Abstract OT3-01-06: A phase I/IIa study of the whole-cell vaccine BriaVax™ in metastatic or locally recurrent breast cancer patients (NCT00095862)

Author(s):  
CL Wiseman ◽  
M Lacher
2013 ◽  
Vol 31 (15_suppl) ◽  
pp. 3087-3087
Author(s):  
Robert Lange Elliott ◽  
Jonathan F. Head

3087 Background: Breast cancer patients were vaccinated in the adjuvant setting with an autologous, allogeneic whole cell vaccine to evaluate the effect on host lymphocyte immunity and disease-specific survival. Methods: We began preparing whole cell preparations for a vaccine study in 1995. Stage I and II breast cancer patients had host lymphocyte immunity against tumors associated antigens evaluated before and after vaccination. Those patients with depressed immunity, determined by a lymphocyte blastogenesis assay (LBA), were offered the whole cell vaccine. Patients were given six intradermal injections (three weekly followed by three monthly). Ten weeks after the last injection the LBA was repeated. Thirty-seven patients were vaccinated in the adjuvant setting with the whole cell autologous, allogeneic vaccine. Results: The vaccine was well tolerated with no severe toxicities. Some patients experienced slight pain and swelling at the injection site and slight chills and fever. The vaccinated patients had a mean follow-up of 12.7 years with mean follow-up of 8.9 and 9.2 years for the patients with normal and depressed immunity, respectively, in the historic control. The 10-year survival was 95% (20 of 21 patients) in the normal immunity historic control, 59% (33 of 56 patients) in the depressed immunity historic control and 89% (33 of 37 patients) in the patients with depressed immunity that were vaccinated in the present clinical trial. Conclusions: The disease-specific survival of the vaccinated patients with depressed immunity in this trial is significantly greater than that of the historic controls of unvaccinated patients with depressed immunity to their tumor associated antigens. This study confirms the importance of maintaining good host lymphocyte immunity after completion of standard therapy and validates the value of cancer immunotherapy in the adjuvant setting.


1979 ◽  
Vol 26 (1) ◽  
pp. 141-145 ◽  
Author(s):  
MICHIO MIYAZAKI ◽  
KAZUHIKO YASUMURA ◽  
SATOSHI II ◽  
YASUAKI TAKATA ◽  
TOSHIAKI KAMI

2019 ◽  
Vol 36 (1) ◽  
pp. 985-991 ◽  
Author(s):  
Sharvari Dharmaiah ◽  
Johnathan Zeng ◽  
Vinay S. Rao ◽  
Zi Ouyang ◽  
Tianjun Ma ◽  
...  

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