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

Primary Purpose

Non Small Cell Lung Cancer Metastatic

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Temozolomide capsules
radiotherapy
Sponsored by
Taizhou Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non Small Cell Lung Cancer Metastatic

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Experimental

    Arm Label

    RT groups

    Drug plus RT groups

    Arm Description

    participants was given radiotherapy only,50Gy in 10 fractions over 2 weeks to metastases synchronously with 25Gy WBRT

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

    Outcomes

    Primary Outcome Measures

    OS
    overall survival

    Secondary Outcome Measures

    iPFS
    intracranial Progress Free Survival
    MMSE scores
    mini 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 rate
    use RECIST 1.1 version

    Full Information

    First Posted
    November 2, 2018
    Last Updated
    January 28, 2019
    Sponsor
    Taizhou Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03732482
    Brief Title
    Temozolomide Combine With Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost for Non Small Cell Lung Cancer Brain Metastases
    Official Title
    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
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    March 1, 2019 (Anticipated)
    Primary Completion Date
    January 31, 2022 (Anticipated)
    Study Completion Date
    May 30, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Taizhou Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Non Small Cell Lung Cancer Metastatic

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2, Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    400 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    RT groups
    Arm Type
    Placebo Comparator
    Arm Description
    participants was given radiotherapy only,50Gy in 10 fractions over 2 weeks to metastases synchronously with 25Gy WBRT
    Arm Title
    Drug plus RT groups
    Arm Type
    Experimental
    Arm Description
    Temozolomide capsules(Jiangsu tasly diyi pharmaceutical Co.,Ltd) Oral Temozolomide capsules 75mg/m2 begins on day 1 and continues until completion of radiotherapy.
    Intervention Type
    Drug
    Intervention Name(s)
    Temozolomide capsules
    Intervention Description
    Temozolomide capsules(Jiangsu tasly diyi pharmaceutical Co.,Ltd) Oral Temozolomide capsules 75mg/m2 begins on day 1 and continues until completion of radiotherapy.
    Intervention Type
    Device
    Intervention Name(s)
    radiotherapy
    Intervention Description
    Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost
    Primary Outcome Measure Information:
    Title
    OS
    Description
    overall survival
    Time Frame
    Duration of time from the start of therapy 3 years or until time of death, whichever occurs first
    Secondary Outcome Measure Information:
    Title
    iPFS
    Description
    intracranial Progress Free Survival
    Time Frame
    Duration of time from the start of therapy to the time of intracranial disease progression, assessed up to 3 years
    Title
    MMSE scores
    Description
    mini 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.
    Time Frame
    up to 2 years
    Title
    overall response rate
    Description
    use RECIST 1.1 version
    Time Frame
    Up to 1 month

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Patients must have an estimated survival of at least 4 weeks Karnofsky Performance Status Scale (KPS) of 60-100. Patients' laboratory values had to meet these restrictions: hemoglobin>8 g/dL, platelets>70*109/L, white blood cells>4*109/L. Patients must sign a study specific informed consent form prior to study entry Exclusion Criteria: Patients had major medical illnesses or psychiatric impairments which will prevent completion of the protocol therapy had received previous brain irradiation could not be regularly followed with leptomeningeal involvement
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Haihua Yang, MD
    Phone
    13819639006
    Email
    yhh93181@hotmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Fengming(spring) Kong, MD
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jian Zhu, MD
    Organizational Affiliation
    Taizhou Hospital, Wenzhou Medical University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

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

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