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The Combination of Adenoviral HSV TK Gene Therapy and Radiation is Effective in Athymic Mouse Glioblastoma Xenografts Without Increasing Toxic Side Effects

Overview
Journal J Neurooncol
Publisher Springer
Date 2004 Apr 10
PMID 15072465
Citations 15
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Abstract

Object: In mouse models of prostate and breast cancer therapeutic effects are enhanced when adenoviral HSV TK gene therapy is combined with ionizing radiation. In the present study, we adopted this approach for the treatment of human glioblastoma xenografts in an athymic mouse model and assessed treatment results as well as toxic side effects.

Methods: About 72 nude mice received intracerebral inoculations of 2 x 10(5) U87deltaEGFR cells. On day 7 after tumor implantation the study population was randomized into six treatment arms: (1) intratumoral buffer inoculation on day 7, (2) intratumoral adenoviral vector injection (2 x 10(9) vp) on day 7, (3) single dose radiation (2.1 Gy) on day 9, (4) adenoviral injection + radiation, (5) adenoviral injection + ganciclovir (GCV) (20 microg/g twice daily from day 8 to 17), (6) adenoviral injection + GCV + radiation. On day 21 half of the animals were sacrificed for histological evaluation of the brain tumors, the other half was assessed for survival.

Results: This study showed significantly prolonged median survival time of 5 days for the GCV treated groups. The addition of radiation decreased the frequency of neurological symptoms and delayed the onset of deficits without altering the expression of thymidine kinase in the tumor cells.

Conclusions: We conclude that adenoviral HSV TK gene therapy in combination with adjuvant radiotherapy does not generate increased toxic side effects in glioblastoma treatment. The prolonged survival time of animals receiving gene therapy and the reduced occurrence of neurological symptoms in irradiated mice constitute promising features of the combined treatment.

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References
1.
Goodman J, Trask T, Chen S, Woo S, Grossman R, Carey K . Adenoviral-mediated thymidine kinase gene transfer into the primate brain followed by systemic ganciclovir: pathologic, radiologic, and molecular studies. Hum Gene Ther. 1996; 7(10):1241-50. DOI: 10.1089/hum.1996.7.10-1241. View

2.
Aghi M, Hochberg F, Breakefield X . Prodrug activation enzymes in cancer gene therapy. J Gene Med. 2000; 2(3):148-64. DOI: 10.1002/(SICI)1521-2254(200005/06)2:3<148::AID-JGM105>3.0.CO;2-Q. View

3.
Freyer J . Role of necrosis in regulating the growth saturation of multicellular spheroids. Cancer Res. 1988; 48(9):2432-9. View

4.
Taghian A, Budach W, Zietman A, Freeman J, Gioioso D, Suit H . Quantitative comparison between the transplantability of human and murine tumors into the brain of NCr/Sed-nu/nu nude and severe combined immunodeficient mice. Cancer Res. 1993; 53(20):5018-21. View

5.
Nestler U, Heinkelein M, Lucke M, Meixensberger J, Scheurlen W, Kretschmer A . Foamy virus vectors for suicide gene therapy. Gene Ther. 1998; 4(11):1270-7. DOI: 10.1038/sj.gt.3300561. View