Completed

Phase I/II Trial of Omega-3 Fatty Acids for Cancer Cachexia

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

omega-3 fatty acid

Dietary Supplement
Who is being recruted

Blood Protein Disorders+15

+ Cardiovascular Diseases

+ Hematologic Diseases

From 18 to 120 Years
See all eligibility criteria
How is the trial designed

Supportive Care Study

Phase 1 & 2
Interventional
Study Start: October 1995
See protocol details

Summary

Principal SponsorAlliance for Clinical Trials in Oncology
Last updated: July 13, 2016
Sourced from a government-validated database.Claim as a partner

Study start date: October 1, 1995

Actual date on which the first participant was enrolled.

OBJECTIVES: Determine whether omega-3 fatty acids will reverse weight loss in advanced cancer patients with cachexia. Determine the maximum tolerated dose (MTD) of omega-3 fatty acids in these patients (phase I completed 12/1999). Determine whether omega-3 fatty acids will result in an antitumor response. OUTLINE: This is a randomized, stratified, dose escalation study. Patients are stratified by the extent of weight loss (2-5 percent or greater than 5 percent in the past month). Patients receive omega-3 fatty acids orally in two equal doses with/after breakfast and lunch for 4 months or until weight loss is observed. Dose is escalated in cohorts of two patients, although dose escalation is allowed in individual patients. The maximum tolerated dose (MTD) is defined as the highest dose level at which no greater than one-third of the patients treated, including escalated patients from a lower dose, experience grade 3 or worse toxicity (phase I completed 12/1999).

NCT00003077
Principal SponsorAlliance for Clinical Trials in Oncology
Last updated: July 13, 2016
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

63 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 120 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Blood Protein DisordersCardiovascular DiseasesHematologic DiseasesHemic and Lymphatic DiseasesHemorrhagic DisordersImmune System DiseasesImmunoproliferative DisordersLymphatic DiseasesLymphoproliferative DisordersNeoplasmsNeoplasms by Histologic TypeParaproteinemiasVascular DiseasesHemostatic DisordersLeukemiaLymphomaMultiple MyelomaNeoplasms, Plasma Cell

Criteria

DISEASE CHARACTERISTICS: Histologically or cytologically proven advanced cancer not amenable to curative therapy (solid tumors and hematologic malignancies eligible except primary and metastatic brain tumors) Cachexia (weight loss at least 2 percent within a one month period) PATIENT CHARACTERISTICS: Age: 18 and over Performance Status: CALBG 0-2 Life Expectancy: At least 2 months Hematopoietic: Granulocytes greater than 1,000/mm3 Platelet count greater than 75,000/mm3 Hemoglobin greater than 8 mg/dL Hepatic: AST less than 3 times upper limit of normal (ULN) Alkaline phosphatase less than 3 times ULN Bilirubin less than 1.5 times ULN Renal: BUN less than 1.5 times ULN Creatinine less than 1.5 times ULN Cardiovascular: No congestive heart failure requiring diuretics within less than 6 months No uncontrolled or severe cardiovascular disease within less than 6 months No myocardial infarction within less than 6 months Other: Not pregnant nor contemplating pregnancy during study Negative pregnancy test No uncontrolled hypercalcemia No metabolic disorders (hyperthyroidism) No poorly controlled diabetes No peripheral edema or ascites requiring diuretics No enteric fistulas, with tracheobronchial fistulas or with aspiration No esophageal or bowel obstruction that would preclude eating Free T4 within normal range No serious medical illness No psychosis No uncontrolled bacterial, viral, or fungal infections No active uncontrolled duodenal ulcers Above laboratory values required unless bone marrow, liver, kidney, or splenic involvement by tumor is documented PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: Prior and concurrent chemotherapy allowed Endocrine therapy: No concurrent steroids such as dronabinol or megestrol acetate (except for adrenal failure) Radiotherapy: No prior or concurrent radiotherapy to abdomen or pelvis Surgery: Greater than 3 weeks since major surgery Greater than 1 week since minor surgery Other: No concurrent diuretics

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Patients receive omega-3 fatty acids orally in two equal doses with/after breakfast and lunch for 4 months or until weight loss is observed. Dose is escalated in cohorts of two patients, although dose escalation is allowed in individual patients. Patients are evaluated for cachexia response every 2 weeks, and tumor response every 4 weeks for a maximum of 4 months. If no response of cachexia or tumor after a 2 month period, patients will be discontinued from study. Patients will be followed for survival post-treatment.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 5 locations

CCOP - Christiana Care Health Services

Wilmington, United StatesOpen CCOP - Christiana Care Health Services in Google Maps

Holden Comprehensive Cancer Center at The University of Iowa

Iowa City, United States

North Shore University Hospital

Manhasset, United States

New York Presbyterian Hospital - Cornell Campus

New York, United States
Completed5 Study Centers