对新辅助化疗完全缓解后持续放化疗可改善肌肉侵袭性尿路上皮癌的预后

Javier J. Lopez Araujo, R. Jacob, C. Baden, J. Fiveash, M. Dobelbower, J. E. Bryant, G. Bolger
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Tumor response was evaluated with an abdomino-pelvic CT scan and cystoscopy 4 weeks after neoadjuvant chemotherapy and 3 months after completion of all therapy. Radiation therapy was delivered using 3DCRT or IMRT to a median dose of 45 Gy to the pelvis and 63 Gy to the bladder (range 41.4 Gy to 71.4 Gy).  Three-year local control (LC) and disease-free survival (DFS) estimates were determined by the Kaplan-Meier method and log rank analysis. Results: The median age was 67.5 years. Median follow-up was 24 months (range 6 to 86). Clinical stage was T2 in 12 patients, T3 in 8, and T4 in 2. Fourteen patients were node-negative while 8 were node-positive. Actuarial 3-year OS, DFS, LC for the entire cohort were 62.2%, 62% and 78.3%, respectively. Furthermore, the 3-year OS and DFS for patients achieving a CR on cystoscopy following neo-adjuvant chemotherapy was 64.6% vs . 57.1% without CR ( p =.046), and 64.3% vs . 57.1% without CR ( p =.03). 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引用次数: 0

摘要

目的:评价局部肌浸润性膀胱癌(MIBC)患者新辅助化疗加持续放化疗(cCRT)的治疗效果。评价新辅助化疗临床完全缓解对膀胱保留患者预后的意义。材料/方法:2002 - 2012年,对22例cT2-4 N0-2 M0 MIBC患者行cCRT保膀胱术。所有患者均被认为医学上不适合手术和/或拒绝膀胱切除术。他们接受最大经尿道肿瘤切除术(turt)和多周期铂双基新辅助化疗,然后进行最终的cCRT。在新辅助化疗后4周和完成所有治疗后3个月,通过腹部-骨盆CT扫描和膀胱镜检查评估肿瘤反应。采用3DCRT或IMRT进行放射治疗,骨盆中位剂量为45 Gy,膀胱中位剂量为63 Gy (41.4 Gy至71.4 Gy)。三年局部控制(LC)和无病生存(DFS)估计值由Kaplan-Meier法和对数秩分析确定。结果:中位年龄67.5岁。中位随访时间为24个月(范围6 - 86)。临床分期为T2 12例,T3 8例,T4 2例。14例淋巴结阴性,8例淋巴结阳性。精算3年OS、DFS和LC在整个队列中分别为62.2%、62%和78.3%。此外,新辅助化疗后膀胱镜检查达到CR的患者的3年OS和DFS为64.6%。无CR者占57.1% (p = 0.046),无CR者占64.3%。无CR的57.1% (p = 0.03)。对新辅助化疗完全缓解的患者3年LC为90.9%。按T分期分层时,T2的3年LC为90.9%,T3为87.5%,T4为0% (p = 0.007)。5例患者中有4例局部衰竭与远处转移有关。2例患者有非侵袭性局部复发,均成功接受膀胱内卡介苗治疗。结论:在3年随访中,最大限度的TURBT、新辅助铂基化疗和最终的cCRT在MIBC中提供了良好的OS、DFS和LC率。新辅助化疗的完全缓解是一个有利的预后因素,3年LC率>90%。
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Continuous chemoradiation following complete response to neo-adjuvant chemotherapy provides improved outcomes in muscle invasive urothelial carcinoma
Purpose: To evaluate the outcomes of patients with localized muscle invasive bladder cancer (MIBC) treated with neo-adjuvant chemotherapy followed by continuous chemo-radiation (cCRT). To evaluate the prognostic significance of clinical complete response to neo-adjuvant chemotherapy in the setting of bladder preservation. Materials/Methods: From 2002 to 2012, twenty-two patients with cT2-4 N0-2 M0 MIBC were treated using cCRT for bladder preservation.  All patients were felt to be medically inoperable and/or refused cystectomy.  They were treated with maximal transurethral tumor resection (TURBT) and multiple cycles of platinum-doublet-based neoadjuvant chemotherapy, followed by definitive cCRT. Tumor response was evaluated with an abdomino-pelvic CT scan and cystoscopy 4 weeks after neoadjuvant chemotherapy and 3 months after completion of all therapy. Radiation therapy was delivered using 3DCRT or IMRT to a median dose of 45 Gy to the pelvis and 63 Gy to the bladder (range 41.4 Gy to 71.4 Gy).  Three-year local control (LC) and disease-free survival (DFS) estimates were determined by the Kaplan-Meier method and log rank analysis. Results: The median age was 67.5 years. Median follow-up was 24 months (range 6 to 86). Clinical stage was T2 in 12 patients, T3 in 8, and T4 in 2. Fourteen patients were node-negative while 8 were node-positive. Actuarial 3-year OS, DFS, LC for the entire cohort were 62.2%, 62% and 78.3%, respectively. Furthermore, the 3-year OS and DFS for patients achieving a CR on cystoscopy following neo-adjuvant chemotherapy was 64.6% vs . 57.1% without CR ( p =.046), and 64.3% vs . 57.1% without CR ( p =.03). The 3-year LC was 90.9% in patients showing complete response to neo-adjuvant chemotherapy. When stratified by T stage, 3-year LC was 90.9% for T2, 87.5% for T3 and 0% for T4 ( p =.007). Local failure was associated with distant metastases in 4 out of 5 patients. Two patients had non-invasive local recurrences and both were successfully treated with intra-vesical BCG. Conclusions: Maximal TURBT followed by neo-adjuvant platinum based chemotherapy and definitive cCRT offers good rates of OS, DFS and LC in MIBC at three-years of follow-up. Complete response to neo-adjuvant chemotherapy is a favorable prognostic factor, achieving LC rates >90% at 3 years.
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