首页> 外文期刊>BMC Cancer >Clinical Phase I/II trial to Investigate Preoperative Dose-Escalated Intensity-Modulated Radiation Therapy (IMRT) and Intraoperative Radiation Therapy (IORT) in patients with retroperitoneal soft tissue sarcoma: interim analysis
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Clinical Phase I/II trial to Investigate Preoperative Dose-Escalated Intensity-Modulated Radiation Therapy (IMRT) and Intraoperative Radiation Therapy (IORT) in patients with retroperitoneal soft tissue sarcoma: interim analysis

机译:I / II期临床试验,研究腹膜后软组织肉瘤患者术前剂量递增的调强放射治疗(IMRT)和术中放射治疗(IORT):中期分析

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Background To report an unplanned interim analysis of a prospective, one-armed, single center phase I/II trial (NCT01566123). Methods Between 2007 and 2013, 27 patients (pts) with primary/recurrent retroperitoneal sarcomas (size?>?5?cm, M0, at least marginally resectable) were enrolled. The protocol attempted neoadjuvant IMRT using an integrated boost with doses of 45–50 Gy to PTV and 50–56 Gy to GTV in 25 fractions, followed by surgery and IOERT (10–12 Gy). Primary endpoint was 5-year-LC, secondary endpoints included PFS, OS, resectability, and acute/late toxicity. The majority of patients showed high grade lesions (FNCLCC G1:18%, G2:52%, G3:30%), predominantly liposarcomas (70%). Median tumor size was 15?cm (6–31). Results Median follow-up was 33?months (5–75). Neoadjuvant IMRT was performed as planned (median dose 50 Gy, 26–55) in all except 2 pts (93%). Gross total resection was feasible in all except one patient. Final margin status was R0 in 6 (22%) and R1 in 20 pts (74%). Contiguous-organ resection was needed in all grossly resected patients. IOERT was performed in 23 pts (85%) with a median dose of 12 Gy (10–20 Gy). We observed 7 local recurrences, transferring into estimated 3- and 5-year-LC rates of 72%. Two were located outside the EBRT area and two were observed after more than 5?years. Locally recurrent situation had a significantly negative impact on local control. Distant failure was found in 8 pts, resulting in 3- and 5-year-DC rates of 63%. Patients with leiomyosarcoma had a significantly increased risk of distant failure. Estimated 3- and 5-year-rates were 40% for PFS and 74% for OS. Severe acute toxicity (grade 3) was present in 4 pts (15%). Severe postoperative complications were found in 9 pts (33%), of whom 2 finally died after multiple re-interventions. Severe late toxicity (grade 3) was scored in 6% of surviving patients after 1?year and none after 2?years. Conclusion Combination of neoadjuvant IMRT, surgery and IOERT is feasible with acceptable toxicity and yields good results in terms of LC and OS in patients with high-risk retroperitoneal sarcomas. Long term follow-up seems mandatory given the observation of late recurrences. Accrual of patients will be continued with extended follow-up. Trial registration NCT01566123 .
机译:背景报道一项前瞻性单臂单中心I / II期试验(NCT01566123)的计划外中期分析。方法2007年至2013年,共纳入27例原发性/复发性腹膜后肉瘤患者(pts≥5?cm,M0,至少可部分切除)。该方案尝试以25倍的PTV剂量45–50 Gy和GTV剂量50–56 Gy的综合剂量进行新辅助IMRT,然后进行手术和IOERT(10–12 Gy)。主要终点为5年LC,次要终点包括PFS,OS,可切除性和急性/晚期毒性。大多数患者表现出高度病变(FNCLCC G1:18%,G2:52%,G3:30%),主要是脂肪肉瘤(70%)。中位肿瘤大小为15?cm(6-31)。结果中位随访时间为33个月(5–75)。除2分(93%)外,所有患者均按计划进行了新辅助IMRT(中位剂量50 Gy,26-55)。除一名患者外,所有患者均可以进行大体全切除。最终保证金状态为6分的R0(22%)和20分的R1(74%)。所有大体切除的患者都需要进行连续器官切除。 IOERT进行了23分(85%),中位剂量为12 Gy(10-20 Gy)。我们观察到7次局部复发,估计3年和5年LC发生率达到72%。其中两个位于EBRT区域以外,超过5年后观察到两个。局部复发情况对局部控制产生了显着的负面影响。在8分中发现了严重的故障,导致3年和5年DC率达到63%。平滑肌肉瘤患者远距离衰竭的风险显着增加。估计3年和5年率的PFS为40%,OS为74%。严重急性毒性(3级)的患者为4分(15%)。术后严重并发症发生率为9分(33%),其中2人经多次干预后最终死亡。 1年后存活的患者中有6%的患者具有严重晚期毒性(3级),而2年后则没有评分。结论新辅助IMRT,手术和IOERT的结合是可行的,具有可接受的毒性,并且在高危腹膜后肉瘤患者中,在LC和OS方面可获得良好的效果。考虑到晚期复发,需要长期随访。继续随访将继续患者的累积。试用注册号NCT01566123。

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