Immunohistochemical analysis of Ki-67, p21waf1/cip1 and apoptosis in marker lesions from patients with superficial bladder tumours treated with vinorelbine intravesical therapy in a preliminary phase I trial

被引:9
作者
Bonfil, RD
Gonzalez, AD
Siguelboim, D
Carrion, FDC
Ciocca, DR
Villaronga, A
Metz, L
Mosso, F
Fayad, E
Reale, M
Schmilovich, AJ
机构
[1] Hosp Med Policial Churruca Visca, Buenos Aires, DF, Argentina
[2] CRICYT, Lab Reprod & Lactat, Mendoza, Argentina
[3] Inst Med Antartida, Buenos Aires, DF, Argentina
[4] Hosp Thompson, San Martin, Buenos Aires, Argentina
[5] Pharmacia Oncol, Buenos Aires, DF, Argentina
关键词
vinorelbine; bladder neoplasms; chemotherapy;
D O I
10.1046/j.1464-410X.2001.02340.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective To investigate Ki-67 and p21(Waf1/Cip1) expression and apoptosis, before and after treatment, in tumour biopsies obtained from patients with superficial bladder cancer who underwent vinorelbine intravesical therapy. Patients and methods Twenty patients with high-risk superficial bladder cancer (including one or more of the following parameters: tumour diameter >3 cm, histological grade 3, or multicentric tumours) were treated 1-6 times (weekly) with intravesical vinorelbine (50 mg/mL) instillations. Transurethral tumour marker biopsies were obtained one week before the first instillation of the drug and one week after the last. The biopsies were immunostained for Ki-67 and p21(Waf1/Cip1) with monoclonal antibodies, on tissue sections derived from paraffin-embedded samples obtained before and after vinorelbine treatments. In addition, apoptosis was determined using a terminal deoxynucleotidyl transferase-mediated dUTP biotin nick-end labelling (TUNEL) technique. Results There were no significant differences in the cell proliferation marker Ki-67 in biopsies taken before or after treatment. However, p21(Waf1/Cip1) showed significantly higher expression in biopsies obtained after vinorelbine treatment, with median (range) values of 40 (20-90)% before and 70 (50-80)% after (P < 0.001, paired nonparametric Wilcoxon test). The apoptotic index was significantly higher after vinorelbine therapy, with median (range) values of 0.89 (0.06-3.8)%, before and 2.25 (0.17-18.7)% after treatment (P < 0.001, paired nonparametric Wilcoxon test). Despite the brief treatment and few patients there was a clinical response in nine patients, together with low toxicity in all. Conclusion The intravesical treatment of tumours with vinorelbine affects p21(Waf1/Cip1) expression without blocking cell proliferation, although increasing apoptosis. The preliminary results suggest that vinorelbine may be useful for treating superficial bladder tumours, and thus a phase II study is warranted.
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收藏
页码:425 / 431
页数:7
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