Herpesvirus 1, Human genetics
Liver Neoplasms secondary
Liver Neoplasms therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1043-0342
- Volume :
- 17
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Human gene therapy
- Publication Type :
- Academic Journal
- Accession number :
- 17107303
- Full Text :
- https://doi.org/10.1089/hum.2006.17.1214