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A Study Comparing Pemetrexed Plus Cisplatin Versus Pemetrexed Alone in NSCLC Patients Who Have Progressed on First Line EGFR-TKI

Primary Purpose

Carcinoma, Non-Small-Cell Lung

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

About this trial

This is an interventional treatment trial for Carcinoma, Non-Small-Cell Lung focused on measuring Failed in First Line EGFR-TKI, EGFR Activating Mutation, Pemetrexed

Eligibility Criteria

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

Inclusion Criteria:

  • Histologically confirmed nonsquamous NSCLC with activating EGFR mutation (on exon 19 deletion or exon 21 L858R mutation)
  • Stage IIIb, IV or recurrent NSCLC (AJCC 7th criteria)
  • Age ≥ 20 years
  • ECOG performance status of 0 or 1
  • At least one measurable lesion by RECIST 1.1
  • Progression after first line treatment with EGFR TKIs for advanced NSCLC
  • Asymptomatic brain metastasis or symptomatic brain metastasis treated with local treatment such as operation, whole brain radiotherapy, or gamma-knife surgery
  • At least 2 weeks later after whole brain radiotherapy or palliative radiotherapy
  • Adequate renal function: estimated creatinine clearance ≥ 45 mL/min
  • Organ function as evidenced by the following; Absolute neutrophil count > 1.5 x 109/L; platelets > 100 x 109/L; total bilirubin ≤1.5 UNL; AST and/or ALT < 3 UNL, in case of known hepatic metastasis, AST/ALT< 5 UNL
  • Written informed consent form
  • No other previous systemic chemotherapy

Exclusion Criteria:

  • Uncontrolled systemic illness such as DM, CHF, unstable angina, hypertension or arrhythmia
  • Patients with post-obstructive pneumonia or uncontrolled serious infection
  • Pregnant or nursing women (Women of reproductive potential have to agree to use an effective contraceptive method)
  • Uncontrolled symptomatic brain metastasis
  • Presence of third space fluid which cannot be controlled by drainage
  • Prior history of malignancy within 5 years from study entry except for adequately treated basal cell or squamous cell skin cancer or in situ cervical cancer, well-treated thyroid cancer.

Sites / Locations

  • Samsung Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Pem/Cis

Pem alone

Arm Description

Pem/Cis IV every 3 weeks

Pem IV alone every 3 weeks

Outcomes

Primary Outcome Measures

progression-free survival

Secondary Outcome Measures

Full Information

First Posted
September 22, 2015
Last Updated
February 9, 2017
Sponsor
Samsung Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03050437
Brief Title
A Study Comparing Pemetrexed Plus Cisplatin Versus Pemetrexed Alone in NSCLC Patients Who Have Progressed on First Line EGFR-TKI
Official Title
A Randomized, Open Label, Phase II Study Comparing Pemetrexed Plus Cisplatin Followed by Pemetrexed Until Progression Versus Pemetrexed Alone Until Progression in Non-small Cell Lung Cancer Patients Who Have Progressed on First Line Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor (EGFR-TKI)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 2013 (undefined)
Primary Completion Date
February 2017 (Anticipated)
Study Completion Date
March 2017 (Anticipated)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
It has not been established whether platinum-based doublets is better than single agent chemotherapy in EGFR mutant NSCLC patients who failed first-line EGFR TKI. In this prospective trial, the investigators try to evaluate whether the progression-free survival of pemetrexed/cisplatin (PC) regimen is longer than that of pemetrexed single(P) regimen in NSCLC patients who have progressed after first line treatment of EGFR-TKI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma, Non-Small-Cell Lung
Keywords
Failed in First Line EGFR-TKI, EGFR Activating Mutation, Pemetrexed

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Pem/Cis
Arm Type
Experimental
Arm Description
Pem/Cis IV every 3 weeks
Arm Title
Pem alone
Arm Type
Active Comparator
Arm Description
Pem IV alone every 3 weeks
Intervention Type
Drug
Intervention Name(s)
Cisplatin
Intervention Description
cisplatin is added to Pem/cis arm
Intervention Type
Drug
Intervention Name(s)
Pemetrexed
Intervention Description
Pem is applied to both arms
Primary Outcome Measure Information:
Title
progression-free survival
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed nonsquamous NSCLC with activating EGFR mutation (on exon 19 deletion or exon 21 L858R mutation) Stage IIIb, IV or recurrent NSCLC (AJCC 7th criteria) Age ≥ 20 years ECOG performance status of 0 or 1 At least one measurable lesion by RECIST 1.1 Progression after first line treatment with EGFR TKIs for advanced NSCLC Asymptomatic brain metastasis or symptomatic brain metastasis treated with local treatment such as operation, whole brain radiotherapy, or gamma-knife surgery At least 2 weeks later after whole brain radiotherapy or palliative radiotherapy Adequate renal function: estimated creatinine clearance ≥ 45 mL/min Organ function as evidenced by the following; Absolute neutrophil count > 1.5 x 109/L; platelets > 100 x 109/L; total bilirubin ≤1.5 UNL; AST and/or ALT < 3 UNL, in case of known hepatic metastasis, AST/ALT< 5 UNL Written informed consent form No other previous systemic chemotherapy Exclusion Criteria: Uncontrolled systemic illness such as DM, CHF, unstable angina, hypertension or arrhythmia Patients with post-obstructive pneumonia or uncontrolled serious infection Pregnant or nursing women (Women of reproductive potential have to agree to use an effective contraceptive method) Uncontrolled symptomatic brain metastasis Presence of third space fluid which cannot be controlled by drainage Prior history of malignancy within 5 years from study entry except for adequately treated basal cell or squamous cell skin cancer or in situ cervical cancer, well-treated thyroid cancer.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ju Yeon Park, RN
Phone
82-2-3410-3459
Email
jy1223.park@samsung.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Myung-Ju Ahn, MD, PhD
Organizational Affiliation
Samsung Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
ZIP/Postal Code
135-710
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Myung-Ju Ahn, Ph.D.
Phone
822-3410-1795
Email
silkahn@skku.edu

12. IPD Sharing Statement

Learn more about this trial

A Study Comparing Pemetrexed Plus Cisplatin Versus Pemetrexed Alone in NSCLC Patients Who Have Progressed on First Line EGFR-TKI

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