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临床试验/NCT04717739
NCT04717739招募中不适用

Use of TTFields in Germany in Routine Clinical Care Study PROgram - Daily Activity, Sleep and Neurocognitive Functioning in Newly Diagnosed Glioblastoma Patients Study

NovoCure Ltd.36 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2021年12月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
NovoCure Ltd.
入组人数
500
试验地点
36
主要终点
Changes in daily physical activity as a potential quality of life parameter in TTFields treatment compared to baseline for up to four months after start of TTFields therapy

研究概览

简要总结

This non-interventional study aims to investigate change over time in cognitive function, sleep quality, and activity in daily life as important determinants of QoL in a large cohort of GBM patients in Germany treated with TTFields in routine clinical care using low-threshold, electronic PRO and modern automated tracking data analyses. The gained results will allow even better understanding of TTFields therapy in daily life of GBM patients and consequently, better informing patients about what to expect when starting this therapy, increasing therapy compliance in the long-term.

详细描述

Glioblastoma (GBM) is the most common malignant primary tumor of the brain with an annual incidence of approximately 3/100.000. Since 2005 the treatment for newly diagnosed GBM consisted of maximal surgical resection, approx. 60 Gy of radiotherapy together with chemotherapy using temozolomide (TMZ), followed by 6 cycles of maintenance chemotherapy. This treatment regimen demonstrated increased median overall survival (OS) from 12.1 to 14.6 months in comparison to surgery and radiotherapy alone in 2005.

Since 2005, despite plenty of clinical phase III trials conducted, Tumor Treating Fields (TTFields) therapy was the first treatment shown to significantly increase median progression-free survival (PFS), OS and one to five year survival rates compared to the previous standard of care. These results led to FDA approval of TTFields for newly diagnosed GBM and were acknowledged since then by several guidelines recommending TTFields for GBM therapy (e.g. NCCN guidelines for CNS cancers V.1.2018, RCC guideline tumörer I hjärna och ryggmärg 2020-01-14 V3.0, DGHO guideline for glioma in adults ICD-10 C71 March 2019). Today, several national committees in Europe already list TTFields as reimbursed treatment (e.g. Austria, Sweden, Germany).

Data with TTFields therapy in real-world setting is limited and therefore further evaluation of different treatment aspects of TTFields therapy in clinical routine are of interest. In particular the QoL-related aspects neurocognitive functioning, daily activity and sleep quality in this patient cohort is of major interest, given the limited life expectancy with this disease.

This non-interventional study aims to investigate change over time in neurocognitive functioning, sleep quality, and activity in daily life as important determinants of QoL in a large cohort of GBM patients in Germany treated with TTFields in routine clinical care using low-threshold, electronic PRO and modern automated tracking data analyses. The gained results will allow even better understanding of TTFields therapy in daily life of GBM patients and consequently, better informing patients about what to expect when starting this therapy, increasing therapy compliance even further in the long-term.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • min.18 years of age
  • Newly diagnosed, histologically confirmed GBM
  • Patient after completion of radiochemotherapy but within first 3 cycles of first-line tumor-specific maintenance chemotherapy
  • Clinical indication of treatment with NovoTTF-200A System (Optune®) according to IFU and medical guidelines
  • Signed informed consent

排除标准

  • Any foreseeable deviation from the IFU of NovoTTF-200T Device

结局指标

主要结局

Changes in daily physical activity as a potential quality of life parameter in TTFields treatment compared to baseline for up to four months after start of TTFields therapy

时间窗: Up to 4 months after start of TTFields treatment compared to baseline

Changes in daily physical activity will be assessed by smartphone app-based clinical monitoring.

Number of TTFields treatment-related SAEs as assessed by the CEC standardized to one year of FU time

时间窗: through study completion, an average of 18 months (mean follow-up time)

Number of TTFields treatment-related SAEs standardized to one year of follow-up (FU) is measured using the collection of SAEs during the follow-up period

Time of usage of TTFields treatment in follow-up derived from monitoring data of the devices, standardised to usage days, as measure of compliance with TTFields treatment.

时间窗: through study completion, an average of 18 months (mean follow-up time)

Time of usage (compliance) of TTFields treatment over time is measured using the treatment compliance report at the Follow-up period

Changes in sleep quality as a potential quality of life parameter in TTFields treatment compared to baseline for up to four months after start of TTFields therapy

时间窗: Up to 4 months after start of TTFields treatment compared to baseline

Changes in sleep quality will be assessed by smartphone app-based clinical monitoring.

Changes in neurocognitive functioning as a potential quality of life parameter in TTFields treatment compared to baseline for up to four months after start of TTFields therapy.

时间窗: Up to 4 months after start of TTFields treatment compared to baseline

Changes in neurocognitive functioning will be assessed by means of MoCA interview tests.

次要结局

未报告次要终点

研究者

发起方
NovoCure Ltd.
申办方类型
Industry
责任方
Sponsor

研究点 (36)

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