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RecruitingNCT07870148MAMTIRUpdated Oct 13, 2026

Cross Immune Response Between Breast Carcinoma and Thyroid Autoimmunity: Impact on Prognosis and Treatment

An interventional study of Aspiration 0 in Breast Cancer, sponsored by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico. Recruiting at 1 site in Italy. Open to female participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico · Not applicable, Interventional, and Diagnostic

From the registry’s dates

  • Registered 2 years 4 months after the study started (first participant enrolled May 2024, registered Oct 2026).
  • Started May 2024; still recruiting 2 years 5 months later.
Updated Oct 13, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
496
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
Female
01

Study summary

Background: Patients with breast cancer (BC) seem to have a higher prevalence of thyroid autoimmunity (TA), and this association has a solid pathogenic rationale: 1) I have discovered that BC tissue expresses thyroid peroxidase (TPO), a major thyroid autoantigen which exists in different isoforms by alternative splicing; 2) the immune system has a key role in both autoimmunity and cancer; 3) immunity and gut microbiota are deeply connected. Serum anti-TPO autoantibodies (TPOAb), the hallmark of TA, are highly prevalent among BC patients and they are associated with a better BC prognosis is retrospective studies. The magnitude of the relationship between BC and TA needs to be defined in longitudinal studies, unbiased by concurrent anti-cancer treatments.

Hypothesis: Patients with both BC and TA have a better BC prognosis, since they express intra-tumoral breast-specific TPO isoforms that are related with TPO-specific immune responses, and microbiota patterns, that contrast neoplastic progression, not present in patients affected with only BC and not associated TA.

Aims: 1) To verify the prevalence and prognostic impact of TA in the first unbiased longitudinal cohort of BC patients, recruited before anti-cancer treatments; 2) To investigate breast-specific TPO isoforms expression in BC tissue; 3) to characterise TPO-specific tissue-resident immune responses in paired human samples derived from BC and thyroid-related tissues/organs; 4) to explore the gut microbiota associated with BC and TA.

Experimental design: Monocentric 5-year longitudinal study. BC patients and non-cancer controls will be sampled from paired blood, stool, tumoral-breast samples (BC only), and neck lymph nodes (LNs). LNs contain thyroid-draining lymphocytes and are easily accessible by ultrasound-guided fine-needle-aspiration, a well-tolerated technique which I routinely operate for research purposes. Methods used to address aims: 1) Serum thyroid function and TPOAb measurement to assess TA; 2) RT-PCR amplification and product sequencing of tumor-derived RNA in BC patients, to identify TPO isoforms expression; 3) Flow-cytometry immunophenotyping of TPO-specific lymphocytes; 4) Metagenomics, metabolomics and metaproteomics for microbiota analysis.

Expected results: BC patients have a higher prevalence of TA than non-cancer controls (Aim 1A). Compared with BC-only patients, those affected with both BC and TA have a better 5-year prognosis (Aim 1B), express breast-specific TPO isoforms (Aim 2), have increased tumor-infiltrating and neck-LN-resident TPO-specific lymphocytes with anti-neoplastic activity, i.e. T follicular helper cells (Tfh) (Aim 3), and show peculiar microbiota signatures (Aim 4).

Impact on cancer: This study will clarify the prognostic role of TA in BC patients by combining paired clinical data, intra-tumoral antigen-expression and related lymphocytic infiltration, and microbiota patterns, generating novel clinical and therapeutic potential applications. Serum thyroid function and TPOAb, as well as intra-tumoral TPO isoforms, may be assessed as routine BC markers. Precision immunotherapy for BC may target TPO isoforms; the benefits of improved tumor control would likely overweight the downside of thyroid adverse effects, easily manageable with levothyroxine replacement treatment. The immune cell subsets identified in this study may suggest other immunotherapies for BC. Finally, future clinical trials of probiotics, antibiotics, or fecal material transplant, may be designed to target the microbiota signatures of BC patients with and without TA.

02

Conditions studied

  • Breast Cancer

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03

In context

Breast Neoplasms

12,815 studies on the registry are indexed under Breast Neoplasms; 2,920 are open to participants now.

This study's planned enrollment of 496 is above the median of 72 across 9,494 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico is the lead sponsor of 232 studies on the registry; 83 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

The study will include patients undergoing mammography (either for screening or for a suspect nodule) who meet all of the following criteria:

  • signed informed consent
  • age 18-80 years
  • female sex

Based on the mammography results and the outcome of any biopsy performed due to the presence of breast nodule(s), patients will subsequently be categorized into cases (diagnosed with breast cancer) and controls (not diagnosed with breast cancer).

Exclusion criteria

Exclusion Criteria:

Subjects who do not meet the mentioned inclusion criteria, or who meet at least one of the following exclusion criteria, will be excluded from recruitment:

  • Pregnancy, within 6 months postpartum, and/or active breastfeeding
  • Prior organ, bone marrow, or hematopoietic stem cell transplantation
  • Prior splenectomy
  • Therapy with biological agents, immunosuppressants, or immunomodulators
  • History of breast cancer
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
496 participants (estimated)

Study arms

  • Other
    Patients with breast cancer

    Other: Aspiration 0

  • Other
    Patients without breast cancer

    Other: Aspiration 0

Interventions

  • OtherAspiration 0

    Ultrasound guided Fine needle aspiration of thyroid and neck

06

What researchers measure

Primary outcomes

  1. Prevalence of thyroid autoimmunity

    Time frame: Participants will be evaluated at recruitment and after 5 years of follow-up

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Study locations

1 of 1 sites recruiting
  • Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico
    Milan, 20122, Italy
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

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Registry details

Key details

Study ID
NCT07870148
Responsible party
Sponsor
First posted
Oct 13, 2026
Start date
May 9, 2024
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2029 (estimated)
Last update
Oct 13, 2026

Study contacts

Ilaria Muller, MD, PHD
Contact
ilaria.muller@unimi.it
+39 02 5503 3332

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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