首页> 外文期刊>Pilot and Feasibility Studies >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
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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

机译:晚期宫颈癌的主动脉旁淋巴结清扫术,用于比较手术分期与PET-CT的安全性,可行性和诊断准确性的方案; PALDISC试用

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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/designIn 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.DiscussionThis 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 registrationNederlands Trial Register/Dutch Trial Registry (www.trialregister.nl), NTR4922. Registered on 24 November 2014.
机译:目前,在国际妇产科联合会(FIGO)IB2期,IIA2-IVA期(局部晚期)宫颈癌中,PET-CT用于评估对主动脉旁淋巴结(PALN)进行大范围放疗的必要性。一项小型研究确定了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的手术分期可能导致更高的诊断准确性。然而,局部晚期宫颈癌的主动脉旁淋巴结的手术分期并不普遍。因此,需要进行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,还将有30名患有FIGO IB2,IIA2-IVA期宫颈癌的成年女性。随机接受手术分期或常规PET-CT分期。干预组应根据淋巴结清扫术的结果以及对照组的PET-CT结果进行大范围放疗。在0、3、6、9和12个月进行随访,以评估与健康相关的生活质量和无进展生存期。将以95%的置信区间计算平均值评估手术分期的主要安全性和可行性。手术时间,并发症数,失血量,主动脉旁淋巴结清扫术后的淋巴结清扫率以及手术分期导致的治疗延迟。将记录并以两组患者为中心的关于生活质量和第一年生存的结果,并进行比较。 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估计值将以95%CI表示。所有分析均将根据治疗原则进行。讨论本研究将评估安全性和可行性,表示为局部晚期宫颈癌的手术分期引起的并发症的数量和严重程度,对生活质量的影响以及治疗延迟。它将提供有关PET-CT的诊断准确性以及因手术分期而遗漏的(微小)转移的检测率的见解。该信息将用于评估进行PET-CT诊断准确性和手术分期的3期研究的必要性。如果认为3期研究是必要的,则可将当前数据用于此类3期研究的样本量计算。试验注册荷兰试验注册/荷兰试验注册(www.trialregister.nl),NTR4922。 2014年11月24日注册。

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