Know Cancer

or
forgot password

Longitudinal Assessment of Arthralgia and Related Symptoms in Breast Cancer Patients Receiving Aromatase Inhibitors


N/A
18 Years
N/A
Open (Enrolling)
Female
Breast Cancer

Thank you

Trial Information

Longitudinal Assessment of Arthralgia and Related Symptoms in Breast Cancer Patients Receiving Aromatase Inhibitors


Study Groups:

If you agree to take part in this study, you will be assigned to one of two groups,
depending on how long you have been receiving anastrozole treatment. If you are within two
months prior to or one month after starting treatment, you will be assigned to Group 1 and
you will be followed through 2 years of treatment. If you have been taking anastrozole for
about 2 years, you will be assigned to Group 2 and you will be followed through your third
year of treatment.

Study Procedures:

You will complete tests and procedures during your regularly scheduled clinic visits.

Assessment 1:

- You will be taught how to use an automated symptom assessment program. For this
program, a telephone system will call you at your home at a time that is convenient for
you. Using the numeric key pad on your telephone, you will rate your pain and how it
interferes with your daily activities.

- You will complete questionnaires about your pain and other symptoms, quality of life,
and your ability to work. Completing the questionnaires should take about 45 minutes.

- You will also complete some cognitive (mental) questionnaires that should take about 30
minutes to complete. The cognitive questionnaires will be given to learn about
problems with attention or mental fatigue that may be related to your treatment. If you
choose not to complete the cognitive questionnaires, you can still participate in this
study.

- Blood (about 2 ½ tablespoons) will be drawn to learn about how certain proteins called
cytokines (found in the blood) change during therapy. Researchers will also measure
the C-reactive protein (CRP) which indicates whether there is inflammation in your
body.

- You will have an exam of your bone joints and you will be shown how to perform a
self-exam on your joints at home using a study joint pain kit. This kit will be mailed
to you if you have a new joint pain.

- Demographic information (name, address, date of birth, weight, height, marital status,
job status, education, medical insurance status, and race) will be collected.

- Participants in Group 2 will complete a medication adherence questionnaire. This
questionnaire contains questions about the dose of anastrozole you are taking, if it
has changed (increased or decreased), and if you have been given any drugs to help
manage symptoms that you may be experiencing. This form should take about 5 minutes to
complete.

- If your doctor in the breast clinic thinks you need to see a specialist because of the
pain or swelling you are experiencing, you will be referred to a rheumatologist here at
M. D. Anderson. The rheumatologist will perform a bone joint examination and may order
a blood draw to test for inflammation in your body.

Telephone System Calls:

The telephone system will call you every 2 weeks at a time convenient to you so that you can
rate your pain and how it interferes with your daily activities. Each phone call will take
about 5 minutes to complete.

While you are on the study, if you report through the telephone system joint pain of a
certain level of severity, a joint pain kit will be mailed to you along with a pre-addressed
stamped envelope. Study staff will call you to let you know the kit is being mailed and
that they can help you complete it, if needed. You will be asked to perform a self exam of
your joints and to mark the area that is painful to you on the body drawing included in the
kit. You will also answer some questions about your pain and about your medication and
supplement use. You will be asked to return the completed kit to the project office in the
pre-addressed stamped envelope included with the kit. This kit should be able to be
completed in about 15 minutes. Once the joint kit arrives in the mail at the project
office, you will be mailed a $20 gift card.

Every Month:

The study coordinator will call you monthly at a time convenient to you so that you can rate
your symptoms and how they interfere with your daily activities.

Every 4 - 6 Months:

Research staff will arrange to meet you at your regularly scheduled clinic visits. These
visits will take about 45 minutes. At these visits, you will have the following exams:

- Demographic information (marital status, job status, education, weight, and medical
insurance status will again be collected.

- Blood (about 2 ½ tablespoons) will be drawn for cytokines and CRP testing.

- You will be asked to complete some questionnaires about your symptoms, ability to work,
and quality of life.

- All participants will repeat the medication adherence questionnaire.

- A brief exam of your bone joints will be performed by the research staff.

- You will be asked to tell researchers about any changes in the medications, both
prescribed and over the counter, and supplements you may be taking.

Annual Visits:

At your regularly scheduled annual visit (up to 2 times while on study), you will complete
the following tests:

-If you agreed at the beginning of the study, you will complete the cognitive
questionnaires. This should take about 45 minutes to complete.

The entire study-related time you will spend at your annual visit will be about 1 hour and
30 minutes.

Research staff will also collect clinical information and test results from your medical
record while you are on study.

Length of Study:

Participants in Group 1 will remain on the study for up to 2 years. Participants in Group 2
will remain on the study for 12-14 months, depending on how follow-up clinic visits are
scheduled.

This is an investigational study. Up to 102 participants will take part in this study. All
will be enrolled at MD Anderson.


Inclusion Criteria:



1. Patients with early stage hormone receptor positive breast cancer who are at these 2
time points in their anastrozole treatment: 1) at the time period between two months
prior or one month after beginning of their anastrozole treatment (Cohort 1); 2)
patients within +/- 2 months of the beginning of the third year of anastrozole
treatment (Cohort 2).

2. Patients >= 18 years old.

Exclusion Criteria:

1. Patients with metastatic disease.

2. Patients who cannot complete the assessment tools.

3. Patients without telephone access.

Type of Study:

Interventional

Study Design:

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Outcome Measure:

Incidence, onset and severity of arthralgia during anastrozole treatment

Outcome Time Frame:

3 Years

Safety Issue:

No

Principal Investigator

Charles Cleeland, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

M.D. Anderson Cancer Center

Authority:

United States: Institutional Review Board

Study ID:

2006-1038

NCT ID:

NCT00738998

Start Date:

June 2008

Completion Date:

Related Keywords:

  • Breast Cancer
  • Breast Cancer
  • Aromatase Inhibitors
  • Symptom Assessment
  • Questionnaire
  • Survey
  • Phone Call
  • Arimidex
  • Anastrozole
  • Arthralgia
  • Breast Neoplasms

Name

Location

UT MD . Anderson Cancer CenterHouston, Texas  77030