Department of Urology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.
Urol Oncol. 2013 Oct;31(7):1270-5. doi: 10.1016/j.urolonc.2012.01.014. Epub 2012 Mar 2.
In bladder-sparing approaches for muscle-invasive bladder cancer (MIBC) involving transurethral resection of the bladder tumor (TURBT) and chemoradiation, survival outcomes are excellent for patients who achieve tumor-free state after TURBT and chemoradiation but poor for those with persistent disease. Since metastatic disease accounts for most bladder cancer deaths, we hypothesized that tumor sensitivity to chemoradiation may reflect metastatic potential in MIBC.
From 1997 to 2010, 179 cT2-4aN0M0 bladder cancer patients underwent TURBT and induction chemoradiation (40 Gy with cisplatin 20 mg/d for 5 days × 2). Study subjects were 73 patients who had had macroscopic disease after TURBT and were evaluated for tumor sensitivity to the induction chemoradiation; of the 73 patients, chemoradiation response was evaluated pathologically in partial and radical cystectomy specimens for 8 and 44 patients, respectively, and clinically for the remaining 21 who did not undergo cystectomy. Tumors were defined as chemoradiation-sensitive when they regressed to T0 pathologically for the 52 patients undergoing cystectomy or clinically for the 21 undergoing no cystectomy; otherwise, they were defined as chemoradiation-resistant. Primary and secondary endpoints were metastasis-free and cancer-specific survival, respectively. The association between chemoradiation sensitivity and development of metastasis was investigated in MIBC patients.
Of the 73 patients, 21 (29%: 13 pathologic and 8 clinical T0) had chemoradiation-sensitive tumors while 52 (71%) had chemoradiation-resistant tumors. Median follow-up was 53 months. Multivariate analysis identified chemoradiation resistance as the strongest independent predictor for the development of metastasis (hazard ratio (HR) 18.9, P < 0.0001). When stratified by chemoradiation sensitivity, 5-year metastasis-free and cancer-specific survival rates were 94.7% and 100%, respectively, for patients with chemoradiation-sensitive tumors, and 45.7% (P = 0.0005) and 41.0% (P < 0.0001), respectively, for patients with chemoradiation-resistant tumors.
Chemoradiation sensitivity predicts the development of metastasis in bladder cancer. Clinical and translational research results indicate that chemoradiation sensitivity is likely to reflect metastatic potential.
在涉及经尿道膀胱肿瘤切除术(TURBT)和放化疗的肌层浸润性膀胱癌(MIBC)的保膀胱方法中,对于 TURBT 和放化疗后达到肿瘤无残留状态的患者,生存结果极佳,但对于仍有疾病残留的患者则较差。由于转移性疾病是膀胱癌死亡的主要原因,我们假设肿瘤对放化疗的敏感性可能反映了 MIBC 的转移潜能。
1997 年至 2010 年,179 例 cT2-4aN0M0 膀胱癌患者接受 TURBT 和诱导放化疗(40Gy,顺铂 20mg/d,连用 5 天×2)。研究对象为 73 例 TURBT 后有肉眼可见疾病的患者,评估其对诱导放化疗的肿瘤敏感性;73 例患者中,8 例和 44 例分别在部分和根治性膀胱切除术标本中评估放化疗的病理反应,21 例未行膀胱切除术的患者进行临床评估。在接受膀胱切除术的 52 例患者中,肿瘤在病理上消退至 T0 或在未接受膀胱切除术的 21 例患者中临床消退至 T0 时,定义为放化疗敏感;否则,定义为放化疗抵抗。主要终点和次要终点分别为无转移生存期和癌症特异性生存期。在 MIBC 患者中研究了放化疗敏感性与转移发展之间的关系。
73 例患者中,21 例(29%:13 例病理 T0 和 8 例临床 T0)肿瘤对放化疗敏感,52 例(71%)肿瘤对放化疗抵抗。中位随访时间为 53 个月。多因素分析显示,放化疗抵抗是转移发展的最强独立预测因素(风险比(HR)18.9,P<0.0001)。按放化疗敏感性分层,放化疗敏感肿瘤患者的 5 年无转移生存率和癌症特异性生存率分别为 94.7%和 100%,放化疗抵抗肿瘤患者分别为 45.7%(P=0.0005)和 41.0%(P<0.0001)。
放化疗敏感性预测膀胱癌的转移发展。临床和转化研究结果表明,放化疗敏感性可能反映转移潜能。