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辅助性全腹调强放疗(IMRT)用于高危FIGO III期卵巢癌患者(OVAR-IMRT-01)——一项I/II期研究的试点试验:研究方案

Adjuvant whole abdominal intensity modulated radiotherapy (IMRT) for high risk stage FIGO III patients with ovarian cancer (OVAR-IMRT-01) - Pilot trial of a phase I/II study: study protocol.

作者信息

Rochet Nathalie, Jensen Alexandra D, Sterzing Florian, Munter Marc W, Eichbaum Michael H, Schneeweiss Andreas, Sohn Christof, Debus Juergen, Harms Wolfgang

机构信息

Department of Radiation Oncology, University of Heidelberg, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany.

出版信息

BMC Cancer. 2007 Dec 19;7:227. doi: 10.1186/1471-2407-7-227.

Abstract

BACKGROUND

The prognosis for patients with advanced epithelial ovarian cancer remains poor despite aggressive surgical resection and platinum-based chemotherapy. More than 60% of patients will develop recurrent disease, principally intraperitoneal, and die within 5 years. The use of whole abdominal irradiation (WAI) as consolidation therapy would appear to be a logical strategy given its ability to sterilize small tumour volumes. Despite the clinically proven efficacy of whole abdominal irradiation, the use of radiotherapy in ovarian cancer has profoundly decreased mainly due to high treatment-related toxicity. Modern intensity-modulated radiation therapy (IMRT) could allow to spare kidneys, liver, and bone marrow while still adequately covering the peritoneal cavity with a homogenous dose.

METHODS/DESIGN: The OVAR-IMRT-01 study is a single center pilot trial of a phase I/II study. Patients with advanced ovarian cancer stage FIGO III (R1 or R2< 1 cm) after surgical resection and platinum-based chemotherapy will be treated with whole abdomen irradiation as consolidation therapy using intensity modulated radiation therapy (IMRT) to a total dose of 30 Gy in 1.5 Gy fractions. A total of 8 patients will be included in this trial. For treatment planning bone marrow, kidneys, liver, spinal cord, vertebral bodies and pelvic bones are defined as organs at risk. The planning target volume includes the entire peritoneal cavity plus pelvic and para-aortic node regions.

DISCUSSION

The primary endpoint of the study is the evaluation of the feasibility of intensity-modulated WAI and the evaluation of the study protocol. Secondary endpoint is evaluation of the toxicity of intensity modulated WAI before continuing with the phase I/II study. The aim is to explore the potential of IMRT as a new method for WAI to decrease the dose to kidneys, liver, bone marrow while covering the peritoneal cavity with a homogenous dose, and to implement whole abdominal intensity-modulated radiotherapy into the adjuvant multimodal treatment concept of advanced ovarian cancer FIGO stage III.

摘要

背景

尽管进行了积极的手术切除和铂类化疗,但晚期上皮性卵巢癌患者的预后仍然很差。超过60%的患者会出现复发性疾病,主要是腹膜内复发,并在5年内死亡。鉴于全腹照射(WAI)能够消除小体积肿瘤,将其用作巩固治疗似乎是一种合理的策略。尽管全腹照射在临床上已被证明有效,但由于与治疗相关的高毒性,卵巢癌放疗的使用已大幅减少。现代调强放射治疗(IMRT)可以在均匀覆盖腹膜腔的同时,使肾脏、肝脏和骨髓免受照射。

方法/设计:OVAR-IMRT-01研究是一项I/II期单中心试点试验。手术切除和铂类化疗后处于国际妇产科联盟(FIGO)III期(R1或R2<1 cm)的晚期卵巢癌患者,将接受调强放射治疗(IMRT)的全腹照射作为巩固治疗,总剂量为30 Gy,每次分割剂量为1.5 Gy。本试验共纳入8名患者。在治疗计划中,骨髓、肾脏、肝脏、脊髓、椎体和骨盆骨被定义为危及器官。计划靶体积包括整个腹膜腔以及盆腔和腹主动脉旁淋巴结区域。

讨论

该研究的主要终点是评估调强全腹照射的可行性以及研究方案。次要终点是在继续进行I/II期研究之前评估调强调强全腹照射的毒性。目的是探索IMRT作为一种新的全腹照射方法的潜力,以降低对肾脏、肝脏、骨髓的剂量,同时均匀覆盖腹膜腔,并将全腹调强放射治疗纳入晚期FIGO III期卵巢癌的辅助多模式治疗方案。

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