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《强度调制盆腔淋巴结和膀胱放疗(IMPART)试验:一项 II 期单中心前瞻性研究》。

The Intensity-Modulated Pelvic Node and Bladder Radiotherapy (IMPART) Trial: A Phase II Single-Centre Prospective Study.

机构信息

Academic Radiotherapy Unit, Institute of Cancer Research, Sutton, Surrey, UK; The Royal Marsden NHS Foundation Trust, Sutton, Surrey, UK.

Academic Radiotherapy Unit, Institute of Cancer Research, Sutton, Surrey, UK; The Royal Marsden NHS Foundation Trust, Sutton, Surrey, UK; Guy's & St. Thomas' NHS Foundation Trust, London, UK.

出版信息

Clin Oncol (R Coll Radiol). 2020 Feb;32(2):93-100. doi: 10.1016/j.clon.2019.07.017. Epub 2019 Aug 8.

Abstract

AIMS

Node-positive bladder cancer (NPBC) carries a poor prognosis and has traditionally been treated palliatively. However, surgical series suggest that a subset of NPBC patients can achieve long-term control after cystectomy and lymph node dissection. There is little published data regarding the use of radiotherapy to treat NPBC patients. This is in part due to concerns regarding the toxicity of whole-pelvis radiotherapy using conventional techniques. We hypothesised that, using intensity-modulated radiotherapy (IMRT), the pelvic nodes and bladder could be treated within a radical treatment volume with acceptable toxicity profiles.

MATERIALS AND METHODS

The Intensity-modulated Pelvic Node and Bladder Radiotherapy (IMPART) trial was a phase II single-centre prospective study designed to assess the feasibility of delivering IMRT to treat the bladder and pelvic nodes in patients with node-positive or high-risk node-negative bladder cancer (NNBC). The primary end point was meeting predetermined dose constraints. Secondary end points included acute and late toxicity, pelvic relapse-free survival and overall survival.

RESULTS

In total, 38 patients were recruited and treated between June 2009 and November 2012; 22/38 (58%) had NPBC; 31/38 (81.6%) received neoadjuvant chemotherapy; 18/38 (47%) received concurrent chemotherapy; 37/38 (97%) patients had radiotherapy planned as per protocol. Grade 3 gastrointestinal and genitourinary acute toxicity rates were 5.4 and 20.6%, respectively. At 1 year, the grade 3 late toxicity rate was 5%; 1-, 2- and 5-year pelvic relapse-free survival rates were 55, 37 and 26%, respectively. The median overall survival was 1.9 years (95% confidence interval 1.1-3.8) with 1-, 2- and 5-year overall survival rates of 68, 50 and 34%, respectively.

CONCLUSION

Delivering IMRT to the bladder and pelvic nodes in NPBC and high-risk NNBC is feasible, with low toxicity and low pelvic nodal recurrence rates. Long-term control seems to be achievable in a subset of patients. However, relapse patterns suggest that strategies targeting both local recurrence and the development of distant metastases are required to improve patient outcomes.

摘要

目的

阳性淋巴结膀胱癌(NPBC)预后不良,传统上采用姑息性治疗。然而,外科系列研究表明,在根治性膀胱切除术和淋巴结清扫术后,NPBC 患者的亚组可以获得长期控制。关于使用放疗治疗 NPBC 患者的文献很少。这部分是由于对使用传统技术进行全骨盆放疗的毒性的担忧。我们假设,使用调强放疗(IMRT),可以在可接受的毒性特征下,在根治性治疗体积内治疗盆腔淋巴结和膀胱。

材料和方法

调强盆腔淋巴结和膀胱放疗(IMPART)试验是一项 II 期单中心前瞻性研究,旨在评估对 NPBC 或高危淋巴结阴性膀胱癌(NNBC)患者进行 IMRT 治疗膀胱和盆腔淋巴结的可行性。主要终点是满足预定的剂量限制。次要终点包括急性和迟发性毒性、盆腔无复发生存率和总生存率。

结果

2009 年 6 月至 2012 年 11 月期间共招募并治疗了 38 例患者;22/38(58%)为 NPBC;31/38(81.6%)接受新辅助化疗;18/38(47%)接受同期化疗;37/38(97%)患者按计划接受放疗。胃肠道和泌尿生殖系统急性毒性 3 级发生率分别为 5.4%和 20.6%。1 年时,3 级迟发性毒性发生率为 5%;1、2 和 5 年盆腔无复发生存率分别为 55%、37%和 26%。中位总生存期为 1.9 年(95%置信区间为 1.1-3.8),1、2 和 5 年总生存率分别为 68%、50%和 34%。

结论

在 NPBC 和高危 NNBC 中对膀胱和盆腔淋巴结进行 IMRT 是可行的,具有低毒性和低盆腔淋巴结复发率。在亚组患者中似乎可以实现长期控制。然而,复发模式表明,需要针对局部复发和远处转移的发展制定策略,以改善患者的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8029/6966321/062814d45347/gr1.jpg

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