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Central Nervous System(CNS) Efficacy of Dacomitinib

Primary Purpose

Non Small Cell Lung Cancer, Brain Metastases

Status
Unknown status
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Dacomitinib
Sponsored by
Samsung Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

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

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Biopsy proven recurrent or metastatic NSCLC (adenocarcinoma) with major EGFR mutation (exon 19 deletion or Leu858Arg mutation without the Thr790Met)
  • No prior systemic treatment of advanced NSCLC (Neoadjuvant or adjuvant chemotherapy are allowed, without limitation on its treatment timing)
  • Age ≥20 years
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1
  • Had at least one measurable intracranial lesion as ≥ 5mm in the longest diameter by magnetic resonance imaging (MRI) (≥ 5mm by thin section (1.2mm) of brain MRI image, ≥ 10mm by less thin section(2.5mm) brain MRI ), which checked within 4 weeks before enrollment. If MRI slice thickness is not appropriate, we need to recheck Brain MRI
  • Number of brain metastasis =>5
  • Adequate organ function
  • Female subjects must either be of non-reproductive potential
  • Subject is willing and able to comply with the protocol
  • Signed written informed consent

Exclusion Criteria:

  • Severe symptomatic brain metastasis, needing urgent control with radiotherapy or high dose steroid: the definition of high dose steroid is the equivalent dose of dexamethasone 10 mg or higher per day (mild symptoms controlled with low dose of steroid can be enrolled)
  • With leptomeningeal seeding
  • Exposure to EGFR-TKIs or other EGFR targeting agents at any time in either neoadjuvant or adjuvant setting
  • Local treatment (stereotatic radiosurgery or whole brain radiotherapy) for brain metastases
  • Uncontrolled systemic illness including uncontrolled hypertension, active bleeding, or active infection.
  • Past medical history of interstitial lung disease, drug induced interstitial lung disease, radiation pneumonitis which required steroid treatment
  • Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the subject's participation for the full duration of the study, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
  • Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.

Sites / Locations

  • Jong-Mu SunRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Study arm

Arm Description

Dacomitinib

Outcomes

Primary Outcome Measures

CNS objective response rate (Complete response or Partial response)
The rate of CR or PR of CNS disease

Secondary Outcome Measures

CNS progression-free survival
Time from enrollment to CNS progression or death
Cumulative incidence of CNS failure by competing risk analysis
To evaluate the CNS efficacy of dacomitinib
Extracranial objective response rate
The rate of CR or PR
Progression-free survival
Time from enrollment to progression or death
Overall survival
Time from enrollment to death of any cause
Safety by Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
The % of side effect

Full Information

First Posted
December 15, 2020
Last Updated
January 1, 2021
Sponsor
Samsung Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04675008
Brief Title
Central Nervous System(CNS) Efficacy of Dacomitinib
Official Title
A Phase II Study of Dacomitinib in Advanced Epidermal Growth Factor Receptor (EGFR)-Mutant Non-small Cell Lung Cancer (NSCLC) Patients Who Have Non-irradiated Brain Metastasis
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 7, 2020 (Actual)
Primary Completion Date
September 1, 2022 (Anticipated)
Study Completion Date
March 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Samsung Medical Center

4. Oversight

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

5. Study Description

Brief Summary
This is a single-arm, phase II study of dacomitinib in advanced EGFR-mutant NSCLC patients who have non-irradiated brain metastasis.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Study arm
Arm Type
Experimental
Arm Description
Dacomitinib
Intervention Type
Drug
Intervention Name(s)
Dacomitinib
Other Intervention Name(s)
Vizimpro
Intervention Description
Secondary generation EGFR-tyrosine kinase inhibitor (TKI) (Dacomitinib) for EGFR mutant NSCLC patients with non irradiated brain metastasis
Primary Outcome Measure Information:
Title
CNS objective response rate (Complete response or Partial response)
Description
The rate of CR or PR of CNS disease
Time Frame
1 year
Secondary Outcome Measure Information:
Title
CNS progression-free survival
Description
Time from enrollment to CNS progression or death
Time Frame
1 year
Title
Cumulative incidence of CNS failure by competing risk analysis
Description
To evaluate the CNS efficacy of dacomitinib
Time Frame
1 year
Title
Extracranial objective response rate
Description
The rate of CR or PR
Time Frame
1 year
Title
Progression-free survival
Description
Time from enrollment to progression or death
Time Frame
1 year
Title
Overall survival
Description
Time from enrollment to death of any cause
Time Frame
1 year
Title
Safety by Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Description
The % of side effect
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Biopsy proven recurrent or metastatic NSCLC (adenocarcinoma) with major EGFR mutation (exon 19 deletion or Leu858Arg mutation without the Thr790Met) No prior systemic treatment of advanced NSCLC (Neoadjuvant or adjuvant chemotherapy are allowed, without limitation on its treatment timing) Age ≥20 years Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 Had at least one measurable intracranial lesion as ≥ 5mm in the longest diameter by magnetic resonance imaging (MRI) (≥ 5mm by thin section (1.2mm) of brain MRI image, ≥ 10mm by less thin section(2.5mm) brain MRI ), which checked within 4 weeks before enrollment. If MRI slice thickness is not appropriate, we need to recheck Brain MRI Number of brain metastasis =>5 Adequate organ function Female subjects must either be of non-reproductive potential Subject is willing and able to comply with the protocol Signed written informed consent Exclusion Criteria: Severe symptomatic brain metastasis, needing urgent control with radiotherapy or high dose steroid: the definition of high dose steroid is the equivalent dose of dexamethasone 10 mg or higher per day (mild symptoms controlled with low dose of steroid can be enrolled) With leptomeningeal seeding Exposure to EGFR-TKIs or other EGFR targeting agents at any time in either neoadjuvant or adjuvant setting Local treatment (stereotatic radiosurgery or whole brain radiotherapy) for brain metastases Uncontrolled systemic illness including uncontrolled hypertension, active bleeding, or active infection. Past medical history of interstitial lung disease, drug induced interstitial lung disease, radiation pneumonitis which required steroid treatment Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the subject's participation for the full duration of the study, or is not in the best interest of the subject to participate, in the opinion of the treating investigator. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jong-Mu Sun, MD
Phone
822-3410-1795
Email
jongmu.sun@samsung.com
Facility Information:
Facility Name
Jong-Mu Sun
City
Seoul
ZIP/Postal Code
06351
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jong-Mu Sun
Phone
82234103459
Ext
82234103459
Email
jongmu.sun@skku.edu

12. IPD Sharing Statement

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Central Nervous System(CNS) Efficacy of Dacomitinib

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