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晚期宫颈癌腹主动脉旁淋巴结切除术:一项比较手术分期与PET-CT的安全性、可行性及诊断准确性的方案;PALDISC试验

Para-aortic lymphadenectomy in advanced stage cervical cancer, a protocol for comparing safety, feasibility and diagnostic accuracy of surgical staging versus PET-CT; PALDISC trial.

作者信息

Tax Casper, Abbink Karin, Rovers Maroeska M, Bekkers Ruud L M, Zusterzeel Petra L M

机构信息

Department of Operating Rooms 715, Radboud University Medical Centre, Radboudumc Institute for Health Sciences, P.O. Box 9101, 6500 HB Nijmegen, the Netherlands.

Department of Gynaecology, Radboud University Medical Centre, Radboudumc Institute for Health Sciences, P.O. Box 9101, 6500 HB Nijmegen, the Netherlands.

出版信息

Pilot Feasibility Stud. 2018 Jan 4;4:27. doi: 10.1186/s40814-017-0218-8. eCollection 2018.

Abstract

BACKGROUND

Currently, a PET-CT is used to assess the need for extended field radiotherapy of para-aortic lymph nodes (PALN) in International Federation of Gynaecology and Obstetrics (FIGO) stage IB2, IIA2-IVA (locally advanced stage) cervical cancer. A small study established a sensitivity and specificity estimate for PALN metastases of 50% (95% CI; 7-93%) and 83% (95% CI; 52-98%), respectively. Surgical staging of PALN may lead to a higher diagnostic accuracy. However, surgical staging of para-aortic lymph nodes in locally advanced stage cervical cancer is not common practice. Therefore, a phase 2 randomised controlled trial is needed to assess its safety and feasibility.

METHODS/DESIGN: In addition to standard imaging (MRI or CT scan) with PET-CT, 30 adult women with FIGO stage IB2, IIA2-IVA cervical cancer will be randomised to receive either surgical staging or usual PET-CT staging. Administering extended field radiotherapy will be based on lymphadenectomy results for the intervention group and on the PET-CT results for the control group. Follow-up visits at 0, 3, 6, 9 and 12 months will assess health-related quality of life and progression-free survival.Primary safety and feasibility outcomes of surgical staging will be assessed by calculating means with 95% confidence intervals for duration of surgery, number of complications, blood loss, nodal yield after para-aortic lymphadenectomy and treatment delay due to surgical staging. Secondary patient-centred outcomes on quality of life and first year survival will be documented and compared between the two groups. Estimates of sensitivity, specificity and negative and positive predictive values of MRI, PET-CT and surgical staging will be presented with 95% CI.. All analysis will be performed according to the intention to treat principle.

DISCUSSION

This study will assess safety and feasibility, expressed as the number and severity of complications, effect on quality of life and the treatment delay due to surgically staging para-aortic lymph nodes in locally advanced cervical cancer. It will provide insight in the diagnostic accuracy of the PET-CT and detection rate of missed (micro)metastases due to surgical staging. This information will be used to assess the necessity for a phase 3 study on the diagnostic accuracy of the PET-CT and surgical staging. If a phase 3 study is deemed necessary, current data can be used for sample size calculation of such a phase 3 study.

TRIAL REGISTRATION

Nederlands Trial Register/Dutch Trial Registry (www.trialregister.nl), NTR4922. Registered on 24 November 2014.

摘要

背景

目前,正电子发射断层显像/X线计算机体层成像(PET-CT)用于评估国际妇产科联盟(FIGO)IB2期、IIA2-IVA期(局部晚期)宫颈癌患者腹主动脉旁淋巴结(PALN)扩大野放疗的必要性。一项小型研究对PALN转移的敏感性和特异性估计分别为50%(95%CI:7-93%)和83%(95%CI:52-98%)。PALN的手术分期可能会带来更高的诊断准确性。然而,局部晚期宫颈癌患者腹主动脉旁淋巴结的手术分期并非普遍做法。因此,需要开展一项2期随机对照试验来评估其安全性和可行性。

方法/设计:除了采用PET-CT进行标准成像(MRI或CT扫描)外,30例FIGO IB2期、IIA2-IVA期宫颈癌成年女性将被随机分组,分别接受手术分期或常规PET-CT分期。扩大野放疗将根据干预组的淋巴结清扫结果和对照组的PET-CT结果来实施。在0、3、6、9和12个月进行随访,以评估健康相关生活质量和无进展生存期。手术分期的主要安全性和可行性结局将通过计算手术持续时间、并发症数量、失血量、腹主动脉旁淋巴结清扫术后淋巴结获取量以及手术分期导致的治疗延迟的95%置信区间均值来评估。两组将记录并比较以患者为中心的生活质量和第一年生存率等次要结局。将给出MRI、PET-CT和手术分期的敏感性、特异性以及阴性和阳性预测值的95%CI估计值。所有分析将按照意向性分析原则进行。

讨论

本研究将评估安全性和可行性,以局部晚期宫颈癌患者腹主动脉旁淋巴结手术分期的并发症数量和严重程度、对生活质量的影响以及治疗延迟来表示。它将深入了解PET-CT的诊断准确性以及手术分期导致的漏诊(微)转移的检出率。这些信息将用于评估是否有必要开展一项关于PET-CT和手术分期诊断准确性的3期研究。如果认为有必要开展3期研究,当前数据可用于此类3期研究的样本量计算。

试验注册

荷兰试验注册中心(www.trialregister.nl),NTR4922。于2014年11月24日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e91/5755440/94fc88c8318a/40814_2017_218_Fig1_HTML.jpg

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