Active specific immunotherapy for stage II and stage III human colon cancer: a randomised trial

JB Vermorken, AME Claessen, H Van Tinteren, HE Gall… - The Lancet, 1999 - thelancet.com
JB Vermorken, AME Claessen, H Van Tinteren, HE Gall, R Ezinga, S Meijer, RJ Scheper…
The Lancet, 1999thelancet.com
Background Colon cancer is curable by surgery, but cure rate depends on the extent of
disease. We investigated whether adjuvant active specific immunotherapy (ASI) with an
autologous tumour cell-BCG vaccine with surgical resection was more beneficial than
resection alone in stage II and III colon cancer. Methods In a prospective randomised trial,
254 patients with colon cancer were randomly assigned postoperative ASI or no adjuvant
treatment. ASI was three weekly vaccinations starting 4 weeks after surgery, with a booster …
Background
Colon cancer is curable by surgery, but cure rate depends on the extent of disease. We investigated whether adjuvant active specific immunotherapy (ASI) with an autologous tumour cell-BCG vaccine with surgical resection was more beneficial than resection alone in stage II and III colon cancer.
Methods
In a prospective randomised trial, 254 patients with colon cancer were randomly assigned postoperative ASI or no adjuvant treatment. ASI was three weekly vaccinations starting 4 weeks after surgery, with a booster vaccination at 6 months with 107 irradiated autologous tumour cells. The first vaccinations contained 107 BCG organisms. We followed up patients for time to recurrence, and recurrence-free and overall survival. Analysis was by intention to treat.
Findings
The 5·3 year median follow-up (range 8 months to 8 years 11 months) showed 44% (95% CI 7–66) risk reduction for recurrence in the recurrence-free period in all patients receiving ASI (p=0·023). Overall, there were 40 recurrences in the control group and 25 in the ASI group. Analysis by stage showed no significant benefit of ASI in stage III disease. The major impact of ASI was seen in patients with stage II disease, with a significantly longer recurrence-free period (p=0·011) and 61% (18–81) risk reduction for recurrences. Recurrence-free survival was significantly longer with ASI (42% risk reduction for recurrence or death [0–68], p=0·032) and there was a trend towards improved overall survival.
Interpretation
ASI gave significant clinical benefit in surgically resected patients with stage II colon cancer. ASI has minimal adverse reactions and should be considered in the management of stage II colon cancer.
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