Nausea or Vomiting in Patients Who Are Receiving Chemotherapy for Breast Cancer or Lung Cancer

Alliance for Clinical Trials in Oncology99 enrolled

Overview

RATIONALE: Understanding how nausea or vomiting caused by chemotherapy effects a patient's treatment decisions may help doctors plan better cancer treatment and may help patients live more comfortably. PURPOSE: This clinical trial is studying nausea or vomiting in patients who are receiving chemotherapy for breast cancer or lung cancer.

OBJECTIVES: * Determine the contribution of nausea or vomiting to the overall importance for a current state of health in patients with breast or lung cancer undergoing chemotherapy. * Determine the average importance for various emetic scenarios in these patients. * Compare the importance of a specific level of chemotherapy-induced nausea or vomiting, defined by the Standard Gamble vs Morrow Assessment of Nausea and Emesis. * Determine the feasibility of using a Standard Gamble technique in patients currently undergoing chemotherapy. OUTLINE: This is a multicenter study. Patients are stratified according to history of chemotherapy-induced nausea or vomiting (yes vs no). Patients undergo a structured interview over 1 hour by a trained interviewer at least 2½ weeks after initiation of the most recent course of chemotherapy and before the new course is administered. Patients complete a Functional Assessment of Cancer Therapy-General questionnaire and Morrow Assessment of Nausea and Emesis questionnaire during the interview. The trained interviewer also administers a Standard Gamble exercise during the interview, in which patients are instructed to imagine various amounts of nausea or vomiting as their current state of nausea and vomiting, and rank their importance to them. They are being asked to answer the question of whether they would choose to accept their current (imagined or real) state of nausea or vomiting or receive a medication that would result (with various probabilities) in either perfect health for 2 years or immediate death.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Breast Cancer Lung Cancer Nausea and Vomiting

Interventions

assessment of therapy complicationsPROCEDURE

quality-of-life assessmentPROCEDURE

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

DISEASE CHARACTERISTICS: * Diagnosis of breast cancer or lung cancer * Must be undergoing chemotherapy with each course lasting 3-6 weeks AND meets all of the following criteria: * Completed ≥ 1 course with ≥ 1 additional course planned * At least 2½ weeks since initiation of the most recent course of chemotherapy PATIENT CHARACTERISTICS: * Common Toxicity Criteria performance status 0-2 * Must have command of written and/or spoken English PRIOR CONCURRENT THERAPY: * See Disease Characteristics

Data from ClinicalTrials.gov

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