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Maintenance Gemcitabine in the Chinese Advanced Lung Cancer (MAGICAL)

Primary Purpose

Non Small Cell Lung Cancer

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Gemcitabine
Best supportive care
Sponsored by
Tongji University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non Small Cell Lung Cancer focused on measuring Advanced NSCLC, Maintenance therapy, Gemcitabine

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologic or cytologic confirmed diagnosis of Stage IV NSCLC according to 2009 the seventh edition of TNM staging of lung tumors.
  • No disease progression after four cycles of first-line chemotherapy with gemcitabine plus cisplatin (running period) within one month before the enrollment.
  • Brain metastases are permitted if treated with full course of whole brain radiotherapy without the presence of symptomatic central nervous system metastases.
  • ECOG score 0-1

Exclusion Criteria:

  • First-line chemotherapy other than combination treatment of gemcitabine plus cisplatin
  • Other therapy including targeted therapy, immunotherapy and prior radiotherapy for the treatment of the primary tumor prior to enrollment.
  • Active infection
  • Inadequate liver and renal function.
  • Serious concomitant systemic disorder incompatible with the study.
  • Second primary malignancy (except in situ carcinoma of the cervix, adequately treated basal cell carcinoma of the skin, T1 vocal cord cancer in remission, or prior malignancy treated more than 5 years prior enrollment without recurrence)
  • Presence of the pregnancy

Sites / Locations

  • Shanghai Pulmonary Hospital Medical Oncology DepartmentRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Best supportive care

Maintenance gemcitabine

Arm Description

Best supportive care

Maintenance therapy of gemcitabine alone

Outcomes

Primary Outcome Measures

Progression free survival
From the start of maintenance therapy or Best Suppotive Care(BSC) until the date of documented progressive disease or death from any cause

Secondary Outcome Measures

Overall Survival
From the start of maintenance therapy or BSC until the date of documented death from any cause
Response Rate
From the start of maintenance therapy or BSC until the date of documented progressive disease
Time to The Progression
From the start of maintenance therapy or BSC until the date of documented progressive disease
Health Related Quality of Life
From the start of maintenance therapy or BSC until the date of documented progressive disease or the termination of study
Number of Participants with treatment-related grade III/IV adverse events
frequency and severity of adverse events and laboratory abnormalities

Full Information

First Posted
April 7, 2011
Last Updated
April 13, 2011
Sponsor
Tongji University
Collaborators
Shanghai Pulmonary Hospital, Shanghai, China
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1. Study Identification

Unique Protocol Identification Number
NCT01336192
Brief Title
Maintenance Gemcitabine in the Chinese Advanced Lung Cancer
Acronym
MAGICAL
Official Title
Maintenance Gemcitabine or Best Supportive Care for the Chinese Advanced NSCLC Patients Without Progression Disease After Given Four Cycles of the Induction Chemotherapy With Gemcitabine Plus Cisplatin
Study Type
Interventional

2. Study Status

Record Verification Date
April 2011
Overall Recruitment Status
Unknown status
Study Start Date
April 2011 (undefined)
Primary Completion Date
April 2012 (Anticipated)
Study Completion Date
April 2013 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Tongji University
Collaborators
Shanghai Pulmonary Hospital, Shanghai, China

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Lung cancer, the most common cancer worldwide, remains the leading cause of cancer death. Approximately two-thirds of all patients with newly diagnosed non-small-cell lung cancer (NSCLC) present with advanced stage that palliative chemotherapy is the only appropriate measure. The standard treatment for this patient population consists of third generation platinum-based doublet regimen for no more than 6 cycles followed by watch and wait until disease progression (PD) before the administration of second-line and third-line systemic anticancer therapeutic agents. Patients who go on to receive second-line therapy represent a selected subgroup with an improved overall prognosis. Switch maintenance therapy with pemetrexed or erlotinib in patients with advanced NSCLC without PD after first-line chemotherapy has been confirmed to improve progression free survival (PFS) and overall survival (OS) significantly compared with placebo in two large randomized controlled studies. However, continuation gemcitabine maintenance therapy in this setting yields conflicting results in the west, i.e.showing a prolongation of PFS without OS improvement. Thus, we investigate the efficacy and safety of continuation of gemcitabine maintenance therapy for patients with metastatic NSCLC with ECOG performance status of 0-1 and without PD after four cycles of first-line chemotherapy with gemcitabine and cisplatin in China.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non Small Cell Lung Cancer
Keywords
Advanced NSCLC, Maintenance therapy, Gemcitabine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Best supportive care
Arm Type
No Intervention
Arm Description
Best supportive care
Arm Title
Maintenance gemcitabine
Arm Type
Experimental
Arm Description
Maintenance therapy of gemcitabine alone
Intervention Type
Drug
Intervention Name(s)
Gemcitabine
Intervention Description
Gemcitabine 1250mg/m^2 Day 1 and 8, 28 days per cycle until PD
Intervention Type
Drug
Intervention Name(s)
Best supportive care
Intervention Description
Best supportive care
Primary Outcome Measure Information:
Title
Progression free survival
Description
From the start of maintenance therapy or Best Suppotive Care(BSC) until the date of documented progressive disease or death from any cause
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Overall Survival
Description
From the start of maintenance therapy or BSC until the date of documented death from any cause
Time Frame
18 months
Title
Response Rate
Description
From the start of maintenance therapy or BSC until the date of documented progressive disease
Time Frame
approximately 4 weeks
Title
Time to The Progression
Description
From the start of maintenance therapy or BSC until the date of documented progressive disease
Time Frame
18 months
Title
Health Related Quality of Life
Description
From the start of maintenance therapy or BSC until the date of documented progressive disease or the termination of study
Time Frame
Approximately 4 weeks
Title
Number of Participants with treatment-related grade III/IV adverse events
Description
frequency and severity of adverse events and laboratory abnormalities
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologic or cytologic confirmed diagnosis of Stage IV NSCLC according to 2009 the seventh edition of TNM staging of lung tumors. No disease progression after four cycles of first-line chemotherapy with gemcitabine plus cisplatin (running period) within one month before the enrollment. Brain metastases are permitted if treated with full course of whole brain radiotherapy without the presence of symptomatic central nervous system metastases. ECOG score 0-1 Exclusion Criteria: First-line chemotherapy other than combination treatment of gemcitabine plus cisplatin Other therapy including targeted therapy, immunotherapy and prior radiotherapy for the treatment of the primary tumor prior to enrollment. Active infection Inadequate liver and renal function. Serious concomitant systemic disorder incompatible with the study. Second primary malignancy (except in situ carcinoma of the cervix, adequately treated basal cell carcinoma of the skin, T1 vocal cord cancer in remission, or prior malignancy treated more than 5 years prior enrollment without recurrence) Presence of the pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Haiping Zhang, MD
Phone
86-21-65115006
Ext
3068
Email
zhp7341@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Di Zheng, MD
Organizational Affiliation
Shanghai Pulmonary Hospital, Shanghai, China
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wen Gao, MD
Organizational Affiliation
Shanghai Pulmonary Hospital, Shanghai, China
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jianfang Xu, MD
Organizational Affiliation
Shanghai Pulmonary Hosptial
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Li Wang, MD
Organizational Affiliation
Shanghai Pulmonary Hospital, Shanghai, China
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Meijun Lv, MD
Organizational Affiliation
Shanghai Pulmonary Hospital, Shanghai, China
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jian Ni, MD
Organizational Affiliation
Shanghai Pulmonary Hospital, Shanghai, China
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jie Zhang, MD
Organizational Affiliation
Shanghai Pulmonary Hospital, Shanghai, China
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Bing Lu, MD
Organizational Affiliation
Shanghai Pulmonary Hospital, Shanghai, China
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ying Xu, MD
Organizational Affiliation
Shanghai Pulmonary Hospital, Shanghai, China
Official's Role
Study Director
Facility Information:
Facility Name
Shanghai Pulmonary Hospital Medical Oncology Department
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200433
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ying Xu, MD
Phone
86-21-65115006
Ext
1053
Email
xuying2186@hotmail.com
First Name & Middle Initial & Last Name & Degree
Di Zheng, MD

12. IPD Sharing Statement

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Maintenance Gemcitabine in the Chinese Advanced Lung Cancer

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