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. Author manuscript; available in PMC: 2010 Aug 1.
Published in final edited form as: Clin Cancer Res. 2009 Jul 28;15(15):4875–4884. doi: 10.1158/1078-0432.CCR-09-0110

Table 3.

Immunologic memory after complete resolution of CT26-KS tumors

A: Mice which resolved their primary CT26-KS tumor after treatment with RFA, huKS-IL2 or combination therapy were challenged simultaneously with CT26 (first exposure) and CT26-KS (2nd exposure) on opposite flanks. Proportions represent tumor-free mice in each treatment group.

B: Fifteen mice were implanted with 5×105 CT26-KS tumor cells s.c. on the abdomen on day 0. Mice were then divided into groups and treated with complete tumor ablation on day 8 (n=3 mice, 40 seconds RFA), complete tumor excision (n = 8) on day 11, or partial RFA (25 sec, day 11) with huKS-IL2 on days 11–15 (n = 4). Mice were monitored for 30 days for evidence of tumor recurrence and were subsequently rechallenged with both CT26-KS and CT26 tumor cells on opposite flanks. Proportions represent tumor-free mice after rechallenge.

Table 3A
Initial Treatment Group Proportion of tumor-free mice after challenge
CT26-KS CT26
Naïve control 0/4 0/4
RFA alone 5/5 1/5 1
huKS-IL2 alone 3/3 3/3 2
RFA + huKS-IL2 9/9 7/9 3
Table 3B
Proportion of tumor-free mice after challenge
Initial Treatment Group CT26-KS1 CT26
RFA 3/3 1/3 3
Surgery 6/8 0/8
RFA + huKS-IL2 4/4 3/4 2
1

p= NS vs. control;

2

p = 0.004 vs. control, p = NS vs. RFA alone;

3

p = 0.004 vs. control, p = 0.018 vs. RFA alone, p = NS (0.90) vs. huKS-IL2 alone

1

No statistical difference among all three treatment groups.

2

p = 0.02 for RFA + huKS-IL2 vs. Surgery, p = NS vs. RFA;

3

p = NS vs. Surgery