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Chemotherapy-Induced Peripheral Neuropathy - Additional Evaluation in Breast Cancer Survivors (NEURO-BREAC-02)

2026年5月17日 更新者:University Hospital Schleswig-Holstein

Chemotherapy-induced Peripheral Neuropathy - Additional Evaluation of a Self-administered Scoring System for Breast Cancer Survivors

The main goal of this trial is to identify the optimal cut-off score of a Scoring System to discriminate between mild chemotherapy-induced peripheral neuropathy (CIPN) and no CIPN in breast cancer survivors previously treated with taxane-based chemotherapy and adjuvant radiotherapy.

研究概览

地位

尚未招聘

条件

详细说明

Adjuvant radiotherapy is a standard procedure following breast-conserving surgery for non-metastatic breast cancer. Depending of the tumor stage and other risk factors, radiotherapy may be indicated also after mastectomy. A considerable number of these patients receive pre- or postoperative chemotherapy. These regimens generally include taxanes (paclitaxel or docetaxel), which are known to be associated with a considerable risk of chemotherapy-induced peripheral neuropathy (CIPN). CIPN can be quite burdensome for the affected patients. According to three review articles, there is no effective prophylactic treatment to prevent peripheral neuropathy (PNP) in general. Moreover, treatment options for existing PNP are limited. The only agent shown to be effective to improve symptoms of PNP in a phase 3 trial is duloxetine, a serotonin an nor-epinephrine dual uptake inhibitor. In addition, physiotherapy may contribute to maintaining or improving the patient's gait function. Close monitoring during the treatment is important to be able to adapt the regimen of neurotoxic chemotherapy very soon after the first symptoms of CIPN occur. To prevent severe neurotoxicity during chemotherapy, the oncology service needs to follow early development of symptoms. In breast cancer patients treated with taxanes, dose reduction due to early development of neuropathy did not change long-term outcomes of toxicity symptoms, suggesting that responses to first doses might be important. In addition, the patient and service burden prohibit frequent out-patient visits to have early detection of toxicity. In clinical neurotoxicity studies a great effort has been put into documenting the validity of grading scales incorporating results from clinical examination with the symptom results. Both approaches require health care resources to document and follow up on CIPN development in order to intervene in the case of severe early toxicity. A scoring system has been developed by members of our group, which is based on patient reported symptoms and signs from self-examination. Depending on number and severity of symptoms identified by the study participants themselves (self-assessment) with the help of a neuropathy tracker, a score ranging between 0 and 44 points is obtained. In a preceding prospective trial, it was shown that the new scoring system can contribute to the identification of moderate to severe CIPN in breast cancer patients who had received taxane-based chemotherapy.

The main goal of this trial is to identify the optimal cut-off score of a scoring system to discriminate between mild CIPN and no CIPN in breast cancer survivors previously treated with taxane-based chemotherapy and adjuvant radiotherapy. To identify the optimal cut-off score of a scoring system to discriminate between mild CIPN and no CIPN in breast cancer survivors previously treated with taxane-based chemotherapy and adjuvant radiotherapy. The scores that range between 0 and 44 points are obtained by using a neuropathy tracker. This tracker is based on self-evaluation of symptoms and signs of CIPN by the study participants. The receiver operating characteristic (ROC) curve is used to show the connection between sensitivity and specificity for every possible cut-off for the Scoring System and select the optimal scoring point for detection of mild CIPN. Secondary aims include satisfaction of the study participants with the scoring system and identification of an optimal cut-off score for the Utah Early Neuropathy Scale to discriminate between mild CIPN and no CIPN.

Sample size calculation: The main goal of this trial is to identify the optimal cut-off score of a scoring system to discriminate between mild CIPN and no CIPN in breast cancer survivors. The discriminative power of the Scoring System will be assessed by calculating the area under the receiver operating characteristic (ROC) curve (AUC). Sample size is calculated to achieve acceptable precision in the estimation of the AUC measured by means of the 90% confidence interval by incorporating a pre-specified probability, which is referred to as assurance, of achieving the desired lower confidence limit. The following assumptions are made:

  • The two-sided significance level is set to 10%
  • An AUC of 0.95 is assumed since this is decided to be an excellent diagnostic accuracy for the Scoring System worth to be considered for future routine use.
  • The pre-specified lower bound of the confidence interval is assumed to be 0.7.
  • The assurance probability is set to 80%.
  • The ratio of standard deviations in patients with no CIPN and patients with mild CIPN is assumed to be 0.67.
  • Approximately 25% of the patients to be included in this study will have no CIPN (according to standard physical examination and medical history), whereas the other 75% will be clinically diagnosed with mild CIPN, i.e. ratio between negative and positive cases is approximately 0.33.

Based on these assumptions above, 26 patients (19 with mild CIPN and 7 without CIPN) are required within the Full Analysis Set. Assuming that roughly 5% of patients will not qualify for Full Analysis Set, a total of 28 patients should be enrolled in the NEURO-BREAC-02 trial.

The Full Analysis Set includes all patients who completed the self-assessment of CIPN.

Statistical considerations: All data recorded in the case report forms describing the study population (demographic and clinical characteristics recorded at baseline), rates of mild CIPN, and safety will be analyzed descriptively. Categorical data will be presented in contingency tables with frequencies and percentages. Continuous data will be summarized with at least the following: frequency, median, quartiles, mean, standard deviation (standard error), minimum and maximum. Number of patients with protocol deviations during the study and listings describing the deviations will be provided. The data analysis will be performed according to the statistical analysis plan (SAP), and which will be finalized prior to database lock and prior to any statistical analysis.

研究类型

介入性

注册 (估计的)

28

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Dirk Rades, Prof. Dr. med., FASTRO
  • 电话号码:45400 0049-451500
  • 邮箱:Dirk.Rades@uksh.de

研究联系人备份

学习地点

    • Schleswig-Holstein
      • Lübeck、Schleswig-Holstein、德国、23562
        • Department of Radiation Oncology, University of Luebeck
        • 接触:
          • Dirk Rades, Prof. Dr. med., FASTRO
          • 电话号码:45400 0049-451500
          • 邮箱:Dirk.Rades@uksh.de
        • 接触:
          • Maria K Streubel, Dr. rer. nat.
          • 电话号码:45420 0049.451-500

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Histologically proven breast cancer
  2. Previous treatment with taxane-based chemotherapy followed by adjuvant radiotherapy
  3. Mild or no CIPN according to the Total Neuropathy Score
  4. Female gender
  5. Age ≥18 years
  6. Written informed consent
  7. Capacity of the patient to consent

Exclusion Criteria:

  1. Disease-related skin disorders of the lower extremities (e.g., related to skin infections, bullous dermatoses, dermatitis, papulo-squamous skin disorders, or urticaria/erythema)
  2. Pregnancy, Lactation
  3. Expected non-compliance

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:诊断
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Breast cancer patients treated with taxane-base chemotherapy
Patients who were previously treated with taxane-base chemotherapy and adjuvant radiotherapy for breast cancer and developed either no or mild chemotherapy-induced peripheral neuropathy
The patients will be asked to complete the self-evaluation of symptoms and signs of neuropathy using a Neuropathy Tracker that questions symptoms quality, severity and distribution and guide the user through a systematic evaluation of pin-prick from a needle and vibration from the mobile on successive levels from the toes to the knee on both legs. Finally, the extension force or both great toes will be self-assessed by the participant. The self-examination is based on the structure of the Utah Early Neuropathy Score.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Number of participants with mild chemotherapy-induced peripheral neuropathy
大体时间:from enrollment to clinical examination at 1 week
Chemotherapy-induced peripheral neuropathy will be assessed with a symptom-based scoring system supported by a neuropathy tracker.
from enrollment to clinical examination at 1 week

次要结果测量

结果测量
措施说明
大体时间
患者满意度
大体时间:从入学到1周的临床检查
患者对基于症状的评分系统的满意度范围从0到44分(较高的分数代表较高的外周神经病等级),将使用特定的问卷进行评估。
从入学到1周的临床检查
Number of participants with mild chemotherapy-induced peripheral neuropathy according to the Utah Early Neuropathy Scale
大体时间:from enrollment to clinical examination at 1 week
Chemotherapy-induced peripheral neuropathy will be assessed with a symptom-based scoring system using the Utah Early Neuropathy Scale.
from enrollment to clinical examination at 1 week

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Dirk Rades, Prof. Dr. med., FASTRO、University of Luebeck, Germany

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月1日

初级完成 (估计的)

2026年8月31日

研究完成 (估计的)

2026年8月31日

研究注册日期

首次提交

2026年5月17日

首先提交符合 QC 标准的

2026年5月17日

首次发布 (实际的)

2026年5月22日

研究记录更新

最后更新发布 (实际的)

2026年5月22日

上次提交的符合 QC 标准的更新

2026年5月17日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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