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Preventive Effects of Zoledronic Acid on Bone Metastasis in Patients With Stage IIIB and IV Lung Cancer

Primary Purpose

Lung Cancer

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Zoledronic acid
Sponsored by
Tang-Du Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Lung Cancer focused on measuring ZOL, Prevention, lung cancer

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age between 18 and 70 years of age, male or female
  2. histologically or cytologically confirmed stage IIIB or IV lung cancer at diagnosis
  3. no evidence of bone metastatic lesions was radiographically confirmed by bone scintigraphy
  4. life expectancy of ≥6 months
  5. adequate renal, hematologic, and hepatic
  6. Eastern Cooperative Oncology Group(ECOG) performance status≤2
  7. All patients provided written informed consent

Exclusion Criteria:

  1. Treatment with other bisphosphonates
  2. Presence of brain metastases
  3. Be allergic to ZOL
  4. attending other unlisted drug clinical trials,currently.

Sites / Locations

  • Department of Oncology,Tangdu Hospital,Fourth Millitary Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

ZOL

Control

Arm Description

Zoledronic acid 4 mg intravenous infusion over at least 15 minutes every 3 months for 12 months.

No investigational treatment

Outcomes

Primary Outcome Measures

Percentage of Participants With Bone Metastases at 12 Months
Percentage of participants developing at least 1 bone metastasis, whether or not symptomatic. Bone scans were scheduled at screening and at 6-monthly intervals after study entry, or when symptoms suggested the presence of bone metastases. Positive bone scans required confirmation by x-ray, magnetic resonance imaging (MRI), or computed tomography (CT).

Secondary Outcome Measures

Progression-Free Survival
Progression-free survival is defined as the time from randomization to the date of the first documented progression or recurrence of disease or death from any cause. Time to disease progression (TTP) was assessed by the Response Evaluation Criteria in Solid Tumors (RECIST) guidelines with evaluations every 3 months.
Percentage of Participants With Overall Survival

Full Information

First Posted
November 30, 2015
Last Updated
July 19, 2017
Sponsor
Tang-Du Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02622607
Brief Title
Preventive Effects of Zoledronic Acid on Bone Metastasis in Patients With Stage IIIB and IV Lung Cancer
Official Title
Preventive Effects of Zoledronic Acid on Bone Metastasis in Patients With Stage IIIB and IV Lung Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 2013 (undefined)
Primary Completion Date
March 2018 (Anticipated)
Study Completion Date
March 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tang-Du Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Bone metastases are common in patients with advanced lung cancer and can have devastating consequences. Preventing or delaying bone metastases may improve outcomes. Bisphosphonates are inhibitors of osteoclast-mediated bone resorption. The current indications for bisphosphonates include the treatment of metabolic disorders of bone metabolism (e.g., osteoporosis and Paget's disease), the treatment of hypercalcaemia of malignancy (HCM), and the prevention of skeletal-related events(SREs)from malignant bone disease. Clinical trials also confirm that bisphosphonates, and zoledronic acid(ZOL) in particular, can prevent bone loss from cancer treatment.There is also emerging evidence that the benefits of bisphosphonate therapy in the oncology setting are more extensive. This study will evaluate whether the addition of ZOL 4 mg every 3 months for up to 1 years in patients with stage IIIB/IV lung cancer could reduce the rate of bone metastases ,improve progression-free survival (PFS) and overall survival(OS), and delay time to bone metastases .
Detailed Description
Bone metastases are common in patients with advanced lung cancer and can have devastating consequences. which can lead to pain, decreased mobility and skeletal complications .Preventing or delaying bone metastases may improve outcomes. Bisphosphonates are inhibitors of osteoclast-mediated bone resorption. The current indications for bisphosphonates include the treatment of metabolic disorders of bone metabolism (e.g., osteoporosis and Paget's disease), the treatment of hypercalcaemia of malignancy (HCM), and the prevention of SREs from malignant bone disease. Clinical trials also confirm that bisphosphonates, and zoledronic acid in particular, can prevent bone loss from cancer treatment.There is also emerging evidence that the benefits of bisphosphonate therapy in the oncology setting are more extensive. This study will evaluate whether the addition of ZOL 4 mg every 3 months for up to 1 years in patients with stage IIIB/IV lung cancer could reduce the rate of bone metastases ,improve progression-free survival (PFS) and overall survival(OS), and delay time to bone metastases .

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer
Keywords
ZOL, Prevention, lung cancer

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ZOL
Arm Type
Experimental
Arm Description
Zoledronic acid 4 mg intravenous infusion over at least 15 minutes every 3 months for 12 months.
Arm Title
Control
Arm Type
No Intervention
Arm Description
No investigational treatment
Intervention Type
Drug
Intervention Name(s)
Zoledronic acid
Other Intervention Name(s)
Zometa
Intervention Description
Zoledronic acid 4 mg in 5 mL concentrated solution prepared with 100 mL calcium free infusion solution (0.9 % sodium chloride)
Primary Outcome Measure Information:
Title
Percentage of Participants With Bone Metastases at 12 Months
Description
Percentage of participants developing at least 1 bone metastasis, whether or not symptomatic. Bone scans were scheduled at screening and at 6-monthly intervals after study entry, or when symptoms suggested the presence of bone metastases. Positive bone scans required confirmation by x-ray, magnetic resonance imaging (MRI), or computed tomography (CT).
Time Frame
Months 12
Secondary Outcome Measure Information:
Title
Progression-Free Survival
Description
Progression-free survival is defined as the time from randomization to the date of the first documented progression or recurrence of disease or death from any cause. Time to disease progression (TTP) was assessed by the Response Evaluation Criteria in Solid Tumors (RECIST) guidelines with evaluations every 3 months.
Time Frame
Up to 24 months
Title
Percentage of Participants With Overall Survival
Time Frame
Months 6, 12, 18, and 24 ]

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18 and 70 years of age, male or female histologically or cytologically confirmed stage IIIB or IV lung cancer at diagnosis no evidence of bone metastatic lesions was radiographically confirmed by bone scintigraphy life expectancy of ≥6 months adequate renal, hematologic, and hepatic Eastern Cooperative Oncology Group(ECOG) performance status≤2 All patients provided written informed consent Exclusion Criteria: Treatment with other bisphosphonates Presence of brain metastases Be allergic to ZOL attending other unlisted drug clinical trials,currently.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
He-Long Zhang, M.D.
Phone
13519128910
Email
zhanghelong@medmail.com.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Mi Jiao, M.M.
Phone
18392467550
Email
mimi10903@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
He-Long Zhang, M.D.
Organizational Affiliation
Department of Oncology,Tangdu Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Oncology,Tangdu Hospital,Fourth Millitary Medical University
City
XI'an
State/Province
Shaanxi
ZIP/Postal Code
710000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
He-Long Zhang, M.D.
Phone
13519128910
Email
zhanghelong@medmail.com.cn
First Name & Middle Initial & Last Name & Degree
Mi Jiao, M.M.
Phone
18392467550
Email
mimi10903@126.com

12. IPD Sharing Statement

Learn more about this trial

Preventive Effects of Zoledronic Acid on Bone Metastasis in Patients With Stage IIIB and IV Lung Cancer

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