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The 'SWIVEL' Study (Switch Vs Effects Relief): Effectiveness of a Medication 'Switch' vs Guideline-Directed Interventions for Relieving Side Effects of Aromatase Inhibitors Among Breast Cancer Patients

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Researchers have learned that about 50% of women do not finish the standard 5-year breast cancer treatment with an aromatase inhibitor. An aromatase inhibitor is hormone therapy that lowers the chance of breast cancer coming back (recurring) after surgery by blocking an enzyme in fat tissue called aromatase; aromatase changes other hormones in the body to estrogen. Women who do not complete the standard 5-year treatment are at higher risk of their cancer coming back. The goal of this research is to prevent breast cancer from coming back after surgery by helping women to stay on treatment with aromatase inhibitors. Researchers believe the best path to help women to stay on treatment is to create a better way to manage (control) side effects.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologic documentation of DCIS or invasive breast cancer by core needle or incisional biopsy.

• The DCIS or invasive cancer must be estrogen receptor alpha (ER)-positive

• The invasive cancer must be HER2-negative (IHC 0-1+, or with a FISH ratio of \<1.8 if IHC is 2+ or if IHC has not been done)

• Clinical Stage I-III invasive breast cancer or DCIS

• Patients for whom adjuvant treatment with one of the following would be clinically indicated: letrozole, anastrozole, exemestane

• Patients who anticipate continuing with adjuvant endocrine therapy for a minimum of 2 years at the time of registration

• Women over 18 years of age who are post-menopausal, defined as last menstrual period \>2 years prior to registration, or \>1 year prior to registration with FSH and estradiol in post-menopausal range.

• Patients must meet the following clinical laboratory criteria:

‣ Absolute neutrophil count (ANC) \>1,000/mm3 and platelet count \> 75,000/mm3

⁃ Total bilirubin \<1.5 x the upper limit of the normal range (ULN).

⁃ Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) \< 3 x ULN.

• Ability to give informed consent.

Locations
United States
New Hampshire
Dartmouth Cancer Center
RECRUITING
Lebanon
Contact Information
Primary
Kristina M. Willey
Kristina.M.Willey@hitchcock.org
603-650-7705
Time Frame
Start Date: 2025-10-17
Estimated Completion Date: 2027-08-05
Participants
Target number of participants: 62
Treatments
Active_comparator: Switch
Participants (people taking part in this study) enrolled to this study will receive treatment with the aromatase inhibitor (AI) Letrozole and fill out surveys to check for side effects to see how the side effects are making their daily life harder. If side effects are reported, the Participant will be randomized (placed by chance) to a group where they will receive either a different AI ('switch') or receive guideline directed intervention GDI using medication and non-medication treatment options.
Active_comparator: Guideline Directed Intervention (GDI)
Participants will receive evidence-based (proven to work) treatment options for side effects according to national guidelines; these may include medications or non-medication options (guideline-directed interventions, GDIs).
Related Therapeutic Areas
Sponsors
Leads: Dartmouth-Hitchcock Medical Center

This content was sourced from clinicaltrials.gov

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