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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02736916
Other study ID # Radiation Oncology 20160101
Secondary ID
Status Recruiting
Phase N/A
First received March 25, 2016
Last updated April 7, 2016
Start date March 2016
Est. completion date December 2018

Study information

Verified date March 2016
Source General Hospital of Ningxia Medical University
Contact Yan-Yang Wang, M.D.
Phone 86-951-6743315
Email fdwyy1981@hotmail.com
Is FDA regulated No
Health authority China: Health and Family Planning Commission of Ningxia Hui Autonomous Region
Study type Interventional

Clinical Trial Summary

Prophylactic cranial irradiation (PCI) is an important treatment modality of patients with limited stage small cell lung cancer (LD-SCLC). However, PCI is also associated with several side effects, such as decline in memory and other cognitive functions. This provides the rationale to explore the clinical feasibility of hippocampal avoidance during WBRT. Previous studies have demonstrated the dosimetric capabilities of IMRT to conformally avoid the hippocampus without detriment to the radiation dose the remaining brain receives. The aims of this study is to evaluate the therapy efficacy and the safety profile of hippocampal-sparing whole-brain radiation therapy (HS-WBRT) for PCI in patients with LD-SCLC.


Description:

Chemotherapy plus thoracic radiation followed by prophylactic cranial irradiation (PCI) is the standard of care in management of limited stage small cell lung cancer patients. However, whole brain radiation therapy (WBRT) is also associated with many side effects including consolidation of new memory, poor attention span/concentration, visual spatial difficulties, difficulty with executive planning, and poor fine motor control. There exists significant preclinical and clinical evidence that radiation induced injury to the hippocampus correlates with neurocognitive decline of patients who received WBRT. Reducing radiation dose to the hippocampus during WBRT has been postulated as an approach to mitigate neurocognitive impairment. The present study hypothesize that hippocampal sparing PCI will allow improved performance on tests of short term memory and executive function compared to a historical control receiving the same dose of conventional PCI. The primary objective of this study is to evaluate performance on the Hopkins Verbal Learning Test-Revised for delayed recall at 6 months following hippocampal-sparing PCI relative to the historical control. Secondary objectives are to estimate: composite cognitive function following hippocampal-sparing PCI relative to the historical control and the rate of metastases in the hippocampus at 2 years following hippocampal-sparing PCI.


Recruitment information / eligibility

Status Recruiting
Enrollment 3
Est. completion date December 2018
Est. primary completion date March 2018
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patient must have newly diagnosed and confirmed small-cell lung cancer (SCLC)

- Patient must have a performance status of 1 or higher

- Patients must not have received previous irradiation to the brain

- Patients must have limited stage disease with CR (complete response) to chemotherapy and consolidative chest radiotherapy that was documented at least on standard chest x-rays within one month of study entry

- Negative MRI or CT scan of the brain at least one month before protocol entry

- Women of child-bearing potential must have a negative pregnancy test and also agree to use adequate contraceptives while on protocol

- Patient must be able to understand and sign the informed consent document

- Patient must be informed of the investigational aspect to this trial prior to singing the informed consent document

Exclusion Criteria:

- Patients receiving prior external beam irradiation to the head or neck, including any form of stereotactic irradiation

- Radiographic evidence of brain metastases and/or ipsilateral lung metastases/malignant pleural effusion

- Planned concurrent chemotherapy or antitumoral agent during PCI

- Concomitant malignancy or malignancy within the past five years other than nonmelanomatous skin cancer or carcinoma in situ of the cervix

- Patients with minimal pleural effusion evident on CXR (chest X-ray); minimal pleural effusion visible on chest CT is allowed.

- Patients with epilepsy requiring permanent oral medication _ Patients must not have a serious medical or psychiatric illness that would, in the opinion of the investigator, prevent informed consent or completion of protocol treatment, and/or follow-up visits.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Intervention

Radiation:
HS-WBRT PCI
LD-SCLC patients with HS-WBRT PCI
Conventional PCI
LD-SCLC patients with conventional PCI

Locations

Country Name City State
China General Hospital of Ningxia Medical University Yinchuan Ningxia

Sponsors (1)

Lead Sponsor Collaborator
General Hospital of Ningxia Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate delayed recall as assessed by the Hopkins Verbal Learning Test-Revised (HVTL-R) 4 months after hippocampal sparing during whole-brain radiotherapy (HS-WBRT) for PCI of limited stage small cell lung cancer patients. The change of the performance on the Hopkins Verbal Learning Test-Revised for delayed recall at 4 months following hippocampal-sparing PCI relative to the control group Yes
Secondary Evaluate the rate of brain metastasis in hippocampal region after HS-WBRT PCI for limited stage small cell lung cancer patients. The metastatic rate between HS-WBRT and control group at 2 years following hippocampal-sparing PCI. Yes
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