Cytokine-enhanced vaccine and suicide gene therapy as surgery adjuvant treatments for spontaneous canine melanoma

被引:26
作者
Finocchiaro, L. M. E. [1 ]
Glikin, G. C. [1 ]
机构
[1] Univ Buenos Aires, Inst Oncol Angel H Roffo, Unidad Transferencia Genet, RA-1417 Buenos Aires, DF, Argentina
关键词
IL-2; GM-CSF; HSV-TK; melanoma vaccine; lipofection; DMRIE;
D O I
10.1038/sj.gt.3303072
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We evaluated the safety, efficacy and anti-tumor effects of a surgery adjuvant treatment on canine patients with malignant melanoma. This approach combined suicide gene therapy with a subcutaneous vaccine composed by formolized tumor cells and irradiated xenogeneic cells producing human interleukin-2 and granulocyte-macrophage colony-stimulating factor. The post-surgical margin of the cavity was infiltrated with lipid-complexed thymidine kinase suicide gene coadministrated with ganciclovir. Toxicity was minimal or absent in all patients. With respect to surgery-treated controls (SC), this combined treatment (CT) significantly increased the fraction of patients local disease-free from 6 to 58% and distant metastases-free from 43 to 78% (Fisher's Exact test). In addition, CT significantly improved both SC overall 78 (23-540) and metastasis-free survival 112 (0-467) days to more than 1312 days (respective ranges: 43-1312 and 0-1312) (Kaplan-Meier analysis). In those patients subjected to partial surgery or presenting local recurrence, the efficacy of CT was verified by a 49% of objective responses that averaged 85% of tumor mass loss, while 22% displayed tumor progression as 94% of SC did. Therefore, surgery adjuvant CT controlled tumor growth, delaying or preventing post-surgical recurrence and distant metastasis, significantly extending survival and recovering the quality of life.
引用
收藏
页码:267 / 276
页数:10
相关论文
共 35 条
[31]   SAFETY AND SHORT-TERM TOXICITY OF A NOVEL CATIONIC LIPID FORMULATION FOR HUMAN GENE-THERAPY [J].
SAN, H ;
YANG, ZY ;
POMPILI, VJ ;
JAFFE, ML ;
PLAUTZ, GE ;
XU, L ;
FELGNER, JH ;
WHEELER, CJ ;
FELGNER, PL ;
GAO, X ;
HUANG, L ;
GORDON, D ;
NABEL, GJ ;
NABEL, EG .
HUMAN GENE THERAPY, 1993, 4 (06) :781-788
[32]   A comparative review of melanocytic neoplasms [J].
Smith, SH ;
Goldschmidt, MH ;
McManus, PM .
VETERINARY PATHOLOGY, 2002, 39 (06) :651-678
[33]   Vaccination with irradiated autologous melanoma cells engineered to secrete human granulocyte-macrophage colony-stimulating factor generates potent antitumor immunity in patients with metastatic melanoma [J].
Soiffer, R ;
Lynch, T ;
Mihm, M ;
Jung, K ;
Rhuda, C ;
Schmollinger, JC ;
Hodi, FS ;
Liebster, L ;
Lam, P ;
Mentzer, S ;
Singer, S ;
Tanabe, KK ;
Cosimi, AB ;
Duda, R ;
Sober, A ;
Bhan, A ;
Daley, J ;
Neuberg, D ;
Parry, G ;
Rokovich, J ;
Richards, L ;
Drayer, J ;
Berns, A ;
Clift, S ;
Cohen, LK ;
Mulligan, RC ;
Dranoff, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13141-13146
[34]   Enhancement of the herpes simplex virus thymidine kinase ganciclovir bystander effect and its antitumor efficacy in vivo by pharmacologic manipulation of gap junctions [J].
Touraine, RL ;
Vahanian, N ;
Ramsey, WJ ;
Blaese, RM .
HUMAN GENE THERAPY, 1998, 9 (16) :2385-2391
[35]   Vaccines for melanoma: translating basic immunology into new therapies [J].
Wolchok, J. D. ;
Livingston, P. O. .
LANCET ONCOLOGY, 2001, 2 (04) :205-211