Fonteyne Valérie, Dirix Piet, Junius Sara, Rammant Elke, Ost Piet, De Meerleer Gert, Swimberghe Martijn, Decaestecker Karel
Department of Radiation-Oncology, Ghent University Hospital, De Pintelaan 185, Ghent, Belgium.
Department of Radiation-Oncology, Iridium Cancer Network, Ghent, Belgium.
BMC Cancer. 2017 May 2;17(1):308. doi: 10.1186/s12885-017-3302-9.
Neo-adjuvant chemotherapy followed by radical cystectomy with extended pelvic lymph node dissection is considered to be the treatment of choice for patients with muscle invasive bladder cancer (MIBC). Despite this aggressive treatment the outcome is poor and ultimately, 30% of the patients with ≥pT3 tumors develop a pelvic recurrence. We hypothesize that postoperative adjuvant external beam radiotherapy (EBRT) might prevent local and lymph node recurrence and improve disease free- and overall survival as loco-regional recurrence is linked to the development of distant metastasis.
We plan to perform a multicentric prospective phase two study including 76 patients. Eligible patients are patients with MIBC, treated with radical cystectomy and presenting with ≥1 of the following characteristics: Pathological (p)T3 stage + presence of lymphovascular invasion on pathological examination pT4 stage <10 lymph nodes removed positive lymph nodes positive surgical margins Patients will have a F-FDG PET-CT to rule out the presence of distant metastasis prior to EBRT. A median dose of 50 Gy in 25 fractions is prescribed to the pelvic lymph node regions with inclusion of the operative bladder bed in case of a positive surgical margin. Patients with suspected lymph nodes on PET- CT can still be included in the trial, but a simultaneous integrated boost to 74Gy to the positive lymph nodes will be delivered. Blood and urine samples will be collected on day-1 and last day of EBRT for evaluation of biomarkers. The primary endpoint is evaluation of acute ≥Grade 3 intestinal or grade 4 urinary toxicity, in case of a neo-bladder reconstruction, within 12 weeks after EBRT. Secondary endpoints are: assessment of QOL, late RTOG toxicity, local control, disease free survival and overall survival. Biomarkers in urine and blood will be correlated with secondary survival endpoints.
This is a prospective phase 2 trial re-assessing the feasibility of adjuvant radiotherapy in high-risk MIBC.
The Ethics committee of the Ghent University Hospital (EC2014/0630) approved this study on 31/07/2014. Trial registration on Clinicaltrials.gov ( NCT02397434 ) on November 19, 2014.
新辅助化疗后行根治性膀胱切除术并扩大盆腔淋巴结清扫术被认为是肌层浸润性膀胱癌(MIBC)患者的首选治疗方法。尽管采用了这种积极的治疗方法,但其预后仍较差,最终,≥pT3肿瘤患者中有30%会出现盆腔复发。我们推测术后辅助外照射放疗(EBRT)可能会预防局部和淋巴结复发,并改善无病生存期和总生存期,因为局部区域复发与远处转移的发生有关。
我们计划开展一项多中心前瞻性二期研究,纳入76例患者。符合条件的患者为接受根治性膀胱切除术的MIBC患者,且具有以下至少一项特征:病理(p)T3期+病理检查发现有淋巴管浸润;pT4期;切除的淋巴结<10个;淋巴结阳性;手术切缘阳性。患者在接受EBRT之前将进行F-FDG PET-CT检查以排除远处转移的存在。盆腔淋巴结区域的处方中位剂量为50 Gy,分25次给予,若手术切缘阳性,则包括手术膀胱床。PET-CT检查怀疑有淋巴结转移的患者仍可纳入试验,但将对阳性淋巴结同时加量至74 Gy。将在EBRT的第1天和最后一天采集血液和尿液样本以评估生物标志物。主要终点是评估在EBRT后12周内(如果进行了新膀胱重建)急性≥3级肠道毒性或4级泌尿系统毒性。次要终点包括:生活质量评估、晚期RTOG毒性、局部控制、无病生存期和总生存期。尿液和血液中的生物标志物将与次要生存终点相关联。
这是一项前瞻性二期试验,重新评估高危MIBC患者辅助放疗的可行性。
根特大学医院伦理委员会(EC2014/0630)于2014年7月31日批准了本研究。于2014年11月19日在Clinicaltrials.gov上注册(NCT02397434)。