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Study of Docosahexaenoic Acid (DHA) in Triple Negative Breast Cancer Survivors

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01849250
Recruitment Status : Completed
First Posted : May 8, 2013
Results First Posted : December 28, 2021
Last Update Posted : December 28, 2021
Sponsor:
Information provided by (Responsible Party):
National Cancer Institute (NCI)

Brief Summary:
This randomized phase II trial studies how well docosahexaenoic acid works in preventing recurrence in breast cancer survivors. Docosahexaenoic acid supplement may prevent recurrence in breast cancer survivors.

Condition or disease Intervention/treatment Phase
Benign Breast Neoplasm Ductal Breast Carcinoma In Situ Invasive Breast Carcinoma Lobular Breast Carcinoma In Situ Paget Disease of the Breast Stage IA Breast Cancer Stage IB Breast Cancer Stage IIA Breast Cancer Stage IIB Breast Cancer Stage IIIA Breast Cancer Stage IIIB Breast Cancer Stage IIIC Breast Cancer Drug: Docosahexaenoic Acid Other: Placebo Phase 2

Detailed Description:

PRIMARY OBJECTIVES:

I. To determine whether treatment with docosahexaenoic acid (DHA) for 12 weeks at 1000 mg twice daily as compared to placebo reduces normal breast tissue levels of tumor necrosis factor-alpha (TNF-alpha) in overweight and obese patients with a history of stage I-III invasive breast cancer, ductal carcinoma in situ (DCIS), Paget's disease, lobular carcinoma in situ (LCIS), or proliferative benign breast disease.

SECONDARY OBJECTIVES:

I. To investigate the effect of DHA at 1000 mg twice daily on tissue biomarkers

  • Change from the baseline in cyclooxygenase-2 (COX-2)/interleukin-1-beta (IL-1beta)/aromatase measured by quantitative real-time polymerase chain reaction (PCR).
  • Change from the baseline in crown-like structures of the breast (CLS-B) measured by immunohistochemical techniques for cluster of differentiation (CD)68.
  • Change from baseline in CLS-B index determined as follows: ([number of slides with evidence of at least one CLS-B]/[total number of slides examined]).
  • Change from baseline in CLS-B/cm^2 defined as the number of CLS-B/cm^2. II. Evaluate age as a predictor of CLS-B and inflammatory biomarkers (TNF-alpha/COX-2/IL-1beta) at baseline and over the time of treatment.

III. Evaluate red blood cell (RBC) fatty acid level as a surrogate of compliance.

OUTLINE: Patients are randomized to 1 of 2 arms.

ARM I: Patients receive docosahexaenoic acid orally (PO) twice daily (BID) for 12 weeks.

ARM II: Patients receive placebo PO BID for 12 weeks.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 65 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Prevention
Official Title: A Multicenter Phase II Study of Docosahexaenoic Acid (DHA) in Patients With a History of Breast Cancer, Premalignant Lesions, or Benign Breast Disease
Actual Study Start Date : May 2013
Actual Primary Completion Date : January 11, 2016
Actual Study Completion Date : April 22, 2020


Arm Intervention/treatment
Experimental: Arm I (Docosahexaenoic Acid)
Docosahexaenoic Acid orally twice a day (PO BID) for 12 weeks.
Drug: Docosahexaenoic Acid
Given PO
Other Name: Fatty Acid 22:6

Placebo Comparator: Arm II (placebo)
Placebo orally twice a day (PO BID) for 12 weeks.
Other: Placebo
Given PO
Other Names:
  • placebo therapy
  • PLCB
  • sham therapy




Primary Outcome Measures :
  1. Normal Breast Tissue Expression of Tumor Necrosis Factor Alpha (TNF-alpha) Levels [ Time Frame: Baseline to 12 weeks ]
    Differences in normal breast tissue levels of TNF-α 12 weeks post-treatment relative to pre-treatment for active treatment and placebo arm, compared using analysis of covariance where the post-treatment measurements were used as a dependent variable and the pretreatment measurements were included as a covariate in the analysis. For the primary study end-point TNF-α levels will be measured by quantitative real-time PCR (mRNA essays) on extracted RNA from breast core biopsies. Relative expression determined using the Computed Tomography (ΔΔCT) analysis protocol.


Secondary Outcome Measures :
  1. Number of Participants With Crown-like Structures of the Breast (CLS-B) at Baseline and Post-treatment [ Time Frame: Baseline to 12 weeks ]
    An indicator of whether a subject is detected with CLS-B or not.

  2. Absolute Change in CLS-B/cm^2 Adjusted for the Pre-treatment Measurements [ Time Frame: Baseline to 12 weeks ]
    To assess the severity of CLS-B using the following formula: number of CLS-B/cm^2. The absolute change in the CLS-B/cm^2 calculated according to the formula; Change in CLS-B/cm^2 = (post-treatment CLS-B/cm^2) - (pre-treatment CLS-B/cm^2).

  3. Breast Tissue Cox 2 mRNA Levels at Baseline and 12 Weeks [ Time Frame: Baseline to 12 weeks ]
    Biomarkers COX-2 are measured by quantitative real-time PCR. Differences between active treatment and placebo arm for each biomarker will be compared using analysis of covariance where the post treatment measurements will be used as a dependent variable and the pretreatment measurements will be included as a covariate in the analysis.

  4. Mean Difference in the Breast Tissue IL- Beta mRNA Levels of Tissue Biomarkers [ Time Frame: Baseline to 12 weeks ]
    Biomarkers IL-1Beta are measured by quantitative real-time PCR. Differences between active treatment and placebo arm for each biomarker will be compared using analysis of covariance where the post treatment measurements will be used as a dependent variable and the pretreatment measurements will be included as a covariate in the analysis.

  5. Mean Difference in the Breast Tissue Aromatase mRNA Levels of Tissue Biomarkers [ Time Frame: Baseline and 12 weeks ]
    Biomarkers Aromatase are measured by quantitative real-time PCR. Differences between active treatment and placebo arm for each biomarker will be compared using analysis of covariance where the post treatment measurements will be used as a dependent variable and the pretreatment measurements will be included as a covariate in the analysis.

  6. Red Blood Cell (RBC) Fatty Acid Level as a Surrogate of Compliance [ Time Frame: Baseline and week 12 ]
    Whole blood samples collected for red blood cell fatty acid analyses at baseline and week 12 (+ 2 weeks). RBC fatty acid composition analyzed by gas chromatography (GC) with flame ionization detection.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Participants must have a history of histologically-confirmed stage I-III invasive breast cancer or ductal carcinoma in situ (DCIS), Paget's disease, lobular carcinoma in situ (LCIS), or proliferative benign breast disease
  • No evidence of disease (in situ or invasive cancer that would normally be treated by resection) at trial entry as determined by the investigator
  • >= 6 months from all previous breast cancer treatment (including surgery for invasive cancer, chest wall radiotherapy, chemotherapy, trastuzumab and endocrine therapy)
  • Participants must have a body mass index (BMI) >= 25, defined as (weight in kilograms/[height in meters]^2)
  • Participants must have adequate accessible breast tissue as determined by the treating physician, consisting of one breast unaffected by invasive cancer, which has not been radiated; a history of prior pre-invasive breast cancer or benign biopsy of this breast will be permitted
  • Daily DHA consumption =< 200 mg/day in the month prior to screening estimated by an abbreviated DHA food frequency questionnaire
  • Mammogram within no more than 6 months prior to the date of informed consent (normal/benign Breast Imaging-Reporting and Data System [BI-RADS] 1 or 2) and no further routine breast imaging planned during the course of the study (12 weeks DHA/placebo)
  • Eastern Cooperative Oncology Group (ECOG) performance status must be =< 2 (Karnofsky >= 60%)
  • Absolute neutrophil count >= 1,500/uL
  • Platelets >= 75,000/uL
  • White blood cells >= 3,000/uL
  • Hemoglobin >= 10 g/dL
  • Total bilirubin within 1.5 times the institution's upper limit of normal (ULN)
  • Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) within 1.5 times the institution's ULN
  • Serum creatinine within 1.5 times the institution's ULN
  • Pregnant women will be excluded; for women of childbearing potential; negative pregnancy testing within 72 hours prior to or on study visit #1 (day 0) and willingness to use adequate contraception during the study intervention OR post-menopausal defined as any one of the following 1) prior hysterectomy, 2) absence of menstrual period for 1 year in the absence of prior chemotherapy or 3) absence of menstrual period for 2 years in women with a prior history of chemotherapy exposure who were pre-menopausal prior to chemotherapy
  • Willingness to comply with all study interventions and follow-up procedures including the ability to swallow the study drug
  • Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria:

  • Any type of active invasive cancer (excluding breast and non-melanoma skin cancer) within the preceding 18 months
  • A history of histologically-confirmed bilateral invasive breast cancer
  • Bilateral mastectomy
  • Prior history or evidence of metastatic breast cancer
  • Prior radiation therapy to the contralateral (unaffected) breast
  • Prior history of contralateral (unaffected) breast augmentation with breast implant placement
  • History of daily use of aspirin or non-steroidal anti-inflammatory drugs (NSAIDs) in the week preceding study entry
  • History of DHA supplementation > 200 mg/day in the month preceding study entry
  • History of autoimmune disorder or any illness that requires therapy with chronic steroids or immunomodulators
  • History of therapeutic doses of anticoagulants including warfarin and low molecular weight heparin (e.g. for prior deep venous thrombosis and pulmonary embolism) in the preceding year
  • Participants may not be receiving any other investigational agents during the study
  • Women who have received cancer surgery, chemotherapy, biological therapy (e.g., trastuzumab), or radiotherapy for the treatment of any cancer within 6 months of study participation
  • Women who are receiving endocrine therapy for breast cancer treatment or chemoprevention including tamoxifen, letrozole, anastrozole, fulvestrant, or exemestane at the time of screening
  • Individuals with severe underlying chronic illness, such as uncontrolled diabetes; ongoing or active infection, psychiatric illness or social situations which in the opinion of the investigator would interfere with study participation
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to DHA or corn/soy oil in placebo agent
  • Pregnant, breastfeeding, or women of childbearing potential unwilling to use a reliable contraceptive method

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01849250


Locations
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United States, Massachusetts
Dana-Farber Cancer Institute
Boston, Massachusetts, United States, 02115
United States, New York
Columbia University/Herbert Irving Cancer Center
New York, New York, United States, 10032
Memorial Sloan-Kettering Cancer Center
New York, New York, United States, 10065
United States, Texas
MD Anderson Cancer Center
Houston, Texas, United States, 77030
Sponsors and Collaborators
National Cancer Institute (NCI)
Investigators
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Principal Investigator: Ayca Gucalp Memorial Sloan Kettering Cancer Center
Study Chair: Powel H. Brown, MD M.D. Anderson Cancer Center
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Responsible Party: National Cancer Institute (NCI)
ClinicalTrials.gov Identifier: NCT01849250    
Other Study ID Numbers: NCI-2013-00859
NCI-2013-00859 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) )
12-474
12-267
N01-CN-2012-00034
DFCI:12- 474 ( Other Identifier: Dana-Farber Cancer Institute (DFCI) )
AAAK6752
MSKCC-12-267 ( Other Identifier: Memorial Sloan Kettering Cancer Center (MSK or MSKCC) )
H-33017
CUMC: AAAK6752
2011-0766 ( Other Identifier: MD Anderson Cancer Center (MDA or MDACC) )
MDA10-16-01 ( Other Identifier: DCP )
N01CN00034 ( U.S. NIH Grant/Contract )
N01CN35159 ( U.S. NIH Grant/Contract )
P30CA016672 ( U.S. NIH Grant/Contract )
First Posted: May 8, 2013    Key Record Dates
Results First Posted: December 28, 2021
Last Update Posted: December 28, 2021
Last Verified: December 2021
Additional relevant MeSH terms:
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Carcinoma
Breast Neoplasms
Carcinoma in Situ
Carcinoma, Ductal, Breast
Breast Carcinoma In Situ
Carcinoma, Intraductal, Noninfiltrating
Carcinoma, Lobular
Paget's Disease, Mammary
Breast Diseases
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms
Neoplasms by Site
Skin Diseases
Carcinoma, Ductal
Adenocarcinoma
Neoplasms, Ductal, Lobular, and Medullary