Ribas A, Bellmunt J, Albanell J, De Torres I, Bermejo B, De Torres J A, Morote J, Gallardo E, Vera R, Carulla J, Sole-Calvo L A
Medical Oncology Section, Hospital General Universitari Vall d'Hebron, Barcelona, Spain.
Tumori. 1996 Nov-Dec;82(6):554-9. doi: 10.1177/030089169608200608.
Several reports on prognostic factors for infiltrating-bladder cancer have given controversial results. We assessed the prognostic value of p53 nuclear overexpression together with known prognostic factors for survival in patients with invasive T2-4 N0 M0 bladder cancer treated with neoadjuvant chemotherapy.
Thirty-five paraffinized tumor samples from initial transurethral resection of patients with bladder cancer were analyzed immunohistochemically to detect overexpression of p53 protein. Patients were treated with 3 to 4 cycles of neoadjuvant methotrexate, carboplatin, and vinblastine (M-CAVI) and then underwent radical cystectomy. Prechemotherapy, treatment, and postchemotherapy factors were analyzed for correlation with survival by univariate and multivariate analysis. Fifty-seven percent of tumors were positive for p53 protein, 71.5% had grade III-IV tumors, and 72% had organ-confined disease. The median follow-up was 20 months (range 5-71+).
By univariate analysis, the significant pretreatment factors were initial tumor (T) stage (P < 0.0001) and the male sex (P = 0.03). Five postchemotherapy variables were found significant: surgery performed according to protocol (P = 0.003), overall clinical (P = 0.004), and overall pathologic (P = 0.02) response to therapy, postchemotherapy pathologic stage (P = 0.0002), and tumor status after surgery (P = 0.0006). By multivariate analysis, the initial prechemotherapy T stage was the only factor that demonstrated independent significance.
Although the median follow-up of the study is still too short, in this group of patients treated with a neoadjuvant carboplatin-based regimen, a classical variable (prechemotherapy T stage) rather than p53 nuclear overexpression was an independent prognostic factor for survival. Further follow-up will be required to assess the value of p53 overexpression as a prognostic factor in invasive bladder cancer patients treated with neoadjuvant carboplatin-based chemotherapy.
多项关于浸润性膀胱癌预后因素的报告结果存在争议。我们评估了p53核过表达以及已知预后因素对接受新辅助化疗的浸润性T2 - 4 N0 M0膀胱癌患者生存的预后价值。
对35例膀胱癌患者经尿道初次切除的石蜡包埋肿瘤样本进行免疫组化分析,以检测p53蛋白的过表达情况。患者接受3至4个周期的新辅助甲氨蝶呤、卡铂和长春碱(M - CAVI)治疗,然后接受根治性膀胱切除术。通过单因素和多因素分析,对化疗前、治疗期间及化疗后的因素与生存情况的相关性进行分析。57%的肿瘤p53蛋白呈阳性,71.5%为III - IV级肿瘤,72%为器官局限性疾病。中位随访时间为20个月(范围5 - 71 +)。
单因素分析显示,显著的化疗前因素为初始肿瘤(T)分期(P < 0.0001)和男性(P = 0.03)。发现5个化疗后变量具有显著性:按方案进行手术(P = 0.003)、总体临床(P = 0.004)和总体病理(P = 0.02)治疗反应、化疗后病理分期(P = 0.0002)以及术后肿瘤状态(P = 0.0006)。多因素分析表明,初始化疗前T分期是唯一具有独立显著性的因素。
尽管该研究的中位随访时间仍然较短,但在这组接受基于卡铂的新辅助治疗方案的患者中,经典变量(化疗前T分期)而非p53核过表达是生存的独立预后因素。需要进一步随访以评估p53过表达作为接受基于卡铂的新辅助化疗的浸润性膀胱癌患者预后因素的价值。