Phase I trial of Vigil® personalized engineered autologous tumor cells (EATC) in ovarian cancer

2018 ◽  
Vol 149 ◽  
pp. 40-41 ◽  
Author(s):  
R.P. Rocconi ◽  
J.M. Scalici ◽  
M. Barve ◽  
L. Manning ◽  
G. Wallraven ◽  
...  
2012 ◽  
Vol 18 (9) ◽  
pp. 2668-2678 ◽  
Author(s):  
Setsuko K. Chambers ◽  
H-H. Sherry Chow ◽  
Mike F. Janicek ◽  
Janiel M. Cragun ◽  
Kenneth D. Hatch ◽  
...  
Keyword(s):  
Phase I ◽  

2020 ◽  
Vol 217 (9) ◽  
Author(s):  
Matthew J. Frank ◽  
Michael S. Khodadoust ◽  
Debra K. Czerwinski ◽  
Ole A.W. Haabeth ◽  
Michael P. Chu ◽  
...  

Here, we report on the results of a phase I/II trial (NCT00490529) for patients with mantle cell lymphoma who, having achieved remission after immunochemotherapy, were vaccinated with irradiated, CpG-activated tumor cells. Subsequently, vaccine-primed lymphocytes were collected and reinfused after a standard autologous stem cell transplantation (ASCT). The primary endpoint was detection of minimal residual disease (MRD) within 1 yr after ASCT at the previously validated threshold of ≥1 malignant cell per 10,000 leukocyte equivalents. Of 45 evaluable patients, 40 (89%) were found to be MRD negative, and the MRD-positive patients experienced early subsequent relapse. The vaccination induced antitumor CD8 T cell immune responses in 40% of patients, and these were associated with favorable clinical outcomes. Patients with high tumor PD-L1 expression after in vitro exposure to CpG had inferior outcomes. Vaccination with CpG-stimulated autologous tumor cells followed by the adoptive transfer of vaccine-primed lymphocytes after ASCT is feasible and safe.


2004 ◽  
Vol 53 (9) ◽  
Author(s):  
Steve Nicholson ◽  
C.C. Bomphray ◽  
H. Thomas ◽  
A. McIndoe ◽  
D. Barton ◽  
...  
Keyword(s):  
Phase I ◽  

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