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Temozolomide Combine With Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost for Non Small Cell Lung Cancer Brain Metastases

A Phase II/III Study of Non Small Cell Lung Cancer Patient With/Without Synchronous Oral Temozolomide Capsules Combine With Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost With Hippocampus Protection

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03732482
Enrollment
400
Registered
2018-11-06
Start date
2019-03-01
Completion date
2022-05-30
Last updated
2019-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non Small Cell Lung Cancer Metastatic

Brief summary

With the improvement of systemic therapeutic effect(especially in the population with driver gene mutation), the incidence of brain metastases had significantly increased. Conventional Whole Brain radiotherapy(WBRT) was less effective, the stereotactic radiosurgery(SRS) technique had improve the local efficacy for 1-3 lesions, but the probability of intracranial recurrence was increased, Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost(SIB-IMRT) is a new radiotherapy technology, Giving a standard radiation dose of whole brain ,at the same time can boost the high-risk region in target, So that it can significantly shorten the treatment time, at the same time can improve the local control rate of brain metastases. In the aspect of normal tissue protecting, SIB was better than WBRT plus SRS sequential treatment pattern. 30Gy to the whole brain had a negative effects on cognitive function, the investigators previous study found that 25Gy to the whole brain while the tumor bed Simultaneous push to 50Gy was safe and effective, while reducing the impact on cognitive function. Hippocampus is a part of the brain located in the temporal lobe, Mainly responsible for long-term memory storage conversion and orientation. Many investigators point out that hippocampus is the main commander of neurocognitive function, Reduce the dose of hippocampus can significant improve the neurocognitive function. Temozolomide capsule is an anti-tumor alkylation agent for glioblastoma multiforme and anaplastic astrocytoma. In recent years, some researchers find that Temozolomide capsules combine with radiotherapy such as SRS, WBRT or The two combined, can improve Objective response(OR) and prolong the Progress Free Survival(PFS),while with tolerable therapeutic toxicity. In order to better reduce the impact on cognitive function and improve the local control rate, the investigators present this trial, under the SIB-IMRT technique, the investigators want to explore the effect of temozolomide in brain metastasis of non-small cell lung cancer with the hippocampal protection technology.

Interventions

DRUGTemozolomide capsules

Temozolomide capsules(Jiangsu tasly diyi pharmaceutical Co.,Ltd) Oral Temozolomide capsules 75mg/m2 begins on day 1 and continues until completion of radiotherapy.

DEVICEradiotherapy

Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost

Sponsors

Taizhou Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patients must have an estimated survival of at least 4 weeks 2. Karnofsky Performance Status Scale (KPS) of 60-100. 3. Patients' laboratory values had to meet these restrictions: hemoglobin\>8 g/dL, platelets\>70\*109/L, white blood cells\>4\*109/L. 4. Patients must sign a study specific informed consent form prior to study entry

Exclusion criteria

1. Patients had major medical illnesses or psychiatric impairments which will prevent completion of the protocol therapy 2. had received previous brain irradiation 3. could not be regularly followed 4. with leptomeningeal involvement

Design outcomes

Primary

MeasureTime frameDescription
OSDuration of time from the start of therapy 3 years or until time of death, whichever occurs firstoverall survival

Secondary

MeasureTime frameDescription
iPFSDuration of time from the start of therapy to the time of intracranial disease progression, assessed up to 3 yearsintracranial Progress Free Survival
MMSE scoresup to 2 yearsmini mental state examination,The MMSE scores included 11 questions and was consisted of orientation to time (5 scores), orientation to place (5 scores), registration (3 scores), attention and calculation (5 scores), recall (3 scores), langue (2 scores), repetition (1 scores), complex commands (6 scores). The minimum score was 0, The maximum score was 30.
overall response rateUp to 1 monthuse RECIST 1.1 version

Contacts

Primary ContactHaihua Yang, MD
yhh93181@hotmail.com13819639006
Backup ContactFengming(spring) Kong, MD

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026