2003
DOI: 10.3816/clc.2003.n.027
|View full text |Cite
|
Sign up to set email alerts
|

Granulocyte-Macrophage Colony-Stimulating Factor Gene–Transfected Autologous Tumor Cell Vaccine: Focus on Non–Small-Cell Lung Cancer

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
15
0

Year Published

2005
2005
2022
2022

Publication Types

Select...
6
2

Relationship

1
7

Authors

Journals

citations
Cited by 18 publications
(15 citation statements)
references
References 111 publications
0
15
0
Order By: Relevance
“…Approximately 20% of the immunized patients achieved long-term survival in excess of 5 years, in spite of the small number of response according to RECIST criteria [178]. Similarly encouraging results have been reported in non-squamous lung cancer, renal cancer and acute myleogenous leukemia with GM-CSF supplemented autologous tumor cell vaccines [179][180][181][182]. The GVAX approach was also tested on patients with HRPC by vaccinating them with 2 different allogeneic prostate tumor cell lines modified to secrete GM-CSF (see section on Genetic modification of whole tumor cells).…”
Section: Granulocyte-marcophage Colony Stimulating Factormentioning
confidence: 84%
“…Approximately 20% of the immunized patients achieved long-term survival in excess of 5 years, in spite of the small number of response according to RECIST criteria [178]. Similarly encouraging results have been reported in non-squamous lung cancer, renal cancer and acute myleogenous leukemia with GM-CSF supplemented autologous tumor cell vaccines [179][180][181][182]. The GVAX approach was also tested on patients with HRPC by vaccinating them with 2 different allogeneic prostate tumor cell lines modified to secrete GM-CSF (see section on Genetic modification of whole tumor cells).…”
Section: Granulocyte-marcophage Colony Stimulating Factormentioning
confidence: 84%
“…On the other hand, GM-CSF can also directly enhance immunogenicity of tumors (Thomas, 2008). In preclinical and clinical studies, the tumor cells genetically engineered to secrete biologically active GM-CSF can generate a systemic antitumor immune response (Tai et al, 2004;Nemunaitis and Nemunaitis, 2003). Analogously, IL-21 is another potent antitumor agent and is a promising candidate for the development of therapeutic tools (Dou et al, 2004;Li and Yee, 2008).…”
Section: Introductionmentioning
confidence: 97%
“…A Phase I/II clinical trial using a modified manufacturing process more suited to commercialization of autologous vaccines was conducted in early-and advancedstage NSCLC patients. Results revealed a dose-related survival advantage [111]. A total of 43 patients initiated vaccine treatment (33 with advanced disease), with injections given biweekly for a total of three to six vaccinations.…”
Section: Gvaxmentioning
confidence: 98%