The role of adjuvant immunotherapy after radical nephrectomy and prognostic factors in pT3N0M0 renal cell carcinoma

Citation
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
Citations number
26
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
19
Issue
6C
Year of publication
1999
Pages
5593 - 5597
Database
ISI
SICI code
0250-7005(199911/12)19:6C<5593:TROAIA>2.0.ZU;2-M
Abstract
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.