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Zoledronate in Preventing Bone Loss in Premenopausal Women Receiving Chemotherapy After Surgery For Early Stage Breast Cancer

Primary Purpose

Breast Cancer, Osteoporosis

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
zoledronic acid
Sponsored by
Herbert Irving Comprehensive Cancer Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer focused on measuring osteoporosis, stage I breast cancer, stage II breast cancer

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Diagnosis of localized breast cancer Stage I or II (T1-3, N0-2, M0) Planned adjuvant chemotherapy (after surgery) of at least 6 months in duration Hormone receptor status: Estrogen receptor and progesterone receptor status known PATIENT CHARACTERISTICS: Age 18 to 50 Sex Female Menopausal status Premenopausal or perimenopausal Performance status Not specified Life expectancy Not specified Hematopoietic Not specified Hepatic Not specified Renal Creatinine less than 2 mg/dL Other No T score of less than 2.0 on bone mineral density (BMD) No fragility fracture No lumbar spine anatomy that would preclude accurate BMD measurement of a minimum of 3 lumbar vertebrae Not pregnant PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy See Disease Characteristics Endocrine therapy Not specified Radiotherapy No concurrent radiotherapy Surgery See Disease Characteristics Other At least 1 month since prior calcitonin At least 12 months since prior bisphosphonates given for more than 1 month duration No concurrent fluoride therapy (10 mg/day or more) No concurrent enrollment in another experimental drug study

Sites / Locations

  • Carl and Dorothy Bennett Cancer Center at Stamford Hospital
  • Valley Hospital - Paramus
  • Herbert Irving Comprehensive Cancer Center at Columbia University

Outcomes

Primary Outcome Measures

Changes in lumbar spine bone mineral density (BMD) at 6 months

Secondary Outcome Measures

Changes in lumbar spine BMD at 12 and 24 months
Total hip and femoral neck BMD at 6, 12, and 24 months
Serum markers of bone turnover (osteocalcin, bone-specific alkaline phosphatase, and cross-linked C-telopeptide of type 1 collagen levels) measured every 6 weeks for 6 months, and at 9 and 12 months
Quality of life as measured by the Short Form-36 instrument at baseline, and at 6 and 12 months
Treatment costs

Full Information

First Posted
November 12, 2002
Last Updated
January 3, 2014
Sponsor
Herbert Irving Comprehensive Cancer Center
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00049452
Brief Title
Zoledronate in Preventing Bone Loss in Premenopausal Women Receiving Chemotherapy After Surgery For Early Stage Breast Cancer
Official Title
A Randomized, Placebo Controlled Trial Of Zoledronic Acid For The Prevention Of Bone Loss In Premenopausal Women With Early Stage Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2007
Overall Recruitment Status
Completed
Study Start Date
December 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Herbert Irving Comprehensive Cancer Center
Collaborators
National Cancer Institute (NCI)

4. Oversight

5. Study Description

Brief Summary
RATIONALE: It is not yet known whether zoledronate is effective in preventing bone loss in premenopausal women who are receiving adjuvant chemotherapy after undergoing surgery for early stage breast cancer. PURPOSE: Randomized phase III trial to determine the effectiveness of zoledronate in preventing bone loss in premenopausal women who are receiving chemotherapy after surgery for early stage breast cancer.
Detailed Description
OBJECTIVES: Compare the changes in bone mineral density (BMD) and bone turnover that occur in premenopausal women with resected early stage breast cancer during and after 6 months of adjuvant chemotherapy. Determine the factors that predict bone loss during chemotherapy, particularly induction of amenorrhea, type of chemotherapeutic regimen, glucocorticoid exposure, and baseline BMD, in these patients. Determine whether zoledronate prevents bone loss in these patients when given during and after adjuvant chemotherapy. Determine the effect of zoledronate on markers of bone turnover in these patients during and after adjuvant chemotherapy. Determine whether the effect on markers of bone turnover predicts response to zoledronate in these patients. OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to estrogen receptor status (positive vs negative), progesterone receptor status (positive vs negative), and adjuvant chemotherapy regimen. Patients are randomized to 1 of 2 treatment arms. Arm I: Patients receive zoledronate IV over 15 minutes on day 1. Arm II: Patients receive placebo IV over 15 minutes on day 1. In both arms, treatment repeats every 3 months for up to 4 courses in the absence of disease progression. Patients also receive calcium and cholecalciferol (vitamin D) supplements daily. Quality of life is assessed at baseline and at 6 and 12 months. Patients are followed at 1 year. PROJECTED ACCRUAL: A total of 120 patients (60 per treatment arm) will be accrued for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Osteoporosis
Keywords
osteoporosis, stage I breast cancer, stage II breast cancer

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 3
Masking
Double
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
zoledronic acid
Primary Outcome Measure Information:
Title
Changes in lumbar spine bone mineral density (BMD) at 6 months
Secondary Outcome Measure Information:
Title
Changes in lumbar spine BMD at 12 and 24 months
Title
Total hip and femoral neck BMD at 6, 12, and 24 months
Title
Serum markers of bone turnover (osteocalcin, bone-specific alkaline phosphatase, and cross-linked C-telopeptide of type 1 collagen levels) measured every 6 weeks for 6 months, and at 9 and 12 months
Title
Quality of life as measured by the Short Form-36 instrument at baseline, and at 6 and 12 months
Title
Treatment costs

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Diagnosis of localized breast cancer Stage I or II (T1-3, N0-2, M0) Planned adjuvant chemotherapy (after surgery) of at least 6 months in duration Hormone receptor status: Estrogen receptor and progesterone receptor status known PATIENT CHARACTERISTICS: Age 18 to 50 Sex Female Menopausal status Premenopausal or perimenopausal Performance status Not specified Life expectancy Not specified Hematopoietic Not specified Hepatic Not specified Renal Creatinine less than 2 mg/dL Other No T score of less than 2.0 on bone mineral density (BMD) No fragility fracture No lumbar spine anatomy that would preclude accurate BMD measurement of a minimum of 3 lumbar vertebrae Not pregnant PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy See Disease Characteristics Endocrine therapy Not specified Radiotherapy No concurrent radiotherapy Surgery See Disease Characteristics Other At least 1 month since prior calcitonin At least 12 months since prior bisphosphonates given for more than 1 month duration No concurrent fluoride therapy (10 mg/day or more) No concurrent enrollment in another experimental drug study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dawn Hershman, MD
Organizational Affiliation
Herbert Irving Comprehensive Cancer Center
Official's Role
Study Chair
Facility Information:
Facility Name
Carl and Dorothy Bennett Cancer Center at Stamford Hospital
City
Stamford
State/Province
Connecticut
ZIP/Postal Code
06904
Country
United States
Facility Name
Valley Hospital - Paramus
City
Paramus
State/Province
New Jersey
ZIP/Postal Code
07652-2509
Country
United States
Facility Name
Herbert Irving Comprehensive Cancer Center at Columbia University
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20022990
Citation
Hershman DL, McMahon DJ, Crew KD, Shao T, Cremers S, Brafman L, Awad D, Shane E. Prevention of bone loss by zoledronic acid in premenopausal women undergoing adjuvant chemotherapy persist up to one year following discontinuing treatment. J Clin Endocrinol Metab. 2010 Feb;95(2):559-66. doi: 10.1210/jc.2009-1366. Epub 2009 Dec 18.
Results Reference
result
PubMed Identifier
18711172
Citation
Hershman DL, McMahon DJ, Crew KD, Cremers S, Irani D, Cucchiara G, Brafman L, Shane E. Zoledronic acid prevents bone loss in premenopausal women undergoing adjuvant chemotherapy for early-stage breast cancer. J Clin Oncol. 2008 Oct 10;26(29):4739-45. doi: 10.1200/JCO.2008.16.4707. Epub 2008 Aug 18.
Results Reference
result

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Zoledronate in Preventing Bone Loss in Premenopausal Women Receiving Chemotherapy After Surgery For Early Stage Breast Cancer

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