Using C3H/He JCr mice bearing the syngeneic MBT-2 bladder tumor, it wa
s found that cyclophosphamide (CYC 100 mg/kg i.p.) treatment, 1 day be
fore and 2 weeks after surgery, followed by postoperative autologous t
umor vaccine immunization can be an effective adjuvant anticancer ther
apy. The shortterm exogeneous addition of low dose II-2 administration
to the protocol provided no further benefit. Suppression of tumor gro
wth was observed in a classical Winn assay when splenocytes were obtai
ned on day 23 from mice receiving this effective adjuvant therapy with
surgery on day 8. Splenocytes from tumor-bearing mice (TBM) treated w
ith CYC were augmented in terms of their proliferative response to con
canavalin A during the first 2 weeks after CYC treatment. Studies usin
g 3-day TBM established that significant suppression of tumor growth a
nd prolonged survivals were dependent upon CYC treatment being combine
d with tumor vaccine and/or interIeukin-2; single agent treatments wer
e ineffective.