Dear Authors,
If you believe that your paper was mistakenly rejected by other leading journals and you do not agree with final decision, the editors of Reports of Practical Oncology and Radiotherapy offer new fast track review. You may submit your manuscript to Reports of Practical Oncology and Radiotherapy together with all prior peer-reviews obtained from the other journal and your rebuttal letter. We guarantee review based decision within 72 hours from the time we will receive your manuscript.

Fast track submission process: Please submit the manuscript with all reviews and rebuttal letter by email to Dr. Michal Masternak (michal.masternak@ucf.edu) for fast review processing. To assure immediate attention the email title must to include: RPOR-fast track- Last Name First Name (of corresponding author).

Volume 6, Number 1, 2001

Gene therapy of cancer

Mackiewicz A.

Summary:

Number of gene therapy clinical trials and patients enrolled increases exponentially. Today there are more than 400 trials and over 4000 patients involved all over the world. However, most of the trails are in the early clinical phases. About 67% of trials are related to cancer. Most of the cancer gene therapy strategies are based on various forms of gene-immunotherapy which include genetically modified tumor vaccines (GMTV), direct intratumoral administration of genes encoding immunostimulatory factors or insertion of these genes into tumor infiltrating lymphocytes (TIL). Other strategies include suicide gene therapy, direct intratumoral administration of genes encoding anti-oncogenes, gene anti-angiogenic therapy or bone marrow cells protection against high dose anti-cancer chemotherapy using MDR genes. Various gene carries are employed in above strategies. Retroviral vectors or Adenoassociated virus vectors are used for GMTV construction, TIL and bone marrow cells modifications. Adenoviral vectors and liposomes are employed for direct intratumoral gene administration. Other carriers such as lentiviral vectors (based on HIV) or SV40 based vectors are in the preclinical studies.

In January 1996 we have initiated melanoma gene-immunotherapy clinical trial using GMTV comprising of irradiated autologous melanoma cells admixed with cells of two allogeneic melanoma cell lines modified to secrete interleukin 6 (IL-6) and agonistic soluble IL-6 receptor (sIL-6R). Until now more than 180 patients were enrolled into study. Phase I trail demonstrated that GMTV is not toxic and possesses therapeutic potential. Phase II trial has shown that in melanoma stage IV with measurable metastatic disease GMTV significantly extended patients' survival. In 16 out of 45 patients (36%) response to the GMTV was observed (4 CR, 4 PR and 8 mixed responses including SD). More than 60% of responding patients survived 2 years while none of non-responders survived that period (rank-log test p<0.0001). CD4+/CD8+ T cells ratio, antibody response, soft tissue metastases and performance status correlated with clinical response. Above results allowed the design of the phase III randomized double blind study which is about to be initiated.

Signature: Rep Pract Oncol Radiother, 2001; 6(1) : 34-34


« back

 
INDEXED IN:

Indexed in: EMBASE®, the Excerpta Medica database, the Elsevier BIOBASE (Current Awareness in Biological Sciences) and in the Index Copernicus.

http://www.sciencedirect.com/science/journal/15071367/19/2