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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03338075
Other study ID # CH-H&N-004
Secondary ID
Status Completed
Phase N/A
First received November 7, 2017
Last updated November 7, 2017
Start date January 1, 2016
Est. completion date August 1, 2017

Study information

Verified date November 2017
Source Chinese Academy of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A propensity- matched study was conducted to investigate the feasibility and safety of adding temozolomide to hypofractionated stereotactic radiotherapy for large brain metastases.


Description:

A previous single arm phase II trial of our institution has shown that HFSRT combined with concurrent TMZ was safe and efficient for patients with BMs of ≥ 6cc in volume. The 1-year local control and overall survival rate was better than the results of a retrospective study using HFSRT alone in treating BMs of ≥ 3cm in diameter. Thus, we hypothesized that adding TMZ to HFSRT should translate to substantive benefits in clinical outcomes compared to HFSRT alone. Propensity score matching method was adopted to decrease potential bias in this retrospective study.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date August 1, 2017
Est. primary completion date August 1, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- (1) primary tumor was pathologically diagnosed and brain metastases were confirmed by gadolinium-enhanced magnetic resonance imaging (MRI) ; (2) age 18 years or older (3) KPS =60, or KPS =50 but symptomatically caused by BMs; (4) the large lesions haven't treated with surgery or SRT.

Exclusion Criteria:

- (1) KPS <60 but not caused by BMs; (2) the large lesions have been treated with surgery or SRT.

Study Design


Intervention

Radiation:
fractionated stereotactic radiotherapy
The regular prescription doses were 52 Gy in 13 fractions or 52.5 Gy in 15 fractions.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Chinese Academy of Medical Sciences

Outcome

Type Measure Description Time frame Safety issue
Primary Local tumor control rate (LTCR) the control rate of treated lesions 3 months after radiation
Secondary Intracranial progression- free survival (IPFS) the interval from the beginning of radiation to any intracranial progression up to 1 year
Secondary Local recurrence- free survival (LRFS) the time from the beginning of radiation to local faliure. up to 1 year
Secondary Overall survival (OS) the time from the beginning of radiation to follow-up or death up to 3 years
Secondary Progression- free survival (PFS) the interval from the beginning of HFSRT to any progression of tumor. up to 1 year
Secondary Brain metastasis-specific survival (BMSS) the internal from the beginning of radiation to death that caused by brain metastases. up to 1 year
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