Assessment of Physical Activity During Chemotherapy and/or Immunotherapy for Non-Small Cell Lung Cancer (NSCLC): Protocol of the APACHIE-01 Study.

IF 2.2 Q2 MEDICINE, GENERAL & INTERNAL
Dirk Rades, Laura Doehring, Christian Staackmann, Maria Karolin Streubel, Stefan Janssen, Tobias Bartscht, Sabine Bohnet
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引用次数: 0

Abstract

Background/objectives: Most patients with non-small cell lung cancer (NSCLC) receive chemo- and/or immunotherapy, which can be associated with adverse events including fatigue. Affected patients may not be able to receive the complete chemo- and/or immunotherapy as planned. In this context, patients may benefit from maintaining their physical activity, which can be challenging. An app reminding patients to perform a certain number of steps may have a positive effect on physical activity during chemo- and/or immunotherapy. Such an app is under development and will be tested in a prospective trial. The current APACHIE-01 study (NCT06993896) is required for proper sample size calculation and design of the planned trial.

Methods: The main goal of the APACHIE-01 study is to evaluate patterns and predictors of physical activity during chemo- and/or immunotherapy for locally advanced or metastatic NSCLC. The primary endpoint is the assessment of the mean number of steps per week during the first three cycles of chemo- and/or immunotherapy for lung cancer. The baseline value is represented by the mean number of steps during the last week prior to chemotherapy and/or immunotherapy. Secondary endpoints include associations between mean number of steps per week and a pain score, a distress score, and a fatigue score. The recruitment of the required 38 patients should be completed within 4 months and the treatment period will be 9-10 weeks (three cycles of chemo- and/or immunotherapy), resulting in a total running time of approximately 6 months. The APACHIE-01 study will contribute to the optimal design of a subsequent prospective trial.

评估非小细胞肺癌(NSCLC)化疗和/或免疫治疗期间的身体活动:APACHIE-01研究方案
背景/目的:大多数非小细胞肺癌(NSCLC)患者接受化疗和/或免疫治疗,这可能与疲劳等不良事件相关。受影响的患者可能无法按计划接受完整的化疗和/或免疫治疗。在这种情况下,患者可能受益于保持他们的身体活动,这可能是具有挑战性的。一款提醒患者完成一定步数的应用程序可能会对化疗和/或免疫治疗期间的身体活动产生积极影响。这样的应用程序正在开发中,并将在前瞻性试验中进行测试。目前的APACHIE-01研究(NCT06993896)需要适当的样本量计算和计划试验的设计。方法:APACHIE-01研究的主要目的是评估局部晚期或转移性NSCLC化疗和/或免疫治疗期间身体活动的模式和预测因素。主要终点是评估肺癌化疗和/或免疫治疗的前三个周期中每周平均步数。基线值由化疗和/或免疫治疗前最后一周的平均步数表示。次要终点包括每周平均步数与疼痛评分、痛苦评分和疲劳评分之间的关联。所需38例患者的招募应在4个月内完成,治疗期为9-10周(三个化疗和/或免疫治疗周期),总运行时间约为6个月。APACHIE-01研究将有助于后续前瞻性试验的优化设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinics and Practice
Clinics and Practice MEDICINE, GENERAL & INTERNAL-
CiteScore
2.60
自引率
4.30%
发文量
91
审稿时长
10 weeks
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