Outpatient Health Care Program for Older Patients Receiving Chemotherapy for Newly Diagnosed Breast Cancer or Colon Cancer

NCT ID: NCT00873600

Last Updated: 2015-03-19

Basic Information

• Recruitment Status: WITHDRAWN
• Study Classification: OBSERVATIONAL
• Study Start Date: 2007-10-31

Brief Summary

RATIONALE: Gathering health information from older patients undergoing chemotherapy may help doctors plan better treatment and improve the quality of life for these patients.

PURPOSE: This randomized clinical trial is studying how well an outpatient health care program works for older patients receiving chemotherapy for newly diagnosed breast cancer or colon cancer.

Detailed Description

OBJECTIVES:

Primary

• Determine the effect of a 1-year geriatric evaluation and management (GEM) program on adherence to adjuvant chemotherapy (defined as tolerance and timely completion of planned dose) in patients with newly diagnosed breast or colon cancer.

Secondary

• Evaluate the effect of a 1-year GEM program on the health-related quality of life and functional, cognitive, and mental status of these patients.
• Evaluate the effect of a 1-year GEM program on 3-year disease-free survival of these patients.
• Compare the number of emergency room visits, acute hospitalizations, and associated Medicare costs within the first 12 months following randomization to a GEM program vs no program.

OUTLINE: Patients are stratified according to tumor site (breast vs colon). Patients are randomized to 1 of 2 arms.

• Arm I (intervention): Patients complete health-related quality-of-life (QOL) and comprehensive geriatric assessment questionnaires at baseline, within 30 days after chemotherapy or at 6 months, and then at 12-13 months to assess functional status (i.e., activities of daily living), comorbidity (i.e., medical problems), medications, mood and memory, nutrition, and social support from family members and friends. Patients receive a home visit from a social worker and visit the Senior Adult Oncology clinic within 1 month after the first course of chemotherapy. The clinic staff develops an individualized care plan for the patient and communicates the results of the assessment questionnaires and their recommendations (e.g., medication and/or specialty referrals) to the patient's primary care provider and oncologist. The staff meets weekly to monitor and update the patient care plan. Patients are followed in the Senior Adult Oncology clinic at least every 3 months for 1 year. Follow-up telephone calls and in-home visits are also conducted as needed. Patients are also assessed prior to each course of chemotherapy for toxicities related to the chemotherapy.
• Arm II (control): Patients complete a health-related QOL questionnaire at baseline, within 30 days after chemotherapy or at 6 months, and then at 12-13 months. Patients receive oncology and primary care by their usual health care providers.

After completion of the study intervention, patients' medical charts are reviewed periodically for up to 2 years.

Conditions

Breast Cancer; Cognitive/Functional Effects; Colorectal Cancer; Psychosocial Effects of Cancer and Its Treatment

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Interventions

chemotherapy

Intervention Type: DRUG

medical chart review

Intervention Type: OTHER

questionnaire administration

Intervention Type: OTHER

adjuvant therapy

Intervention Type: PROCEDURE

assessment of therapy complications

Intervention Type: PROCEDURE

cognitive assessment

Intervention Type: PROCEDURE

psychosocial assessment and care

Intervention Type: PROCEDURE

quality-of-life assessment

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed adenocarcinoma, including one of the following:

• Breast cancer (female), meeting the following criteria:

• Stage I-III (T1-4, N0-3, M0) disease
• Has undergone complete surgical removal of invasive cancer by mastectomy or lumpectomy
• Has undergone either sentinel lymph node dissection or axillary lymph node dissection with adequate TNM staging
• Colon cancer (male or female), meeting the following criteria:

• Stage I-III (T1-3, any N, M0) disease
• Has undergone appropriate surgical resection with TNM staging
• Newly diagnosed disease
• Scheduled to receive chemotherapy

• Agrees to receive chemotherapy AND is able to receive chemotherapy within 3 months after surgery
• No distant metastases
• Hormone receptor status not specified

PATIENT CHARACTERISTICS:

• Menopausal status not specified
• Life expectancy ≥ 6 months
• Fluent in English
• Not living in a nursing home
• No end-stage disease
• No severe dementia
• No other clinically active malignancy within the past 5 years or within 3 months after diagnosis of current malignancy

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• No prior chemotherapy for the malignancy
• More than 1 year since prior treatment on an inpatient/outpatient geriatric evaluation and management unit

• Minimum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Case Comprehensive Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Ireland Cancer Center at University Hospitals Case Medical Center, Case Comprehensive Cancer Center

Principal Investigators

Cynthia Owusu, MD, MSC

Role: PRINCIPAL_INVESTIGATOR

Ireland Cancer Center at University Hospitals Case Medical Center, Case Comprehensive Cancer Center

Related Links

http://clinicaltrials.gov/ct2/results?term=case4y07

Clinical trial summary from the National Cancer Institute's PDQ® database

Other Identifiers

P30CA043703

Identifier Type: NIH

Identifier Source: secondary_id

View Link

CASE4Y07

Identifier Type: OTHER

Identifier Source: secondary_id

CASE4Y07

Identifier Type: -

Identifier Source: org_study_id