Ignite Creation Date:
2024-10-26 @ 3:40 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06608108
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-09
Brief Title:
The Clinical Efficacy of CT-Guided All-in-One Adaptive Emergency Radiotherapy for Spinal Cord Compression Caused by Spinal Metastases
Sponsor:
None
Organization:
None
Study Overview
Official Title:
The Clinical Efficacy of CT-Guided All-in-One Adaptive Emergency Radiotherapy for Spinal Cord Compression Caused by Spinal Metastases
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The aim of this study is to implement a new protocol for concurrent and sequential dose-escalation radiotherapy based on CT-guided all-in-one adaptive emergency radiotherapy for spinal cord compression due to spinal metastases MSCC This protocol is designed to assess the clinical efficacy in MSCC patients with the goals of improving local control rates functional relief and optimizing treatment outcomes and safety The study also seeks to provide reliable data and guidance for future radiotherapy protocol design and clinical practice Additionally the study records and analyzes the treatment time required for the all-in-one emergency radiotherapy aiding in the evaluation of its operational efficiency and clinical feasibility and providing data support for its broader adoption and dissemination
Detailed Description:
Spinal Cord Compression Syndrome SCCS is a clinical syndrome caused by space-occupying lesions within the spine or spinal canal These lesions exert pressure on the spinal cord spinal nerve roots and the blood vessels supplying the spinal cord leading to neurological deficits and ultimately spinal cord dysfunction Spinal cord compression caused by primary malignant tumors or distant metastases of malignant tumors is referred to as Malignant Spinal Cord Compression MSCC a common complication in advanced cancer Approximately 40 of cancer patients develop metastatic spinal disease and 10-20 of these patients will experience spinal cord compression symptoms MSCC is characterized by its rapid onset short course and fast progression Early symptoms often manifest as localized or radiating pain As the condition progresses patients may experience muscle weakness sensory deficits impaired voluntary movement particularly loss of bowel and bladder control and even complete paralysis If not diagnosed and treated promptly MSCC can severely affect quality of life of patients
Radiation therapy is one of the most commonly used and effective treatments for MSCC Radiotherapy reduces tumor burden alleviates localized bone pain prevents pathological fractures and vertebral collapse promotes the healing of pathological fractures and relieves spinal cord compression thereby improving mobility function and quality of life of patients However conventional radiotherapy workflows are complex and involve multiple steps Patients typically need to visit different departments multiple times and may face days of waiting before receiving treatment which is far from ideal in the emergency context of MSCC The domestic innovative radiotherapy equipment uRT-linac506C was developed to address this need It integrates diagnostic-grade spiral CT and linear accelerator technology into a single workflow allowing for seamless rapid transitions from simulation CT scanning intelligent contouring and modification of tumor targets and organs-at-risk to treatment plan design evaluation verification and implementation of the first radiation therapy Without compromising standardized procedures this significantly shortens waiting and treatment times realizing All-in-One image-guided diagnosis-treatment integration that seamlessly connects the various stages of radiotherapy This approach reduces the time from patient positioning to treatment from several days with conventional radiotherapy to approximately 30 minutes enabling rapid and precise radiation therapy to relieve spinal cord compression and improve patient outcomes Investigators refer to this integrated approach as All-in-One emergency radiotherapy
Although radiotherapy has become the primary treatment for spinal cord compression especially when surgery is not feasible emergency radiotherapy has significantly improved the timeliness and effectiveness of treatment allowing patients to receive rapid relief and care in urgent situations and preventing severe consequences from delayed treatment However there is still debate about the specific implementation of radiation therapy for spinal metastases Various fractionation regimens have been reported in the literature ranging from single-fraction to multi-fraction radiation therapy There is no consensus on the optimal treatment regimen for bone metastases in terms of treatment volume total dose or fractionation For patients with a short expected survival shorter courses of radiotherapy 1-5 fractions with doses ranging from 8 to 20 Gy are commonly used to reduce treatment time and minimize patient suffering For patients with a longer expected survival eg more than 6 months the risk of disease progression or in-field recurrence must be considered and longer courses of radiotherapy such as the commonly used 10 3 Gy regimen are more appropriate
In previous large retrospective studies patient survival was not considered and many patients did not live long enough to experience local recurrence which may have led to biased results in local control Therefore it is reasonable to investigate whether patients with a longer prognosis can benefit from increased radiation doses beyond the traditional 10 3 Gy For these longer-surviving patients exploring more precise and individualized radiotherapy regimens is necessary This may include higher radiation doses and longer treatment durations to achieve better disease control and prolong progression-free and overall survival
With advances in imaging and radiotherapy technology Simultaneous Integrated Boost Intensity-Modulated Radiotherapy SIB-IMRT has emerged as a radiotherapy technique that applies differential doses to high-risk and low-risk regions within the same radiation field maximizing normal tissue protection while increasing the dose to the target area Sequential Boost Radiotherapy involves delivering additional doses to tumors or high-risk areas after the standard radiotherapy course is completed further increasing the cumulative radiation dose Based on long-term experience investigators have developed the ability to escalate the planned gross tumor volume PGTV from the traditional 3 Gy per fraction to 4 Gy per fraction while maintaining organ-at-risk dose limits within tolerance Moreover the number of sequential boost sessions has been increased from the traditional 10 to 12 sessions with promising initial results
Therefore this study aims to evaluate the efficacy of Simultaneous Integrated and Sequential Boost Radiotherapy in patients with MSCC receiving All-in-One adaptive emergency radiotherapy guided by CT for spinal metastases Investigators seek to validate its safety and efficacy while also recording and analyzing the overall treatment duration of All-in-One emergency radiotherapy Ultimately investigators hope to improve patient quality of life and extend survival providing scientific evidence and guidance for clinical practice
Supplement
Dear Professor
Investigators sincerely appreciate the review of this clinical trial application by the professor Further clarification regarding the study design and type is provided Since 2018 the radiation oncology center has employed this dose-fractionation regimen to treat patients with malignant spinal cord compression Recently due to clinical demand an advanced accelerator system integrated with diagnostic-grade CT has been introduced which is now routinely applied in clinical practice This study is conducted within this clinical context All enrolled participants regardless of their involvement in the study will receive the same treatment methods and protocols and the research itself will not influence the treatment Therefore this study qualifies as a prospective non-interventional study
Should the professor have any further questions or suggestions please feel free to reach out
Best regards
Radiation therapy is one of the most commonly used and effective treatments for MSCC Radiotherapy reduces tumor burden alleviates localized bone pain prevents pathological fractures and vertebral collapse promotes the healing of pathological fractures and relieves spinal cord compression thereby improving mobility function and quality of life of patients However conventional radiotherapy workflows are complex and involve multiple steps Patients typically need to visit different departments multiple times and may face days of waiting before receiving treatment which is far from ideal in the emergency context of MSCC The domestic innovative radiotherapy equipment uRT-linac506C was developed to address this need It integrates diagnostic-grade spiral CT and linear accelerator technology into a single workflow allowing for seamless rapid transitions from simulation CT scanning intelligent contouring and modification of tumor targets and organs-at-risk to treatment plan design evaluation verification and implementation of the first radiation therapy Without compromising standardized procedures this significantly shortens waiting and treatment times realizing All-in-One image-guided diagnosis-treatment integration that seamlessly connects the various stages of radiotherapy This approach reduces the time from patient positioning to treatment from several days with conventional radiotherapy to approximately 30 minutes enabling rapid and precise radiation therapy to relieve spinal cord compression and improve patient outcomes Investigators refer to this integrated approach as All-in-One emergency radiotherapy
Although radiotherapy has become the primary treatment for spinal cord compression especially when surgery is not feasible emergency radiotherapy has significantly improved the timeliness and effectiveness of treatment allowing patients to receive rapid relief and care in urgent situations and preventing severe consequences from delayed treatment However there is still debate about the specific implementation of radiation therapy for spinal metastases Various fractionation regimens have been reported in the literature ranging from single-fraction to multi-fraction radiation therapy There is no consensus on the optimal treatment regimen for bone metastases in terms of treatment volume total dose or fractionation For patients with a short expected survival shorter courses of radiotherapy 1-5 fractions with doses ranging from 8 to 20 Gy are commonly used to reduce treatment time and minimize patient suffering For patients with a longer expected survival eg more than 6 months the risk of disease progression or in-field recurrence must be considered and longer courses of radiotherapy such as the commonly used 10 3 Gy regimen are more appropriate
In previous large retrospective studies patient survival was not considered and many patients did not live long enough to experience local recurrence which may have led to biased results in local control Therefore it is reasonable to investigate whether patients with a longer prognosis can benefit from increased radiation doses beyond the traditional 10 3 Gy For these longer-surviving patients exploring more precise and individualized radiotherapy regimens is necessary This may include higher radiation doses and longer treatment durations to achieve better disease control and prolong progression-free and overall survival
With advances in imaging and radiotherapy technology Simultaneous Integrated Boost Intensity-Modulated Radiotherapy SIB-IMRT has emerged as a radiotherapy technique that applies differential doses to high-risk and low-risk regions within the same radiation field maximizing normal tissue protection while increasing the dose to the target area Sequential Boost Radiotherapy involves delivering additional doses to tumors or high-risk areas after the standard radiotherapy course is completed further increasing the cumulative radiation dose Based on long-term experience investigators have developed the ability to escalate the planned gross tumor volume PGTV from the traditional 3 Gy per fraction to 4 Gy per fraction while maintaining organ-at-risk dose limits within tolerance Moreover the number of sequential boost sessions has been increased from the traditional 10 to 12 sessions with promising initial results
Therefore this study aims to evaluate the efficacy of Simultaneous Integrated and Sequential Boost Radiotherapy in patients with MSCC receiving All-in-One adaptive emergency radiotherapy guided by CT for spinal metastases Investigators seek to validate its safety and efficacy while also recording and analyzing the overall treatment duration of All-in-One emergency radiotherapy Ultimately investigators hope to improve patient quality of life and extend survival providing scientific evidence and guidance for clinical practice
Supplement
Dear Professor
Investigators sincerely appreciate the review of this clinical trial application by the professor Further clarification regarding the study design and type is provided Since 2018 the radiation oncology center has employed this dose-fractionation regimen to treat patients with malignant spinal cord compression Recently due to clinical demand an advanced accelerator system integrated with diagnostic-grade CT has been introduced which is now routinely applied in clinical practice This study is conducted within this clinical context All enrolled participants regardless of their involvement in the study will receive the same treatment methods and protocols and the research itself will not influence the treatment Therefore this study qualifies as a prospective non-interventional study
Should the professor have any further questions or suggestions please feel free to reach out
Best regards
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None