Sh. Jeon et al., The role of adjuvant immunotherapy after radical nephrectomy and prognostic factors in pT3N0M0 renal cell carcinoma, ANTICANC R, 19(6C), 1999, pp. 5593-5597
Five-year overall survival after radical nephrectomy in pT3N0M0 renal cell
carcinoma is 35-50%. In light of immunotherapy, which has shown some activi
ty in advanced diseases with increasing efficacy in limited metastatic inva
sion, we decided to explore the theoretical advantage of adjuvant immunothe
rapy in radically resected stage pT(3)N(0)M(0) renal cell carcinoma. We stu
died several factors including tumor size, nuclear grade, mean nuclear area
and expression of p53 protein to find out which factor is concerned with d
isease progression. A total of 10 patients with pT3N0M0 RCC who received ra
dical nephrectomy from February 1992 to April 1999 were randomly assigned t
o receive treatment with either interferon-alpha alone or interferon-alpha
plus vinblastine. Eight patients with PT3N0M0 RCC who received only radical
nephrectomy from January 1984 to February 1993 were analyzed and the resul
ts were compared with the first group. Six out of 10 (60%) patients in the
adjuvant immunotherapy group are alive with no evidence of disease. Metasta
ses were documented in 4 patients (40%) with a median interval to progressi
on of 17.5 months. All of them died of turner. In the surgery only group, 5
out of 8 patients (62.5%) are still alive with no evidence of disease. Two
patients (25%) developed distant metastases and both of them died of tumor
. The median progression interval was 11 months. There were no statistical
differences in time to progression and survival rate between the two groups
. In the univariate analysis using a log-rank test, the expression of p53 p
rotein seemed to be associated with shorter survival (p = 0.0591). However,
in the multivariate analysis rising Cox's proportional hazard model, no pa
rameter had significant independent prognostic value. We concluded that adj
uvant immunotherapy did not improve the survival of patients with pT3N0M0 R
CC. Furthermore, MT failed to find significant prognostic factors in patien
ts with pT(3)N(0)M(0) RCC.