A Phase II Randomized Trial to Evaluate the Impact of Targeted Nutritional Apport and Exercise on the Modulation of Metabolic and Immune-related Gene Expression Signatures in Early Breast Cancer (eBC) Patients Candidate to Neoadjuvant Therapy (NAT)

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

NEOMET is an exploratory randomized prospective, multicenter study whose primary aim is to explore if metabolomic signatures can be modified by a lifestyle intervention including dietary supplements and physical exercise intervention, in eBC patients candidate to NAT. Eligible patients will be randomised to one of 4 groups: A. NAT, according to molecular subtype; B. NAT plus nutritional supplementation; C. NAT plus supervised physical exercise; D. NAT plus supervised physical exercise plus nutritional supplementation. Nutritional supplementazion will consist of two main long-chain polyunsaturated fatty acids omega-3 (n-3 Lc-PUFA), EPA (eicosapentaenoic acid) and DHA (docosahexaenoic acid) plus a source of palmitoleic acid (hexadecenoic acid).

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

• \- Women (regardless of menopausal status) ≥ 18 years of age

• Pathologic confirmation of breast cancer by tumor biopsy

• Immunohistochemical assessment (as per local standards) of ER and PgR status, HER2 status;

• Stage I-III breast cancer without evidence of distant metastases

• Being candidate to standard neoadjuvant therapy

• Having available tumor tissue from breast and/or lymph node at baseline

• Ability to fill a nutritional daily diary

• Medical clearance for non-agonistic physical activity

• Written informed consent to study-specific procedures

Locations
Other Locations
Italy
AOU Maggiore della Carità
RECRUITING
Novara
Contact Information
Primary
Carmen Branni, BSc
carmen.branni@uniupo.it
+3903213732292
Backup
Ida Taglialatela, MD
ida.taglialatela@maggioreosp.novara.it
+3903213732292
Time Frame
Start Date: 2024-09-01
Estimated Completion Date: 2026-12
Participants
Target number of participants: 160
Treatments
No_intervention: A - treatment of physician choice
Conventional anti-cancer treatment, according to the molecular subtype and standard of care; all patients in Arm A will also receive general recommendations on lifestyle, including weight control and physical activity as indicated by WHO and EUSOMA criteria (control arm).
Experimental: B - nutritional supplementation
Conventional anti-cancer treatment, according to the molecular subtype plus nutritional supplementation.~Patients will be required to take on a daily basis two main long-chain polyunsaturated fatty acids omega-3 (n-3 Lc-PUFA), EPA (eicosapentaenoic acid) and DHA (docosahexaenoic acid), respectively at a dose of 700mg and 240mg, through 1 softgel twice a day. Besides, patients will be provided with a source of palmitoleic acid (hexadecenoic acid) equivalent to 1000mg of pure palmitoleic acid on a daily basis, through one daily 7 ml vial.
Experimental: C - physical activity
Conventional anti-cancer treatment, according to the molecular subtype plus indication for supervised physical exercise
Experimental: D - nutritional supplementation plus physical activity
Conventional anti-cancer treatment, according to the molecular subtype plus indication for supervised exercise training plus nutritional supplementation
Related Therapeutic Areas
Sponsors
Leads: University of Eastern Piedmont

This content was sourced from clinicaltrials.gov